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Differences in response to corticotropin-releasing factor after short- and long-term consumption of a high-fat diet

Authors :
Legendre, Ariadne
Papakonstantinou, Emilia
Roy, Marie-Claude
Richard, Denis
Harris, Ruth B.S.
Source :
The American Journal of Physiology. Sept, 2007, Vol. 293 Issue 3, pR1076, 10 p.
Publication Year :
2007

Abstract

We previously reported an exaggerated endocrine and weight loss response to stress in rats fed a high-fat (HF) diet for 5 days. Others report blunted stress-induced anxiety in rats made obese on a HF diet. Experiments described here tested whether sensitivity to stress-related peptides was changed in obese and nonobese HF-fed rats. Third ventricle infusion of corticotropin-releasing factor (CRF) in rats made obese on HF diet (40% kcal fat) produced an exaggerated hypophagia, which is thought to be mediated by CR[F.sub.2] receptors. Obese rats responded to a lower dose of CRF for a longer time than rats fed a low-fat (LF) diet (12% kcal fat). CRF-induced release of corticosterone, which is thought to be mediated by CR[F.sub.1] receptors, was not exaggerated in obese HF-fed rats. In contrast, rats fed HF diet for 5 days showed the same food intake and corticosterone response to CRF as LF-fed rats. CRF mRNA expression in the paraventricular nucleus of the hypothalamus was stimulated by mild stress (ip saline injection and placement in a novel cage) in LF-fed rats but not in rats fed HF diet for 5 days because of a nonsignificant increase in expression in nonstressed HF-fed rats. In addition, nonstressed levels of urocortin (UCN) I mRNA expression in the Edinger-Westphal nucleus were significantly inhibited in HF-fed rats. These data suggest that rats that have become obese on a HF diet show a change in responsiveness to stress peptides, whereas the increased stress response in nonobese HF-fed rats may he associated with changes in basal CRF and UCN I mRNA expression. rats; food intake; corticosterone; corticotropin-releasing factor mRNA; urocortin I mRNA

Details

Language :
English
ISSN :
00029513
Volume :
293
Issue :
3
Database :
Gale General OneFile
Journal :
The American Journal of Physiology
Publication Type :
Academic Journal
Accession number :
edsgcl.169085910