INCREASE IN NEUROTENSIN RECEPTOR EXPRESSION IN RAT-BRAIN INDUCED BY CHRONIC TREATMENT WITH THE NONPEPTIDE NEUROTENSIN RECEPTOR ANTAGONIST SR-48692

被引:23
作者
AZZI, M
NICOT, A
GULLY, D
KITABGI, P
BEROD, A
ROSTENE, W
机构
[1] HOP ST ANTOINE, INSERM, U339, F-75012 PARIS, FRANCE
[2] SANOFI RECH, F-31036 TOULOUSE, FRANCE
[3] CNRS, IPCM, F-06560 VALBONNE, FRANCE
关键词
NEUROTENSIN RECEPTOR; IN SITU HYBRIDIZATION; VENTRAL MESENCEPHALON; CENTRAL NERVOUS SYSTEM; DOPAMINERGIC NEURON;
D O I
10.1016/0304-3940(94)90671-8
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
In the present study, we examined the regulation of neurotensin receptor following a chronic pharmacological blockade of the neurotensin transmission with a nonpeptide neurotensin receptor antagonist, SR 48692. Our results showed that treatment of the rats for five days with SR 48692, at a dose of 1 mg/kg, i.p., induced an increase of both the number of binding sites for I-125-neurotensin to whole brain membrane homogenates and neurotensin receptor mRNA levels in the ventral mesencephalon. This study brings the first evidence for an in vivo up-regulation of neurotensin receptors following their pharmacological blockade, and suggests that endogenous neurotensin exerts a tonic inhibitory control on neurotensin receptor mRNA levels.
引用
收藏
页码:97 / 100
页数:4
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