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pubmed-article:16166201pubmed:abstractTextApolipoprotein (apo) A-IV is an anorexigenic gastrointestinal peptide that is also synthesized in the hypothalamus. The goal of these experiments was to determine whether apo A-IV interacts with the central melanocortin (MC) system in the control of feeding. The third ventricular (i3vt) administration of a subthreshold dose of apo A-IV (0.5 microg) potentiated i3vt MC-induced (metallothionein-II, 0.03 nmol) suppression of 30-min feeding in Long-Evans rats. A subthreshold dose of the MC antagonist (SHU9119, 0.1 nmol, i3vt) completely attenuated the anorectic effect of i3vt apo A-IV (1.5 microg). The i3vt apo A-IV significantly elevated the expression of c-Fos in neurons of the paraventricular nucleus of the hypothalamus, but not in the arcuate nucleus or median eminence. In addition, c-Fos expression was not colocalized with proopiomelanocortin-positive neurons. These data support a synergistic interaction between apo A-IV and melanocortins that reduces food intake by acting downstream of the arcuate.lld:pubmed
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pubmed-article:16166201pubmed:articleTitleApolipoprotein A-IV interacts synergistically with melanocortins to reduce food intake.lld:pubmed
pubmed-article:16166201pubmed:affiliationDepartment of Psychiatry, University of Cincinnati, 2170 East Galbraith Road, Cincinnati, OH 45237, USA.lld:pubmed
pubmed-article:16166201pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:16166201pubmed:publicationTypeResearch Support, N.I.H., Extramurallld:pubmed
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