Khan M W, Priyamvada S, Khan S A, Khan S, Gangopadhyay A, Yusufi A N K
Department of Biochemistry, Faculty of Life Sciences, Aligarh Muslim University, Aligarh, Uttar Pradesh, India Cell Biology and Physiology Division, Council of Scientific and Industrial Research (CSIR)-Indian Institute of Chemical Biology, Jadavpur, Kolkata, West Bengal, India.
Department of Biochemistry, Faculty of Life Sciences, Aligarh Muslim University, Aligarh, Uttar Pradesh, India Department of Medicine, University of Illinois at Chicago, Chicago, IL, USA.
Hum Exp Toxicol. 2016 Mar;35(3):302-11. doi: 10.1177/0960327115586207. Epub 2015 May 10.
Sodium nitroprusside (SNP) is an antihypertensive drug with proven toxic effects attributed mainly to the production of nitric oxide (NO). Polyunsaturated fatty acids (PUFAs) are widely regarded as functional foods and have been shown to ameliorate the harmful effects of many toxicants. This study examined whether feeding of fish oil (FO)/flaxseed oil (FXO) would have any protective effect against SNP-induced hepatotoxicity and cell death. Male Wistar rats were fed either on normal diet or with 15% FO/FXO for 15 days, following which SNP (1.5 mg/kg body weight) was administered intraperitoneally for 7 days. Animals were killed after treatment, and livers were collected for further analysis. We observed that SNP significantly elevated tissue nitrite levels and lipid peroxidation (LPO) with concomitant perturbation in antioxidant defense systems accompanied with dysregulated glucose metabolism and pronounced cellular death. FO/FXO supplementation to SNP-treated rats caused reversal of tissue injury/cell death and markedly decreased LPO and improved antioxidant defense systems. FO/FXO appear to protect against SNP-induced hepatotoxicity by improving energy metabolism and antioxidant defense mechanism.
硝普钠(SNP)是一种降压药,已证实其毒性作用主要归因于一氧化氮(NO)的产生。多不饱和脂肪酸(PUFAs)被广泛认为是功能性食品,并已显示出可减轻许多毒物的有害影响。本研究考察了喂食鱼油(FO)/亚麻籽油(FXO)是否对SNP诱导的肝毒性和细胞死亡具有任何保护作用。雄性Wistar大鼠分别喂食正常饮食或含15% FO/FXO的饮食15天,之后腹腔注射SNP(1.5 mg/kg体重)7天。处理后处死动物,收集肝脏进行进一步分析。我们观察到,SNP显著提高了组织亚硝酸盐水平和脂质过氧化(LPO),同时抗氧化防御系统受到干扰,伴有葡萄糖代谢失调和明显的细胞死亡。给SNP处理的大鼠补充FO/FXO可导致组织损伤/细胞死亡的逆转,并显著降低LPO,改善抗氧化防御系统。FO/FXO似乎通过改善能量代谢和抗氧化防御机制来保护机体免受SNP诱导的肝毒性。