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The Journal of Neuroscience, December 1, 1998, 18(23):10128-10135
Brainstem Application of Melanocortin Receptor Ligands Produces
Long-Lasting Effects on Feeding and Body Weight
Harvey J.
Grill1,
Abigail B.
Ginsberg1,
Randy
J.
Seeley2, and
Joel M.
Kaplan1
1 Department of Psychology and Institute of
Neurological Sciences, University of Pennsylvania, Philadelphia,
Pennsylvania 19104, and 2 Department of Psychiatry,
University of Cincinnati, Cincinnati, Ohio 45267
Recent evidence suggests that the central melanocortin (MC) system
is a prominent contributor to food intake and body weight control. MC
receptor (MC-R) populations in the arcuate and paraventricular nuclei are considered probable sites of action mediating the orexigenic effects of systemically or intracerebroventricularly
administered ligands. Yet, the highest MC4-R density in the brain is
found in the dorsal motor nucleus of the vagus nerve, situated
subjacent to the commissural nucleus of the solitary tract, a
site of pro-opiomelanocortin mRNA expression. We evaluated the
contribution of the caudal brainstem MC system by (1) performing
respective dose-response analyses for an MC-R agonist (MTII) and
antagonist (SHU9119) delivered to the fourth ventricle,
(2) comparing, in the same rats, the fourth intracerebroventricular
dose-response profiles to those obtained with lateral
intracerebroventricular delivery, and (3) delivering an effective dose
of MTII or SHU9119 to rats before a 24 hr period of food deprivation.
Fourth intracerebroventricular agonist treatment yielded a
dose-dependent reduction of short-term (2 and 4 hr) and longer-term (24 hr) food intake and body weight. Fourth intracerebroventricular
antagonist treatment produced the opposite pattern of results:
dose-related increases in food intake and corresponding increases in
body weight change for the 24-96 hr observation period. Comparable
dose-response functions for food intake and body weight were observed
when these compounds were delivered to the lateral ventricle. Results
from deprived rats (no effect of MTII or SHU9119 on weight loss)
support the impression derived from the dose-response analyses that
the body weight change that follows MC treatments is secondary to their respective effects on food intake. Results support the relevance of the
brainstem MC-R complement to the control of feeding.
Key words:
fourth ventricle; lateral ventricle; food intake; water
intake; MTII; SHU9119; dorsal motor nucleus; caudal brainstem; POMC; arcuate nucleus; solitary nucleus
Copyright © 1998 Society for Neuroscience 0270-6474/98/182310128-08$05.00/0
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