THE CALCITONIN-GENE-RELATED PEPTIDE ANTAGONIST CGRP(8-37) INCREASES THE LATENCY TO WITHDRAWAL RESPONSES IN RATS

被引:63
作者
YU, LC
HANSSON, P
LUNDEBERG, T
机构
[1] KAROLINSKA INST, DEPT REHABIL MED, NEUROGEN PAIN UNIT, S-17176 STOCKHOLM, SWEDEN
[2] BEIJING MED UNIV, DEPT PHYSIOL, BEIJING 100083, PEOPLES R CHINA
关键词
CALCITONIN GENE-RELATED PEPTIDE; CGRP(8-37); CGRP ANTAGONIST; CGRP RECEPTOR; SUBSTANCE P; HINDPAW WITHDRAWAL LATENCY; INTRATHECAL INJECTION;
D O I
10.1016/0006-8993(94)90393-X
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The present study explored the effects of calcitonin gene-related peptide (CGRP) and its antagonist CGRP(8-37) 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 CGRP(8-37), but not 1 nmol, induced a significant increase in hindpaw withdrawal latency. (3) Intrathecal administration of CGRP(8-37) 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 CGRP(8-37) has a possible antinociceptive effect, and CGRP receptors in the spinal cord may be involved.
引用
收藏
页码:223 / 230
页数:8
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