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熊果酸作为一种新型抗结核药物的前景:当前进展和挑战。

Promising Ursolic Acid as a Novel Antituberculosis Agent: Current Progress and Challenges.

机构信息

Department of Pharmacology and Clinical Pharmacy, Faculty of Pharmacy, Universitas Padjadjaran, Sumedang, 45363, Indonesia.

Center of Excellence in Higher Education for Pharmaceutical Care Innovation, Universitas Padjadjaran, Sumedang, 45363, Indonesia.

出版信息

Drug Des Devel Ther. 2024 May 31;18:1969-1979. doi: 10.2147/DDDT.S454399. eCollection 2024.

Abstract

Tuberculosis (TB) stands as the second most prevalent cause of global human mortality from infectious diseases. In 2022, the World Health Organization documented an estimated number of global TB cases reaching 7.5 million, which causes death for 1.13 million patients. The continuous growth of drug-resistant TB cases due to various mutations in the (MTB) strain, raises the urgency of the exploration of novel anti-TB treatments. Ursolic acid (UA) is a natural pentacyclic triterpene found in various plants that has shown potential as a novel anti-TB agent. This review aims to provide an overview of the therapeutic prospects of UA against MTB, with a particular emphasis on in silico, in vitro, and in vivo studies. Various mechanisms of action of UA against MTB are briefly recapped from in silico studies, such as enoyl acyl carrier protein reductase inhibitors, FadA5 (Acetyl-CoA acetyltransferase) inhibitors, tuberculosinyl adenosine transferase inhibitors, and small heat shock protein 16.3 inhibitor. The potential of UA to overcome drug resistance and its synergistic effects with existing antituberculosis drugs are briefly explained from in vitro studies using a variety of methods, such as Microplate Alamar Blue Assay, Mycobacteria Growth Indicator Tube 960 and Resazurin Assays, morphological change evaluation using transmission electron microscopy, and in vivo studies using BALB/C infected with multi drug resistant clinical isolates. Besides its promising mechanism as an antituberculosis drug, its complex chemical composition, limited availability and supply, and lack of intellectual property are also reviewed as those are the most frequently occurring challenges that need to be addressed for the successful development of UA as novel anti-TB agent.

摘要

结核病(TB)是全球传染病导致人类死亡的第二大主要原因。2022 年,世界卫生组织(WHO)记录了全球结核病病例估计数达到 750 万,导致 113 万患者死亡。由于结核分枝杆菌(MTB)菌株的各种突变导致耐药性结核病病例不断增加,迫切需要探索新的抗结核治疗方法。熊果酸(UA)是一种天然五环三萜,存在于各种植物中,具有作为新型抗结核药物的潜力。本综述旨在概述 UA 对 MTB 的治疗前景,特别强调计算机模拟、体外和体内研究。从计算机模拟研究中简要回顾了 UA 对 MTB 的各种作用机制,例如烯酰基辅酶 A 还原酶抑制剂、FadA5(乙酰辅酶 A 乙酰转移酶)抑制剂、结核酰基腺苷转移酶抑制剂和小热休克蛋白 16.3 抑制剂。从使用各种方法的体外研究中简要解释了 UA 克服耐药性的潜力及其与现有抗结核药物的协同作用,例如微量板 Alamar Blue 测定法、分枝杆菌生长指示剂管 960 和 Resazurin 测定法、使用透射电子显微镜进行形态变化评估,以及使用 BALB/C 感染多药耐药临床分离株的体内研究。除了作为抗结核药物的有前途的机制外,其复杂的化学成分、有限的可用性和供应以及缺乏知识产权也被审查,因为这些是成功开发 UA 作为新型抗结核药物所必需解决的最常见挑战。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/370a/11149632/94bfb09d85fd/DDDT-18-1969-g0001.jpg

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