ausblenden:
Schlagwörter:
Animals, Neurons/*metabolism, Pro-Opiomelanocortin/metabolism, Mice, Transgenic, Hunger/physiology, alpha-MSH/*metabolism, Arcuate Nucleus of Hypothalamus/*metabolism, Energy Metabolism/*physiology, Hypothalamus/metabolism, Nerve Net/*physiology, Synaptic Potentials/*physiology
Zusammenfassung:
Arcuate nucleus (ARC) neurons sense the fed or fasted state and regulate hunger. Agouti-related protein (AgRP) neurons in the ARC (ARC(AgRP) neurons) are stimulated by fasting and, once activated, they rapidly (within minutes) drive hunger. Pro-opiomelanocortin (ARC(POMC)) neurons are viewed as the counterpoint to ARC(AgRP) neurons. They are regulated in an opposite fashion and decrease hunger. However, unlike ARC(AgRP) neurons, ARC(POMC) neurons are extremely slow in affecting hunger (many hours). Thus, a temporally analogous, rapid ARC satiety pathway does not exist or is presently unidentified. Here we show that glutamate-releasing ARC neurons expressing oxytocin receptor, unlike ARC(POMC) neurons, rapidly cause satiety when chemo- or optogenetically manipulated. These glutamatergic ARC projections synaptically converge with GABAergic ARC(AgRP) projections on melanocortin-4 receptor (MC4R)-expressing satiety neurons in the paraventricular hypothalamus (PVH(MC4R) neurons). Transmission across the ARC(Glutamatergic)→PVH(MC4R) synapse is potentiated by the ARC(POMC) neuron-derived MC4R agonist, α-melanocyte stimulating hormone (α-MSH). This excitatory ARC→PVH satiety circuit, and its modulation by α-MSH, provides insight into regulation of hunger and satiety.
