首页 | 本学科首页   官方微博 | 高级检索  
     


Modulatory role of Emblica officinalis against alcohol induced biochemical and biophysical changes in rat erythrocyte membranes
Authors:Vaddi Damodara Reddy  Pannuru Padmavathi  Maturu Paramahamsa  Nallanchakravarthula Varadacharyulu
Affiliation:1. Department of Biochemistry, Sri Krishnadevaraya University, Anantapur 515 003, India;2. Department of Microbiology and Immunology, J.G. Brown Cancer Center, University of Louisville Health Sciences, Louisville, KY 40202, USA
Abstract:This study investigated the protective effect of Emblica officinalis against alcohol-induced biochemical and biophysical changes in rat erythrocyte membranes. Thirty-two male rats were divided into four groups (= 8 in each group): control (C), alcohol (A), alcohol plus Emblica fruit extract (A + EFE) and Emblica fruit extract (EFE) alone. Administration of twenty percent alcohol (5 g/kg body weight) to rats significantly increased cholesterol/phospholipid (C/P) ratio, lipid peroxidation and the activities of Na+/K+ and Mg2+ ATPases in erythrocyte membranes as well as augmented nitric oxide (NO) levels. However, membrane fluidity studies using the fluorescent probe DPH (1,6 diphenyl 1,3 hexatriene) reveals that alcohol administration significantly (p < 0.05) increased membrane anisotropic values and altered membrane individual phospholipid content. Administration of EFE (250 mg/kg body weight) to alcoholic rats resulted in significant (p < 0.05) reduction of NO levels, erythrocyte membrane lipid peroxidation, C/P ratio, activities of Na+/K+ and Mg2+ ATPases and fluorescent anisotropic values. Further, EFE administration to alcoholic rats beneficially modulated membrane properties as evidenced from the contents of total phospholipids as well individual phospholipid classes. The tannoid principles present in Emblica offers protection against alcohol induced adverse effects in rats.
Keywords:Alcohol   ATPases   Emblica officinalis   Erythrocyte membrane   Fluidity   Nitric oxide
本文献已被 ScienceDirect 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号