EEDQ reduces the striatal neurotensin mRNA response to haloperidol

被引:2
作者
Adams, MR
Dobie, DJ
Merchant, KM
Unis, A
Dorsa, DM
机构
[1] SEATTLE VA MED CTR, CTR GERIATR RES EDUC & CLIN, SEATTLE, WA 98108 USA
[2] UPJOHN CO, CNS DIS RES, KALAMAZOO, MI 49001 USA
[3] UNIV WASHINGTON, DEPT PSYCHIAT & BEHAV SCI, SEATTLE, WA 98195 USA
关键词
neurotensin/neuromedin N; dorsolateral striatum; EEDQ; antipsychotic; drugs; haloperidol; dopamine;
D O I
10.1016/S0196-9781(97)87957-0
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
Haloperidol is believed to induce neurotensin/neuromedin N (NT/N) gene expression in the dorsolateral striatum (DLST) of the rat brain via dopamine D2 receptor blockade, but is also known to interact with other receptors as well. To further characterize haloperidol's effects, rats were treated with the irreversible monoaminergic receptor antagonist N-ethoxycarbonyl-2-ethoxy-1,2 hydroxyquinolone (EEDQ). In situ hybridization was performed for NT/N mRNA. D2-like and sigma receptor autoradiography was performed using I-125-sulpride and H-3-1,3-di-o-tolylguanidine (DTG), respectively. Despite antagonism of D2 receptors, pretreatment with EEDQ failed to significantly reduce the NT/N mRNA response when given 3 days prior to the haloperidol challenge. These data suggest that the acute effects of haloperidol on NT/N mRNA expression in large part result from D2 receptor antagonism. Nonetheless, a contribution of other receptors can not be excluded. (C) 1997 Elsevier Science Inc.
引用
收藏
页码:527 / 535
页数:9
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