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[内皮细胞对平滑肌张力调节的意义——内皮舒张因子的形成]

[Significance of endothelial cells for the regulation of the tone of smooth muscle--formation of an endothelial, relaxing factor].

作者信息

Förstermann U

出版信息

Z Kardiol. 1986 Oct;75(10):577-83.

PMID:2878541
Abstract

Vascular endothelium is not only a mechanical, non-thrombogenetic barrier in the blood vessel wall, but probably plays a substantial role in the regulation of vascular smooth muscle tone. Besides the ability to metabolize vasoactive compounds like catecholamines and angiotensins, endothelial cells possess an active biochemical machinery for the production of vasoactive compounds (e.g. prostacyclin). During recent years it has become apparent that a large variety of vasodilator compounds require intact endothelial cells to exert their relaxing action. These endothelium-dependent relaxations are not mediated by prostacyclin of endothelial origin, but by an unknown substance that is referred to as endothelium-derived relaxing factor (EDRF). EDRF is a chemically unstable humoral substance and has a biological half-life in the range of seconds. Although EDRF is not a prostaglandin or leukotriene, several findings suggest possible relationships of its production with the eicosanoid system. Both stimulation of phospholipase A2 and inhibition of lysolecithin acyltransferase induce the production of EDRF. This suggests that cleavage of phospholipids may be an important step in the formation of EDRF. EDRF-mediated vascular relaxations (like relaxations induced by nitrovasodilators) were found to be associated with increases in cyclic GMP in vascular smooth muscle. Endothelial cells produce a factor that directly stimulates the enzymatic activity of soluble guanylate cyclase. Several points of evidence indicate that this factor may be identical with EDRF. Thus the mechanism of action of the EDRF formed endogenously may be similar to that of nitrovasodilators.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

血管内皮不仅是血管壁中的机械性、非血栓形成屏障,而且可能在调节血管平滑肌张力方面发挥重要作用。除了能够代谢儿茶酚胺和血管紧张素等血管活性化合物外,内皮细胞还拥有用于产生血管活性化合物(如前列环素)的活跃生化机制。近年来,很明显,多种血管舒张化合物需要完整的内皮细胞才能发挥其舒张作用。这些内皮依赖性舒张不是由内皮源性前列环素介导的,而是由一种未知物质介导的,这种物质被称为内皮衍生舒张因子(EDRF)。EDRF是一种化学性质不稳定的体液物质,其生物半衰期在数秒范围内。尽管EDRF不是前列腺素或白三烯,但一些研究结果表明其产生与类花生酸系统可能存在关系。磷脂酶A2的刺激和溶血卵磷脂酰基转移酶的抑制都会诱导EDRF的产生。这表明磷脂的裂解可能是EDRF形成的重要步骤。发现EDRF介导的血管舒张(如硝基血管舒张剂诱导的舒张)与血管平滑肌中环鸟苷酸的增加有关。内皮细胞产生一种直接刺激可溶性鸟苷酸环化酶酶活性的因子。几点证据表明该因子可能与EDRF相同。因此,内源性形成的EDRF的作用机制可能与硝基血管舒张剂的作用机制相似。(摘要截短至250字)

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