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神经和药物诱导的兔主动脉中腺嘌呤核苷和核苷酸的释放。

Nerve and drug-induced release of adenine nucleosides and nucleotides from rabbit aorta.

作者信息

Sedaa K O, Bjur R A, Shinozuka K, Westfall D P

机构信息

Department of Pharmacology, University of Nevada School of Medicine, Reno.

出版信息

J Pharmacol Exp Ther. 1990 Mar;252(3):1060-7.

PMID:2319458
Abstract

The purpose of the present study was to assess the possible sites which contribute to the nerve stimulation- and alpha-agonist-induced overflow of endogenous adenine nucleosides and nucleotides in vascular tissue. Particular attention was focused on the endothelium because it is known that endothelial cells have a high concentration of ATP and its metabolites. Segments of rabbit thoracic aorta, some denuded of endothelial cells by rubbing the lumen of the vessel, were incubated in organ baths and subjected to transmural nerve stimulation or stimulated with the alpha-1 adrenoceptor agonist methoxamine. A portion of the bathing solution was processed for the determination of norepinephrine by high-performance liquid chromatography with electrochemical detection and a portion for determination of ATP, ADP, AMP and adenosine by high-performance liquid chromatography with fluorescence detection. Transmural stimulation led to a significant release of both norepinephrine and the adenine nucleosides and nucleotides in a ratio of 1 to 350. Removal of the endothelium did not change the release of norepinephrine but reduced the release of adenosine and its derivatives by 90%. Methoxamine also caused the release of adenosine and the adenine nucleotides which was reduced by 93% by removal of the endothelium. Thus, the endothelium seems to be a major source of transmural nerve stimulation and alpha-agonist induced overflow of adenosine and adenine nucleotides. The endothelium is not the exclusive source of these purine congeners, however. In the case of transmural stimulation there is approximately 10% of the total which is independent of the endothelium.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

本研究的目的是评估在血管组织中,可能导致神经刺激和α-激动剂诱导内源性腺嘌呤核苷和核苷酸外溢的部位。特别关注内皮,因为已知内皮细胞中ATP及其代谢产物浓度很高。将兔胸主动脉段(部分通过摩擦血管内腔去除内皮细胞)置于器官浴中,进行跨壁神经刺激或用α-1肾上腺素能受体激动剂甲氧明刺激。一部分浴液用高效液相色谱-电化学检测法测定去甲肾上腺素,一部分用高效液相色谱-荧光检测法测定ATP、ADP、AMP和腺苷。跨壁刺激导致去甲肾上腺素以及腺嘌呤核苷和核苷酸显著释放,其比例为1比350。去除内皮并未改变去甲肾上腺素的释放,但使腺苷及其衍生物的释放减少了90%。甲氧明也导致腺苷和腺嘌呤核苷酸的释放,去除内皮后释放减少了93%。因此,内皮似乎是跨壁神经刺激和α-激动剂诱导腺苷和腺嘌呤核苷酸外溢的主要来源。然而,内皮并非这些嘌呤类似物的唯一来源。在跨壁刺激的情况下,约10%的总量与内皮无关。(摘要截短于250字)

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