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气道中的肽受体。

Peptide receptors in the airways.

作者信息

Regoli D

机构信息

Department of Pharmacology, Medical School, University of Sherbrooke, Quebec, Canada.

出版信息

Am Rev Respir Dis. 1987 Dec;136(6 Pt 2):S35-9. doi: 10.1164/ajrccm/136.6_Pt_2.S35.

DOI:10.1164/ajrccm/136.6_Pt_2.S35
PMID:2446539
Abstract

Two categories of peptides exert opposing effects on the isolated guinea pig trachea. Neurokinins (substance P [SP] and congeners) provoke contraction, and kinins (bradykinin) provoke relaxation. Both peptide categories promote the release of relaxing prostaglandins that oppose the contractions induced by neurokinins and mediate entirely the relaxations by the kinins. Receptors for neurokinins have been characterized by comparing the effects of a variety of agonists (naturally occurring or synthetic peptides) in the guinea pig trachea and in other selective preparations. It has been found that the guinea pig trachea contains receptors for neurokinin A (NKA) and for substance P. This has been demonstrated by showing that selective activators of the neurokinin A receptor type are potent stimulants of contraction, and that selective stimulants of the receptors for SP are also active contractile agonists. The order of potency for the neurokinins is NKA greater than NKB greater than SP. The relaxations of guinea pig trachea provoked by bradykinin is not due to the activation of B1 or B2 receptors since it is not modified by specific B1 or B2 antagonists. It is suggested that bradykinin may promote the release of prostaglandins either through a third receptor or by an unknown mechanism. These studies show that the isolated guinea pig trachea is a complex preparation, composed of various tissues and containing different types of neurokinin receptors. The preparation also contains endogenous active agents (e.g., prostaglandins) that are released by the peptides and that may modify or partially or entirely mediate the biologic effects of peptides.

摘要

两类肽对分离的豚鼠气管产生相反的作用。神经激肽(P物质[SP]及其同类物)引起收缩,而激肽(缓激肽)引起舒张。这两类肽都能促进舒张性前列腺素的释放,这些前列腺素可对抗神经激肽引起的收缩,并完全介导激肽引起的舒张。通过比较多种激动剂(天然存在的或合成的肽)在豚鼠气管和其他选择性制剂中的作用,对神经激肽受体进行了表征。已发现豚鼠气管含有神经激肽A(NKA)受体和P物质受体。这已通过以下方式得到证明:表明神经激肽A受体类型的选择性激活剂是有效的收缩刺激剂,并且P物质受体的选择性刺激剂也是有活性的收缩激动剂。神经激肽的效力顺序为NKA大于NKB大于SP。缓激肽引起的豚鼠气管舒张不是由于B1或B2受体的激活,因为它不受特异性B1或B2拮抗剂的影响。有人提出缓激肽可能通过第三种受体或未知机制促进前列腺素的释放。这些研究表明,分离的豚鼠气管是一种复杂的制剂,由各种组织组成,含有不同类型的神经激肽受体。该制剂还含有内源性活性剂(例如前列腺素),这些活性剂由肽释放,并且可能改变或部分或完全介导肽的生物学效应。

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1
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Am Rev Respir Dis. 1987 Dec;136(6 Pt 2):S35-9. doi: 10.1164/ajrccm/136.6_Pt_2.S35.
2
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3
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8
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