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   DMPCl220
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   DMPCl221
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

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