PMID- 15049859 OWN - NLM STAT- MEDLINE DCOM- 20040615 LR - 20131121 IS - 0953-8194 (Print) IS - 0953-8194 (Linking) VI - 16 IP - 3 DP - 2004 Mar TI - Roles of corticotropin-releasing factor, neuropeptide Y and corticosterone in the regulation of food intake in Xenopus laevis. PG - 279-88 AB - In mammals, hypothalamic control of food intake involves counterregulation of appetite by an orexigenic peptides such as corticotropin-releasing factor (CRF), and orexigenic peptides such as neuropeptide Y (NPY). Glucocorticoids also stimulate food intake by inhibiting CRF while facilitating NPY actions. To gain a better understanding of the diversity and evolution of neuroendocrine feeding controls in vertebrates, we analysed the effects of CRF, NPY and glucocorticoids on food intake in juvenile Xenopus laevis. We also analysed brain CRF and NPY mRNA content and plasma corticosterone concentrations in relation to nutritional state. Intracerebroventricular (i.c.v.) injection of ovine CRF suppressed food intake while CRF receptor antagonist alpha helical CRF(9-41) significantly increased food intake relative to uninjected and placebo controls. By contrast, i.c.v. injection of frog NPY and short-term corticosterone treatment increased food intake. Semi-quantitative reverse transcription-polymerase chain reaction analyses showed that CRF and NPY mRNA fluctuated with food intake in the brain region containing the mid-posterior hypothalamus, pretectum, and optic tectum: CRF mRNA decreased 6 h after a meal and remained low through 31 days of food deprivation; NPY mRNA content also decreased 6 h after a meal, but increased to prefeeding levels by 24 h. Plasma corticosterone concentration increased 6 h after a meal, returned to prefeeding levels by 24 h, and did not change with prolonged food deprivation. This postprandial increase in plasma corticosterone may be related to the subsequent increase in plasma glucose and body water content that occurs 24 h postfeeding. Overall, our data support the conclusion that, similar to other vertebrates, CRF is anorexigenic while NPY is orexigenic in X. laevis, and CRF secretion modulates food intake in the absence of stress by exerting an inhibitory tone on appetite. Furthermore, the stress axis is activated in response to food intake, but in contrast to mammals and birds is not activated during periods of food deprivation. FAU - Crespi, E J AU - Crespi EJ AD - Department of Molecular, Cellular, and Developmental Biology, University of Michigan, Ann Arbor, MI 48109-1048, USA. ejcrespi@umich.edu FAU - Vaudry, H AU - Vaudry H FAU - Denver, R J AU - Denver RJ LA - eng GR - T32-HD07048/HD/NICHD NIH HHS/United States PT - Comparative Study PT - Journal Article PT - Research Support, U.S. Gov't, Non-P.H.S. PT - Research Support, U.S. Gov't, P.H.S. PL - United States TA - J Neuroendocrinol JT - Journal of neuroendocrinology JID - 8913461 RN - 0 (Neuropeptide Y) RN - 0 (RNA, Messenger) RN - 9015-71-8 (Corticotropin-Releasing Hormone) RN - W980KJ009P (Corticosterone) SB - IM MH - Adaptation, Physiological MH - Animals MH - Appetite Regulation/*physiology MH - Corticosterone/blood/*physiology MH - Corticotropin-Releasing Hormone/genetics/*physiology MH - Feeding Behavior/physiology MH - Hypothalamus/physiology MH - Neuropeptide Y/genetics/*physiology MH - Postprandial Period/physiology MH - RNA, Messenger/analysis MH - Superior Colliculi/physiology MH - Xenopus laevis/*physiology EDAT- 2004/03/31 05:00 MHDA- 2004/06/16 05:00 CRDT- 2004/03/31 05:00 PHST- 2004/03/31 05:00 [pubmed] PHST- 2004/06/16 05:00 [medline] PHST- 2004/03/31 05:00 [entrez] AID - JNE1168 [pii] AID - 10.1111/j.0953-8194.2004.01168.x [doi] PST - ppublish SO - J Neuroendocrinol. 2004 Mar;16(3):279-88. doi: 10.1111/j.0953-8194.2004.01168.x.