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内皮细胞作为动脉血管舒张的介质。

Endothelial cells as mediators of vasodilation of arteries.

作者信息

Furchgott R F, Cherry P D, Zawadzki J V, Jothianandan D

出版信息

J Cardiovasc Pharmacol. 1984;6 Suppl 2:S336-43. doi: 10.1097/00005344-198406002-00008.

Abstract

A brief review is first presented of findings during the past few years by the authors and by others on the nonprostaglandin endothelium-dependent relaxation of isolated arteries by a large number of vasoactive agents. Among these agents are acetylcholine (ACh); the calcium ionophore A23187; ATP and ADP; substance P; bradykinin (canine, human, and porcine arteries); histamine, acting via an H1-receptor (rat arteries); thrombin (canine arteries); serotonin (canine coronary artery); and norepinephrine, acting via an alpha2-receptor (canine coronary artery). The endothelium-derived relaxing factor (EDRF) released by ACh and other agents has not yet been identified. Our original hypothesis that arachidonic acid is the precursor of EDRF is not supported by the finding that other unsaturated fatty acids in addition to arachidonic acid, and even stearic acid, elicited nonprostaglandin endothelium-dependent relaxations. Methylene blue and hemoglobin (but not methemoglobin) rapidly inhibited relaxation of rabbit aorta by ACh or A23187, suggesting that our proposal that EDRF is a labile free radical may be correct. The endothelium-dependent relaxation by each of these agents was shown to be preceded by an endothelium-dependent increase in cyclic GMP in the smooth muscle--a finding consistent with the hypothesis that EDRF stimulates guanylate cyclase in the muscle, leading to an increase in cyclic GMP that somehow activates relaxation. Some questions relating to the potential physiological important of endothelium-dependent relaxations are discussed.

摘要

首先简要回顾一下作者及其他研究人员在过去几年中关于大量血管活性药物对离体动脉非前列腺素内皮依赖性舒张作用的研究结果。这些药物包括乙酰胆碱(ACh);钙离子载体A23187;ATP和ADP;P物质;缓激肽(犬、人及猪动脉);通过H1受体起作用的组胺(大鼠动脉);凝血酶(犬动脉);5-羟色胺(犬冠状动脉);以及通过α2受体起作用的去甲肾上腺素(犬冠状动脉)。由ACh和其他药物释放的内皮源性舒张因子(EDRF)尚未得到鉴定。我们最初提出的花生四烯酸是EDRF前体的假设,并未得到以下研究结果的支持:除花生四烯酸外,其他不饱和脂肪酸甚至硬脂酸也能引发非前列腺素内皮依赖性舒张。亚甲蓝和血红蛋白(而非高铁血红蛋白)能迅速抑制ACh或A23187引起的兔主动脉舒张,这表明我们提出的EDRF是一种不稳定自由基的观点可能是正确的。研究表明,这些药物中的每一种引起的内皮依赖性舒张之前,平滑肌中内皮依赖性环鸟苷酸(cGMP)都会增加——这一发现与EDRF刺激肌肉中的鸟苷酸环化酶,导致cGMP增加并以某种方式激活舒张的假设一致。文中还讨论了一些与内皮依赖性舒张潜在生理重要性相关的问题。

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