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青蒿素及其衍生物的抗疟机制与耐药状况

Antimalarial Mechanisms and Resistance Status of Artemisinin and Its Derivatives.

作者信息

Zheng Dan, Liu Tingting, Yu Shasha, Liu Zhilong, Wang Jing, Wang Ying

机构信息

Department of Tropical Medicine, College of Military Preventive Medicine, Army Medical University, Chongqing 400038, China.

School of Public Health, The Key Laboratory of Environmental Pollution Monitoring and Disease Control, Ministry of Education, Guizhou Medical University, Guiyang 561113, China.

出版信息

Trop Med Infect Dis. 2024 Sep 20;9(9):223. doi: 10.3390/tropicalmed9090223.

Abstract

Artemisinin is an endoperoxide sesquiterpene lactone isolated from and is often used to treat malaria. Artemisinin's peroxide bridge is the key structure behind its antimalarial action. Scientists have created dihydroartemisinin, artemether, artesunate, and other derivatives preserving artemisinin's peroxide bridge to increase its clinical utility value. Artemisinin compounds exhibit excellent efficacy, quick action, and minimal toxicity in malaria treatment and have greatly contributed to malaria control. With the wide and unreasonable application of artemisinin-based medicines, malaria parasites have developed artemisinin resistance, making malaria prevention and control increasingly challenging. Artemisinin-resistant strains have been found in many countries and regions. The mechanisms of antimalarials and artemisinin resistance are not well understood, making malaria prevention and control a serious challenge. Understanding the antimalarial and resistance mechanisms of artemisinin drugs helps develop novel antimalarials and guides the rational application of antimalarials to avoid the spread of resistance, which is conducive to malaria control and elimination efforts. This review will discuss the antimalarial mechanisms and resistance status of artemisinin and its derivatives, which will provide a reference for avoiding drug resistance and the research and development of new antimalarial drugs.

摘要

青蒿素是一种从植物中分离出来的内过氧化物倍半萜内酯,常用于治疗疟疾。青蒿素的过氧化物桥是其抗疟作用的关键结构。科学家们已研制出双氢青蒿素、蒿甲醚、青蒿琥酯等保留青蒿素过氧化物桥的衍生物,以提高其临床应用价值。青蒿素类化合物在疟疾治疗中显示出优异的疗效、快速的作用和最小的毒性,为疟疾控制做出了巨大贡献。随着以青蒿素为基础的药物的广泛不合理应用,疟原虫已产生青蒿素耐药性,使得疟疾防控日益具有挑战性。在许多国家和地区都发现了对青蒿素耐药的疟原虫株。抗疟药物及青蒿素耐药性的机制尚未完全明确,这使得疟疾防控成为一项严峻的挑战。了解青蒿素类药物的抗疟及耐药机制有助于开发新型抗疟药物,并指导抗疟药物的合理应用以避免耐药性的传播,这有利于疟疾控制和消除工作。本综述将讨论青蒿素及其衍生物的抗疟机制和耐药现状,这将为避免耐药性及新型抗疟药物的研发提供参考。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bfa5/11435542/6138fb3b3744/tropicalmed-09-00223-g001.jpg

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