Antioxidant and hepatoprotective activities of phenolic rich fraction of Seabuckthorn (Hippophae rhamnoides L.) leaves

被引:179
作者
Maheshwari, D. T. [1 ]
Kumar, M. S. Yogendra [1 ]
Verma, Saroj K. [1 ]
Singh, Vijay K. [1 ]
Singh, Som Nath [1 ]
机构
[1] Def Res & Dev Org, Def Inst Physiol & Allied Sci, Delhi 110054, India
关键词
Seabuckthorn; Phenolic compounds; Antioxidant enzymes; Lipid peroxidation; Protein oxidation; Total phenol; TETRACHLORIDE-INDUCED HEPATOTOXICITY; CARBON-TETRACHLORIDE; LIPID-PEROXIDATION; OXIDATIVE DAMAGE; EXTRACT;
D O I
10.1016/j.fct.2011.06.061
中图分类号
TS2 [食品工业];
学科分类号
100403 [营养与食品卫生学];
摘要
Present study was aimed to investigate antioxidant and hepatoprotective activities of phenolic rich fraction (PRF) of Seabuckthorn leaves on CCl4 induced oxidative stress in Sprague Dawley rats. Total phenolic content was found to be 319.33 mg gallic acid equivalent (GAE)/g PRF and some of its phenolic constituents, such as gallic acid, myricetin, quercetin, kaempferol and isorhamnetin were found to be in the range of 1.935-196.89 mg/g of PRF as determined by reverse-phase high-performance liquid chromatography (RP-HPLC). Oral administration of PRF at dose of 25-75 mg/kg body weight significantly protected from CCl4 induced elevation in aspartate aminotransferase (AST), alanine aminotransferase (ALT), gamma-glutamyl transpeptidase (GGT) and bilirubin in serum, elevation in hepatic lipid peroxidation, hydroperoxides, protein carbonyls, depletion of hepatic reduced glutathione (GSH) and decrease in the activities of hepatic antioxidant enzymes; superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GPX), glutathione reductase (GR) and glutathione-S-transferase (GST). The PRF also protected against histopathological changes produced by CCl4 such as hepatocytic necrosis, fatty changes, vacuolation, etc. The data obtained in the present study suggests that PRF has potent antioxidant activity, prevent oxidative damage to major biomolecules and afford significant protection against CCl4 induced oxidative damage in the liver. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2422 / 2428
页数:7
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