ISSN: 2161-069X

Journal of Gastrointestinal & Digestive System
Open Access

Our Group organises 3000+ Global Conferenceseries Events every year across USA, Europe & Asia with support from 1000 more scientific Societies and Publishes 700+ Open Access Journals which contains over 50000 eminent personalities, reputed scientists as editorial board members.

Open Access Journals gaining more Readers and Citations
700 Journals and 15,000,000 Readers Each Journal is getting 25,000+ Readers

This Readership is 10 times more when compared to other Subscription Journals (Source: Google Analytics)

Momordica charantia mitigates hepatic injury following adjuvant treatment with antiretroviral drugs in diabetic and non-diabetic animal models

International Conference on Gastrointestinal Cancer and Therapeutics & 4th World Congress on Digestive & Metabolic Diseases & 26th Annual Congress on Cancer Science and Targeted Therapies

Offor U, Naidu ECS and Azu OO

University of KwaZulu-Natal, South AfricaUniversity of Namibia, Namibia

Posters & Accepted Abstracts: J Gastrointest Dig Syst

DOI: 10.4172/2161-069X-C8-086

Abstract
Hepatogenous diabetes and hepatoxicity traced to highly active antiretroviral therapy (HAART) is a significant threat to the health of mankind and calls for urgent attention. Momordica charantia (M. charantia) is a medicinal plant, used in Ayurveda for treating various diseases, including diabetes mellitus. This study investigated the possible protective effect of M. charantia against HAART and streptozotocin STZ induced hepatoxicity. 78 adult male Sprague Dawley rats were divided into two groups (non-diabetic and diabetic) and treated according to protocols. Diabetes was induced with streptozotocin (STZ) by intraperitoneal injection (45 mg/kg body weight). The animals were euthanized on the tenth week with livers removed for examination and blood obtained via cardiac puncture and centrifuged to collect the serums. Blood glucose levels (BGL) were consistently and significantly raised in all groups not receiving the adjuvant M. charantia (p<0.05). Treatment with M. charantia reverses the increase in BGL to near normal. Markers of liver injury assayed showed a significant increase (p<0.05) in AST, ALP and ALT levels in diabetic groups not receiving M. charantia. Adjuvant HAART and M. charantia caused significant declines in the liver enzymes (p<0.05). Serum GGT was not markedly altered. Treatment with M. charantia significantly restored liver enzymes elevations to near normal comparable to control. Histopathological observations ranged from severe hepatocellular distortions, necrosis and massive fibrosis following treatment of HAART in diabetic and non-diabetic groups. M. charantia did not show any sign of hepatotoxicity as judged from the histological and biochemical observations.
Biography

E-mail: ugochukwuoffor@yahoo.com

 

Top