Document Type : Original Article
Department of Biochemistry, Arunai Medical College and Hospital, Tiruvanamalai-606603, Tamilnadu, India
Department of Biochemistry, Meenakshi Ammal Dental College and Hospital, Chennai-600095, Tamilnadu, India
Department of Physiology, Konaseema Institute of Medical Sciences and Research Foundation, Amalapuram, East Godavari Dt-533201, Andhra Pradesh, India
Department of Physiology, Krishnadevaraya College of Dental Science and Hospital, Bangalore, Karnadaka, India
Department of Biochemistry, Zydus Medical College and Hospital, Dahod-389151, Gujarat, India
Background: Among many human diet-related disorders, Diabetes mellitus (DM) stands on the top of the table, its persistent and perdurable threat/stress response to systemic functions and endocrine control makes it's more popular. The management of diabetes and related chronic diseases has focused on the use of indigenous natural compounds, derived from plant sources that possess medicinal properties.
Methods: Wistar albino rats were fed with high-fat diet comprising 2% cholesterol, 1% cholic acid, 30% coconut oil, 67 % percent regular rat feed, and 25% fructose through drinking water for 60 days to induce type-2diabetic. After induction, type-2 diabetic rats were treated with β-Carophyllene (50, 100, 200, and 400mg/kg body weight once a day, orally) for 30 days, respectively. Fasting Blood glucose, liver and kidney function markers were analyzed.
Results: Diabetic animals showed elevated blood glucose level when compared to control. Treatment with 50 and 100 mg/kg b.wt β-Carophyllene did not reach control level. Whereas, 200 and 400 mg/kg b.wt doses effectively reduced the blood glucose levels in diabetic animals.
Conclusion: Liver function markers such as ALT, AST, and ALP and kidney function markers like urea and creatinine were also found to be elevated in diabetic animals. β-Carophyllene effectively reduced it. No toxicity was found in 200 and 400 mg/kg b.wt β-Carophyllene treated animals. Since blood glucose was restored to normal range at 200 mg dose itself, the same dose was selected as optimal dose for further study to elucidate the anti-diabetic potential.