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降钙素基因相关肽拮抗剂CGRP8 - 37可延长大鼠撤药反应的潜伏期。

The calcitonin gene-related peptide antagonist CGRP8-37 increases the latency to withdrawal responses in rats.

作者信息

Yu L C, Hansson P, Lundeberg T

机构信息

Department of Physiology and Pharmacology, Karolinska Institutet, Stockholm, Sweden.

出版信息

Brain Res. 1994 Aug 8;653(1-2):223-30. doi: 10.1016/0006-8993(94)90393-x.

Abstract

The present study explored the effects of calcitonin gene-related peptide (CGRP) and its antagonist CGRP8-37 on the latency to hindpaw withdrawal responses induced by both thermal and mechanical stimulation in rats. (1) Intrathecal injection of 10 nmol of CGRP had no effects on the latency to hindpaw withdrawal; intrathecal injection of 5 nmol of substance P (SP) decreased the latency to both withdrawal responses. (2) Intrathecal administration of 5 nmol or 10 nmol of CGRP8-37, but not 1 nmol, induced a significant increase in hindpaw withdrawal latency. (3) Intrathecal administration of CGRP8-37 not only reversed the SP-induced decrease in latency to both withdrawal responses but also mediated a significant increase in response latency compared to basal levels. The demonstrated results suggest that intrathecal administration of CGRP8-37 has a possible antinociceptive effect, and CGRP receptors in the spinal cord may be involved.

摘要

本研究探讨了降钙素基因相关肽(CGRP)及其拮抗剂CGRP8 - 37对大鼠热刺激和机械刺激诱发的后爪退缩反应潜伏期的影响。(1)鞘内注射10 nmol的CGRP对后爪退缩潜伏期无影响;鞘内注射5 nmol的P物质(SP)可缩短两种退缩反应的潜伏期。(2)鞘内给予5 nmol或10 nmol的CGRP8 - 37(而非1 nmol)可显著延长后爪退缩潜伏期。(3)鞘内给予CGRP8 - 37不仅可逆转SP诱导的两种退缩反应潜伏期缩短,而且与基础水平相比,还可介导反应潜伏期显著延长。研究结果表明,鞘内给予CGRP8 - 37可能具有抗伤害感受作用,脊髓中的CGRP受体可能参与其中。

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