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1.
Am J Physiol Regul Integr Comp Physiol ; 288(6): R1492-8, 2005 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-15731400

RESUMEN

Many mammals experience spontaneous declines in their food intake and body weight near the end of life, a stage we refer to as senescence. We have previously demonstrated that senescent rats have blunted food intake responses to intracerebroventricular injections of neuropeptide Y (NPY). In the present study, we tested the hypothesis that responsiveness to GABA, a putative potentiator of NPY's effect, is also diminished. Young and old male F344 rats received injections of NPY, muscimol, (MUS, a GABA-A receptor agonist), combinations of these two agents, and vehicle [artificial cerebrospinal fluid (aCSF)] into the hypothalamic paraventricular nucleus (PVN). Both young and old presenescent rats increased their food intake in response to NPY, MUS, and the combination of the two (in comparison to injections of aCSF). The combination treatment was generally more effective than either NPY or MUS alone. These data are consistent with suggestions that both NPY and GABA play a role in the regulation of feeding behavior. Senescent rats exhibited an attenuated NPY-induced food intake, no increase in response to MUS, and a response to NPY + MUS that was no larger than that of NPY alone. We conclude that PVN injections of GABA, as well as NPY, are less effective in stimulating feeding in senescent rats and suggest that alterations in their signaling pathways play a role in the involuntary feeding decrease seen near the end of life.


Asunto(s)
Envejecimiento/fisiología , Estimulantes del Apetito/farmacología , Ingestión de Alimentos/efectos de los fármacos , Ingestión de Alimentos/fisiología , Agonistas del GABA/farmacología , Muscimol/farmacología , Neuropéptido Y/farmacología , Agonistas alfa-Adrenérgicos/farmacología , Animales , Estimulantes del Apetito/administración & dosificación , Peso Corporal/efectos de los fármacos , Peso Corporal/fisiología , Interacciones Farmacológicas , Agonistas del GABA/administración & dosificación , Agonistas de Receptores de GABA-A , Masculino , Microinyecciones , Muscimol/administración & dosificación , Neuropéptido Y/administración & dosificación , Norepinefrina/farmacología , Núcleo Hipotalámico Paraventricular/fisiología , Ratas , Ratas Endogámicas F344
2.
Am J Physiol Regul Integr Comp Physiol ; 287(1): R69-75, 2004 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-15044185

RESUMEN

Many mammals, nearing the end of life, spontaneously decrease their food intake and body weight, a stage we refer to as senescence. The spontaneous decrease in food intake and body weight is associated with attenuated responses to intracerebroventricular injections of neuropeptide Y (NPY) compared with old presenescent or with young adult rats. In the present study, we tested the hypothesis that this blunted responsiveness involves the number and expression of hypothalamic paraventricular nucleus (PVN) Y(1) and/or Y(5) NPY receptors, both of which are thought to mediate NPY-induced food intake. We found no significant difference in mRNA levels, via quantitative PCR, for Y(1) and Y(5) receptors in the PVN of senescent vs. presenescent rats. In contrast, immunohistochemistry indicated that the number of PVN neurons staining for Y(1) receptor protein was greater in presenescent compared with senescent rats. We conclude that a decreased expression and number of Y(1) or Y(5) receptors in the PVN cannot explain the attenuated responsiveness of the senescent rats to exogenous NPY.


Asunto(s)
Envejecimiento/metabolismo , Núcleo Hipotalámico Paraventricular/metabolismo , Receptores Acoplados a Proteínas G/biosíntesis , Receptores de Neuropéptido Y/biosíntesis , Receptores de Neuropéptido/biosíntesis , Animales , Peso Corporal/fisiología , ADN Complementario/análisis , ADN Complementario/biosíntesis , Inmunohistoquímica , Masculino , Neuronas/metabolismo , Núcleo Hipotalámico Paraventricular/crecimiento & desarrollo , ARN Mensajero/biosíntesis , ARN Mensajero/genética , Ratas , Ratas Endogámicas F344 , Reacción en Cadena de la Polimerasa de Transcriptasa Inversa
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