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孤束核中神经肽Y的Y2受体介导降压反应。

Y2 receptors for neuropeptide Y in the nucleus of the solitary tract mediate depressor responses.

作者信息

Barraco R A, Ergene E, Dunbar J C, Ganduri Y L, Anderson G F

机构信息

Department of Physiology, Wayne State University, School of Medicine, Detroit, MI 48201.

出版信息

Peptides. 1991 Jul-Aug;12(4):691-8. doi: 10.1016/0196-9781(91)90121-5.

Abstract

In anesthetized, spontaneously breathing rats, microinjections of selective agonists of neuropeptide Y (NPY) receptor subtypes were made into the medial region of the caudal nucleus of the solitary tract (NTS) at the level of the area postrema. This region of the rat NTS exhibits very high densities of NPY binding sites. Microinjections of the long C-terminal NPY fragment, NPY(13-36), a selective agonist at Y2 receptors, into the caudal NTS elicited pronounced, dose-related reductions in blood pressure and respiratory minute volume. Moreover, the specific pattern of cardiorespiratory responses elicited by NPY(13-36) was remarkably similar, over approximately the same dosage range, with the cardiorespiratory response pattern elicited by intact NPY. In contrast to the potent NTS-mediated responses evoked by NPY(13-36), similar microinjections conducted with either NPY(26-36), an inactive C-terminal NPY fragment, or [Leu31,Pro34]NPY, a NPY analog with specific agonist properties at Y1 receptors, into the same caudal NTS sites did not appreciably affect cardiorespiratory parameters even at 10-20-fold higher dosages. The present results with selective agonists for NPY receptor subtypes suggest that the depressor responses and reductions in minute volume elicited by microinjections of intact NPY and NPY(13-36) were mediated by Y2 receptors in the caudal NTS, likely distributed at presynaptic sites in the medial region of the subpostremal NTS.

摘要

在麻醉状态下自主呼吸的大鼠中,将神经肽Y(NPY)受体亚型的选择性激动剂微量注射到最后区水平的孤束核尾侧核的内侧区域。大鼠孤束核的这个区域显示出非常高的NPY结合位点密度。将长C末端NPY片段NPY(13 - 36)(一种Y2受体的选择性激动剂)微量注射到尾侧孤束核中,可引起血压和呼吸分钟量显著的、剂量相关的降低。此外,在大约相同的剂量范围内,NPY(13 - 36)引发的心肺反应的特定模式与完整NPY引发的心肺反应模式非常相似。与NPY(13 - 36)引起的强大的孤束核介导的反应相反,将无活性的C末端NPY片段NPY(26 - 36)或在Y1受体具有特定激动剂特性的NPY类似物[Leu31,Pro34]NPY微量注射到相同的尾侧孤束核部位,即使在高10 - 20倍的剂量下,也不会明显影响心肺参数。目前使用NPY受体亚型选择性激动剂的结果表明,完整NPY和NPY(13 - 36)微量注射引起的降压反应和分钟量减少是由尾侧孤束核中的Y2受体介导的,可能分布在最后区下核内侧区域的突触前部位。

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