A Review- Phytomedicines Used in Treatment of Diabetes

 

Mohd. Yaqub Khan*, Irfan Aziz1, Bipin Bihari2, Hemant Kumar3, Maryada Roy4,

Vikas Kumar Verma2

1Azad Institute of Pharmacy and Research, Azadpur,

Adjacent CRPF Camp, Bijnour, Lucknow - 226 002, Uttar Pradesh, India

2Saroj Institute of Technology and Management, Ahimamau P.O.

Arjunganj Sultanpur Road, Lucknow-226002,Uttar Pradesh, India

3Hygia Institute of Pharmacy, Lucknow, Uttar Pradesh, India

4Mangalayatan University, Aligarh, Uttar Pradesh, India

*Corresponding Author E-mail: venkipharma75@gmail.com

 

ABSTRACT:

Diabetes mellitus (DM), both insulin-dependent DM (IDDM) and non-insulin dependent DM (NIDDM) is a common and serious metabolic disorder throughout the world. Traditional plant treatments have been used throughout the world for the therapy of diabetes mellitus. Among many medications and other alternative medicines, several herbs have been known to cure and control diabetes; additionally they have no side effects. The present paper is an attempt to list of the plants with anti-diabetic and related beneficial effects originating from different parts of world. History showed that medicinal plants have been used in traditional healing around the world for a long time to treat diabetes; this is because such herbal plants have hypoglycemic properties and other beneficial properties, as reported in scientific literature. The medicinal plants, besides having natural therapeutic values against various diseases and considerable works have been done on these plants to treat diabetes mellitus, describes that the antidiabetic activity of medicinal plants is due to the presence of phenolic compounds, avonoids, terpenoids, coumarins and other constituents which show reduction in blood glucose levels. Some of these herbal plants and their active chemical constituents which have a role in the management of diabetes mellitus are compiled here and discussed in this review.

 

KEY WORDS: Diabetes mellitus, hypoglycemic agents, herbal medicines, sulphonylureas, biguanides.

 


 

INTRODUCTION:

Diabetes mellitus is a group of metabolic diseases characterized by high blood sugar (glucose) levels that result from defects in insulin secretion, or action, or both. Diabetes mellitus, commonly referred to as diabetes (as it will be in this article) was first identified as a disease associated with "sweet urine," and excessive muscle loss in the ancient world. Elevated levels of blood glucose (hyperglycemia) lead to spillage of glucose into the urine, hence the term sweet urine. Normally, blood glucose levels are tightly controlled by insulin, a hormone produced by the pancreas. Insulin lowers the blood glucose level. When the blood glucose elevates (for example, after eating food), insulin is released from the pancreas to normalize the glucose level.

 

In patients with diabetes, the absence or insufficient production of insulin causes hyperglycemia.

 

Diabetes is a chronic medical condition, meaning that although it can be controlled, it lasts a lifetime. 1

 

Blood sugar level in normal and diabetic patients

Category of a person

Fasting Value

Post Prandial

 

Minimum Value

Maximum Value

Value 2 hours after consuming glucose

Normal

70

100

Less than 140

Early Diabetes

101

126

140 to 200

Established Diabetes

More than 126

-

More than 200

* All values are in mg/100ml

 

Causes of Diabetes

Insufficient production of insulin (either absolutely or relative to the body's needs), production of defective insulin (which is uncommon), or the inability of cells to use insulin properly and efficiently leads to hyperglycemia and diabetes. This latter condition affects mostly the cells of muscle and fat tissues, and results in a condition known as "insulin resistance." This is the primary problem in type 2 diabetes. The absolute lack of insulin, usually secondary to a destructive process affecting the insulin producing beta cells in the pancreas, is the main disorder in type 1 diabetes. In type 2 diabetes, there also is a steady decline of beta cells that adds to the process of elevated blood sugars. Essentially, if someone is resistant to insulin, the body can, to some degree, increase production of insulin and overcome the level of resistance. After time, if production decreases and insulin cannot be released as vigorously, hyperglycemia develops.

 

Glucose is a simple sugar found in food. Glucose is an essential nutrient that provides energy for the proper functioning of the body cells. Carbohydrates are broken down in the small intestine and the glucose in digested food is then absorbed by the intestinal cells into the bloodstream, and is carried by the bloodstream to all the cells in the body where it is utilized. However, glucose cannot enter the cells alone and needs insulin to aid in its transport into the cells. Without insulin, the cells become starved of glucose energy despite the presence of abundant glucose in the blood stream. In certain types of diabetes, the cells' inability to utilize glucose gives rise to the ironic situation of "starvation in the midst of plenty". The abundant, unutilized glucose is wastefully excreted in the urine.

 

Insulin is a hormone that is produced by specialized cells (beta cells) of the pancreas. (The pancreas is a deep-seated organ in the abdomen located behind the stomach.) In addition to helping glucose enter the cells, insulin is also important in tightly regulating the level of glucose in the blood. After a meal, the blood glucose level rises. In response to the increased glucose level, the pancreas normally releases more insulin into the bloodstream to help glucose enter the cells and lower blood glucose levels after a meal. When the blood glucose levels are lowered, the insulin release from the pancreas is turned down. It is important to note that even in the fasting state there is a low steady release of insulin than fluctuates a bit and helps to maintain a steady blood sugar level during fasting. In normal individuals, such a regulatory system helps to keep blood glucose levels in a tightly controlled range. As outlined above, in patients with diabetes, the insulin is either absent, relatively insufficient for the body's needs, or not used properly by the body. All of these factors cause elevated levels of blood glucose (hyperglycemia).2

 

Herbal Treatment of Diabetes Mellitus

BITTER MELON

 

Biological source

It is obtained from edible fruit of Momordica charantia, belonging to the family Cucurbitaceae.

 

Chemical constituents

The plant contains several biologically active compounds-

a) Chiefly momordicin I and momordicin II, cucurbitacin B

b) Glycosides (momordin, charantin, charantosides, goyaglycosides)

c) Terpenoid compounds- momordicinin, momordicilin, momordol

d) Cytotoxic (ribosome inactivating) proteins such as momorcharin and momordin.3

 

Uses

Bitter melon is used as anti-diabetic. It contains lectin that has insulin like activity due to its non- protein specific linking together to insulin receptors. This lectin lowers blood glucose level by acting on peripheral tissues. Lectin is a major contributor to hypoglycemic effect.4

 

Scientific work done- Triterpenoids Isolated from Bitter Melon has showed antidiabetic

activity.5

 

Dosage form

It is used as fresh juice, tincture, juice extract and powered leaf.

 

Dose

Fresh juice- 57-113 gm daily, Tincture- 1.3 ml/ twice/ daily, Juice extract- 300-600 mg, Powered leaf- 1-2 gm

 

FIERY COSTUS

 

Biological Source

It is obtained from the leaves of the plant Costus igneus, belonging to the family Costaceae.

 

Chemical Constituents

The main chemical constituents are Beta-carotene, deoxyribose, phenol, flavonoids, and insulin precursors.

 

Uses- The leaves of insulin plant reduced the fasting and postprandial blood sugar levels, bringing them down towards normal. Reduction in the fasting and the postprandial blood sugar levels with leaves of insulin plant was comparable with that obtained with Glibenclamide 500 µg/kg at 250 mg/kg/day and 500 mg/kg/day of powdered leaves of the insulin plant.

 

The hypoglycemic action can be due to release of insulin, insulin-sensitizing action or a combination of both. Hence further studies need to be undertaken to determine the mechanism of action by measurement of either insulin or 'C' peptide level.6

 

Scientific work done Costus igneus has showed effect on hyperglycemia.7

 

Dosage Forms- It is used as oral hypoglycemic agent, or as i.v. injection

Dose- Tablet- 1 tablet/ day

 

Dandelion

 

Biological Source

It is obtained from the leaves of Taraxacum officinale, belonging to the family Asteraceae.

 

Chemical Constituents

1. Sesquiterpene lactones (bitters): taraxinic acid (taraxacin), tetrahydroridentin B

2. Triterpenoids and sterols: taraxasterol, taraxerol, cycloartenol, beta-sitosterol

3.Other: Vitamin A, Vitamin C, tannins, alkaloids, pectin, inulin, starch, potassium, beta carotene, caffeic acid, flavonoids (apigenin)8

 

Uses

It is a good antidiabetic drug. It can lower the blood glucose level .Tests on diabetic mice show that dandelion extract may help regulate blood sugar and keep cholesterol in check.9

 

Scientific work done

Dandelion has showed antihyperglycemic effect.10

 

Dosage forms

Capsules, tinctures, and teas containing dandelion leaves, roots, flowers, or the entire plant is used.

 

Doses

Capsules- taken after each meal

Adult doses: There is disagreement on the optimal form and dose of dandelion. Reputable physicians and herbalists recommend a range of doses

Fresh leaves: 4-10 grams daily

Dried leaves: 4-10 grams daily

Fresh leaf juice: 1 tsp (4-8 ml) twice daily

Fluid extract: 1-2 teaspoons daily

Fresh roots: 2-8 grams daily

Dried powdered extract: 250-1000 mg three to four times daily

Tea: Pour 2 cups boiling water over one ounce of fresh leaves and steep for 10 minutes.

Or, boil 1 cup of water with 2-3 tsp of dried, cut root for 15 minutes. Cool.

Pediatric dosages: Unknown

 

French Lilac

 

Biological Source

It consists of the aerial parts of the plant, flowers, leaf, stem, seeds of the plant Galega officinalis, belonging to the family Fabaceae.

 

Chemical Constituents

Oleanane and ursane type triterpinoids like sophoradiol, soyasapogenol b, and 9-sitosterol, Sophorediol, galactogil, galegine, peganine, hydroxygalegine, vasicinone, alkaloids like lutein, pentahydroxy flavone 5 glucoside, luteoline, galuteoline, luteoline 5 glucosides, flavonoids, saponines etc.11

 

Uses

It has been known since the Middle Ages for relieving the symptoms of diabetes mellitus. Upon analysis, it turned out to contain compounds related to guanidine, a substance that decreases blood sugar by mechanisms including a decrease in insulin resistance, but was too toxic for human use. Georges Tanret identified an alkaloid from this plant (galegine) that was less toxic, and this was evaluated in clinical trials in patients with diabetes in the 1920s and 1930s.

 

Other related compounds were being investigated clinically at this time, including biguanide derivatives. This work led ultimately to the discovery of metformin (Glucophage), currently recommended in international guidelines for diabetes management as the first choice for antidiabetic pharmacotherapy alongside diet and exercise 12 and the older agent phenformin, which has been withdrawn in most countries due to an unacceptable risk of lactic acidosis (the risk of lactic acidosis with metformin is no higher than with other antidiabetic therapies when it is prescribed according to its label)13 The study of galegine and related molecules in the first half of the 20th century is regarded as an important milestone in the development of oral antidiabetic pharmacotherapy.14

 

Dosage form

It is used as herbal infusion, tincture and leaves.

 

Doses- Herbal infusion- twice daily, Tincture- thrice daily

 

GULVEL

 

Biological source

It is obtained from the stems and roots of Tinospora cordifolia, belonging to the family Menispermaceae.

 

Chemical Constituents

The active adaptogenic constituents are diterpene compounds including tinosporone, tinosporic acid, cordifolisides A to E, syringen, the yellow alkaloid, berberine, Giloin, crude Giloininand, a glucosidal bitter principle as well as polysaccharides, including arabinogalactan polysaccharide (TSP). Picrotene and bergenin were also found in the plant. The active principles of Tinospora cordifolia, a traditional Indian medicinal plant were found to possess anticomplementary and immunomodulatory activities.15

Use

It is used as antidiabetic16.

 

Scientific work done

Tinospora cordifolia has showed Anti-diabetic activity.17

 

Dosage form

Aqueous extract of roots is used.

 

Dose

Aqueous extract of root- 2.5g, 5 g/ kg body weight

 

TURMERIC

 

Biological Source

It consists of dried fresh rhizomes of the plant Curcuma longa belonging to the family Zingiberaceae.

 

Chemical Constituents

Turmeric contains 5% of volatile oil, resin, zingiberaceous starch grains and yellow coloured curcuminoids. The chief component of curcuminoids is known as curcumin. Volatile oil is composed of mono and sesquiterpens such as alpha and beta pinene, alpha- phellandrene, camphor, camphene, zingiberene, alpha and beta curcumenes.18

 

Use- It is used as anti- diabetic drug.19

 

Scientific works done

1. Turmeric has showed hypoglycemic, hypolipidemic and antioxidant activity20

2. Turmeric has shown effect in diabetes.21

 

Dosage form

Powdered form of turmeric is used.

 

Dose

Powdered turmeric- 500-8000 mg/ day.

 

GURMAR

 

Biological source

It is obtained from leaves and roots of Gymnema sylvestre, belonging to the family Asclepiadaceae.

 

Chemical constituents

The principal active ingredient is gymnemic acid. The other compounds found are calcium oxalate, anthraquinone compound, tartaric acid, cellulose but no tannin is present22.

 

Uses

1) This is one of the main herbs used for healing diabetes mellitus.

2) Gymnema removes sugar from pancreas, restores pancreatic function.

3) Gymnema stimulates circulatory system, increases urine secretion.23

 

Scientific works done

1. Gymnema sylvestre has shown Enzyme changes and glucose utilization.24

2. Gymnema sylvestre has showed effect in controlling blood glucose level.25

 

Dosage forms

It is used as water soluble acidic solution and as powered leaf.

 

Doses

Power leaf- 2-4 mg/daily, Water soluble acidic solution- 400 mg/day

 

BAEL

 

Biological source

It consists of unripe or half ripe fruits of the plant known as Aegle marmelos, belonging to the family Rutaceae.

 

Chemical constituents

The chief constituent of the drug is marmelosinn (0.5%) which is a furocoumarin. Other coumarins are marmesin, psoralin, umbelliferone. The drug also contains carbohydrate, protein, volatile oil and tannins. The pulp also contains good amount of vitamin A and C. Two alkaloids, Omethylhalfordinol and isopentylhalfordinol has been isolated from fruits.26

 

Use

It is used as anti-diabetic drug.27

Scientific work done

Leaf and callus extract of Aegle marmelos has shown antidiabetic activity. 28

 

Dosage forms

It is used as aqueous decoction and aqueous leaf extract.

 

Doses

Aqueous decoction- 1 ml/ 100 mg, Aqueous leaf extract- 1 gm/ kg

 

AMLA

 

Biological Source

It is obtained from the dried as well as fresh fruits of Emblica officinalis, belonging to the family

Euphorbiaceae.

 

Chemical Constituents

Amla is a rich natural source of vitamin C. It contains 0.5% fat, phyllemblin, 5% tannin. It also contains phosphorus, iron and calcium. It contains pectin and 75% moisture29.

 

Use- It is used as anti-diabetic30.

 

Scientific work done

Emblica officinalis has shown Anti-diabetic activity in animal models. 31

 

Dosage form

It is used as amalaki capsules.

 

Dose

Capsule- 1 capsule/ twice a day before meal

 

FENUGREEK

 

Biological source

It is obtained from the leaves and seeds of Trigonella foenum- graecum, belonging to the family Fabaceae.

 

Chemical constituents

The nicotinic acid, alkaloid trogonelline, and coumarin contained by defatted section of the seed of fenugreek prove to be the responsible active ingredient for its anti-diabetic properties. 32

 

Uses

It is used as anti-diabetic. The fiber-rich fraction of fenugreek seeds can lower blood sugar levels in people with type II diabetes.33

 

Scientific works done-

Metabolic and molecular action of Trigonella foenum-graecum (fenugreek) and trace metals has been shown in experimental diabetic tissues.34

 

2. Fenugreek Seed has shown the postprandial hypoglycemic activity35

 

Dosage forms

The leaves and seeds of fenugreek are used in therapeutic purpose.

 

Doses

Leaves- 5-30 gm/ thrice daily with meal, Seeds- 3 ˝ ounces/ daily.

 

GINSENG

 

Biological Source

It is obtained from the dried roots of Panax ginseng, belonging to the family Araliaceae.

 

Chemical Constituents

Ginseng contains a mixture of several saponin glycosides, belonging to triterpenoid group. They are grouped as follows-

 

1) Ginsenosides

2) Panaxosides

3) Chikusetsusaponin

 

Ginsenosides contain aglycone dammarol while panaxosides have oleanolic acid as aglycone.

 

About 13 ginsenosides have been identified. Panaxosides give oleanolic acid, panaxadiol and

panaxatriol on decomposition.36

 

Use

It is used as hypoglycemic agent.37

 

Scientific works done

1. Use of Ginseng in diabetes.38

2. Ginseng has shown hypoglycemic effect.39

 

Dosage forms

Dried root and tincture are used.

 

Doses

Dried root- 0.5- 9 gm/ daily, Tincture- 0.2- 3/ one to three times daily

 

INDIAN KINO TREE

 

Biological source

It is obtained from the dried juice of the plant Pterocarpus marsupium and obtained by making vertical incisions to the stem bark and it belongs to the family Leguminaceae.

 

Chemical constituents

It contains about 70%- 80% of kinotannic acid, kino- red, k- pyrocatechin (catechol), resin and gallic acid. Kinotannic acid is glucosidal tannin, while kino- red is anhydride of kinoin. Kinoin is an insoluble phlobaphene and is produced by action of oxydase enzyme. It is darker in colour than kinotannic acid.

 

If the juice is boiled during drying, enzyme gets destroyed and thus insolubilisation and darkening is

prevented.40

 

Uses

The heartwood of the plant is used in treatment of diabetes. The gum resin is the only herbal product ever found to regenerate B cells that make insulin in the pancreas.41

 

Scientific works done

1. Phenolics from Pterocarpus marsupium has shown antihyperglycemic activity.42

2. Hypoglycaemic activity of Pterocarpus marsupium has been seen.43

 

Dosage forms

The wood extracts and bark decoction is used.

 

Doses

Wood extract (pterostilbene) – 10 mg/ kg, Bark decoction- 1 gm/ 100 mg body weight for 10 days.

 

NAYANTARA

 

Biological source

It is obtained from the dried whole plant of Catharanthus roseus, belonging to the family Apocynaceae.

 

Chemical constituents

The main active compounds here are alkaloids and tannins. The major alkaloid is vincamine. Aclosely related semi-synthetic derivative of vincamine is vinpocetin. There are over 130 constituents with an indole or dihydroindole structure, including the principal component vindoline, vinblastine, vincristine, learocristine, vinine, ajmalicine, leurocine, vinomine etc.44

 

Use

t is used as antihyperglycemic agent.45

 

Scientific works done

1. Effect of an antidiabetic extract of Catharanthus roseus has been seen.46

2. The juice of fresh leaves of Catharanthus roseus has shown reduction blood glucose.47

 

Dosage forms

It is used as tincture and infusion.

 

Doses

Tincture- 1-2 ml/ 3 times daily, Infusion- 2-3 cups daily.

 

NEEM

Biological source

It is obtained from the leaves of Azadirachta indica, belonging to the family Meliaceae.

 

Chemical constituents

It contains glycerides of saturated and unsaturated fatty acids. The main fatty acids are oleic (50%) and stearic (20%) acids. The oil contains 2.0% of bitters, which are sulpher containing compounds,

nimbidin, nimbin, nimbinin, nimbidol. The unsaponifiable part contains nimbosterol (0.03%). The main limonoid that it contains is azadirachtin but it also contains azadiradione, fraxinellone,

nimbin, salannin, salannol, vepinin, vilasinin.48

 

Use

It is used in diabetes.49

 

Scientific work done

Azadirachta indica leaf extract has shown antihyperglycemic and antidyslipidemic activity.50

 

Dosage form

Capsules are used.

 

Dose

Capsule- 1-2 capsules/ twice daily.

 

CINNAMON

 

Biological source

It consists of dried inner bark of shoots of coppiced trees of Cinnamomum zeylanicum, belonging to the family Lauraceae.

Chemical constituents

Cinnamon bark contains volatile oil, tannins, mucilage, calcium oxalate, starch and mannitol. Cinnamon oil contains cinnamaldehyde, other terpenes like phellandrene, pinene, cymene, caryophyllene.51

 

Uses

Cinnamon is used in the treatment of type II diabetes mellitus and insulin resistance.52

 

Scientific works done

1. Alcoholic Extract of Cinnamomum zeylanicum Leaves has shown antidiabetic Activity.53

2. Cinnamon improves glucose and lipid of people54

 

Dosage form

It is mostly used as powdered form.

 

Dose

Powder- ˝ teaspoon daily

 

SAPTRANGI

 

Biological source

It is obtained from the stem, root and leaves of Salacia oblonga, belonging to the family Hippocrateaceae.

 

Chemical constituents

It contains 2 potent alpha- glycosidase inhibitors- salicinol, kotalanol, sesquiterpene (salasol A and B), triterpenes (salasones A-E, salaquinones A and B) 55

 

Uses

It is used as anti-diabetic. It binds to intestinal enzymes alpha- glucosidases that break down carbohydrate into glucose in body56

 

Scientific work done

Salacia oblonga has shown antidiabetic potential57

 

Dosage form

Aqueous extract of the root bark is used.

 

Dose

Aqueous extract of root bark- 250 ml/ kg

 

ONION

 

Biological source- It is obtained from the bulb of the plant Allium cepa, belonging to the family

Liliaceae.

 

Chemical constituents- It contains essential amino acid composition of arginine, histidine, lysine, tryptophan, phenylalanine, methionine, threonine, leucine and isoleucine. The bulb on steam distillation yields an essential oil known as onion oil. The bulb contains several phenolic acid, such as protocatechuic acid, p-hydroxybenzoic acid, vanillic acid, caffeic acid, and o and p- coumaric acids. Citric, abietic, oxalic and mialic acids are also present. It also contains several oligo- saccharides.58

 

Uses- Onion consists of an active ingredient called APDS (allyl propyl disulphide). APDS has been shown to block the breakdown of insulin by the liver and possibly to stimulate insulin production by the pancreas, thus increasing the amount of insulin and reducing sugar levels in the blood. It is found to lower lipid levels, inhibit platelet aggregation and are antihypertensive. So, liberal use of onion is recommended for diabetes patients.59

 

Scientific work done

Clinical Hypoglycemic effect of Allium cepa (Red onion) has been seen.60

 

Dosage forms

Raw and boiled onion extracts are used. APDS can also be administered orally.

 

Dose

APDS- 125 mg/ kg to fasting humans.

 

GARLIC

 

Biological source

It consists of bulbs of the plant known as Allium sativum, belonging to the Liliaceae.

 

Chemical constituents

Garlic bulbs contain 29% of carbohydrate, about 56% of proteins (albumin), 0.1% of fat, mucilage, and 0.06- 0.1% of volatile oil. It also contains phosphorus, iron and copper. Volatile oil of the drug is the chief active constituent, and contains allyl propyl disulphide, diallyl disulphide, alliin and allicin. Alliin by action of enzyme allinlyase is converted into allicin. Garlic oil is yellow in colour.61

 

Uses

Garlic cloves lower blood sugar significantly. Subsequently, scientific studies have proven that the presence of disulfides in garlic such as allyl propyl and diallyl sulfide have played a role in the decrease of blood glucose levels. They have been seen to have actions similar to Tolubutamide, a sulfonylurea drug of the first generation. They act on the pancreas and stimulate the production of insulin so as to control the sugar levels in the blood. It is those patients with type 2 diabetes who benefit the most out of this.62

 

Scientific work done

Anti-diabetic and hypolipidaemic properties of garlic has been seen.63

 

Dosage form

Juice extract of it is used.

 

Dose

Juice extract- 50 ml / daily

 

OPUNTIA

Biological source

It is obtained from the stems of Opuntia ficusindica, belonging to the family Cactaceae.

 

Chemical constituents

The main chemical constitutes are 3- methoxytyramine64, candicine65, hordinine66, N- methyltyramine67, tyramine68 etc.

 

Use

It is used in the treatment of type II diabetes.

 

Scientific work done

Polysaccharides from Opuntia has shown antidiabetic effects. 69

 

Dosage form

Boiled stems are used.

Dose-

Oiled stem- 100-500/ daily

 

BLUEBERRY

 

Biological source

It is obtained from the leaves of Vaccinium myrtillus, belonging to the family Ericaceae.

 

Chemical constituents

The main chemical constituents are· flavonoids (hyperoside, isoquercitrin, quercitrin, astragaline), ·anthocyanosides (myrtillin, malvidin, cyanidin, delphinidin and others), catechin tannins (2-10%), others (carbohydrates including invertose, organic acids, pectins, alkaloids) 70

 

Uses

Blueberry is a natural herb of controlling or lowering blood sugar levels when they are slightly elevated. It contains an active agent known as myrtillin which is an anthocyanoside. It is weaker and less toxic than insulin.71

 

Scientific works done

1. Vaccinium myrtillus has shown antidiabetic activity.72

2. Vaccinium myrtillus has shown hypoglycaemic effect.73

 

Dosage form- Leaf extracts are used.

 

Dose- Leaf extract- 3 cups/ day

 

Blackberry

 

Biological Source

It is obtained from the edible fruits of the plant Rubus fruticosus belonging to the family Rosaceae.

 

Chemical Constituents

The principal compounds isolated from red blackberry leaves are hydrolyzable tannins. Simple compounds such as 1,2,6-tri-O -galloyl-glucose74 and penta- O -galloyl glucose are oxidatively coupled through galloyl groups to form more complex compounds such as casuarictin, pendunculagin, sanguin H-675 and lambertianin A76, with as many as 15 galloyl groups coupled to 3 glucose units77.

Common flavonoids have also been isolated from the leaves. Rutin was isolated78, as were kaempferol, quercitin, quijaverin, and kaempferol- 3- O -â-D-glucuronopyranoside79. Major leaf volatiles studied by GC-MS include the monoterpenes geraniol and linalool as well as 1- octane-3-ol and decanal80. Phenolic acids common to the Rosaceae family have also been identified.81

 

Use

It is used as anti-diabetic.

 

Dosage form-

It is used as fruit powder.

 

Dose

Dried fruit powder- 20 mg/day.

 

Blond Psyllium (Blond Plantago)

Blond psyllium seed husk orally seems to significantly reduce postprandial serum glucose, insulin levels, serum total cholesterol, and low-density lipoprotein (LDL) cholesterol levels in patients with Type II diabetes and hypercholesterolemia. Blond psyllium seems to reduce postprandial blood glucose levels by about 14% to 20%, total cholesterol by about 9%, and LDL cholesterol by 13%. Blonde psyllium also seems to lower postprandial glucose levels in patients with Type I diabetes. Blond psyllium's maximum effect on the glucose levels occurs when psyllium is mixed and consumed with foods. Blond psyllium does not lower postprandial glucose in people who do not have diabetes.

 

Devil’s Claw

Devil's Claw is native to south and central Africa. Its medicinal value lies in its fleshy roots, which are sliced, chopped, or pulverized while fresh.

 

Some evidence shows that this herb might decrease blood glucose and have additive effects with medication used in diabetes.

 

Ginger (Zingiber officinale)

Preliminary research suggests ginger might increase insulin levels. Theoretically, it could have an additive effect with medication used to treat diabetes and cause hypoglycemia.

 

Glucomannan (Konnyaku root):

A member of the yam family, this herb is high in fiber and can help normalize blood sugar, relieve stress on the pancreas.

 

Holy Basil (Hot Basil)

Preliminary evidence suggests that holy leaf extract may decrease fasting (17.6%) and postprandial blood glucose in patients with Type II diabetes.

 

Jambolan (Syzygium cumini)

A close relative of the clove tree Syzygium aromaticum, Jambolan is native to east India and the Malay Peninsula, but has spread as far as China and Australia and is grown in the Caribbean.

 

Only the bark of the Jambolan has proven medicinal value, although the seeds are often used as well. In Asian medicine, it is used for diabetes, diarrhea, sore throat, and diseases of the spleen.

 

Kudzu

Kudzu is native to Japan and China, however it grows extremely well in the Southern United states. This vine, when left uncontrolled, will eventually grow over almost any fixed object or other vegetation.

 

Kudzu or its constituents might have hypoglycemic, hypocholesterolemic, and antioxidant activity.

 

Prickly Pear Cactus (Nopal)

There is some preliminary clinical evidence that prickly pear cactus used orally can decrease blood glucose levels in patients with Type II diabetes. Single doses can decrease blood glucose levels by 17% to 46% in some patients. However, it is not known if extended daily use can consistently lower blood glucose levels and decrease HbA1c levels. Only the broiled stems of the specific species Opuntia streptacantha seem to be beneficial and raw or crude stems do not seem to decrease glucose levels. Other prickly pear cactus species do not seem to significantly lower blood glucose levels.

 

Red Sandalwood (Pterocarpus marsupium)

Like Gymnema Sylvestre, this is a traditional herb used in India to help rejuvenate the insulin-producing pancreatic beta cells. One group of researchers investigating diabetic rats compared Pterocarpus' observed effects on blood glucose levels to those of metformin, a drug familiar to many diabetics.

 

Stevia (Sweet Herb)

Stevia is a non-caloric herb, native to Paraguay, which has been used as a sweetener and flavor enhancer for centuries. Clinical research suggests that stevioside, a constituent of Stevia, might reduce postprandial glucose levels by 18% in people with Type II diabetes.

 

Herbal Home Remedies for Diabetes82

Diabetes has been referred to as 'Madhumeh' by Ayurveda. This desease is caused by imbalance of the hormone insulin (which controls the sugar level of blood) that has to be taken externally by a diabetes patient regularly. Ayurvedic therapies recommend many Indian herbs and general practices to improve the secretion of insulin through natural ways. Some of the home and herbal remedies prescribed by Ayurveda are described below.

 

·         Include turmeric and cinnamon in your diets. You can even take one teaspoon of cinnamon powder daily.

·         Soak one teaspoon of fenugreek seeds in 1 cup of water overnight. Drink this water in the morning on an empty stomach and eat the seeds.

·         Take a bitter gourd, remove the seeds and saturate in a cup of water. Drain this preparation and drink every morning.

·         Boil around fifteen mango leaves in one cup of water. Keep it over night and filter in the morning. Drink every morning on an empty stomach.

·         Avoid oily, fried and starchy foodstuffs.

·         Avoid coffee, sugar, refined flour and alcohol.

·         Eat smaller meals (low fat diet) five to six times a day instead of having three large meals.

·          Increase intake of vegetables like spinach, cucumber, tomatoes, onion, sprouts, beans, garlic etc.

·          Refrain from taking stress.

·         Do regular exercise. Walk for at least 40 minutes a day.

·         Avoid red meat and excessive salt in your meals. Fish and soy can be taken due to their good protein value.

·         Bitter herbs like Azadirachta Indica (Neem), bitter gourd and fenugreek are like miracle drugs for diabetics. Take them in any form you can.

·         Avoid white bread, rice, potatoes, sweet and sugary foods.

·         Chew 8-10 curry leaves (Meetha Neem) on an empty stomach. It is very effective for bringing the urine and blood sugar to their normal levels, even in hereditary diabetic patients.

·          Emblica officinalis or Indian gooseberry (Amla) is very beneficial for diabetic patients. Prepare a fine powder of dry amala and put this powder in water. Allow it to stand for some time. Then filter the solution and mix some lemon juice in it. Take this early in the morning. You can even use extract of amla easily available in the market.

·         Syzygium cumini or Indian plum (Jamun) is considered a panacea for diabetes. Eating this fruit is very beneficial for patients of diabetes. In fact, more than fruit, the seeds of jamun fruit is beneficial when taken in powdered form mixed with some water.

·         The holy fruit of India- the bel fruit or the Aegle marmelos has anti-diabetic properties. The herbal extract of its leaves should be taken preferably with a pinch of black pepper.

·         Garlic contains allicin that helps in reducing sugar level in blood.

·         The leaves of Butea monosperma (Palas) tree are very useful in diabetes. They reduce blood sugar and are useful in glycosuria- the presence of large amount of glucose inurine.

·          Tenner’s cassia (Tarwar) is an effective remedy for diabetes. A decoction of the whole plant or bubs is used to treat diabetes. The powder of the herb, mixed with honey, is very effective. Seeds can also be used in the similar manner as flowers.


 

Some marketed Antidiabetic Polyherbal Formulations83

Name

Company

Ingredients

Diabecon

Himalaya

Gymnema sylvestre, Pterocarpus marsupium, Glycyrrhiza glabra, Casearia esculenta, Syzygium cumini, Asparagus racemosus, Boerhavia diffusa, Sphaeranthus indicus, Tinospora cordifolia, Swertia chirata, Tribulus terrestris, Phyllanthus amarus, Gmelina arborea, Gossypium herbaceum, Berberis aristata, Aloe vera, Triphala, Commiphora wightii, shilajeet, Momordica charantia, Piper nigrum, Ocimum sanctum, Abutilon indicum, Curcuma longa, Rumex maritimus.

Diasulin

Tobbest Busindo

Cassia auriculata, Coccinia indica, Curcuma longa, Emblica officinalis, Gymnema sylvestre, Momordica charantia, Scoparia dulcis, Syzygium cumini, Tinospora cordifolia, Trigonella foenum graecum.

Bitter gourd Powder

Garry and Sun natural remedies

Momordica charantia

Dia-care

Admark Herbals Limited

Sanjeevan Mool; Himej, Jambu beej, Kadu, Namejav, Neem chal.

Diabetes- Daily Care

Nature’s Health Supply

Alpha Lipoic Acid, Cinnamon 4% Extract, Chromax, Vanadium, Fenugreek 50% extract, Gymnema sylvestre 25% extract Momordica charantia 7% extract, Licorice Root 20% extract

Gurmar powder

Garry and Sun natural Remedies

Gymnema sylvestre

Epinsulin

Swastik Formulations

Pterocarpus marsupium

Diabecure

Nature beaute santé

Juglans regia, Berberis vulgaris,  Erytherea centaurium, Millefolium, Taraxacum

Diabeta

Ayurvedic cure Ayurvedic Herbal Health Products

Gymnema sylvestre, Vinca rosea, Curcuma longa, Azadirachta indica, Pterocarpus marsupium, Momordica charantia, Syzygium cumini, Acacia arabica, Tinospora cordifolia, Zingiber officinale

Syndrex

Plethico Laboretaries

Germinated Fenugreek seed extract

 


Mineral Supplementation  

The treatment of diabetes requires nutritional supplementation, as these patients have a greatly increased need for many nutrients. Supplying the diabetic with additional key nutrients has been shown to improve blood sugar control as well as help prevent or ameliorate many major complications of diabetes.

 

Chromium:

Chromium is an essential micronutrient for humans. Considerable experimental and epidemiological evidence now indicates that chromium levels are a  major determinant of insulin sensitivity, as it functions as a cofactor in all insulin- regulating activities.84 Chromium facilitates insulin binding and subsequent uptake of  glucose into the cell. Supplemental chromium has been shown to decrease fasting glucose levels, improve glucose tolerance, lower insulin levels, and decrease total cholesterol and triglycerides, while increasing HDL cholesterol in normal, elderly, and type 2 diabetic subjects.85, 86 Without chromium, insulin's action is blocked and glucose levels are elevated.87

 

Chromium picolinate, trivalent chromium (Cr3+), is one of the forms of chromium that exhibits biological activity.88 A large clinical study on 180 diabetic patients documents the benefit of chromium picolinate for type 2 diabetic patients. In the study, while patients continued their normal medication, they were placed in one of three groups:  placebo group, 100 mcg chromium picolinate twice daily, or 500 mcg chromium picolinate twice daily. There were significant dose- and time-dependent decreases in  glycosylated hemoglobin, fasting glucose, two-hour postprandial glucose levels, fasting  and two-hour postprandial insulin values, and total cholesterol, particularly in the 500  mcg twice daily group.89 However, not all studies on chromium have yielded positive  results. In a controlled six-month study to determine the effect of 200 mcg/day chromium picolinate on individuals with type 2 diabetes, Lee and Reasner reported a decrease in triglycerides but no statistical difference between control and chromium-treated subjects with respect to measured parameters of glucose control.90 This dosage is considerably smaller than that found effective at lowering glucose in other studies so may explain the disparate findings among studies. 

 

Although no recommended daily allowance (RDA) has been established for chromium, over 200 mcg/day appears necessary for optimal blood sugar regulation. A good supply of chromium is assured by supplemental chromium91 in addition to dietary sources. Good dietary sources are brewer's yeast63 and barley flour, 92 while refined sugars, white flour products, and lack of exercise can deplete chromium levels.   Trivalent chromium has long been considered to be a safe nutritional supplement.93 Although the hexavalent form of chromium is a known human respiratory tract carcinogen when inhaled in high-exposure industrial settings, there is no evidence of any carcinogenesis in humans from the trivalent form of chromium found in chromium supplements.94, 95 Further evaluation of the safety and efficacy of trivalent chromium in diabetes treatment may be warranted.

 

Vanadium:

Prior to the discovery of insulin in 1922, vanadium was used for the control of blood sugar. Two small studies (one with six type 2 diabetic patients, one with seven type 2 diabetic patients) have confirmed the effectiveness of vanadyl sulfate at a dose of 100 mg/day in improving insulin sensitivity.96, 97

 

Magnesium:

A deficiency of magnesium is significantly more common in type 2  diabetics than in the general population.98 Magnesium deficiency has been associated with complications of diabetes, retinopathy in particular. One study found patients with the most severe retinopathy were also lowest in magnesium.99

 

Physical Interventions: Acupuncture and Hydrotherapy  

Acupuncture is best known in the United States as an alternative therapy for chronic pain.  However, it has been used for the treatment of diabetes and related complications during the past several decades. There are numerous Chinese publications on the use of acupuncture for diabetes, but only those published in English will be cited here.

 

Acupuncture may be effective in treating not only diabetes, but also in preventing and managing complications of the disease.100 The effects of acupuncture on diabetes have been observed experimentally and clinically.101, 102 Animal experiments have shown that acupuncture can activate glucose-6- phosphatase (an important enzyme in carbohydrate metabolism) and affect the  hypothalamus.103 Acupuncture can act on the pancreas to enhance insulin synthesis, increase the number of receptors on target cells, and accelerate the utilization of glucose,  resulting in lowering of blood sugar.104 Data from other studies have shown the beneficial  anti-obesity effect of acupuncture,105 which is the most modifiable risk factor for type 2  diabetes. It appears that the therapeutic effect of acupuncture on diabetes is not the result of its action on one single organ, but on multiple systems. 

 

Four commonly used points are:

(1) Zusanli point, located three inches below the lateral knee depression, one finger width from the lateral side of the anterior crest of the tibia;

(2) Sanyinjiao point, located three inches above the tip of the inner ankle, on the posterior margin of the metatarsal bone; (3) Feishu point, located 1.5 inches lateral and inferior to the spinous process of the third thoracic vertebra in a prone position; and

(4) Shenshu point, located 1.5 inches lateral to the posterior midline, lateral and inferior to the spinous process of the second lumbar vertebra in a prone position. These acupuncture points were selected based on traditional Chinese medicine theory. During the treatment, other points can be added according to symptoms and signs.106 Other methods have also been employed such as point injection with normal saline, small dose insulin, and Chinese herbal medicine extracts. Treatment is generally given once daily or once every other day as a course of 14-21 treatments. It is believed that the longer the course of treatment, the more marked will be the effect. Acupuncture can be effective in treating complications of diabetes, often with marked improvement in clinical symptoms. Better therapeutic results are obtained in patients with dietary control than in those without it. Physical exercise, breathing exercises, and massage can help improve the therapeutic effect. 

 

Although acupuncture shows some effectiveness in treating diabetes, its mechanisms of action are still obscure. Since hot-tub therapy can increase blood flow to skeletal muscles, it has been recommended for patients with type 2 diabetes who are unable to exercise.107 A study reported that eight patients were asked to sit in a hot tub for 30 minutes daily for three weeks. During the study period, patients' weight, mean plasma glucose level, and mean glycosylated hemoglobin decreased.107 Caution should be taken that the water not be too hot as neuropathy may prevent the patient from noticing they are burning themselves. In addition, poor circulation can result in increased metabolic demands when feet become heated demands that cannot be met by the diabetic patient. Proper water sanitation and appropriate guidance should be considered when prescribing hot-tub therapy for diabetic patients.108

 


Medicinal plants with antidiabetic and their reported effect on experimental models

Botanical Name

Family

Antidiabetic and other beneficial effects

References

Achiliea santolina L.

Asteraceae

Hypoglycemic, antioxidant

109

Artemisia patterns

Asteraceae

Hypoglycemic, increases peripheral glucose utilization

110

Areca catechu L.

Arecaceae

Hypoglycemic

111

Beta vulgaris L.

Chenopodiaceae

Increases glucose tolerance in OGTT

112

Boerhaavia diffusa L.

Nyctaginaceae

Decreases blood glucose level and increases plasma insulin levels, antioxidant

113

Bombax ceiba L.

Malvaceae

Hypoglycemic

114

Butea manosperma (Lam)

Caesalpinaceae

Anti-hyperglycemic

115

Carum carvi L.

Apiaceae

Potent anti-hyperglycemic

116

Cogniauxia podoleana Baillon

Cucurbitaceae

Hypoglycemic and anti-hyperglycemic

117

Commelina communis L.

Conimelinaceae

Anti-hyperglycemic, management of non-insulin-dependent diabetes.

118

Croton cajucara Benth

Euphorbiaceae

Anti-hyperglycemic

119,120

Curcuma longa L.

Zingiberaceae

Hypoglycemic, plays a role in PPAR-gamma activation

121

Cynodon dactylon Pers

Poaceae

Anti-hyperglycemic

122

Enicostemma littorale Blume

Gentianaceae

Decreases plasma glucose level, glycosylated haemoglobin and glucose-6-phosphatase activity in liver

123

Eriobotrya japonica Lindl.

Rosaceae

Hypoglycemic

124

Gentiana olivieri L.

Gentianaceae

Hypoglycemic, anti-hyperlipidemic

125

Ginkgo biloba L.

Ginkgoaceae

Hypoglycemic, increases pancreatic beta-cell in NIDDM

126,127

Globularia alypum L.

Globulariaceae

Hypoglycemic, increases plasma insulin levels

128

Glycyrrhiza uralensis Fish.

Papilionaceae

PPAR-gamma ligand-binding activity, decreases the blood glucose levels

129

Gymnema nwntanum Hook

Asclepiadaceae

Anti-peroxidative, antioxidant, may prevent the cholinergic neural and retinal complications of hyperglycemia in diabetes

130

Gymnema sylvestre R. Br.

Asclepiadaceae

Hypoglycemic. Hypolipidemic

131

Hintonia standleyana

Rubiaceae

Anti-hyperglycemic

132

Ibervillea sonorae S.

Cucurbitaceae

Acute and chronic hypoglycemic

133

Ipomoea aquatic Forsk.

Convolvulaceae

Decreases serum glucose concentration by 29.4% in Type II diabetic patients. hypoglycemic

134

Kalopanax pictus Thumb.

Araliaceae

Anti-diabetic activity, hypocholesterolmic and hypolipidemic

135

Lagerstroemia speciosa L.

Lythraceae

Insulin-like actions, glucose uptake, anti-adipogenesis

136,137

Medicago saliva L.

Fabaceae

Anti-hyperglycemic, insulin-releasing and insulin-like activity

138

Morus alba L.

Moraceae

Protects pancreatic beta cells from degeneration anddiminishes lipid peroxidation

139

Morus indica. L.

Moraceae

Hypoglycemic

140,141

Morus inignis L.

Moraceae

Hypoglycemic

142

Murraya koenigii L.

Rutaceae

Hypoglycemic, increases glycogenesis,decreases gluconeogenesis and glycogenolysis

143

Nelumbo nucifera L.

Neluntbonaceae

Improves glucose tolerance and potentiates the action of exogenouslyinjected insulin

144

Nigella saliva Gaertn.

Ranunculaceae

Decreases oxidative stress and preserves pancreatic beta-cell integrity.

145

Ocimum gratissinuim L. Var.

Lamiaceae

Hypoglycemic

146

Pandanus odorus Ridl.

Pandanaceae

Hypoglycemic, increases serum insulin levels and liver glycogen

147

Parmentieru edulis A.DC

Bignoniaceae

Hypoglycemic

148

Phyllanthus sellowianus Mull.Arg.

Euphorbiaceae

Hypoglycemic

149

Psacalium decompositum (Gray) H.

Asteraceae

Hypoglycemic

150

Psacalium peltatum (Kunth)

Asteraceae

Anti-hyperglycemic

151

Punica granatum L.

Punicaceae

Improves postprandial hyperglycemia in type 2 diabetes and obesity by inhibiting intestinal alpha-glucosidase activity

152

Solaria oblonga

Celastraceae

Hypoglycemic and possess anti-oxidant activity

153

Sambucus nigra L.

Adoxaceae

Insulin-releasing and insulin-like activity

154

Sanguis draxonis

Apocynaceae

Increase insulin sensitivity and improve the development of insulin resistance in rats

155

Sclerocarya birea (A.Rich)

Anacardiaceae

Hypoglycemic

156

Scoparia dulcis L.

Scrophariaceae

Hypoglycemic, antihyperlipidemic, antidiabetic

157,158

Swertia chirayita (Roxb)

Gentianaceae

Stimulates insulin release from islets

159

Syzygium alternifolium (Wt) Walp.

Myrtaceae

Hypoglycemic, antihyperglycemic and antihyperlipidemic

160,161

Terminalia bellirica (Gaertn)

Combretaceae

Stimulates insulin secretion. Enhances insulin action andinhibits both protein glycation and starch digestion

162

Terminalia chebula Retz.

Combretaceae

Dose-dependent glucose lowering effect, antidiabetic and renoprotective, decreases hepatic and skeletal muscle glycogen content, increases insulin release from the pancreatic islets

163,164

Teucriumpolium

Lamiaceae

Increases insulin release, antioxidant and hypoglycemic

165

Tinospora cordifolia Miers..

Menispermaceae

Hypoglycemic

166

Tinospora crispa (L) Hook.

Menispermaceae

Anti-hyperglycemic, stimulates insulin release from islets

167

Urtica dioica L.

Urticaceae

Anti-hyperglycemic

168

Urtica pilulifera L.

Urticaceae

Hypoglycemic

169

Vinca rosea L.

Apocynaceae

Anti-hyperglycemic

170

Withania soimifera (L) Dunal

Solanaceae

Hypoglycemic, antioxidant, diuretic and hypocholesterolemic

171,172

Withania coagulans Dunal

Solanaceae

Anti-hyperglycemic, anti-hyperlipidemic and hypoglycemic

173,174

Zizyphus sativa Gaertn

Rhamnaceae

Hypoglycemic

175

Zizyphus spina-christi L.

Rhamnaceae

Insulinotropic, hypoglycemic anddepressant effect on the central nervous system

176

Zygophyllum gaetulum Emb

Zygophyllaceae

Hypoglycemic, increases plasma insulin levels

177

 

 


Traditional phytotherapies

1. Antidiabetic Extracts

a. Adhatoda vasica Nees:

Extract obtained from the fresh leaves of plant mixed with water. About 10 ml of extract is used thrice a day to treat sugar.

 

b. Aloe vera Nill + Fagonia indica L. + Tylophora hirsuta L.:

Equal quantity of extract obtained from the fresh aerial parts of Fagonia indica, fresh leaves and stem of Aloe vera and fresh branches of Tylophora hirsuta L. Then these three extracts are mixed and used small teaspoon thrice a day. According to the rural inhabitants of the area this formula is very old and 100% effective to lower the blood glucose level of diabetics.

 

c. Ficus bengalensis L.:

The latex obtained from the aerial parts of the plant (leaves and young branches) and mixed with honey and used orally to control high blood glucose level.

 

d. Psidium guajava L.:

Hot water extract made from the dried leaves of plant is used to reduce blood glucose level of diabetics. This hot tea was very common among the local people of the area.

 

e. Momordica charantia L.:

The juice of fresh fruits, used, one small cup daily. This juice exhibits an antidiabetic property.

 

f. Cajanus cajan and Vigna mungo (Burm. f.) Walp:

The pulse obtained from the seeds of these plants is cooked and is recommended to diabetics.

 

g. Allium cepa L.:

The juice obtained from the underground bulb is used, one tea spoon thrice a day. This is given for the control of blood sugar and high blood pressure amongst the diabetics.

 

h. Caralluma edulis (L.) Benth ex Hook. f.:

The aerial parts are cooked as vegetables by the local people for diabetes mellitus.

 

2. Antidiabetic leaves

a. Zizyphus jujuba Mill:

4-5 fresh leaves are chewed daily to lower blood glucose level.

 

b. Dodonaea viscosa (L.) Jacq:

2-3 Fresh leaves of the plant are masticated twice a day with glass of water.

 

3. Antidiabetic powder (Safoof)

a. Ocimum sanctum L. + Ocimum album L.:

Leaves of these plant species are dried under shade, then ground to make powder (Safoof). One gm power is given with water twice a day for prophylactic and the treatment of diabetes.

 

b. Momordica charantia L.:

The fruits of the plant are dried under shade, then ground to obtain powder. One table spoon is administered twice a day to lower blood glucose level.

 

c. Syzygium cumini Skeels:

Seeds of the plant are dried under shade, then ground to make powder About 25 gm powder is used thrice a day with water. This decreases blood glucose level very significantly.

 

d. Kickxia ramosissima (Wall) Janchen:

The whole plant is dried under shade and is ground to make powder. This powder is prescribed for treatment of diabetes by the inhabitants of the study area.

 

e. Cichorium intybus L.:

The roots are dried under shade and then ground to obtain powder. About 15 gm of this powder is taken with glass of water twice a day before meal to lower blood glucose level.

 

f. Melia azedarach L.: The dried fruits of the plant are ground to make powder. About half small teaspoon is given with glass of water before breakfast daily for a month. It is claimed by the inhabitants that it is an effective therapy for the treatment of diabetes.

 

g. Hordeum vulgare L. + Cicer arietinum L. + Elettaria cardamomum Maton:

Seeds of Hordeum vulgare 125 gram are roasted and mixed with each of 50 gm of Cicer arietinum and Elettaria cardamomum and used @ half teaspoon with water thrice a day to control blood glucose level.

 

4. Antidiabetic bread:

Equal quantity of Cicer arietinum (Seeds), Daucus carrota ((Dried form), Hordeum vulgare (Seeds), Oryza sativa (Seeds), Triticum aestivum (Seeds) and Zea mays (yellow variety) are ground and made into powder. The bread is cooked from this mixed flour and taken as breakfast with fresh butter of cow for 2-month. This remedy is used as dietary supplement to control diabetes.

 

5. Antidiabetic seeds

a. Trigonella foenum-graecum L.:

Twenty five gm seeds are given daily for 21 days with water. The inhabtants claimed that it is one of the effective treatments to reduce blood glucose in diabetic patients.

 

b. Withania coagulens (L.) Dunal.

Fifteen gm seeds of the plant are soaked in water for the whole night. This is given early morning before breakfast to diabetic patients.

 

6. Antidiabetic Potherbs/Vegetables

a. Solanum nigrum L.:

Fresh aerial parts of the plant are cooked as vegetable and are recommended to control diabetes.

b. Taraxicum officinale Weber:

Fresh leaves are cooked as vegetable (locally-called Saag).

c. Cajanus cajan and Vigna mungo (Burm. F.) Walp.:

The pulses obtained from the seeds of these plants are cooked and is recommended to diabetic patients.

d. Allium sativum L.:

The under ground bulb is cooked or uncooked is used for diabetes and hypertension amongst diabetics.

e. Caralluma edulis (L.) Bth. ex Hk. F.:

The aerial parts are cooked as vegetables by local people for diabetes mellitus.

7. Antidiabetic fruits

a. Vigna sinensis (L.) Savi ex Hassk: The immature pods of the plant are used to reduce blood glucose level.

b. Syzygium cuminii Skeels: The fresh fruits are used for diabetes.

c. Olea ferruginea Royle: Fruit fresh in summer season are collected, dried and recommended to diabetics in winter season for reducing blood glucose level.

 

8. Antidiabetic herbal mixtures

a. The seeds in 25 gm of Syzygium cumini, Momordica charantia, 12 gm of Cyperus rotundus and Rosa alba are made into powder. This compound is given successfully for lowering blood glucose by the inhabitants of an area.

 

b. The equal quantity of Tylophlra hirsuta (leaves), Trigonella foenum-graecum (seeds) and aerial parts of Fumaria indica is ground and made into powder. This mixture is claimed a significant therapy to reduce blood sugar of diabetic patients.

 

Clinical research of CAM supplements in diabetes

Currently, there is not yet sufficient evaluation of herbs, vitamins, and mineral supplements for glucose control in diabetes. Aside from relatively poor study methodological quality, this area of supplement research has been fraught with several complications. First, the multiple constituent nature of botanical products has made standardization a challenging task. Proponents of herbal remedies caution that in standardizing to one constituent, resulting extracts may have lost a proportion of benefit as compared with the whole plant 178. Precise considerations of purity, chemical composition, and potency of derivatives may be grossly influenced by the age of the plant (especially of roots), the source location, the season of harvest, the method of drying and crude preparation, etc. In the literature we examined, several herb studies used “homemade” or otherwise unspecified preparations. Although individual companies have begun to standardize supplements, there is a general lack of consistency across the market. With vitamin and mineral supplements, these issues are less relevant. In addition, the development of proper supplement regulation and safety codes has been slow. Currently, all dietary supplements (including herbal products) are regulated under the Dietary Supplement Health and Education Act of 1994 (DSHEA), which specifically differentiates supplements from drugs.  Consequently, DSHEA does not require the extensive premarket approval that the Food and Drug Adminstration requires for a prescription drug, and although it calls for “good manufacturing practices [GMP],” the burden of proof that a supplement is unsafe lies with the government, leaving manufacturers to operate unchecked. This has contributed to scepticism among clinicians, and makes it especially difficult for physicians to responsibly recommend supplements to patients. In the absence of external regulation, the industry has taken steps to police itself. For example, the National Nutritional Foods Association (NNFA), representing about one-third to one-half of retailers and manufacturers of natural products in the U.S., has encouraged the adoption of strict, self-imposed GMP standards, as well as initiatives such as the TruLabel program (in which products are subjected to random laboratory testing by independent third-party auditors to verify contents) 179. Research of vitamin and mineral supplements has also been hindered by a lack of accurate and meaningful assays that detect functional micronutrient deficiencies. In the case of chromium, for example, it is postulated that supplementation of targeted individuals might be more beneficial. Some speculate that positive results seen in large studies in diabetic patients in China may be due to the population’s relative chromium deficiency. However, without reliable assays, these theories have remained difficult to test 180. Finally, the existing literature in this area includes a considerable amount of study population heterogeneity. Future research may need to more precisely define targeted diabetic populations with regard to disease classification, severity, optimal adjunctive interventions, and perhaps nutrient deficiencies. It will also be important to further elucidate mechanisms of action so that applicability to type 1 or type 2 diabetes can be clarified.

 

CONCLUSION:

Diabetes mellitus is the most common endocrine disorder, affecting more than 300 million people worldwide. For this, therapies developed along the principles of western medicine (allopathic) are often limited in efficacy, carry the risk of adverse effects and are often too costly, especially for the developing world. Therefore, treating diabetes mellitus with plant derived compounds which are accessible and do not require laborious pharmaceutical synthesis seems highly attractive. All the herbal drugs discussed in the review exhibit significant clinical and pharmacological activity. The potency of herbal drugs is significant and they have negligible side effects than the synthetic anti diabetic drugs. In this review article an attempt has been made to focus on hypoglycemic plants and maybe useful to the health professionals, scientists and scholars working in the field of pharmacology and therapeutics to develop evidence based alternative medicine to cure different kinds of diabetes in man and animals.

 

Isolation and identification of active constituents from these plants, preparation of standardized dose and dosage regimen can play a significant role in improving the hypoglycemic action.

 

REFERENCES:

1.        Medscape.com. Type 2 Diabetes Mellitus.

2.        Medscape.com. Type 2 Diabetes Mellitus.

3.        Text Book Of Pharmacognosy- C. K. Kokate, A.P. Purohit, S.B. Gokhale, P: 218

4.        Text Book Of Pharmacognosy, C. K. Kokate, A.P. Purohit, S.B. Gokhale, P: 219

5.        Min-Jia Tan, Ji-Ming Ye, Nigel Turner, Cordula Hohnen-Behrens, Chang- Qiang Ke, Chun-Ping Tang, Tong Chen, Hans-Christoph Weiss, Ernst- Rudolf Gesing, Alex Rowland, David E. James and Yang Ye – Antidiabetic Activities of Triterpenoids Isolated from Bitter Melon Associated with Activation of the AMPK Pathway.

6.        Shukla R., Sharma S. B., Buri D., Probhu K. M., Medicinal plants for the treatment of Diabetes Mellitus, Indian J Clin Biochem, 15 (2000), P: 169

7.        Ghaisas Saket M. - Effect of the insulin plant (Costus igneus) leaves on dexamethasone-induced hyperglycemia.

8.        Text Book Of Pharmacognosy, C. K. Kokate, A.P. Purohit, S.B. Gokhale, P: 156

9.        Text Book Of Pharmacognosy, C. K. Kokate, A.P. Purohit, S.B. Gokhale, P: 157

10.     Akhtar M.S., Khan Q.M., Khaliq T. - Effects of Portulaca oleracae (Kulfa) and Taraxacum officinale (Dhudhal) in normoglycaemic and alloxan-treated  hyperglycaemic rabbits. J Pak Med Assoc 1985; 35:207-210.

11.     Wadkar K.A., Magdum C.S., Patil S.S.,” Antidiabetic Potential and Indian Medicinal plants- A Review Article”, Journal of Herbal Medicine and Toxicology 2 (1); 2008, P: 45-50

12.     Nathan D.M., Buse J.B., Davidson M.B., Ferrannini E., Holman R.R., Sherwin R., Zinman B., (2009). "Medical Management of Hyperglycemia in Type 2 Diabetes: A Consensus Algorithm for the Initiation and Adjustment of Therapy: A consensus statement of the American Diabetes Association and the European Association for the Study of Diabetes". Diabetes Care 32 (1): 193–203. doi:10.2337/dc08-9025.  PMC 2606813.PMID 18945920.http://www.pubmedcentral.nih.gov/articlerender.fcg i?tool=pmcentrezandartid=2606813

13.     Salpeter S., Greyber E., Pasternak G., Salpeter E. - Risk of fatal and nonfatal lactic acidosis with metformin use in type 2 diabetes mellitus. Cochrane Database Syst Rev 2006 Jan 25 ;( 1):CD002967.

14.     Bailey C.J., Day, C. - (2004). "Metformin: its botanical background". Practical Diabetes Int 21 (3): 115–117. doi:10.1002/pdi.606

15.     Text Book Of Pharmacognosy, C. K. Kokate, A.P. Purohit, S.B. Gokhale, P: 573

16.     Text Book Of Pharmacognosy, C. K. Kokate, A.P. Purohit, S.B. Gokhale, P: 573

17.     Rajalakshmi M., Eliza J., Priya Cecilia Edel, Nirmala A., Daisy P. - Anti-diabetic properties of Tinospora cordifolia stemextracts on streptozotocin- induced diabetic rats.

18.     Text Book Of Pharmacognosy, C. K. Kokate, A.P. Purohit, S.B. Gokhale, P: 414

19.     Text Book Of Pharmacognosy, C. K. Kokate, A.P. Purohit, S.B. Gokhale, P: 415

20.     Halim Eshrat M., Hussain Ali- Hypoglycemic, hypolipidemic and antioxidant properties of combination of curcumin from Curcuma longa, Linn, and partially purified product from Abroma augusta, Linn. in streptozotocin induced diabetes.

21.     Rai P.K., Jaiswal D., Mehta S., Rai D.K.,  Sharma B., Watal G.- Effect of curcuma longa freeze dried rhizome powder with milk in STZ induced diabetic rat.

22.     Text Book Of Pharmacognosy, C. K. Kokate, A.P. Purohit, S.B. Gokhale, P: 253-254

23.     Text Book Of Pharmacognosy, C. K. Kokate, A.P. Purohit, S.B. Gokhale, P: 254

24.     Shanmugasundaram K.R., Panneerselvam C., Samudram P., Shanmugasundaram E.R.- Enzyme changes and glucose utilisation in diabetic rabbits: the effect of Gymnema sylvestre.

25.     Shanmugasundaram E.R., Rajeswari G., Baskaran K., et al- Use of Gymnema sylvestre leaf in the control of blood glucose in insulin-dependent diabetes mellitus.

26.     Text Book Of Pharmacognosy, C. K. Kokate, A.P. Purohit, S.B. Gokhale, P: 152

27.     Text Book Of Pharmacognosy, C. K. Kokate, A.P. Purohit, S.B. Gokhale, P: 152

28.     Sevugan arumugam, Subhramanian Kavimani, Balamuthu Kadalmani, Abdul Bakrudeen Ali Ahmed, Mohammed Abdulkadar Akbarsha, Mandali Venkateswara Rao- Antidiabetic activity of leaf and callus extract of Aegle marmelos in rabbits.

29.     Text Book Of Pharmacognosy, C. K. Kokate, A.P. Purohit, S.B. Gokhale, P: 264

30.     Text Book Of Pharmacognosy, C. K. Kokate, A.P. Purohit, S.B. Gokhale, P: 264

31.     Rakesh Kumar Singh, Dolly Jaiswal, Prashant Kumar Rai, (November 2009) - Anti-diabetic activity of Emblica officinalis in animal models.

32.     Hannan J.M., Ali L., Rokeya B., Khaleque J., Akhter M., Flatt P.R., Abdel- Wahab Y.H.-Soluble dietary fibre fraction of Trigonella foenum-graecum (fenugreek) seed improves glucose homeostasis in animal models of type 1 and type 2 diabetes by delaying carbohydrate digestion and absorption, and enhancing insulin action.

33.     Hannan J.M., Ali L., Rokeya B., Khaleque J., Akhter M., Flatt P.R., Abdel- Wahab Y.H.-Soluble dietary fibre fraction of Trigonella foenum-graecum (fenugreek) seed improves glucose homeostasis in animal models of type 1 and type 2 diabetes by delaying carbohydrate digestion and absorption, and enhancing insulin action.

34.     Najma Zaheer Baquer, Pardeep Kumar, Asia Taha, RK Kale, SM Cowsik and P  Mclean- Metabolic and molecular action of Trigonella foenum-graecum (fenugreek) and trace metals in experimental diabetic tissues.

35.     Bawadi Hiba A., Maghaydah Sofyan N.; Tayyem Rabab F., Tayyem Reema F.- The Postprandial Hypoglycemic Activity of Fenugreek Seed and Seeds’ Extract in Type 2 Diabetics: A Pilot Study.

36.     Text Book of Pharmacognosy, C. K. Kokate, A.P. Purohit, S.B. Gokhale, P: 222.

37.     Text Book Of Pharmacognosy, C. K. Kokate, A.P. Purohit, S.B. Gokhale, P: 223

38.     Jing Tian Xie, Sangeeta Mehendale and Chun-Su Yuan- Ginseng and Diabetes.

39.     Ng T.B., Yeung H.W. – Hypoglycemic constituents of Panax ginseng.

40.     Text Book Of Pharmacognosy, C. K. Kokate, A.P. Purohit, S.B. Gokhale, P: 270

41.     Text Book Of Pharmacognosy, C. K. Kokate, A.P. Purohit, S.B. Gokhale, P: 270

42.     Manickam M., Ramanathan M., Farboodniay Jahromi M. A., Chansouria J. P. N., and Ray A. B.- Antihyperglycemic Activity of Phenolics from Pterocarpus marsupium.

43.     Dhanaba S. P., Kokate C. K., Ramanathan M., Kumar E. P., Suresh B. - Hypoglycaemic activity of Pterocarpus marsupium Roxb.

44.     Text Book Of Pharmacognosy, C. K. Kokate, A.P. Purohit, S.B. Gokhale, P: 486

45.     Text Book Of Pharmacognosy, C. K. Kokate, A.P. Purohit, S.B. Gokhale, P: 487

46.     Som Nath Singh, Praveen Vats, Shoba Suri, Radhey Shyam, Kumria M.M.L., Ranganathan S., Sridharan K. - Effect of an antidiabetic extract of Catharanthus roseus on enzymic activities in streptozotocin induced diabetic rats.

47.     Srinivas Nammi, Boini Murthy K ., Lodagala Srinivas D. and Behar Ravindra Babu S.- The juice of fresh leaves of Catharanthus roseus Linn. Reduces blood glucose in normal and alloxan diabetic rabbits.

48.     Text Book Of Pharmacognosy, C. K. Kokate, A.P. Purohit, S.B. Gokhale, P: 296

49.     Text Book Of Pharmacognosy, C. K. Kokate, A.P. Purohit, S.B. Gokhale, P: 296

50.     Shradha Bisht, Sisodia S.S. - Anti- Hyperglycemic And Antidyslipidemic Potential Of Azadirachta indica Leaf Extract In STZ- Induced Diabetes Mellitus.

51.     Text Book Of Pharmacognosy, C. K. Kokate, A.P. Purohit, S.B. Gokhale, P: 35

52.     Text Book Of Pharmacognosy, C. K. Kokate, A.P. Purohit, S.B. Gokhale, P: 357

53.     Mukul Tailang, Gupta Bhaskar K., Amrish Sharma. - Antidiabetic Activity of Alcoholic Extract of Cinnamomum zeylanicum Leaves in Alloxon Induced Diabetic Rats.

54.     Khan A., Safdar M., Ali Khan M.M., Khattak K.N., Anderson R.A. - Cinnamon improves glucose and lipids of people with type 2 diabetes.

55.     Williams J.A., Choe Y.S., Noss M.J., Baumgartner C.J., Mustad V.A.- Extract of Salacia oblonga lowers acute glycemia in patients with type 2 diabetes

56.     Williams J.A., Choe Y.S., Noss M.J., Baumgartner C.J., Mustad V.A.- Extract of Salacia oblonga lowers acute glycemia in patients with type 2 diabetes

57.     Savariraj Sahayam C., Dubey G.P., Rajamanickaam G.V. and Brindha. P. - Comparative study of anti diabetic potential of Salacia species in Hippocrateaceae family.

58.     Text Book Of Pharmacognosy, C. K. Kokate, A.P. Purohit, S.B. Gokhale, P: 267

59.     Text Book Of Pharmacognosy, C. K. Kokate, A.P. Purohit, S.B. Gokhale, P: 268

60.     Imad M. Taj Eldin, Elhadi M. Ahmed and Abd. Elwahab H. M- Priliminary study of the Clinical Hypoglycemic effect of Allium cepa (Red onion) in type 1 and type 2 diabetic patients.

61.     Text Book Of Pharmacognosy, C. K. Kokate, A.P. Purohit, S.B. Gokhale, P: 360

62.     Text Book Of Pharmacognosy, C. K. Kokate, A.P. Purohit, S.B. Gokhale, P: 361

63.     Martha Thomson, Al-Amin Zainab M., Al-Qattan Khaled K., Shaban Lemia H. and Muslim Ali- Anti-diabetic and hypolipidaemic properties of garlic (Allium sativum) in streptozotocininduced diabetic rats.

64.     Confirmed in Opuntia subulata: Trenary (1997)

65.     Confirmed in Opuntia subulata: Trenary (1997)

66.     Confirmed in Opuntia aurantiaca (.014%), O. clavata, O. ficus-indica (.01%), O. maldonandensis (.01%): Trenary (1997)

67.     Confirmed in Opuntia clavata, O. ficusindica, O. invicta: Trenary (1997)

68.     Confirmed in Opuntia clavata, O. ficusindica, O. invicta: Trenary (1997)

69.     Ning Yang, Mouming Zhao, , Banghao Zhu, Bao Yang, Chunhui Chen, Chun Cui Yueming Jiang -Anti-diabetic effects of polysaccharides from Opuntia monacantha cladode in normal and streptozotocin-induced diabetic rats.

70.     Skrede G., Wrolstad R.E., Durst R.W. - “Changes in anthocyanins and polyphenolics during juice processing of highbush blueberries (Vaccinium myrtillus L.),” Journal of Food Science, 2000, 65:357-364.

71.     Skrede G., Wrolstad R.E., Durst R.W. - “Changes in anthocyanins and polyphenolics during juice processing of highbush blueberries (Vaccinium myrtillus L.),” Journal of Food Science, 2000, 65:357-364.

72.     Cignarella A., Nastasi M., Cavalli E., et al- Novel lipid-lowering properties of Vaccinium myrtillus L. leaves, a traditional antidiabetic treatment, in several models of rat dyslipidaemia: a comparison with ciprofibrate. Thromb Res.

73.     Bever B., Zahnd G. (1979) - Vaccinium myrtillus with oral hypoglycemic action.

74.     Haddock E., et al. The metabolism of gallic acid and hexahydroxydiphenic acid in plants. Part É. Introduction. Naturally occurring galloyl esters. J Chem Soc 1982; 11:2515.

75.     Nonaka G., et al. A dimeric hydrolysable tannin, Sanguin H-6 from Sanguisorba officinalis L. Chem Pharm Bull 1982; 30(6):2255.

76.     Tanaka T., et al. Tannins and related compounds. CXXII. New dimeric, trimeric and tetrameric ellagitannins, lambertianins A-D, from Rubus lambertianus Seringe. Chem Pharm Bull 1993; 41(7):1214.

77.     Gupta R., et al. The metabolism of gallic acid and hexahydroxydiphenic acid in plants. Part 2. Esters of (S) - hexahydroxydiphenic acid with Dglucopyranose ( 4 C 1 ). J Chem Soc 1982; 11:2525.

78.     Khabibullaeva L., et al. Phytochemical study of raspberry leaves. Mater Yubileinoi Resp Nauchn Konf Farm 1972; 98. Chem Abs 1972; 83:4960z.

79.     Gudej J., et al. Flavonoid compounds from the leaves of Rubus idaeus L. Herba Pol 1996; 42(4):257.

80.     Maga J., et al. Bramble leaf volatiles. Dev Food Sci 1992; 29:145.

81.     Krzaczek T. - Phenolic acids in some tannin drugs from the Rosaceae family. Farm Pol 1984; 40(8):475. CA 102:146198s.

82.     health.indiamart.com.

83.     J. Clin Biochem Nutr. (2007, May) 40(3): 163-173.

84.     Offenbacher EG, Pi-Sunyer FX. Beneficial effect of chromium-rich yeast on glucose tolerance and blood lipids in elderly subjects. Diabetes 1980; 29:919-925. 

85.     Mooradian AD, Failla M, Hoogwerf B, et al. Selected vitamins and minerals in diabetes. Diabetes Care 1994; 17:464-479. 

86.     Baker B. Chromium supplements tied to glucose control. Fam Pract News 1996; 15:5. 

87.     Mooradian AD, Failla M, Hoogwerf B, et al. Selected vitamins and minerals in diabetes. Diabetes Care 1994; 17:464-479. 

88.     Mertz M. Chromium occurrence and function in biologic systems. Physiol Rev 1969; 49:163-237.

89.      Anderson RA, Cheng N, Bryden NA, et al. Elevated intakes of supplemental chromium improve glucose and insulin variables in individuals with type 2 diabetes.  Diabetes 1997; 46:1786-1791. 

90.     Lee NA, Reasner CA. Beneficial effect of chromium supplementation on serum triglyceride levels in NIDDM. Diabetes Care 1994; 17:1449-1452. 

91.     Anderson RA, Bryden NA, Polansky MM. Dietary chromium intake. Freely chosen diets, institutional diet, and individual foods. Biol Trace Element Res1992; 32:117-121.

92.     Castro VR. Chromium in a series of Portuguese plants used in the herbal treatment of diabetes. Biol Trace Elem Res 1998; 62:101-106.

93.     Nielsen FH. Chromium. In: Shils ME, Olson JA, Shike M, eds. Modern Nutrition in Health and Disease, 8th ed. Philadelphia, PA: Lea and Febiger; 1994:264-268.

94.     Reading SA. Chromium picolinate. J Fla Med Assoc 1996; 83:29-31.

95.     Stearns DM, Wetterhahn KE. Chromium picolinate. FASEB J 1996; 10:367-369.

96.     Cohen N, Halberstam M, Shlimovich P, et al. Oral vanadyl sulfate improves hepatic and peripheral insulin sensitivity in patients with non-insulin-dependent diabetes mellitus. J Clin Invest 1995; 95:2501-2509. 

97.     Halberstam M, Cohen N, Shlimovich P, et al. Oral vanadyl sulfate improves insulin sensitivity in NIDDM but not in obese nondiabetic subjects. Diabetes 1996; 45:659-666. 

98.     Sjogren A, Floren CH, Nilsson A. Magnesium, potassium and zinc deficiency in subjects with type II diabetes mellitus. Acta Med Scand 1988; 224:461-466. 

99.     McNair P, Christiansen C, Madsbad S, et al. Hypomagnesemia, a risk factor in diabetic retinopathy. Diabetes 1978; 27:1075-1077. 

100.  Hu H. A review of treatment of diabetes by acupuncture during the past forty years. J Tradit Chin Med 1995; 15:145-154. 

101.  Chen JF, Wei J. Changes of plasma insulin level in diabetics treated with acupuncture. J Tradit Chin Med 1985; 5:79-84. 

102.  Huang KC. Diabetes mellitus. In: Huang KC, ed. Acupuncture: The Past and the Present, 1st ed. New York: Vantage Press; 1996:202. 

103.  Hui H. A review of treatment of diabetes by acupuncture during the past forty years. J Tradit Chin Med 1995; 15:145-154. 

104.  Hui H. A review of treatment of diabetes by acupuncture during the past forty years. J Tradit Chin Med 1995; 15:145-154. 

105.  Huang KC. Diabetes mellitus. In: Huang KC, ed. Acupuncture: The Past and the Present, 1st ed. New York: Vantage Press; 1996:202.

106.  Hu H. A review of treatment of diabetes by acupuncture during the past forty years. J Tradit Chin Med 1995; 15:145-154. 

107.  Hooper PL. Hot-tub therapy for type 2 diabetes mellitus. N Engl J Med 1999; 341:924-925. 

108.  Hooper PL. Hot-tub therapy for type 2 diabetes mellitus. Reply to discussion. N Engl J Med 2000; 342:218-219. 

109.  Yazdanparast R, Ardestani A, Jamshidi S. Experimental diabetes treated with Achillea santolina: effect on pancreatic oxidative parameters, J Ethnopharmacol 2007, 112, 13-8

110.  Subramoniam A, Pushpangadan P, Rajasekharan S, Evans DA, Latha PG, Valsaraj R. Effects of Artemisia pollens Wall. On blood glucose levels in normal andalloxan-induced diabetic rats. J Ethnopharmacol 1996, 50, 13-17.

111.  Chempakam, B. Hypogiycemic activity of arecoline in betel nut Areca catechu L. Ind J Exp Biol 1993, 31, 474-475.

112.  Yoshikawa M, Murakami T, Kadoya M, Matsuda H, Muraoka O, Yamahara J, Murakami N.Medicinal foodstuff. III. Sugar beet. Hypoglycemic oleanotic acid oligoglycosides,betavulgarosides 1, II, III and IV, from the root of Beta vulgaris L. Chemical and Pharmaceutical Bulletin 1996, 44, 1212-1217.

113.  Pari L, Amarnath Satheesh M. Anlidiabetic activity of Boerhaavia diffusa L. effect on hepatickeyenzymes in experimental diabetes. J Ethnopharmacol 2004, 91, 109-13

114.  Saleem R, Ahmad M, Hussain SA, Qazi AM, Ahmad SI, Qazi MH, Ali M, Faizi S, Akhtar S, Husnain SN. Hypotensive, hypoglycemic and toxicological studies on the flavonol C-glycosideshamimin from Bombax ceiba. Planta Medica 1999, 5, 331-334.

115.  Somani R, Kasture S, Singhai AK. Antidiabetic potential of Butea monospenna in rats. Fitoterapia 2006, 77, 86-90.

116.  Eddouks M, Lemhadri A, Michel JB.Caraway and caper: potential antihyperglycaemie plants in diabetic rats. J Ethnopharmacol 2004, 94, 143- 148.

117.  Diatewa M, Samba CB, Assah TC, Abena AA.Hypoglycemic and antihyperglycemic effects of diethyl ether fraction isolated from theaqueous extract of the leaves of Cogniauxia podoleana Baillon in normal and alloxan-induced diabetic rats. J Ethnopharmacol 2004, 92, 229-232.

118.  Youn JY, Park HY, Cho KH. Anti-hyperglycemic activity of CommeUna communis L.: inhibition of alpha-glucosidase. Diabetes Res CHn Pract 2004, 66, S149-S155.

119.  Farias RA, Rao VS, Viana GS, Silveira ER, Maciel MA, Pinto AC. Hypoglycemic effect of trans-dehydrocrotonin, a nor-clerodanc diterpene from Crotoncajucara. Planta Med 1997, 63, 558-560.

120.  Rodrigues G, Marcolin E, Bona S, Porawski M, Lehmann M, Marroni NP. Hepatics alterations and genotoxic effects of Croton cajucara Benth (SACACA) indiabetic rats. Arq Gastroenterol 2010, 47, 301-305.

121.  Kuroda M, Mimaki Y, Nishiyama T, Mae T, Kishida H, Tsukagawa M, Takahashi K, Kawada T, Nakagawa K, Kitahara M. Hypoglycemic effects of turmeric (Curcuma longa L. rhizomes) on genetically diabeticKK-Ay mice. Biol Pharm Bull 2005, 28, 937-939.

122.  Jarald EE, Joshi SB, Jain DC. Antidiabetic activity of aqueous extract and non-polysaccharide fraction of Cynodondactylon Pers. Indian J Exp Biol 2008, 46, 660-667.

123.  Vijayvargia R, Kumar M, Gupta S. Hypoglycemic effect of aqueous extract of Enicostemma littorale Blume (chhotachirayata) on alfoxan induced diabetes mellitus in rats. Indian J Exp Bioi 2000, 38, 781-784.

124.  Tanaka K, Nishizono S, Makino N, Tamaru S, Terai O, Ikeda I. Hypoglycemic activity of Eriobotrya japonica seeds in type 2 diabetic rats and mice.Biosci Biotechnol Biochem 2008, 72, 686-693.

125.  Sezik E, Aslan M, Yesilada E, Ito S. Hypoglycaemic activity of Gentiana olivieri and isolation of the active constituent through bioassay-directed fractionation techniques. Life Sci 2005, 76, 1223- 1238.

126.  Sugiyama T, Kubota Y, Shinozuka K, Yamada S, Wu J, Umegaki K. Ginkgo biloba extract modifies hypoglycemic action of tolbutainide via hepatic cytochrome P450 mediated mechanism in aged rats. Life Sci 2004, 75, 1113-1122.

127.  Kudolo GB. The effect of 3-month ingestion of Ginkgo biloba extract (EGb 761) on pancreatic beta-cell functionin response to glucose loading in individuals with non-insulin-dependent diabetes mellitus. J Clin Pharmacol 2001, 41, 600-611.

128.  Skim F, Lazrek HB, Kaaya A, el Amri H, Jana M. Pharmacological studies of two antidiabetic plants: Globularia alypum and Zygophyllum gaetulum. Therapie 1999, 54, 711-715.

129.  Kuroda M, Mimaki Y, Sashida Y, Mae T, Kishida H, Nishiyama T, Tsukagawa M, Konishi E, Takahashi K, Kawada T, Nakagawa K, Kitahara M. Phenolics with PPAR-gamma ligand-binding activity obtained from licorice (Glycyrrhizauralensis roots) and ameliorative effects of glycyrin on genetically diabetic KK-A(y) mice. Bioorg Med ChemLett 2003, 13, 4267-4272.

130.  Ramkumar KM, Latha M, Ashokkumar N, Pari L, Ananthan R. Modulation of impaired cholinesterase activity in experimental diabetes: effect of Gymnema montanum leaf extract. J Basic Clin Physiol Pharmacol 2005, 16, 17-35.

131.  Daisy P, Eliza J, Mohamed Farook KA. A novel dihydroxy gymnemic triacetate isolated from Gymnema sylvestre possessing normoglycemic and hypolipidemic activity on STZ-induced diabetic rats. J Ethnopharmacol 2009, 126, 339-344.

132.  Guerrero-Analco JA, Hersch-Martínez P, Pedraza-Chaverri J, Navarrete A, Mata R.Antihyperglycemic effect-of constituents from Hintonia standleyana in streptozotocin-induced diabetic rats. Planta Med 2005, 71, 1099-1105.

133.  Alarcon-Aguilar FJ, Calzada-Bermejo F, Hernandez-Galicia E, Ruiz- Angeles C, Roman-Ramos R. Acute and chronic hypoglycemic effect of Ibervillea sonorae root extracts-11. J Ethnopharmacol 2005, 97, 447- 452.

134.  Malalavidhane TS, Wickramasinghe SM, Perera MS, Jansz ER. Oral hypoglycaemic activity of Ipomoea aquatica in streptozotocin-induced, diabetic wistar rats and Type II diabetics. Phytother Res 2003, 17, 1098- 1100.

135.  Park HJ, Kim DH, Choi JW, Park JH, Han YN. A potent anti-diabetic agent from Kalopan axpictus.Arch Pharm Res 1998, 21, 24-29.

136.  Hattori K, Sukenobu N, Sasaki T, Takasuga S, Hayashi T, Kasai R, Yamasaki K, Hazeki O. Activation of insulin receptors by lagerstroemin J Pharmacol Sci 2003, 93, 69-73.

137.  Klein G, Kim J, Himmeldirk K, Cao Y, Chen X. Antidiabetes and Antiobesity Activity of Lagerstroemia speciosa. Evid Based Complement Alternat Med 2007, 4, 401-407.

138.  Gray AM, Flatt PR. Pancreatic and extra-pancreatic effects of the traditional anti-diabetic plant, Medicago saliva (lucerne). Br J Nutr 1997, 78, 325-334

139.  Singab AN, El-Beshbishy HA, Yonekawa M, Nomura T, Fukai T. Hypoglycemic effect of Egyptian Moms albaroot bark extract: effect on diabetes and lipid peroxidation of streptozotocin-induced diabetic rats. J T-Etnnopharmacol 2005, 100, 333-338.

140.  Devi VD, Urooj A. Hypoglycemic potential of Moms indica. L and Costus igneus. Nak.—a preliminary study. Indian J Exp Biol 2008, 46, 614-616.

141.  Andallu B, Suryakantham V, Lakshmi Srikanthi B, Reddy GK. Effect of mulberry (Morus indica L.) therapy on plasma and erythrocyte membrane lipids in patients with type 2 diabetes. Clin Chim Acta 2001, 314, 47-53.

142.  Basnet P, Kadota S, Terashima S, ShimizuM, Namba T. Two new 2- arylbenzofuran derivatives from hypoglycemic activity-bearing fractions of Morus insignis. Chem Pharm Bull (Tokyo) 1993, 41, 1238- 1243.

143.  Khan BA, Abraham A, Leelamma S.Hypoglycemic action of Murraya koenigii (curry leaf) and Brassica juncea (mustard) mechanism of action. Ind J Biochem Biophys 1995, 32, 106-108.

144.  Mukherjee PK, Saha K, Pal M, Saha BP.Effect of Nelumbo nucifera rhizome extract on blood sugar level in rats. J Ethnopharmacol 1997, 58, 207-213.

145.  Kanter M, Coskun O, Korkmaz A, Oter S. Effects of Nigella sativa on oxidative stress and beta-cell damage in streptozotocin-induced diabetic rats. Anat Rec A Discov Mol Cell Evol Biol 2004, 279, 685-691.

146.  Aguiyi JC, Obi CI, Gang SS, Igweh AC. Hypoglycaemic activity of Ocimum gratissimum in rats. Fitoterapia 2000, 71, 444-446.

147.  Peungvicha P, Temsiririrkkul R, Prasain JK, Tezuka Y, Kadota S, Thirawarapan SS, Watanabe H.4-Hydroxybenzoic acid: a hypoglycaemic constituent of aqueous extract of Pandanus odorus root. J Ethnopharmacol 1998, 62, 79-84.

148.  Perez RM, Perez C, Zavala MA, Perez S, Hernandez H, Lagunes F. Hypoglycemic effects of lactucin-8-O-melhyl aery late of Parmentiera edulis fruit. J Ethnopharmacol 2000, 71, 391-394.

149.  Hnatyszyn O, Mińo J, Ferraro G, Acevedo C. The hypoglycemic effect of Phyllanthus sellowiamts fractions in streptozotocin-induced diabetic mice. Phytomedicine 2002, 9, 556-559.

150.  Alarcon-Aguilar FJ, Jimenez-Estrada M, Reyes-Chilpa R, Roman- Ramos R. Hypoglyceraic effect of extracts and fractions from Psacalium decompositum inhealthy and alloxan-diabetic mice. J Ethnopharmacol 2000, 72, 21-27.

151.  Contreras-Weber C, Perez-Gutierrez S, Alarcon-Aguilar F, Roman- Ramos R. Anti-hyperglycemic effect of Psacalium peltatum. ProcWest Pharmacol Soc 2002, 45, 134-136.

152.  Li Y, Wen S, Kota BP, Peng G, Li GQ, Yamahara J, Roufogalis BD. Punica granatum flower extract, a potent alpha-glucosidase inhibitor, improves postprandial hyperglycemia in Zucker diabetic fatty rats. J Ethnopharmacol 2005, 99, 239-244.

153.  Krishnakumar K, Augusti KT, Vijayammal PL. Hypoglycaemic and anti-oxidant activity of Salacia oblonga Wall, extract instreptozotocininduced diabetic rats. Indian J Physiol Pharmacol 1999, 43, 510-514.

154.  Gray AM, Abdel-Wahab YH, Flatt PR. The traditional plant treatment, Sambucus nigra (elder), exhibits insulin-like and insulin-releasing actions in vitro. J Nutr 2000, 130, 15-20.

155.  Hou Z, Zhang Z, Wu H. Effect of Sanguis draxonis (a Chinese traditional herb) on the formation of insulin resistancein rats. Diabetes Res Clin Pract 2005, 68, 3-11.

156.  Ojewole JA. Hypoglycemic effect of Sclerocarya birrea [(A. Rich.)Hochst.Anacardiaceae] stem-bark aqueous extract in rats. Phytomedicine 2003, 10, 675-681.

157.  Beh JE, Latip J, Abdullah MP, Ismail A, Hamid M. Scoparia dulcis (SDF7) endowed with glucose uptake properties on L6 myotubes comparedinsulin. J Ethnopharmacol 2010, 129, 23-33.

158.  Pari L, Latha M. Antihyperlipidemic effect of Scoparia dulcis (sweet broomweed) in streptozotocin diabetic rats. J Med Food 2006, Spring, 9, 102-107.

159.  Saxena AM, Bajpai MB, Murthy PS, Mukherjee SK. Mechanism of blood sugar lowering by a Swerchirin containing hexane fraction (SWI) of Swertia chirayita. Ind J Exp Biol 1993, 31, 178-181.

160.  Rao BK, Rao CH. Hypoglycemic and antihyperglycemic activity of Syzygium alternifblium (Wt.) Walp. Seed extracts in normal and diabetic rats. Phytomedicine 2001, 8, 88-93.

161.  Kasetti RB, Rajasekhar MD, Kondeti VK, Fatima SS, Kumar EG, Swapna S, Ramesh B, Rao CA. Antihyperglycemic and antihyperlipidemic activities of methanol:water (4:1) fraction isolated from aqueous extract of Syzygium alternifolium seeds in streptozotocin induced diabetic rats. Food ChemToxicol 2010, 48, 1078-1084.

162.  Kasabri V, Flatt PR, Abdel-Wahab YH. Terminalia bellirica stimulates the secretion and action of insulin and inhibits starchdigestion and protein glycation in vitro. Br J Nutr 2010, 103, 212-217.

163.  Singh I, Singh PK, Bhansali S, Shafiq N, Malhotra S, Pandhi P, Pal Singh A. Effects of three different doses of a fruit extract of Terminalia chebula on metabolic components of metabolic syndrome, in a rat model. Phytother Res 2010, 24, 107-112.

164.  Rao NK, Nammi S. Antidiabetic and renoprotective effects of the chloroform extract of Terminalia chebula Retz.seeds in streptozotocininduced diabetic rats. BMC Complement AlternMed 2006, 6, 17.

165.  Murali YK, Anand P, Tandon V, Singh R, Chandra R, Murthy PS. Long-term effects of Terminalia chebula Retz.on hyperglycemia and associated hyperlipidemia, tissue glycogen content and in vitro release of insulin in streptozotocin induced diabetic rats. Exp Clin Endocrinol Diabetes 2007, 115, 641-646.

166.  Esmaeili MA, Zohari F, Sadeghi H. Antioxidant and protective effects of major flavonoids from Teucrium polium on beta-cell destruction in a model of streptozotocin-induced diabetes. Planta Med 2009, 75, 1418- 1420.

167.  Sengupta S, Mukherjee A, Goswami R, Basu S. Hypoglycemic activity of the antioxidant saponarin, characterized as alpha-glucosidase inhibitor present in Tinospora cordifolia. J Enzyme Inhib Med Chem 2009, 24, 684-690.

168.  Noor H, Ashcroft SJ. Pharmacological characterization of the antihyperglycemic properties of Tinospora crispa extract. J Ethnopharmacol 1998, 62, 7-13.

169.  Bnouham M, Merhfour FZ, Ziyyat A, Mekhfi H, Aziz M, Legssyer A. Antihyperglycemic activity of the aqueous extract of Urtica dioica.Fitoterapia 2003, 74, 677-681.

170.  Kavalali G, Tuncel H, Göksel S, Hatemi HH. Hypoglycemic activity of Urtica p'dulifera in streptozotocin-diabetic rats. J Ethnopharmacol 2003, 84, 241-245.

171.  Chattopadhyay RR, Sarkar SK, Ganguly S, Banerjee RN, Basu TK. Hypoglycemic and anti-hyperglycemic effect of Vinca rosea Linn.Ind. J Physiof Pharmacol 1991, 35, 145-151.

172.  Adallu B, Radhika B. Hypoglycemic, diuretic and hypocholesterolemic effect of winter cherry (Withaniasomnifera, Dunal) root. Indian J Exp Biol 2000, 38, 607-609.

173.  Udayakumar R, Kasthurirengan S, Vasudevan A, Mariashibu TS, Rayan JJ, Choi CW, Ganapathi A, Kim SC. Antioxidant effect of dietary supplement Withania somnifera L. reduce bloodglucose levels in alloxan-induced diabetic rats. Plant Foods Hum Nutr 2010, 65, 91-98.

174.  Hoda Q, Ahmad S, Akhtar M, Najmi AK, Pillai KK, Ahmad SJ. Antihyperglycaemic and antihyperlipidaemic effect of poly-constituents, in aqueous andchloroform extracts, of Withania coagulans Dunal in experimental type 2 diabetes mellitus in rats. Hum Exp Toxicol 2010, 29, 653-658.

175.  Hemalatha S, Wahi AK, Singh PN, Chansouria JP. Hypoglycemic activity of Dunal in streptozotocin induced diabetic rats. J Ethnopharmacol 2004, 93, 261-264.

176.  Anand KK, Singh B, Chand D, Chandan BK, Gupta VN. Effect of Zizyphus saliva leaves on blood glucose levels in normal and alloxandiabeticrats. J Ethnopharmacol 1989, 27, 121-127.

177.  Abdel-Zaher AO, Salim SY, Assaf MH, Abdel-Hady RH. Antidiabetic activity and toxicity of Zizyphus spina-chnsti leaves. J Ethnopharmacol 2005, 101, 129-138.

178.  Goldman P: Herbal medicines today and the roots of modern pharmacology. Ann Intern Med 135:594–600, 2001

179.  Chitwood M: Botanical therapies for diabetes: on the cutting edge. Diabetes Care and Education 20:3–20, 1999

180.  Althuis MD, Jordan NE, Ludington EA, Wittes JT: Glucose and insulin responses to dietary chromium supplements: a meta-analysis. Am J Clin Nutr 76:148– 155, 2002

 

 

Received on 17.06.2014          Accepted on 30.07.2014        

© Asian Pharma Press All Right Reserved

Asian J. Pharm. Res. 4(3): July-Sept. 2014; Page 135-154