Ansar S, Iqbal M
Department of Clinical Laboratory Sciences, College of Applied Medical Science, King Saud University, Riyadh, Saudi Arabia
Biotechnology Research Institute, Universiti Malaysia Sabah, Jalan UMS, Kota Kinabalu Sabah, Malaysia.
Hum Exp Toxicol. 2016 Dec;35(12):1305-1311. doi: 10.1177/0960327116629723. Epub 2016 Jan 28.
The present study was undertaken to evaluate the effect of diallylsulphide (DAS) against mercuric chloride (HgCl)-induced oxidative stress in rat livers. Rats were randomly divided into four groups of six rats each and exposed to HgCl (50 mg/kg/body weight (b.w.)) intraperitoneally and/or DAS (200 mg/kg/b.w.) by gavage. HgCl administration enhanced alanine aminotransferase (AST) and aspartate aminotransferase (ALT) levels (p < 0.05) with reduction in the levels of superoxide dismutase (SOD), catalase (CAT) and glutathione peroxidase (GSH-Px). However, treatment with DAS markedly attenuated HgCl-induced biochemical alterations in liver and serum transaminases (AST and ALT; p < 0.05). Further, biochemical results were confirmed by histopathological changes as compared to HgCl-intoxicated rats. Histopathology of liver also showed that administration of DAS significantly reduced the damage generated by HgCl The present study suggests that DAS shows antioxidant activity and plays a protective role against mercury-induced oxidative damage in the rat livers.
本研究旨在评估二烯丙基硫醚(DAS)对氯化汞(HgCl)诱导的大鼠肝脏氧化应激的影响。将大鼠随机分为四组,每组六只,通过腹腔注射给予HgCl(50 mg/kg体重(b.w.))和/或通过灌胃给予DAS(200 mg/kg/b.w.)。给予HgCl会提高丙氨酸转氨酶(AST)和天冬氨酸转氨酶(ALT)水平(p < 0.05),同时超氧化物歧化酶(SOD)、过氧化氢酶(CAT)和谷胱甘肽过氧化物酶(GSH-Px)水平降低。然而,用DAS治疗可显著减轻HgCl诱导的肝脏生化改变和血清转氨酶(AST和ALT;p < 0.05)。此外,与HgCl中毒大鼠相比,组织病理学变化证实了生化结果。肝脏组织病理学还显示,给予DAS可显著减少HgCl产生的损伤。本研究表明,DAS具有抗氧化活性,对汞诱导的大鼠肝脏氧化损伤起到保护作用。