Reproductive Biology and Toxicology Laboratory, UNESCO Satellite center of Trace Element Research & School of Studies in Zoology, Jiwaji University, Gwalior, (M.P.) 474011, India.
Environ Toxicol Pharmacol. 2010 Mar;29(2):97-103. doi: 10.1016/j.etap.2009.11.002. Epub 2009 Dec 31.
Mercury is one of the most toxic non-radioactive heavy metals. Chelation therapy has been the basis for the medical treatment of mercury poisoning. Male albino rats were administered dimethylmercury (1.5mg/kg) orally for 21 days. Chelation therapy with N-acetyl cysteine along with combination of antioxidants viz. zinc and selenium was given for 5 days after 24h of toxicant administration. All animals were sacrificed after 48h of last treatment and various blood biochemical parameters were performed. Toxicant caused rise in bilirubin, γ-GT, cholesterol, triglycerides, urea, creatinine, the uric acid content with a decline in albumin. A significant elevation was observed in LPO content and mercury concentration, along with concomitant decline in GSH levels after toxicant administration in liver, kidney and brain. Noticeable fall was also observed in AChE enzyme. Histopathological analysis was consistent with the biochemical observations and led to conclude that combination therapy provided protection against mercury toxicity.
汞是毒性最强的非放射性重金属之一。螯合疗法一直是治疗汞中毒的基础。雄性白化大鼠经口给予二甲基汞(1.5mg/kg),连续 21 天。在给予毒物后 24 小时,给予 N-乙酰半胱氨酸螯合治疗,并与抗氧化剂锌和硒联合使用,共 5 天。最后一次治疗后 48 小时,所有动物均被处死,并进行了各种血液生化参数检测。毒物导致胆红素、γ-GT、胆固醇、甘油三酯、尿素、肌酐、尿酸含量升高,白蛋白含量下降。在肝脏、肾脏和大脑中,毒物给药后 LPO 含量和汞浓度显著升高,同时 GSH 水平下降。AChE 酶也明显下降。组织病理学分析与生化观察结果一致,表明联合治疗可提供针对汞毒性的保护。