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学術論文

Central amygdala circuits modulate food consumption through a positive-valence mechanism

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Douglass,  Amelia M.
Department: Molecules-Signaling-Development / Klein, MPI of Neurobiology, Max Planck Society;

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Kucukdereli,  Hakan
Department: Molecules-Signaling-Development / Klein, MPI of Neurobiology, Max Planck Society;

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Ponserre,  Marion
Department: Molecules-Signaling-Development / Klein, MPI of Neurobiology, Max Planck Society;

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Strobel,  Cornelia
Department: Molecules-Signaling-Development / Klein, MPI of Neurobiology, Max Planck Society;

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Alcala Morales,  Pilar L.
Department: Molecules-Signaling-Development / Klein, MPI of Neurobiology, Max Planck Society;

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Klein,  Rüdiger
Department: Molecules-Signaling-Development / Klein, MPI of Neurobiology, Max Planck Society;

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引用

Douglass, A. M., Kucukdereli, H., Ponserre, M., Markovic, M., Gruendemann, J., Strobel, C., Alcala Morales, P. L., Conzelmann, K.-K., Luethi, A., & Klein, R. (2017). Central amygdala circuits modulate food consumption through a positive-valence mechanism. Nature Neuroscience, 20(10), 1384-1394. doi:10.1038/nn.4623.


引用: https://hdl.handle.net/11858/00-001M-0000-002E-0AF4-4
要旨
The complex behaviors underlying reward seeking and consumption are integral to organism survival. The hypothalamus and mesolimbic dopamine system are key mediators of these behaviors, yet regulation of appetitive and consummatory behaviors outside of these regions is poorly understood. The central nucleus of the amygdala (CeA) has been implicated in feeding and reward, but the neurons and circuit mechanisms that positively regulate these behaviors remain unclear. Here, we defined the neuronal mechanisms by which CeA neurons promote food consumption. Using in vivo activity manipulations and Ca2+ imaging in mice, we found that GABAergic serotonin receptor 2a (Htr2a)-expressing CeA neurons modulate food consumption, promote positive reinforcement and are active in vivo during eating. We demonstrated electrophysiologically, anatomically and behaviorally that intra-CeA and long-range circuit mechanisms underlie these behaviors. Finally, we showed that CeA(Htr2a) neurons receive inputs from feeding-relevant brain regions. Our results illustrate how defined CeA neural circuits positively regulate food consumption.