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P物质、神经激肽A和降钙素基因相关肽在人体皮肤中的作用及其与感觉神经介导反应的关系。

Effects of substance P, neurokinin A and calcitonin gene-related peptide in human skin and their involvement in sensory nerve-mediated responses.

作者信息

Wallengren J, Håkanson R

机构信息

Department of Dermatology, Malmö, Sweden.

出版信息

Eur J Pharmacol. 1987 Nov 10;143(2):267-73. doi: 10.1016/0014-2999(87)90542-5.

Abstract

The effects evoked by intradermal injections of substance P (SP), neurokinin A (NKA) or calcitonin gene-related peptide (CGRP) were studied in 51 non-atopic subjects. SP and NKA produced flare and weal, and CGRP produced an indurated erythema. The reactions to SP were strong, the flare being maximal 3-5 min after injection and the weal after 10-15 min. NKA evoked a much weaker flare and a slightly weaker weal than did SP. CGRP produced a prominent long-lasting, indurated erythema with pseudopodia surrounded by a pallor edge. The mode of action of the three peptides was studied by pretreatment of the skin with the histamine-releasing compound 48/80, the H1-antagonist mepyramine or the local anesthetic xylocaine. The results suggest that mast-cell histamine and an intact sensory nerve supply are essential for the flare response to both SP and NKA. The weal response to SP was somewhat reduced by pretreatment with either 48/80 or xylocaine. The weal response to NKA, however, did not seem to depend upon either mast cells or sensory nerve fibres. The erythema evoked by CGRP was not suppressed by pretreatment with xylocaine, compound 48/80 or mepyramine, suggesting a direct action of CGRP on the blood vessels. The interaction between SP and CGRP was studied in subjects receiving a low dose of CGRP and increasing doses of SP or a low dose of SP and increasing doses of CGRP. CGRP did not potentiate the SP-evoked flare and weal and SP did not seem to enhance the response to CGRP.

摘要

在51名非特应性受试者中研究了皮内注射P物质(SP)、神经激肽A(NKA)或降钙素基因相关肽(CGRP)所引起的效应。SP和NKA产生风团和潮红,而CGRP产生硬结性红斑。对SP的反应强烈,注射后3 - 5分钟潮红达到最大,10 - 15分钟后风团达到最大。NKA引起的潮红比SP弱得多,风团也稍弱。CGRP产生显著的持久硬结性红斑,有伪足并被苍白边缘环绕。通过用组胺释放化合物48/80、H1拮抗剂美吡拉敏或局部麻醉药利多卡因对皮肤进行预处理,研究了这三种肽的作用方式。结果表明,肥大细胞组胺和完整的感觉神经供应对于对SP和NKA的潮红反应至关重要。用48/80或利多卡因预处理可使对SP的风团反应有所减弱。然而,对NKA的风团反应似乎不依赖于肥大细胞或感觉神经纤维。利多卡因、化合物48/80或美吡拉敏预处理均未抑制CGRP引起的红斑,提示CGRP对血管有直接作用。在接受低剂量CGRP并递增剂量SP或低剂量SP并递增剂量CGRP的受试者中研究了SP与CGRP之间的相互作用。CGRP未增强SP引起的潮红和风团,SP似乎也未增强对CGRP的反应。

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