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四氢生物蝶呤生物合成作为磺胺类药物的非靶标。

Tetrahydrobiopterin biosynthesis as an off-target of sulfa drugs.

机构信息

EPFL, Institute of Chemical Sciences and Engineering, Institute of Bioengineering, National Centre of Competence in Research in Chemical Biology, 1015 Lausanne, Switzerland.

出版信息

Science. 2013 May 24;340(6135):987-91. doi: 10.1126/science.1232972.

Abstract

The introduction of sulfa drugs for the chemotherapy of bacterial infections in 1935 revolutionized medicine. Although their mechanism of action is understood, the molecular bases for most of their side effects remain obscure. Here, we report that sulfamethoxazole and other sulfa drugs interfere with tetrahydrobiopterin biosynthesis through inhibition of sepiapterin reductase. Crystal structures of sepiapterin reductase with bound sulfa drugs reveal how structurally diverse sulfa drugs achieve specific inhibition of the enzyme. The effect of sulfa drugs on tetrahydrobiopterin-dependent neurotransmitter biosynthesis in cell-based assays provides a rationale for some of their central nervous system-related side effects, particularly in high-dose sulfamethoxazole therapy of Pneumocystis pneumonia. Our findings reveal an unexpected aspect of the pharmacology of sulfa drugs and might translate into their improved medical use.

摘要

1935 年,磺胺类药物被引入用于细菌性感染的化学疗法,这彻底改变了医学。尽管人们已经了解了它们的作用机制,但大多数副作用的分子基础仍不清楚。在这里,我们报告说,磺胺甲恶唑和其他磺胺类药物通过抑制蝶呤还原酶来干扰四氢生物蝶呤的生物合成。结合磺胺类药物的蝶呤还原酶的晶体结构揭示了结构多样的磺胺类药物如何特异性地抑制该酶。磺胺类药物在基于细胞的测定中对四氢生物蝶呤依赖性神经递质生物合成的影响为它们的一些中枢神经系统相关副作用提供了依据,特别是在高剂量磺胺甲恶唑治疗肺囊虫肺炎时。我们的发现揭示了磺胺类药物药理学的一个意外方面,这可能会转化为它们在医学上的更好应用。

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