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吩噻嗪类药物作为抗结核药物:作用机制的见解与临床意义。

Phenothiazines as anti-tubercular agents: mechanistic insights and clinical implications.

机构信息

Post Graduate Institute of Medical Education & Research, Department of Biochemistry, Chandigarh-160012, India.

出版信息

Expert Opin Investig Drugs. 2011 Dec;20(12):1665-76. doi: 10.1517/13543784.2011.628657. Epub 2011 Oct 21.

Abstract

INTRODUCTION

Tuberculosis (TB) chemotherapy has been rendered ineffective by the emergence of multi-drug resistant (MDR), extensively drug resistant (XDR) and totally drug resistant strains reinforcing the need for the development of new drugs as a global health priority. Reconsidering phenothiazines for the improvement of TB chemotherapy seems to be a rational option especially in view of their role as inhibitors of type II NADH dehydrogenase, a key component of respiratory chain of Mycobacterium tuberculosis, thus raising the speculation that they can be effective against latent TB as well.

AREAS COVERED

This article offers a detailed description of the chemotherapeutic efficacy of phenothiazine compounds against susceptible, drug resistant and latent TB. Furthermore, their clinical implications and molecular mechanisms of action have been reviewed extensively.

EXPERT OPINION

Phenothiazines are currently being evaluated for the treatment of TB and have been shown to be effective against M. tuberculosis through a number of in vitro, ex vivo and in vivo studies. In addition, recent clinical studies have implicated their role in the treatment of MDR/XDR TB also. Therefore, phenothiazines, particularly thioridazine, hold great potential to be considered as safe and effective antimycobacterial agents in near future.

摘要

简介

结核病(TB)化疗因出现耐多药(MDR)、广泛耐药(XDR)和完全耐药菌株而失效,这凸显了将开发新药作为全球卫生重点的必要性。重新考虑吩噻嗪类药物在改善结核病化疗中的作用似乎是一个合理的选择,特别是考虑到它们作为 II 型 NADH 脱氢酶抑制剂的作用,NADH 脱氢酶是结核分枝杆菌呼吸链的关键组成部分,因此推测它们也可以有效对抗潜伏性结核病。

涵盖领域

本文详细描述了吩噻嗪类化合物对敏感、耐药和潜伏性结核病的化学治疗效果。此外,还广泛回顾了它们的临床意义和作用机制。

专家意见

吩噻嗪类药物目前正在评估用于治疗结核病,多项体外、离体和体内研究表明它们对结核分枝杆菌有效。此外,最近的临床研究表明,它们在治疗耐多药/广泛耐药结核病方面也有作用。因此,吩噻嗪类药物,特别是噻吨嗪,极有希望在不久的将来被视为安全有效的抗分枝杆菌药物。

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