INCREASED EXPRESSION OF PREPROTACHYKININ, CALCITONIN GENE-RELATED PEPTIDE, BUT NOT VASOACTIVE-INTESTINAL-PEPTIDE MESSENGER-RNA IN DORSAL-ROOT GANGLIA DURING THE DEVELOPMENT OF ADJUVANT MONOARTHRITIS IN THE RAT

被引:155
作者
DONALDSON, LF
HARMAR, AJ
MCQUEEN, DS
SECKL, JR
机构
[1] ROYAL EDINBURGH & ASSOCIATED HOSP,MRC BRAIN METAB UNIT,EDINBURGH,SCOTLAND
[2] UNIV EDINBURGH,DEPT PHARMACOL,EDINBURGH EH8 9YL,MIDLOTHIAN,SCOTLAND
来源
MOLECULAR BRAIN RESEARCH | 1992年 / 16卷 / 1-2期
基金
英国惠康基金;
关键词
PREPROTACHYKININ; SUBSTANCE-P; CALCITONIN GENE-RELATED PEPTIDE; VASOACTIVE INTESTINAL POLYPEPTIDE; ADJUVANT MONOARTHRITIS; INFLAMMATION; DORSAL ROOT GANGLIA; INSITU HYBRIDIZATION; GENE EXPRESSION;
D O I
10.1016/0169-328X(92)90204-O
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
Neuropeptides in dorsal root ganglia (DRG) have been implicated in the pathogenesis of pain and neurogenic inflammation in experimental and clinical arthritis. Recently we demonstrated increased levels of substance P (SP) and calcitonin gene-related peptide (CGRP) confined to innervating DRG in adjuvant-mediated monoarthritis. We have now investigated whether changes in peptide content are reflected in altered neuropeptide gene expression and the time course involved. Using in situ hybridization we found marked increases in expression of beta-preprotachykinin (PPT; 81 +/- 24% rise) and alpha-CGRP (44 +/- 6% rise) mRNAs in innervating (ipsilateral L5) DRG neurones only. These increases occured at the onset of acute inflammation (8 h) and persisted until chronic arthritis developed after 14 days. There were no changes in the proportion of DRG neurones expressing PPT or CGRP mRNAs. Messenger RNA encoding vasoactive intestinal polypeptide (VIP) was not induced. These data suggest that increased synthesis of PPT and CGRP peptides in DRG may play a role in the pathogenesis both of adjuvant-mediated acute inflammation and chronic arthritis.
引用
收藏
页码:143 / 149
页数:7
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