首页 | 本学科首页   官方微博 | 高级检索  
     


Oral administration of Nigella sativa oil ameliorates the effect of cisplatin on brush border membrane enzymes,carbohydrate metabolism and antioxidant system in rat intestine
Authors:Faaiza Shahid  Zeba Farooqui  Sana Rizwan  Subuhi Abidi  Iqbal Parwez  Farah Khan
Affiliation:1. Department of Biochemistry, Faculty of Life Sciences, Aligarh Muslim University, Aligarh 202002, U.P., India;2. Department of Zoology, Faculty of Life Sciences, Aligarh Muslim University, Aligarh 202002, U.P., India
Abstract:Cisplatin (CP) is an effective chemotherapeutic agent that induces gastrointestinal toxicity. Nigella sativa oil (NSO) has been shown to be beneficial in a wide range of gastrointestinal disorders. The present study investigates the possible protective effect of NSO on CP-induced gastrointestinal toxicity. NSO administration (2 ml/kg bwt, orally), prior to and following, a single dose CP treatment (6 mg/kg bwt. ip), significantly attenuated the CP-induced decrease in brush border membrane (BBM) enzyme activities in intestinal homogenates and BBM vesicles (BBMV). NSO administration also mitigated CP induced alterations in the activities of carbohydrate metabolism enzymes and in the enzymatic and non-enzymatic antioxidant parameters in the intestine. The results suggest that NSO by empowering the endogenous antioxidant system improves intestinal redox and metabolic status and restores BBM integrity in CP treated rats. Histopathological studies supported the biochemical findings. Thus, NSO may help prevent the accompanying gastrointestinal dysfunction in CP chemotherapy.
Keywords:ACPase  acid phosphatase  ALP  alkaline phosphatase  BBM  brush border membrane  BBMV  BBM vesicles  CAT  catalase  CP  cisplatin  FBPase  fructose 1,6-bisphosphatase  G6Pase  glucose 6-phosphatase  G6PDH  glucose 6-phosphate dehydrogenase  GGTase  γ-glutamyl transferase  GR  glutathione reductase  GSH  glutathione reduced  GSH  Px- glutathione peroxidase  GST  glutathione S-transferase  HK  hexokinase  hydrogen peroxide  LAP  leucine aminopeptidase  LDH  lactate dehydrogenase  LPO  lipid peroxidation  MDA  malondialdehyde  MDH  malate dehydrogenase  ME  malic enzyme  NAD  nicotinamide adenine dinucleotide  NADH  nicotinamide adenine dinucleotide reduced  NADPH  nicotinamide adenine dinucleotide phosphate reduced  NADP  nicotinamide adenine dinucleotide phosphate  NSO  ROS  reactive oxygen species  SH  sulfhydryl  SOD  superoxide dismutase  TCA  tricarboxylic acid  TR  thioredoxin reductase  Cisplatin  Carbohydrate metabolism  Antioxidant system  Gastrointestinal toxicity
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