Serotonin reciprocally regulates melanocortin neurons to modulate food intake
LK Heisler, EE Jobst, GM Sutton, L Zhou, E Borok… - Neuron, 2006 - cell.com
LK Heisler, EE Jobst, GM Sutton, L Zhou, E Borok, Z Thornton-Jones, HY Liu, JM Zigman…
Neuron, 2006•cell.comThe neural pathways through which central serotonergic systems regulate food intake and
body weight remain to be fully elucidated. We report that serotonin, via action at serotonin1B
receptors (5-HT 1B Rs), modulates the endogenous release of both agonists and
antagonists of the melanocortin receptors, which are a core component of the central
circuitry controlling body weight homeostasis. We also show that serotonin-induced
hypophagia requires downstream activation of melanocortin 4, but not melanocortin 3 …
body weight remain to be fully elucidated. We report that serotonin, via action at serotonin1B
receptors (5-HT 1B Rs), modulates the endogenous release of both agonists and
antagonists of the melanocortin receptors, which are a core component of the central
circuitry controlling body weight homeostasis. We also show that serotonin-induced
hypophagia requires downstream activation of melanocortin 4, but not melanocortin 3 …
Summary
The neural pathways through which central serotonergic systems regulate food intake and body weight remain to be fully elucidated. We report that serotonin, via action at serotonin1B receptors (5-HT1BRs), modulates the endogenous release of both agonists and antagonists of the melanocortin receptors, which are a core component of the central circuitry controlling body weight homeostasis. We also show that serotonin-induced hypophagia requires downstream activation of melanocortin 4, but not melanocortin 3, receptors. These results identify a primary mechanism underlying the serotonergic regulation of energy balance and provide an example of a centrally derived signal that reciprocally regulates melanocortin receptor agonists and antagonists in a similar manner to peripheral adiposity signals.
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