Feeding during the rest phase promotes circadian conflict in nuclei that control energy homeostasis and sleep–wake cycle in rats
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Food intake during the rest phase promotes circadian desynchrony, which has been associated with metabolic diseases. However, the link between circadian rhythm and metabolic alterations is not well understood. To investigate this issue, we explored the circadian rhythm of c-Fos immunoreactivity (IR) in rats fed during the day, during the night or with free access to food for 3 weeks. The analysis was focused on the hypothalamic nuclei, which are interconnected and involved in the control of energy homeostasis and/or arousal: lateral hypothalamus (LH), perifornical area, arcuate, ventrolateral pre-optic (VLPO) and tuberomammillary nuclei. The results show that food intake during the rest phase flattened the circadian c-Fos expression in the LH and perifornical area, and induced a phase shift in the VLPO area. In addition, c-Fos expression was analyzed in the orexin and melanin-concentrating hormone (MCH) neurons of the LH, which are involved in the control of food intake and arousal, and in α-melanin-stimulating hormone and neuropeptide Y (NPY) cells in the arcuate nucleus, all of which are involved in feeding–fasting cycles, energy homeostasis and sending projections to the LH. The results indicate that feeding during the rest phase decreased orexin neuron activation in the light in comparison with the other groups. Feeding during this phase also flattened the activity rhythm of MCH and α-melanin-stimulating hormone neurons and increased NPY IR when the light was turned on. This evidence indicates that mealtime differentially affected the hypothalamic nuclei under investigation leading to a circadian conflict that might account for metabolic impairment. © 2017 Federation of European Neuroscience Societies and John Wiley %26 Sons Ltd
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Food intake during the rest phase promotes circadian desynchrony, which has been associated with metabolic diseases. However, the link between circadian rhythm and metabolic alterations is not well understood. To investigate this issue, we explored the circadian rhythm of c-Fos immunoreactivity (IR) in rats fed during the day, during the night or with free access to food for 3 weeks. The analysis was focused on the hypothalamic nuclei, which are interconnected and involved in the control of energy homeostasis and/or arousal: lateral hypothalamus (LH), perifornical area, arcuate, ventrolateral pre-optic (VLPO) and tuberomammillary nuclei. The results show that food intake during the rest phase flattened the circadian c-Fos expression in the LH and perifornical area, and induced a phase shift in the VLPO area. In addition, c-Fos expression was analyzed in the orexin and melanin-concentrating hormone (MCH) neurons of the LH, which are involved in the control of food intake and arousal, and in α-melanin-stimulating hormone and neuropeptide Y (NPY) cells in the arcuate nucleus, all of which are involved in feeding–fasting cycles, energy homeostasis and sending projections to the LH. The results indicate that feeding during the rest phase decreased orexin neuron activation in the light in comparison with the other groups. Feeding during this phase also flattened the activity rhythm of MCH and α-melanin-stimulating hormone neurons and increased NPY IR when the light was turned on. This evidence indicates that mealtime differentially affected the hypothalamic nuclei under investigation leading to a circadian conflict that might account for metabolic impairment. © 2017 Federation of European Neuroscience Societies and John Wiley & Sons Ltd
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arcuate nucleus; circadian rhythms; lateral hypothalamus; orexin; ventrolateral pre-optic nucleus melanin concentrating hormone; neuropeptide Y; protein c fos; hypophysis hormone; hypothalamus hormone; melanin; melanin-concentrating hormone; neuropeptide Y; orexin; protein c fos; animal cell; animal experiment; animal tissue; arcuate nucleus; Article; circadian rhythm; controlled study; diet restriction; energy metabolism; feeding; food intake; hypothalamus nucleus; immunoreactivity; lateral hypothalamus; male; nonhuman; priority journal; protein expression; rat; rest; sleep waking cycle; thalamus ventral nucleus; tuberomammillary nucleus; animal; cytology; eating; feeding behavior; homeostasis; hypothalamus; metabolism; nerve cell; periodicity; physiology; sleep; Wistar rat; Activity Cycles; Animals; Circadian Rhythm; Eating; Energy Metabolism; Feeding Behavior; Homeostasis; Hypothalamic Hormones; Hypothalamus; Male; Melanins; Neurons; Neuropeptide Y; Orexins; Pituitary Hormones; Proto-Oncogene Proteins c-fos; Rats; Rats, Wistar; Sleep
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