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鉴定参与P物质诱导清醒大鼠心血管和行为反应的中枢速激肽受体亚类。

Identification of the central tachykinin receptor subclass involved in substance P-induced cardiovascular and behavioral responses in conscious rats.

作者信息

Itoi K, Tschöpe C, Jost N, Culman J, Lebrun C, Stauss B, Unger T

机构信息

Department of Pharmacology, University of Heidelberg, Germany.

出版信息

Eur J Pharmacol. 1992 Sep 4;219(3):435-44. doi: 10.1016/0014-2999(92)90485-m.

DOI:10.1016/0014-2999(92)90485-m
PMID:1385176
Abstract

To identify the tachykinin receptor subclass involved in the central cardiovascular and behavioral actions of substance P (SP), we compared the central actions of SP with those of neurokinin A (NKA) and senktide in conscious chronically instrumented rats. Intracerebroventricular (i.c.v.) injection of SP (an NK1 agonist) and NKA (an NK2 agonist) increased mean arterial pressure (MAP) and heart rate (HR) dose dependently and these cardiovascular responses were associated with the behavioral responses, comprising excessive grooming and exploring. Both peptides were equipotent to produce the cardiovascular and the behavioral responses. Senktide (a highly selective NK-3 agonist), injected i.c.v. increased the HR markedly. The behavioral response, 'wet dog shakes', was observed most frequently after senktide and was dissociated from the HR response. Pretreatment with a peripheral NK-1-selective antagonist, L-668,169, attenuated the NKA-induced cardiovascular and behavioral responses but not the SP-induced responses. However, pretreatment with a peripheral NK-2-selective antagonists, L-659,877, attenuated the SP-induced responses but not the NKA-induced responses. These results suggest that the central cardiovascular and behavioral actions of SP and NKA are mediated by different subclasses of receptors and that the receptor subclasses which are specific for the central nervous system differ from those which mediate the peripheral actions of the two tachykinins.

摘要

为了确定参与P物质(SP)中枢心血管和行为作用的速激肽受体亚类,我们在有意识的慢性植入仪器的大鼠中比较了SP与神经激肽A(NKA)和senktide的中枢作用。脑室内(i.c.v.)注射SP(一种NK1激动剂)和NKA(一种NK2激动剂)剂量依赖性地增加平均动脉压(MAP)和心率(HR),并且这些心血管反应与行为反应相关,包括过度梳理和探索。两种肽产生心血管和行为反应的效力相当。脑室内注射senktide(一种高度选择性的NK-3激动剂)显著增加心率。在注射senktide后最常观察到“湿狗抖”的行为反应,并且该反应与心率反应分离。用外周NK-1选择性拮抗剂L-668,169预处理可减弱NKA诱导的心血管和行为反应,但不减弱SP诱导的反应。然而,用外周NK-2选择性拮抗剂L-659,877预处理可减弱SP诱导的反应,但不减弱NKA诱导的反应。这些结果表明,SP和NKA的中枢心血管和行为作用由不同的受体亚类介导,并且中枢神经系统特有的受体亚类与介导这两种速激肽外周作用的受体亚类不同。

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