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定量评估通过谷胱甘肽(GSH)途径对SD大鼠肝毒性微囊藻毒素-LR的解毒作用。

Quantitatively evaluating detoxification of the hepatotoxic microcystin-LR through the glutathione (GSH) pathway in SD rats.

作者信息

Guo Xiaochun, Chen Liang, Chen Jun, Xie Ping, Li Shangchun, He Jun, Li Wei, Fan Huihui, Yu Dezhao, Zeng Cheng

机构信息

College of Fisheries, Huazhong Agricultural University, Wuhan, 430070, Hubei, China.

Donghu Experimental Station of Lake Ecosystems, State Key Laboratory of Freshwater Ecology and Biotechnology, Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan, 430072, Hubei, China.

出版信息

Environ Sci Pollut Res Int. 2015 Dec;22(23):19273-84. doi: 10.1007/s11356-015-5531-2. Epub 2015 Oct 21.

Abstract

Glutathione (GSH) plays crucial roles in antioxidant defense and detoxification metabolism of microcystin-LR (MC-LR). However, the detoxification process of MC-LR in mammals remains largely unknown. This paper, for the first time, quantitatively analyzes MC-LR and its GSH pathway metabolites (MC-LR-GSH and MC-LR-Cys) in the liver of Sprague-Dawley (SD) rat after MC-LR exposure. Rats received intraperitoneal (i.p.) injection of 0.25 and 0.5 lethal dose 50 (LD50) of MC-LR with or without pretreatment of buthionine-(S,R)-sulfoximine (BSO), an inhibitor of GSH synthesis. The contents of MC-LR-GSH were relatively low during the experiment; however, the ratio of MC-LR-Cys to MC-LR reached as high as 6.65 in 0.5 LD50 group. These results demonstrated that MC-LR-GSH could be converted to MC-LR-Cys efficiently, and this metabolic rule was in agreement with the data of aquatic animals previously reported. MC-LR contents were much higher in BSO + MC-LR-treated groups than in the single MC-LR-treated groups. Moreover, the ratio of MC-LR-Cys to MC-LR decreased significantly after BSO pretreatment, suggesting that the depletion of GSH induced by BSO reduced the detoxification of MCs. Moreover, MC-LR remarkably induced liver damage, and the effects were more pronounced in BSO pretreatment groups. In conclusion, this study verifies the role of GSH in the detoxification of MC-LR and furthers our understanding of the biochemical mechanism for SD rats to counteract toxic cyanobacteria.

摘要

谷胱甘肽(GSH)在微囊藻毒素-LR(MC-LR)的抗氧化防御和解毒代谢中发挥着关键作用。然而,MC-LR在哺乳动物体内的解毒过程仍 largely未知。本文首次对MC-LR暴露后Sprague-Dawley(SD)大鼠肝脏中的MC-LR及其GSH途径代谢产物(MC-LR-GSH和MC-LR-Cys)进行了定量分析。大鼠腹腔注射0.25和0.5致死剂量50(LD50)的MC-LR,同时给予或不给予谷胱甘肽合成抑制剂丁硫氨酸-(S,R)-亚砜胺(BSO)预处理。实验过程中MC-LR-GSH的含量相对较低;然而,在0.5 LD50组中,MC-LR-Cys与MC-LR的比值高达6.65。这些结果表明,MC-LR-GSH可以有效地转化为MC-LR-Cys,并且这种代谢规律与先前报道的水生动物数据一致。BSO+MC-LR处理组中的MC-LR含量远高于单一MC-LR处理组。此外,BSO预处理后,MC-LR-Cys与MC-LR的比值显著降低,表明BSO诱导的GSH耗竭降低了MCs的解毒作用。此外,MC-LR显著诱导肝脏损伤,并且在BSO预处理组中这种作用更为明显。总之,本研究验证了GSH在MC-LR解毒中的作用,并进一步加深了我们对SD大鼠对抗有毒蓝藻的生化机制的理解。

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