Peptidase inhibitors improve recovery of substance P and calcitonin gene-related peptide release from rat spinal cord slices

被引:35
作者
Chen, JJ
Barber, LA
Dymshitz, J
Vasko, MR
机构
[1] INDIANA UNIV, SCH MED, DEPT PHARMACOL & TOXICOL, INDIANAPOLIS, IN 46202 USA
[2] INDIANA UNIV, SCH MED, DEPT ANESTHESIA, INDIANAPOLIS, IN 46202 USA
关键词
substance P; calcitonin gene-related peptide; release; peptidase inhibitors; capsaicin; spinal cord slices;
D O I
10.1016/0196-9781(95)02091-8
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The purpose of present study was to determine whether peptidase activity affects the release of substance P (SP) and calcitonin gene-related peptide (CGRP) from spinal cord slices. When slices were exposed to various inhibitors of endopeptidase 24.11, the resting and capsaicin-stimulated release of SP were less than 0.04% and 0.20% total content per minute, respectively. Resting CGRP release was approximately 0.10% and stimulated release was 0.40%. The combination of 20 mu M bacitracin, 100 mu M phenylalanylalanine (Phe-Ala), and 50 mu M p-chloromercuriphenylsulfonic acid (PCMS) significantly increased both resting and stimulated release of SP and CGRP at least two- or threefold. Doubling the concentration of PCMS and Phe-Ala did not further improve peptide release. These results demonstrate that recovery of peptides released from spinal cord slices is dependent in part on activity of multiple peptidases in the tissues.
引用
收藏
页码:31 / 37
页数:7
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