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生物活化在青蒿素类抗疟药药理学和毒理学中的作用。

The role of bioactivation in the pharmacology and toxicology of the artemisinin-based antimalarials.

作者信息

Mercer Amy E

机构信息

MRC Centre for Drug Safety Science, The Department of Pharmacology and Therapeutics, The University of Liverpool, UK.

出版信息

Curr Opin Drug Discov Devel. 2009 Jan;12(1):125-32.

Abstract

Artemisinin and artemisinin-based antimalarials are currently recommended as the frontline antimalarial treatment, with over 100 million courses administered annually. Despite possessing excellent therapeutic activity and tolerability, neurotoxicity and embryotoxicity have been reported in cross-species animal models. The endoperoxide group contained within the artemisinins is essential for pharmacologic and toxicological activity and it is hypothesized that its bioactivation to toxic C-centered radical species is the mechanistic basis for activity. The chemical nature of this activation and the ultimate toxic species remain controversial and this review will focus upon studies published on this topic over the past year. Furthermore, the possibility of chemical dissociation of pharmacology and toxicology in novel artemisinins will be discussed.

摘要

青蒿素及以青蒿素为基础的抗疟药物目前被推荐作为一线抗疟治疗药物,每年有超过1亿疗程的药物被使用。尽管具有出色的治疗活性和耐受性,但在跨物种动物模型中已报道有神经毒性和胚胎毒性。青蒿素中含有的内过氧化物基团对于药理和毒理活性至关重要,据推测其生物活化为有毒的碳中心自由基物种是活性的机制基础。这种活化的化学性质以及最终的有毒物种仍存在争议,本综述将聚焦于过去一年中关于该主题发表的研究。此外,还将讨论新型青蒿素中药理学和毒理学化学解离的可能性。

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