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吡嗪酰胺:揭示分枝杆菌作用机制的重要性。

Pyrazinamide: the importance of uncovering the mechanisms of action in mycobacteria.

机构信息

LIONEX Diagnostics and Therapeutics GmbH, Salzdahlumer Straße 196, D-38126, Braunschweig, Germany.

出版信息

Expert Rev Anti Infect Ther. 2015 May;13(5):593-603. doi: 10.1586/14787210.2015.1021784. Epub 2015 Mar 6.

Abstract

Pyrazinamide (PZA) is still one of the key drugs used in current therapeutic regimens for tuberculosis (TB). Despite its importance for TB therapy, the mode of action of PZA remains unknown. PZA has to be converted to its active form pyrazinoic acid (POA) by the nicotinamidase PncA and is then excreted by an unknown efflux pump. At acidic conditions, POA is protonated to HPOA and is reabsorbed into the cell where it causes cellular damage. For a long time, it has been thought that PZA/POA has no defined target of action, but recent studies have shown that both PZA and POA have several different targets interfering with diverse biochemical pathways, especially in the NAD(+) and energy metabolism. PZA resistance seems to depend not only on a defective pyrazinamidase but is also rather a result of the interplay of many different enzyme targets and transport mechanisms.

摘要

吡嗪酰胺(PZA)仍然是目前结核病(TB)治疗方案中使用的关键药物之一。尽管它对结核病治疗很重要,但 PZA 的作用模式仍不清楚。PZA 必须由烟酰胺酶 PncA 转化为其活性形式吡嗪酸(POA),然后通过未知的外排泵排出。在酸性条件下,POA 质子化形成 HPOA 并被重新吸收到细胞内,从而导致细胞损伤。长期以来,人们一直认为 PZA/POA 没有明确的作用靶点,但最近的研究表明,PZA 和 POA 都有几个不同的靶点,干扰多种生化途径,特别是在 NAD(+)和能量代谢中。PZA 耐药似乎不仅取决于缺陷的吡嗪酰胺酶,而且还是许多不同的酶靶点和转运机制相互作用的结果。

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