Hepatoprotective effect of food preservatives (butylated hydroxyanisole, butylated hydroxytoluene) on carbon tetrachloride-induced hepatotoxicity in rat

被引:34
作者
Dassarma, Barsha [1 ]
Nandi, Dilip K. [2 ]
Gangopadhyay, Somnath [3 ]
Samanta, Saptadip [1 ]
机构
[1] Midnapore Coll, Dept Physiol, Midnapore 721101, W Bengal, India
[2] Raja NL Khan Womens Coll, Dept Physiol & Nutr, Midnapore 721102, W Bengal, India
[3] Univ Calcutta, Univ Coll Sci & Technol, Occupat Ergon Lab, Dept Physiol, 92 APC Rd, Kolkata 700009, W Bengal, India
关键词
Butylated hydroxyanisole; Butylated hydroxytoluene; Hepatoprotection; CCl4 - intoxicated rats;
D O I
10.1016/j.toxrep.2017.12.009
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Carbon tetrachloride (CCl4), a hepatotoxic agent is widely used to study the toxic mechanisms in experimental animals. This study was carried out to establish the hepatoprotective measures of food preservative antioxidants butylated hydroxyanisole and butylated hydroxytolune (BHA, BHT) when mixed with food towards carbon tetrachloride (CCl4) intoxication (230 mg/ kg b wt/rat/day) in rat. Biochemical markers like serum glutamate pyruvate tranaminase (AST), serum glutamate oxaloacetate transaminase (ALT), alkaline phosphatase (ALP) and bilirubin content, antioxidant enzymes such as SOD, CAT, GPx, and malondialdehyde (MDA) as the end product of lipid peroxidanion were measured. The results had shown the elevated level of AST (121.16%), ALT (124.68%), ALP (122.41%) an, bilirubin content (57.14%) after CCl4 treatment. Marked decrease of activity of antioxidant enzymes such as SOD (85.36%), CAT (67.47%), GPx (50.7%) had indicated that the ROS mediated toxicity and pretreatment of BHA and BHT restored the activity of these enzymes. High level of MDA content with reduced GSH value was also observed due to oxidative stress. The hepatic antioxidant status was restored with the food preservative (BHA, BHT) antioxidant treatment which had indicated the significant protective effect against CCl4 induced hepatotoxicity and finally confirmed by histopathological studies.
引用
收藏
页码:31 / 37
页数:7
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