Suppr超能文献

对不同阶段疟原虫包括引起复发的休眠子的抑制活性。

Artemisinin-independent inhibitory activity of sp. infusions against different stages including relapse-causing hypnozoites.

机构信息

Sorbonne Université, Institut National de la Santé et de la Recherche Médicale (INSERM), Centre National pour la Recherche Scientifique (CNRS), Centre d'Immunologie et des Maladies Infectieuses, CIMI, Paris, France.

Unité d'Epidémiologie Moléculaire du Paludisme, Institut Pasteur du Cambodge, Phnom Penh, Cambodia.

出版信息

Life Sci Alliance. 2021 Dec 2;5(3). doi: 10.26508/lsa.202101237. Print 2022 Mar.

Abstract

Artemisinin-based combination therapies (ACT) are the frontline treatments against malaria worldwide. Recently the use of traditional infusions from (from which artemisinin is obtained) or (lacking artemisinin) has been controversially advocated. Such unregulated plant-based remedies are strongly discouraged as they might constitute sub-optimal therapies and promote drug resistance. Here, we conducted the first comparative study of the anti-malarial effects of both plant infusions in vitro against the asexual erythrocytic stages of and the pre-erythrocytic (i.e., liver) stages of various species. Low concentrations of either infusion accounted for significant inhibitory activities across every parasite species and stage studied. We show that these antiplasmodial effects were essentially artemisinin-independent and were additionally monitored by observations of the parasite apicoplast and mitochondrion. In particular, the infusions significantly incapacitated sporozoites, and for and , disrupted the hypnozoites. This provides the first indication that compounds other than 8-aminoquinolines could be effective antimalarials against relapsing parasites. These observations advocate for further screening to uncover urgently needed novel antimalarial lead compounds.

摘要

青蒿素类复方疗法(ACT)是全球治疗疟疾的一线药物。最近,有人有争议地提倡使用传统的草药浸剂(从中提取青蒿素)或(缺乏青蒿素)。由于这些不受监管的植物性药物可能构成次优治疗方法并促进耐药性,因此强烈不鼓励使用。在这里,我们首次对这两种植物浸剂在体外对抗疟原虫无性红细胞期和各种疟原虫种的前红细胞(即肝)期的抗疟效果进行了比较研究。低浓度的浸剂对研究中的每一种寄生虫物种和阶段都具有显著的抑制活性。我们表明,这些抗疟效果基本上与青蒿素无关,并且通过观察寄生虫的类质体和线粒体得到了进一步的监测。特别是,这些浸剂显著地使孢子虫失活,并且对于 和 ,破坏了休眠子。这首次表明,除了 8-氨基喹啉类化合物之外,其他化合物可能是针对复发寄生虫的有效抗疟药物。这些观察结果主张进一步筛选以发现急需的新型抗疟先导化合物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f87d/8675911/442e4506841f/LSA-2021-01237_Fig1.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验