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四氢生物蝶呤与内皮功能。

Tetrahydrobiopterin and endothelial function.

作者信息

Cosentino F, Lüscher T F

机构信息

University Hospital and Cardiovascular Research, Institute of Physiology, Zürich, Switzerland.

出版信息

Eur Heart J. 1998 Jul;19 Suppl G:G3-8.

PMID:9717048
Abstract

Tetrahydrobiopterin is an essential co-factor required for catalytic activity of nitric oxide synthases. A close link between tetrahydrobiopterin and nitric oxide synthesis has been recently demonstrated in a number of different cell types, including endothelial cells. The precise role of tetrahydrobiopterin in regulation of nitric oxide synthase activity is not completely understood; however, it may function as both an allosteric and redox co-factor. In peripheral and cerebral arteries, administration of tetrahydrobiopterin can stimulate production of nitric oxide. By contrast, in arteries depleted of tetrahydrobiopterin, nitric oxide production is impaired. Evidence indicates that, under certain pathological conditions, decreased availability of tetrahydrobiopterin may be responsible for a dysfunction of nitric oxide synthase leading to a shift in the balance between the production of protective nitric oxide and deleterious oxygen-derived free radicals. This concept may have important implications in understanding the mechanisms of endothelial dysfunction and oxidative vascular injury described in a number of vascular diseases, including atherosclerosis. This review will discuss the complex interaction between tetrahydrobiopterin and nitric oxide synthase and its role in the control of vascular tone.

摘要

四氢生物蝶呤是一氧化氮合酶催化活性所需的一种必需辅助因子。最近在包括内皮细胞在内的多种不同细胞类型中证实了四氢生物蝶呤与一氧化氮合成之间存在密切联系。四氢生物蝶呤在调节一氧化氮合酶活性中的精确作用尚未完全明确;然而,它可能同时作为变构和氧化还原辅助因子发挥作用。在外周动脉和脑动脉中,给予四氢生物蝶呤可刺激一氧化氮的产生。相比之下,在四氢生物蝶呤缺乏的动脉中,一氧化氮的产生受损。有证据表明,在某些病理条件下,四氢生物蝶呤可用性降低可能导致一氧化氮合酶功能障碍,进而导致保护性一氧化氮生成与有害氧衍生自由基生成之间的平衡发生改变。这一概念对于理解包括动脉粥样硬化在内的多种血管疾病中所描述的内皮功能障碍和氧化性血管损伤机制可能具有重要意义。本综述将讨论四氢生物蝶呤与一氧化氮合酶之间的复杂相互作用及其在控制血管张力中的作用。

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