Home

DiaMedBase 

Diabetes Medicinal Plant Database

Browse    A B C D E F G H I J K L M N O P Q R S T U V W X Y Z     Plants List
Caesalpinia
Cajanus
Calamintha
Camellia
Capparis
Capsicum
Caralluma
Carissa
Carum
Casearia
Cassia
Castanospermum
Catharanthus
Cecropia
Centaurea
Centaurium
Cephalandra
Chamaemelum
Chelidonium
Chrysanthemum
Chrysobalanus
Cicer
Cichorium
Cimicifuga
Cinnamomum
Cirsium
Cissus
Citrullus
Citrus
Clausena
Cleome
Cnidium
Cnidoscolus
Coccinia
Cogniauxia
Colocassia
Commelina
Commiphora
Convallaria
Convolvulus
Coptis
Coriandrum
Corni
Cornus
Coscinium
Costus
Cressa
Crotalaria
Croton
Cryptolepis
Cucumis
Cucurbita
Cuminum
Curcuma
Cyamopsis
Cyclocarya
Cymbopogon


 
DiaMedBase ID   DMPCf143
Medicinal Plant   Artemisia roxburghiana, Salvia coccinia, Monstera deliciosa, Abies pindrow, Centaurea iberica, Euphorbia helioscopia, Bauhinia variegate, Bergenia himalacia, Taraxacum officinale, Viburnum foetens, Adhatoda vasica, Cassia fistula, Chrysanthemum leucanthemum, Morus alba, Plectranthus rugosus, Peganum harmala and Olea ferruginea
Plant part(s)   Whole plant
Objective  

To know the effects of medicinal plants on diabetes

Journal Source   Phytother Res, 2004; 18(1):73-77
Title  

The effect of medicinal plants of Islamabad and Murree region of Pakistan on insulin secretion from INS-1 cells

Authors   Hussain Z, Waheed A, Qureshi RA, Burdi DK, Verspohl EJ, Khan N, Hasan M
Address  

Department of Chemistry, Quaid-i-Azam University, Islamabad Pakistan. chem63@yahoo.com

Abstract  

In vitro testing of the extracts of medicinal plants collected from Islamabad and the Murree region on insulin secretagogue activity was carried out. Dried ethanol extracts of all plants (ZH1-ZH19) were dissolved in ethanol and DMSO, and tested at various concentrations (between 1 and 40 microg/mL) for insulin release from INS-1 cells in the presence of 5.5 mM glucose. Glibenclamide was used as a control. Promising insulin secretagogue activity in various plant extracts at 1, 10, 20 and 40 microg/mL was found, while in some cases a decrease in insulin secretion was also observed. Artemisia roxburghiana, Salvia coccinia and Monstera deliciosa showed insulin secretagogue activity at 1 microg/mL (p < 0.05) while Abies pindrow, Centaurea iberica and Euphorbia helioscopia were active at 10 microg/mL (p < 0.05). Extracts of Bauhinia variegata and Bergenia himalacia showed effects at 20 microg/mL (p < 0.05), and Taraxacum officinale and Viburnum foetens at 40 microg/mL (p < 0.05). Insulin secretagogue activity could not be detected in the extracts of Adhatoda vasica, Cassia fistula, Chrysanthemum leucanthemum, Morus alba, Plectranthus rugosus, Peganum harmala and Olea ferruginea. The results suggest that medicinal plants of Islamabad and the Murree region of Pakistan may be potential natural resources for antidiabetic compounds.

Diseases   Disease Link
DiaMedBase ID   DMPCa144
Medicinal Plant   Momordica charantia, Melia azadirachta, Pterocarpus marsupium, Tinospora cordifolia , Gymnema sylvestre, Enicostemma littorale, Emblica officinalis, Eugenia jambolana, Cassia auriculata and Curcuma longa
Plant part(s)   Whole plant
Objective   To investigate the antihyperglycaemic and antioxidant activity in STZ-induced diabetic rats
Journal Source   J Pharm Pharmacol, 2004; 56(11):1435-1442
Title  

Antihyperglycaemic and antioxidant effect of hyponidd, an ayurvedic herbomineral formulation in streptozotocin-induced diabetic rats

Authors   Babu PS, Stanely Mainzen Prince P
Address  

Department of Biochemistry, Annamalai University, Annamalai Nagar-608 002, Tamil Nadu, India

Abstract  

Hyponidd is a herbomineral formulation composed of the extracts of ten medicinal plants ( Momordica charantia, Melia azadirachta, Pterocarpus marsupium, Tinospora cordifolia , Gymnema sylvestre, Enicostemma littorale, Emblica officinalis, Eugenia jambolana, Cassia auriculata and Curcuma longa). We have investigated hyponidd for its possible antihyperglycaemic and antioxidant effect in diabetic rats. Rats were rendered diabetic by streptozotocin (STZ) (45 mg kg(-1) body weight). Oral administration of hyponidd (100 mg kg(-1) and 200 mg kg(-1)) for 45 days resulted in significant lowered levels of blood glucose and significant increased levels of hepatic glycogen and total haemoglobin. An oral glucose tolerance test was also performed in experimental diabetic rats in which there was a significant improvement in blood glucose tolerance in the rats treated with hyponidd. Hyponidd administration also decreased levels of glycosylated haemoglobin, plasma thiobarbituric acid reactive substances, hydroperoxides, ceruloplasmin and alpha-tocopherol in diabetic rats. Plasma reduced glutathione and vitamin C were significantly elevated by oral administration of hyponidd. The effect of hyponidd at a dose of 200 mg kg(-1) was more effective than glibenclamide (600 microg kg(-1)) in restoring the values to near normal. The results showed that hyponidd exhibits antihyperglycaemic and antioxidant activity in STZ-induced diabetic rats.

Diseases   Disease Link
DiaMedBase ID   DMPCt145
Medicinal Plant   Cassia tora
Plant part(s)   Fiber
Objective   To study the effect of serum lipids in korean diabetic patients.
Journal Source   Journal of Medicinal Food, 2005; 8(3): 311-318
Title   Effects of Cassia tora Fiber Supplement on Serum Lipids in Korean Diabetic Patients
Authors   Sung-Hee Cho1, Tae-Hee Kim1, Nan-Hee Lee1, Ho-Sang Son2, Il-Jin Cho3, Tae-Youl Ha3
Address   1Department of Food Science and Nutrition, Catholic University of Daegu, Gyeongbuk, 2Department of Medicine, Catholic University of Daegu, Daegu, 3Korea Food Research Institute, Gyeonggi-do, Korea
Abstract   Cassia tora fiber supplement consisting of 2 g of soluble fiber extracted from Cassia semen (C. tora L.), 200 mg of -tocopherol, 500 mg of ascorbic acid, and 300 mg of maltodextrin was formulated in a pack, and given to 15 type II diabetic subjects (seven men and eight women 57.1 ± 2.9 years old) with instructions to take two packs per day for 2 months. Placebo contained maltodextrin only with a little brown caramel color. Lifestyle factors and dietary intakes of the subjects were not altered during the 2-month period. Serum total cholesterol was moderately (P < .1) decreased in the C. tora group compared with the age- and gender-matched placebo group, as was the ratio of apolipoprotein B to apolipoprotein A1 (P < .1). Levels of serum triglycerides and low-density lipoprotein-cholesterol tended to decrease more in the C. tora-supplemented group than in the placebo group. Serum -tocopherol was increased (P < .01) but lipid peroxides were not significantly lower in the C. tora group. Fasting blood glucose, hemoglobin A1c, blood urea nitrogen, creatinine, and activities of serum aspartate aminotransferase and alanine aminotransferase were not changed by the fiber supplement. We concluded that C. tora supplements can help improve serum lipid status in type II diabetic subjects without serious adverse effects.
Diseases   Disease Link
DiaMedBase ID   DMPCa146
Medicinal Plant   Gymnema sylvestre, Eugenia jambolana, Momordica charantia, Azadirachta indica, Cassia auriculata, Aegle marmelose, Withania somnifera and Curcuma longa
Plant part(s)   Leaves
Objective   To study the hypoglycemic activity in normal and streptozotocin induced diabetic mice
Journal Source   Phytother, 2005; 19(5):409-415
Title  

Effect of Dianex, a herbal formulation on experimentally induced diabetes mellitus

Authors   Mutalik S, Chetana M, Sulochana B, Devi PU, Udupa N
Address   College of Pharmaceutical Sciences, Manipal, Karnataka, India
Abstract   Dianex, a polyherbal formulation consisting of the aqueous extracts of Gymnema sylvestre, Eugenia jambolana, Momordica charantia Azadirachta indica, Cassia auriculata, Aegle marmelose, Withania somnifera and Curcuma longa was screened for hypoglycemic activity in normal and streptozotocin induced diabetic mice. Dianex was administered in different doses of 100-500 mg/kg/day orally in acute (6 h) and long-term (6 weeks) studies. Blood glucose levels were checked 2-6 h after treatment in acute studies and every 2 weeks in long-term studies. Body weight was recorded on the first and final day of the treatment in the long-term studies with diabetic mice. After 6 weeks, high-density lipoprotein, triglycerides, total cholesterol, alanine transaminase (ALT), aspertate transaminase (AST), urea and creatinine were estimated in serum of the diabetic mice. Glycogen and total protein levels were estimated in the liver. Also, the liver and pancreas was subjected to histological examination. Oral glucose tolerance and in vitro free radical scavenging activity was also studied.Dianex produced significant (p<0.05) hypoglycemic activity at 250-500 mg/kg doses in both normal and diabetic mice in acute and long-term studies. The body weight of diabetic mice significantly (p<0.05) increased with all tested doses of Dianex. The elevated triglycerides, cholesterol, ALT, AST, urea and creatinine levels in diabetic mice were significantly (p<0.05) reduced at the doses of 250 and 500 mg/kg. The liver glycogen and protein levels were both significantly (p<0.05) increased in diabetic mice at 250 and 500 mg/kg doses. Dianex increased the glucose tolerance significantly (p<0.05) in both normal and diabetic mice at all the doses tested. Histopathological examination showed that the formulation decreased streptozotocin induced injury to the tissues at all the doses tested. It produced significant (p<0.05) free radical scavenging activity against ABTS+, DPPH and hydroxyl free radicals at the concentrations ranging between 10-1000 microg/ml.Thus, in the present study, Dianex produced significant hypoglycemic activity in both normal and diabetic animals. It also reversed other diabetic complications in diabetic mice at 250 and 500 mg/kg doses. In our earlier study, Dianex was well tolerated in laboratory animals at higher doses (upto 10 g/kg in mice, acute toxicity; up to 2.5 g/kg in rats, subacute toxicity studies for 30 days) without exhibiting any toxic manifestation. Hence, Dianex may be useful in the treatment of diabetes mellitus.
Diseases   Disease Link
DiaMedBase ID   DMPCa147
Medicinal Plant   Cassia alata
Plant part(s)   Leaves
Objective   To study the hypoglycemic effect
Journal Source   J Ethnopharmacol., 1988; 22(1):81-90
Title   Effect of Cassia alata leaf extract on hyperglycemic rats
Authors   Palanichamy S, Nagarajan S, Devasagayam M
Address   Department of Chemistry, Bharathidasan University, Tiruchirapalli, India
Abstract   The oral effectiveness of Cassia alata leaf extract on streptozotocin-induced hyperglycemia in rats has been studied and the results compared with glybenclamide. While the extract has no effect on glucose levels in normoglycemic animals, it reduced the blood sugar value in streptozotocin-induced hyperglycemic animals.
Diseases   Disease Link
DiaMedBase ID   DMPCo148
Medicinal Plant   Bearberry (Arctostaphylos uva-ursi), golden seal (Hydrastis canadensis), mistletoe (Viscum album), tarragon (Artemisia dracunculus), bayberry (Cinnamomum tamala), meadowsweet (Filipendula ulmaria), senna (Cassia occidentalis)
Plant part(s)   Herbal mixture of all plants
Objective   To study blood glucose levels
Journal Source   Acta Diabetol Lat., 1989; 26(1):51-55
Title  

Evaluation of traditional plant treatments for diabetes: studies in streptozotocin diabetic mice

Authors   Swanston-Flatt SK, Day C, Bailey CJ, Flatt PR
Address  

Department of Biological and Biomedical Sciences, University of Ulster, Coleraine, U.K

Abstract   Seven plants and a herbal mixture used for traditional treatment of diabetes were studied in streptozotocin diabetic mice. The treatments were supplied as 6.25% by weight of the diet for 9 days. Consumption of diets containing bearberry (Arctostaphylos uva-ursi), golden seal (Hydrastis canadensis), mistletoe (Viscum album) and tarragon (Artemisia dracunculus) significantly reduced the hyperphagia and polydipsia associated with streptozotocin diabetes, but bayberry (Cinnamomum tamala), meadowsweet (Filipendula ulmaria), senna (Cassia occidentalis) and the herbal mixture did not alter these parameters. Bearberry, mistletoe and tarragon retarded the body weight loss but none of the eight treatments significantly altered plasma glucose or insulin concentrations. These studies suggest that bearberry, golden seal, mistletoe and tarragon may counter some of the symptoms of streptozotocin diabetes without, however, affecting glycemic control.
Diseases   Disease Link
DiaMedBase ID   DMPCf149
Medicinal Plant   Cajanus cajan L. and Cassia fistula L
Plant part(s)   Leaves and Stems
Objective   To study the effects of Cajanus cajan L. and of Cassia fistula L. on carbohydrate metabolism in mice
Journal Source   Rev Med Panama. 1991; 16(1):39-45
Title  

Evaluation of traditional medicine: effects of Cajanus cajan L. and of Cassia fistula L. on carbohydrate metabolism in mice

Authors   Esposito Avella M, Diaz A, de Gracia I, de Tello R, Gupta MP
Address   Departamento de Farmacologia, Universidad de Panama
Abstract  

The authors report the results of pharmacologic evaluation of two medicinal plants: Cajanus cajan (L.) Millsp and Cassia fistula, which are used in Panamanian folk medicine for the treatment of diabetes. It was found that the aqueous fraction of the leaves and stems of C. cajan did not produce any hypo blood sugar effect in normoglycemic mice; instead, it produced a hyperglycemia with doses of 500 mg/kg and 1000 mg/kg (p less than 0.001). Only with a dose of 300 mg/kg a short lived decrease in the glycemia was seen at one hour. On the contrary, the folk use of the leaves of C. fistula for diabetes seems to have some correlation with the popular frek use. The aqueous fraction produced a significant decrease in the glycemia (p less than 0.001) at 4 and 24 hours with doses of 300 and 500 mg/kg, and at one and four hours after the dose of 1000 mg/kg (p less than 0.001). In the glucose tolerance test, the aqueous fraction of C. cajan produced a significant and short lasting decrease (p less than 0.05) with the dose of 300 mg/kg, while the dose of 500 mg/kg did at 0.25, 0.5 and 1 hour (p less than 0.01). The 1000 mg/kg dose produced a significant increase in glucose tolerance at 1 and 2 hours (p less than 0.05). The aqueous fraction of C. fistula produced a significant decrease (p less than 0.05) with the dose of 500 mg/kg at 0.25 and 0.5 hours. The 1000 mg/kg dose produced a significant increase (p less than 0.001) at 0.25 and 2 hours.

Diseases   Disease Link
DiaMedBase ID   DMPCa150
Medicinal Plant   Azardirachta indica, Cassia auriculata and Momordica charantia
Plant part(s)   Leaves
Objective  

To investigate Diamed for its possible antihyperglycaemic action in rats with alloxan-induced experimental diabetes

Journal Source   J Pharm Pharmacol, 2001; 53(8):1139-1143
Title   Antihyperglycaemic effect of Diamed, a herbal formulation, in experimental diabetes in rats
Authors   Pari L, Ramakrishnan R, Venkateswaran S
Address  

Department of Biochemistry, Annamalai University, Tamil Nadu, India. paribala@sancharnet.in

Abstract  

Diamed is a herbal formulation composed of the aqueous extracts of three medicinal plants (Azardirachta indica, Cassia auriculata and Momordica charantia). We have investigated Diamed for its possible antihyperglycaemic action in rats with alloxan-induced experimental diabetes. Oral administration of Diamed (1.39 (0.25 g), 1.67 (0.30 g) or 1.94 (0.35 g) mL kg(-1)) for 30 days resulted in a significant reduction in blood glucose, glycosylated haemoglobin, and an increase in plasma insulin and total haemoglobin. The effect was highly significant after administration of the 1.94 mL (0.35 g) g(-1) body weight dose. Diamed also prevented a decrease in body weight. An oral glucose tolerance test was performed in experimental diabetic rats in which there was a significant improvement in glucose tolerance in the animals treated with Diamed. The effect was compared with 600 microg kg(-1) glibenclamide. The results showed that Diamed had antihyperglycaemic action in experimental diabetes in rats.

Diseases   Disease Link
DiaMedBase ID   DMPCa151
Medicinal Plant   Cassia auriculata
Plant part(s)   Flower
Objective   To study the effect of Cassia auriculata flower extract (CFEt) on hepatic glycolytic and gluconeogenic enzymes
Journal Source   Clinical and Experimental Pharmacology and Physiology, 2003; 30(1-2):38
Title   Antihyperglycaemic effect of Cassia auriculata in experimental diabetes and its effects on key metabolic enzymes involved in carbohydrate metabolism
Authors   Muniappan Latha and Leelavinothan Pari
Address  

Department of Biochemistry, Faculty of Science, Annamalai University, Annamalai Nagar, Tamil Nadu, India

Abstract   1. In experimental diabetes, enzymes of glucose and fatty acid metabolism are markedly altered. Persistent hyperglycaemia is a major contributor to such metabolic alterations, which lead to the pathogenesis of diabetic complications. To our knowledge, there are no available reports on the enzymes of hepatic glucose metabolism of Cassia auriculata flower against diabetes. The present study was designed to study the effect of Cassia auriculata flower extract (CFEt) on hepatic glycolytic and gluconeogenic enzymes. 2. Streptozotocin diabetic rats were given CFEt (0.15, 0.30 and 0.45 g/kg) or 600 µg/kg glibenclamide for 30 days. At the end of 30 days, blood glucose, plasma insulin, haemoglobin, glycosylated haemoglobin, glycolytic and gluconeogenic enzymes were assessed. 3. Administration of CFEt at 0.45 g/kg significantly decreased blood glucose, glycosylated haemoglobin and gluconeogenic enzymes and increased plasma insulin, haemoglobin and hexokinase activity. Similarly, administration of glibenclamide showed a significant effect; however, CFEt at 0.15 and 0.30 g/kg did not show any significant effect. 4. In conclusion, the observations show that the aqueous extract of CFEt possesses an antihyperglycaemic effect and suggest that enhanced gluconeogenesis during diabetes is shifted towards normal and that the extract enhances the utilization of glucose through increased glycolysis. The effect of CFEt was more prominent than that of glibenclamide.
Diseases   Disease Link

         Copyright © 2006 ProGene Biosciences
            Last modified: March, 2006
             info@progenebio.in