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1.
Endocrine ; 21(2): 163-7, 2003 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-12897381

RESUMEN

We previously demonstrated that daily melatonin administration to middle-aged rats to restore youthful plasma melatonin levels also decreased body weight, visceral fat, plasma leptin, and plasma insulin to more youthful levels, without detectable changes in consumption of chow diet. We now evaluate: (a) whether melatonin alters consumption of a more precisely quantifiable liquid diet similar in high-fat content to the typical American diet; (b) differences between melatonin-induced endocrine responses in the fasted vs fed state; and (c) time course of these responses. Ten-month-old male Sprague- Dawley rats received liquid diet containing either 0.2 micro g/mL melatonin (MELATONIN) or vehicle (CONTROL) (n = 14/treatment); the diet was available throughout each night, but was removed for the final 10 h of each daytime. MELATONIN rats gained 4% body weight during the first 2 wk and then stabilized, whereas CONTROL rats continued to gain for an additional week, achieving 8% gain (p < 0.05 vs MELATONIN). During the first 3 wk, afternoon tail-blood leptin, but not insulin, levels decreased in melatonin-treated rats (p < 0.05 vs CONTROL). After 8 wk, half of the rats were killed at the midpoint of the dark period (NIGHT; fed) and half at the end of the light period (DAYTIME; fasted). NIGHT but not DAYTIME plasma leptin levels were decreased in MELATONIN rats, whereas DAYTIME but not NIGHT plasma insulin levels were decreased (p < 0.05 vs CONTROL). Melatonin treatment did not alter cumulative food consumption. Thus, melatonin decreased weight gain in response to high-fat diet, decreased plasma leptin levels within 3 wk-before decreasing plasma insulin-and exerted these metabolic effects independent of total food consumption.


Asunto(s)
Grasas de la Dieta/metabolismo , Ingestión de Alimentos/fisiología , Melatonina/fisiología , Aumento de Peso/fisiología , Factores de Edad , Animales , Ritmo Circadiano , Ayuno/fisiología , Insulina/sangre , Leptina/sangre , Masculino , Melatonina/sangre , Ratas , Ratas Sprague-Dawley
2.
Endocrine ; 21(2): 169-73, 2003 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-12897382

RESUMEN

We previously demonstrated that daily melatonin administration to middle-aged rats, restoring nocturnal plasma melatonin to young adult levels, decreased body weight and suppressed visceral fat and plasma leptin. In some species, metabolic and some neuronal responses to melatonin are mediated or dependent at least in part on gonadal steroid levels. Thus, melatonin-induced changes in gonadal steroid secretion may have mediated the aging-dependent melatonin-induced metabolic responses in our previous studies. To address this issue, melatonin (0.4 micro g/mL) or vehicle (0.01% ethanol) was administered for 10 wk in the drinking water of both castrate and sham-operated Sprague-Dawley male rats, starting 1 mo after surgery at 9 mo of age. Melatonin treatment decreased (p < 0.05) body weight in sham-operated rats by 7 +/- 2% relative to control (n = 7/treatment), comparable to our previous results; melatonin likewise decreased (p < 0.05) body weight in castrate rats by 6 +/- 2% relative to control (n = 7/treatment). Melatonin treatment also decreased both intraabdominal fat and plasma leptin levels in both intact and castrate rats, with no significant differences of percentage suppression in the intact versus castrate rats. These results demonstrate that suppression of body weight, visceral adiposity, and plasma leptin levels by daily melatonin administration to middle-aged rats was independent of gonadal function.


Asunto(s)
Peso Corporal/fisiología , Metabolismo Energético/fisiología , Melatonina/fisiología , Testículo/fisiología , Testosterona/sangre , Tejido Adiposo/metabolismo , Factores de Edad , Animales , Composición Corporal/fisiología , Castración , Ritmo Circadiano , Ingestión de Alimentos/fisiología , Ayuno/fisiología , Insulina/sangre , Leptina/sangre , Masculino , Ratas , Ratas Sprague-Dawley , Testículo/metabolismo , Testosterona/metabolismo
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