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吉比林波尔B的合成类似物在……中诱导生物能量损伤和钙失衡。

Synthetic Analogues of Gibbilimbol B Induce Bioenergetic Damage and Calcium Imbalance in .

作者信息

Amaral Maiara, Varela Marina T, Kant Ravi, Christodoulides Myron, Fernandes João Paulo S, Tempone Andre G

机构信息

Instituto de Medicina Tropical, Faculdade de Medicina, Universidade de São Paulo, São Paulo 05403-000, Brazil.

Centre for Parasitology and Mycology, Instituto Adolfo Lutz, São Paulo 01246-000, Brazil.

出版信息

Life (Basel). 2023 Feb 28;13(3):663. doi: 10.3390/life13030663.

Abstract

Chagas disease is an endemic tropical disease caused by the protozoan , which affects around 7 million people worldwide, mostly in development countries. The treatment relies on only two available drugs, with severe adverse effects and a limited efficacy. Therefore, the search for new therapies is a legitimate need. Within this context, our group reported the anti- activity of gibbilimbol B, a natural alkylphenol isolated from the plant . Two synthetic derivatives, LINS03018 (1) and LINS03024 (2), demonstrated a higher antiparasitic potency and were selected for mechanism of action investigations. Our studies revealed no alterations in the plasma membrane potential, but a rapid alkalinization of the acidocalcisomes. Nevertheless, compound 1 exhibit a pronounced effect in the bioenergetics metabolism, with a mitochondrial impairment and consequent decrease in ATP and reactive oxygen species (ROS) levels. Compound 2 only depolarized the mitochondrial membrane potential, with no interferences in the respiratory chain. Additionally, no macrophages response of nitric oxide (NO) was observed in both compounds. Noteworthy, simple structure modifications in these derivatives induced significant differences in their lethal effects. Thus, this work reinforces the importance of the mechanism of action investigations at the early phases of drug discovery and support further developments of the series.

摘要

恰加斯病是一种由原生动物引起的地方性热带疾病,全球约有700万人受其影响,主要分布在发展中国家。治疗该病仅依赖两种现有药物,它们具有严重的副作用且疗效有限。因此,寻找新的治疗方法是合理的需求。在此背景下,我们团队报道了从植物中分离出的天然烷基酚吉比林酚B的抗[此处原文缺失相关寄生虫名称]活性。两种合成衍生物LINS03018(1)和LINS03024(2)表现出更高的抗寄生虫效力,并被选用于作用机制研究。我们的研究表明,质膜电位没有变化,但酸性钙小体迅速碱化。然而,化合物1对生物能量代谢有显著影响,导致线粒体损伤,进而使ATP和活性氧(ROS)水平降低。化合物2仅使线粒体膜电位去极化,对呼吸链没有干扰。此外,两种化合物均未观察到巨噬细胞产生一氧化氮(NO)的反应。值得注意的是,这些衍生物的简单结构修饰导致其致死效应存在显著差异。因此,这项工作强化了在药物发现早期进行作用机制研究的重要性,并为该系列药物的进一步开发提供了支持。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf84/10052702/9ef903b3117b/life-13-00663-g001.jpg

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