|  Help  |  About  |  Contact Us

Publication : mTORC1 Signaling in AgRP Neurons Is Not Required to Induce Major Neuroendocrine Adaptations to Food Restriction.

First Author  de Souza GO Year  2023
Journal  Cells Volume  12
Issue  20 PubMed ID  37887286
Mgi Jnum  J:359137 Mgi Id  MGI:7544274
Doi  10.3390/cells12202442 Citation  de Souza GO, et al. (2023) mTORC1 Signaling in AgRP Neurons Is Not Required to Induce Major Neuroendocrine Adaptations to Food Restriction. Cells 12(20)
abstractText  Hypothalamic mTORC1 signaling is involved in nutrient sensing. Neurons that express the agouti-related protein (AgRP) are activated by food restriction and integrate interoceptive and exteroceptive signals to control food intake, energy expenditure, and other metabolic responses. To determine whether mTORC1 signaling in AgRP neurons is necessary for regulating energy and glucose homeostasis, especially in situations of negative energy balance, mice carrying ablation of the Raptor gene exclusively in AgRP-expressing cells were generated. AgRP(DeltaRaptor) mice showed no differences in body weight, fat mass, food intake, or energy expenditure; however, a slight improvement in glucose homeostasis was observed compared to the control group. When subjected to 5 days of food restriction (40% basal intake), AgRP(DeltaRaptor) female mice lost less lean body mass and showed a blunted reduction in energy expenditure, whereas AgRP(DeltaRaptor) male mice maintained a higher energy expenditure compared to control mice during the food restriction and 5 days of refeeding period. AgRP(DeltaRaptor) female mice did not exhibit the food restriction-induced increase in serum corticosterone levels. Finally, although hypothalamic fasting- or refeeding-induced Fos expression showed no differences between the groups, AgRP(DeltaRaptor) mice displayed increased hyperphagia during refeeding. Thus, some metabolic and neuroendocrine responses to food restriction are disturbed in AgRP(DeltaRaptor) mice.
Quick Links:
 
Quick Links:
 

Expression

Publication --> Expression annotations

 

Other

8 Bio Entities

Trail: Publication

0 Expression