Centre Suisse de Recherches Scientifiques en Côte d'Ivoire, 01 BP 1303, Abidjan 01, Côte d'Ivoire.
Trends Parasitol. 2011 Feb;27(2):73-81. doi: 10.1016/j.pt.2010.11.006. Epub 2010 Dec 18.
Artemisinins are efficacious antimalarial drugs widely employed as first-line treatment in endemic countries under the form of combined therapies. Different molecular modes of action have been postulated to explain the parasiticidal effect of these compounds; however, none has been unequivocally accepted, and their physiological relevance is still questioned. Similarly, no definite genetic determinant of Plasmodium sensitivity to artemisinins has been identified so far. A better understanding of the mode of action of artemisinins and the genetic basis of laboratory-induced or field-observed altered susceptibility is crucial for malaria control. In this review different models of artemisinins' molecular action are briefly presented, focusing on recent advances, and the evidence of potential association between various gene polymorphisms and artemisinin resistance is comprehensively reviewed.
青蒿素是一种有效的抗疟药物,在流行地区广泛用作联合疗法的一线治疗药物。已经提出了不同的分子作用模式来解释这些化合物的杀虫作用;然而,没有一种模式被明确接受,它们的生理相关性仍存在疑问。同样,到目前为止,也没有确定的遗传决定因素表明疟原虫对青蒿素的敏感性。更好地了解青蒿素的作用模式和实验室诱导或现场观察到的敏感性改变的遗传基础对于疟疾控制至关重要。在这篇综述中,简要介绍了青蒿素分子作用的不同模型,重点介绍了最新进展,并全面回顾了各种基因多态性与青蒿素耐药性之间潜在关联的证据。