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百草枯研究:限制其毒性的最新进展是否使其使用更安全?

Paraquat research: do recent advances in limiting its toxicity make its use safer?

机构信息

REQUIMTE, Laboratory of Toxicology, Department of Biological Sciences, Faculty of Pharmacy, University of Porto, Portugal.

出版信息

Br J Pharmacol. 2013 Jan;168(1):44-5. doi: 10.1111/j.1476-5381.2012.02017.x.

Abstract

The use of the herbicide paraquat (1,1'-dimethyl-4,4'-bipyridylium dichloride; PQ) has been fiercely challenged due to its severe acute toxicity, putative neurotoxicity after long-term exposure and lack of antidotes. Breakthrough research on PQ is therefore required for an effective risk control and to allow a safer use of PQ in the future. The silencing or inhibition of quinone oxidoreductase 2, a NAD(P)H-independent flavoenzyme, was shown to significantly attenuate PQ toxicity in vitro, in primary pneumocytes and astroglial U373 cells, and to strongly antagonize PQ-induced systemic toxicity and animal mortality. The novel results reported in this issue of BJP, added to recent findings using sodium salicylate and lysine acetylsalicylate, in which full survival of PQ-intoxicated rats was also achieved, open the door for new preventative and therapeutic strategies that may lead to safer use of this effective pesticide.

摘要

由于百草枯(1,1'-二甲基-4,4'-联吡啶二氯化物;PQ)具有严重的急性毒性、长期暴露后的潜在神经毒性以及缺乏解毒剂,其使用受到了强烈的质疑。因此,需要在百草枯方面取得突破性的研究进展,以实现有效的风险控制,并允许未来更安全地使用百草枯。研究表明,醌氧化还原酶 2(一种 NAD(P)H 非依赖性黄素酶)的沉默或抑制可显著减轻体外、原代肺细胞和星形胶质细胞 U373 细胞中的百草枯毒性,并强烈拮抗百草枯引起的全身毒性和动物死亡率。本研究在 BJP 发表的新发现,加上最近使用水杨酸钠和赖氨酸乙酰水杨酸钠的研究结果,其中也实现了百草枯中毒大鼠的全部存活,为新的预防和治疗策略打开了大门,这些策略可能会导致更安全地使用这种有效的农药。

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