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Multiple metabolic signals in the CeA regulate feeding: The role of AMPK.
- Source :
-
Molecular and cellular endocrinology [Mol Cell Endocrinol] 2024 Aug 01; Vol. 589, pp. 112232. Date of Electronic Publication: 2024 Apr 10. - Publication Year :
- 2024
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Abstract
- Background: The central nucleus of the amygdala (CeA) is part of the dopaminergic reward system and controls energy balance. Recently, a cluster of neurons was identified as responsive to the orexigenic effect of ghrelin and fasting. However, the signaling pathway by which ghrelin and fasting induce feeding is unknown. AMP-activated protein kinase (AMPK) is a cellular energy sensor, and its Thr172 phosphorylation (AMPKThr172) in the mediobasal hypothalamus regulates food intake. However, whether the expression and activation of AMPK in CeA could be one of the intracellular signaling activated in response to ghrelin and fasting eliciting food intake is unknown.<br />Aim: To evaluate the activation of AMPK into CeA in response to ghrelin, fasting, and 2-deoxy-D-glucose (2DG) and whether feeding accompanied these changes. In addition, to investigate whether the inhibition of AMPK into CeA could decrease food intake.<br />Methods: On a chow diet, eight-week-old Wistar male rats were stereotaxically implanted with a cannula in the CeA to inject several modulators of AMPKα1/2Thr172 phosphorylation, and we performed physiological and molecular assays.<br />Key Findings: Fasting increased, and refeeding reduced AMPKThr172 in the CeA. Intra-CeA glucose injection decreased feeding, whereas injection of 2DG, a glucoprivation inductor, in the CeA, increased food intake and blood glucose, despite faint increases in AMPKThr172. Intra-CeA ghrelin injection increased food intake and AMPKThr172. To further confirm the role of AMPK in the CeA, chronic injection of Melanotan II (MTII) in CeA reduced body mass and food intake over seven days together with a slight decrease in AMPKThr172.<br />Significance: Our findings identified that AMPK might be part of the signaling machinery in the CeA, which responds to nutrients and hormones contributing to feeding control. The results can contribute to understanding the pathophysiological mechanisms of altered feeding behavior/consumption, such as binge eating of caloric-dense, palatable food.<br />Competing Interests: Declaration of competing interest None. The authors declared no financial/personal interest or belief that could affect their objectivity.<br /> (Copyright © 2024 Elsevier B.V. All rights reserved.)
- Subjects :
- Animals
Male
Phosphorylation drug effects
Rats
Signal Transduction drug effects
Deoxyglucose pharmacology
Deoxyglucose metabolism
Feeding Behavior drug effects
Glucose metabolism
Rats, Wistar
Ghrelin metabolism
Ghrelin pharmacology
AMP-Activated Protein Kinases metabolism
Fasting
Central Amygdaloid Nucleus metabolism
Eating drug effects
Eating physiology
Subjects
Details
- Language :
- English
- ISSN :
- 1872-8057
- Volume :
- 589
- Database :
- MEDLINE
- Journal :
- Molecular and cellular endocrinology
- Publication Type :
- Academic Journal
- Accession number :
- 38604549
- Full Text :
- https://doi.org/10.1016/j.mce.2024.112232