Altered Expression of Hypothalamic Neuropeptide mRNAs in Food-Restricted and Food-Deprived Rats

Linda S. Brady, Mark A. Smith, Philip W. Gold, Miles Herkenham

Neuroendocrinology · 2008 · 646 citations · 0 references

Concepts

TL;DR

Hypothalamic neuropeptides regulate appetite and body weight. The study used 2‑week food restriction and 4‑day deprivation in male and female rats, applying in‑situ hybridization to measure hypothalamic peptide mRNA changes, mainly in the arcuate nucleus. Food restriction increased NPY and decreased POMC, GAL, and CRH mRNAs in the arcuate and paraventricular nuclei, with larger, sex‑dependent effects than deprivation, indicating these peptides may drive compensatory eating behavior linked to disorders.

Abstract

Hypothalamic neuropeptides play a role in appetite and weight regulation. Food restriction for 2 weeks and food deprivation for 4 days were used as models to characterize the effects of weight loss on hypothalamic peptide gene expression in male and female rats. We used in situ hybridization to examine the mRNA levels of hypothalamic peptides which stimulate and inhibit food intake and found selective effects primarily in the arcuate nucleus. Neuropeptide Y (NPY) mRNA was increased and pro-opiomelanocortin (POMC) and galanin (GAL) mRNA were decreased in the hypothalamic arcuate nucleus and corticotropin-releasing hormone (CRH) mRNA was decreased in the hypothalamic paraventricular nucleus in male and female food-restricted and food-deprived rats. Food restriction produced larger changes in peptide mRNA expression than did food deprivation. Changes in NPY, POMC and CRH gene expression induced by food restriction were greater in male than female rats. Elevated NPY and reduced CRH gene expression may be a compensatory physiological response to restore food intake in food-restricted and food-deprived animals. The discrete changes in NPY, POMC, GAL and CRH gene expression in food-restricted and food-deprived animals suggest the involvement of these peptides in abnormal appetitive behavior and weight loss associated with human eating disorders.