Suppr超能文献

神经肽Y诱导大鼠肠系膜动脉床儿茶酚胺合成减弱。

Neuropeptide Y induced attenuation of catecholamine synthesis in the rat mesenteric arterial bed.

作者信息

Westfall Thomas C, Naes Linda, Gardner Alice, Yang Chun-Lian

机构信息

Department of Pharmacological and Physiological Science, Saint Louis University School of Medicine, St Louis, MO 63104, USA.

出版信息

J Cardiovasc Pharmacol. 2006 Jun;47(6):723-8. doi: 10.1097/01.fjc.0000211761.06271.15.

Abstract

The effect of neuropeptide Y (NPY) on the basal and nerve stimulation-induced increase in norepinephrine synthesis was studied in the isolated and perfused mesenteric arterial bed of the rat. Tyrosine hydroxylation, the rate-limiting step in catecholamine (CA) biosynthesis, was assessed by measuring the accumulation of DOPA in the perfusate/superfusate overflow after perfusion of the mesenteric arterial bed with the decarboxylase inhibitor m-hydroxybenzyl hydralazine (NSD-1015). Treatment with NDS-1015 resulted in a time-dependent increase in DOPA production and nerve stimulation (8 Hz, supramaximal voltage, 2 ms duration) increased DOPA production even further. NPY 1 to 100 nM was observed to produce a concentration-dependent attenuation in both the basal and nerve stimulation-induced increase in DOPA formation. To come to an understanding of the NPY receptor subtype mediating the inhibition of CA synthesis, the rank order of potency of a series of NPY analogs with varying selectivity for NPY receptor subtypes including intestinal polypeptide (PYY), PYY 13-36, Leu36 Pro34 NPY, human pancreatic polypeptide (h-PP), and rat pancreatic polypeptide (r-PP) were determined. In addition, the effect of various selective NPY antagonists on the inhibitory effect of NPY was also examined. These included the Y1 antagonist BIB03304, the Y2 antagonist BIIE0246, and the Y5 antagonist CGP71683. The IC50's for NPY, PYY, PYY13-36, Leu31 Pro34 NPY, and hPP in inhibiting CA synthesis were 5, 7, 15, 30, and 33 nM respectively. rPP failed to inhibit CA synthesis. All 3 of the NPY antagonists produced attenuation of the NPY-induced inhibition of CA synthesis, but it took a combination of all 3 to completely block the effect of a maximal inhibitory concentration of NPY. These results demonstrate that NPY inhibits CA synthesis in the perfused mesenteric arterial bed and can do so by activation of a variety of receptors including the Y1, Y2, and Y5.

摘要

在大鼠离体灌注肠系膜动脉床中,研究了神经肽Y(NPY)对基础状态及神经刺激诱导的去甲肾上腺素合成增加的影响。通过在肠系膜动脉床灌注脱羧酶抑制剂间羟基苄基肼(NSD - 1015)后,测量灌注液/超滤液溢流中多巴(DOPA)的蓄积,评估儿茶酚胺(CA)生物合成的限速步骤——酪氨酸羟化作用。用NSD - 1015处理导致DOPA生成呈时间依赖性增加,并且神经刺激(8 Hz,超最大电压,持续2 ms)使DOPA生成进一步增加。观察到1至100 nM的NPY对基础状态及神经刺激诱导的DOPA生成增加均产生浓度依赖性减弱作用。为了解介导CA合成抑制作用的NPY受体亚型,测定了一系列对NPY受体亚型具有不同选择性的NPY类似物的效价顺序,这些类似物包括肠肽(PYY)、PYY 13 - 36、Leu36 Pro34 NPY、人胰多肽(h - PP)和大鼠胰多肽(r - PP)。此外,还研究了各种选择性NPY拮抗剂对NPY抑制作用的影响。这些拮抗剂包括Y1拮抗剂BIB03304、Y2拮抗剂BIIE0246和Y5拮抗剂CGP71683。NPY、PYY、PYY13 - 36、Leu31 Pro34 NPY和hPP抑制CA合成的IC50分别为5、7、15、30和33 nM。rPP未能抑制CA合成。所有3种NPY拮抗剂均使NPY诱导的CA合成抑制作用减弱,但需要这3种拮抗剂联合使用才能完全阻断最大抑制浓度NPY的作用。这些结果表明,NPY在灌注的肠系膜动脉床中抑制CA合成,并且可以通过激活包括Y1、Y2和Y5在内的多种受体来实现。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验