Chronic non-peptide neurokinin receptor antagonist treatment alters striatal tachykinin peptide and receptor gene expression in the rat

被引:4
作者
McCarson, KE
Krause, JE
McLean, S
机构
[1] Washington Univ, Sch Med, Dept Anat & Neurobiol, St Louis, MO 63110 USA
[2] Pfizer Inc, Div Cent Res, Dept Neurosci, Groton, CT 06340 USA
关键词
substance P; neurokinin receptor; basal ganglia; gene expression; rat tachykinin peptide; non-peptide antagonist;
D O I
10.1016/S0304-3940(98)00514-X
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The neurokinin-l receptor (NK-1R) and the tachykinin peptide substance P (SP) are found throughout the central nervous system (CNS) and are involved in the regulation of sensory, cardiovascular, and inflammatory function. Selective antagonists for the NK-1R such as CP-122,721 block NK-1R-mediated responses both in vitro and in vivo. This study investigated the effects of long-term daily CP-122,721 treatment on gene expression of SP and the NK-1R in the striatum and hindbrain of the rat. The striatum and hindbrain of rats receiving CP122,721 (5, 30, or 150 mg/kg) once-daily for 30 days were assayed for SP- and NK-1R-encoding mRNAs using solution hybridization-nuclease protection assays. Results show that treatment with CP-122,721 significantly increased SP-encoding mRNA and NK-1R mRNA levels in the striatum, but not in the hindbrain. The ability of CP122,721 to alter SP and NK-1R gene expression may provide a use for non-peptide neurokinin receptor antagonists in the modulation of systems regulated by NK-1R function. (C) 1998 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:113 / 116
页数:4
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