The role of CRF2 receptors in corticotropin-releasing factor- and urocortin-induced anorexia

被引:124
|
作者
Smagin, GN
Howell, LA
Ryan, DH
De Souza, EB
Harris, RBS
机构
[1] Louisiana State Univ, Pennington Biomed Res Ctr, Baton Rouge, LA 70808 USA
[2] Neurocrine Biosci Inc, San Diego, CA 92121 USA
关键词
antisense oligonucleotides; corticosterone; HPA axis; selective antagonist;
D O I
10.1097/00001756-199805110-00063
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
THE experiments presented in this study were designed to assess corticotropin-releasing factor (CRF) receptor subtype mediation of CRF-and urocortin (UCN)-induced decrease in food intake. Male Sprague-Dawley rats were treated with antisense and sense oligonucleotides (ON) to CRF2 receptor mRNAs for 36 h and then received an intracerebroventricular injection of CRF, UCN (3 mu g) or saline. Antisense treatment significantly attenuated CRF- and UCN-induced suppression in food intake and HPA activation. Administration of CRF1 receptor antagonist did not affect the decrease in food intake or activation of the HPA axis induced by ICV infusion of 3 mu g CRF. The data suggest that down-regulation of CRF2 receptors selectively attenuates CRF-and UCN-induced anorexia and hypothalamo-pituitary-adrenocortical activation in rats. (C) 1998 Rapid Science Ltd.
引用
收藏
页码:1601 / 1606
页数:6
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