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Estradiol decreases the orexigenic effect of neuropeptide Y, but not agouti-related protein, in ovariectomized rats

Producción científica: Articlerevisión exhaustiva

71 Citas (Scopus)

Resumen

Available data suggest that estradiol exerts an inhibitory effect on food intake by modulating the actions of multiple gut- and brain-derived peptides implicated in the control of food intake. For example, recent studies have shown that estradiol decreases the orexigenic effects of ghrelin and melanin-concentrating hormone. In the present study, we examined estradiol's ability to decrease the actions of two additional orexigenic peptides, neuropeptide Y (NPY) and agouti-related protein (AgRP). Food intake was monitored following lateral ventricular infusions of 5 μg NPY, 10 μg AgRP, or saline vehicle in ovariectomized rats treated with either 1 μg estradiol or sesame oil vehicle. NPY increased food intake for 2 h in both oil- and estradiol-treated ovariectomized rats. During this interval, the orexigenic effect of NPY was significantly greater in oil-treated rats, relative to estradiol-treated rats. In contrast to the short-term action of NPY, a single injection of AgRP increased food intake for 3 days in oil- and estradiol-treated rats. Meal pattern analysis revealed that the orexigenic effect of AgRP is mediated by an increase in meal size, not meal number. Unlike that observed following NPY treatment, estradiol failed to modulate the magnitude by which AgRP increased food intake and meal size. We conclude that a physiological regimen of estradiol treatment decreases the orexigenic effect of NPY, but not AgRP, in ovariectomized rats.

Idioma originalEnglish
Páginas (desde-hasta)173-177
Número de páginas5
PublicaciónBehavioural Brain Research
Volumen191
N.º2
DOI
EstadoPublished - ago 22 2008

Nota bibliográfica

Funding Information:
This work was supported by a grant from the NIH (DK-073936) and an NIH Joint Neuroscience Predoctoral Training Grant (NIH, NIDCR, NIGMS, NIMH, NINDS, NINR).

Financiación

This work was supported by a grant from the NIH (DK-073936) and an NIH Joint Neuroscience Predoctoral Training Grant (NIH, NIDCR, NIGMS, NIMH, NINDS, NINR).

FinanciadoresNúmero del financiador
National Institutes of Health (NIH)
National Institute of Mental Health
National Institute of Nursing Research
National Institute of General Medical Sciences
National Institute of Diabetes and Digestive and Kidney DiseasesR01DK073936
National Institute of Neurological Disorders and Stroke
National Institute of Dental and Craniofacial Research

    ASJC Scopus subject areas

    • Behavioral Neuroscience

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