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β-内啡肽(1-31)和强啡肽(1-13)可能参与了α-甲基多巴的中枢性降压作用机制。

Possible involvement of beta endorphin(1-31) and dynorphin(1-13) in the central hypotensive mechanism of action of alpha methyldopa.

作者信息

van Giersbergen P L, Wiegant V M, de Jong W

机构信息

Rudolf Magnus Institute for Pharmacology, Medical Faculty, State University of Utrecht, The Netherlands.

出版信息

Neuroendocrinology. 1989 Jan;49(1):71-9. doi: 10.1159/000125093.

Abstract

The present study was performed to gain more information on the nature of the opioid peptide(s) involved in the mechanism of action of alpha-methyldopa. Conscious, normotensive Wistar rats were used and all treatments were given intracisternally. For blood pressure and heart rate, pretreatment with a midportion beta-endorphin antiserum resulted in a parallel shift to the right of the dose-response curve for alpha-methyldopa. In addition, when rats were pretreated with various dilutions of this antiserum and treated with a constant dose of alpha-methyldopa, the antiserum dose-dependently inhibited alpha-methyldopa-induced hypotension and bradycardia. Using antisera specifically recognizing the C-terminus of beta-, gamma- and alpha-endorphin, respectively, revealed that only the beta-endorphin antiserum inhibited the decrease in blood pressure seen after administration of alpha-methyldopa. An antiserum against [Met5]enkephalin did not influence the cardiovascular responses following alpha-methyldopa. On the other hand, a dynorphin(1-13) antiserum also inhibited in a dose-dependent manner the hypotension induced by alpha-methyldopa. When administered 3 h after the injection of alpha-methyldopa, the beta-endorphin and dynorphin(1-13) antisera failed to reverse the hypotension induced by alpha-methyldopa. The results favor a role for beta-endorphin(1-31) and dynorphin(1-13) in the hypotension centrally mediated by alpha-methyldopa.

摘要

本研究旨在获取更多关于参与α-甲基多巴作用机制的阿片肽性质的信息。使用清醒的、血压正常的Wistar大鼠,所有处理均经脑池内给药。对于血压和心率,用中部β-内啡肽抗血清预处理导致α-甲基多巴剂量-反应曲线平行右移。此外,当用该抗血清的各种稀释液预处理大鼠并给予恒定剂量的α-甲基多巴时,抗血清剂量依赖性地抑制α-甲基多巴诱导的低血压和心动过缓。分别使用特异性识别β-、γ-和α-内啡肽C末端的抗血清,结果显示只有β-内啡肽抗血清能抑制给予α-甲基多巴后出现的血压下降。抗[Met5]脑啡肽抗血清对α-甲基多巴后的心血管反应没有影响。另一方面,强啡肽(1-13)抗血清也以剂量依赖性方式抑制α-甲基多巴诱导的低血压。在注射α-甲基多巴3小时后给予β-内啡肽和强啡肽(1-13)抗血清,未能逆转α-甲基多巴诱导的低血压。结果表明β-内啡肽(1-31)和强啡肽(1-13)在α-甲基多巴中枢介导的低血压中起作用。

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