4.8 Article

VTA Glutamatergic Neurons Mediate Innate Defensive Behaviors

Journal

NEURON
Volume 107, Issue 2, Pages 368-+

Publisher

CELL PRESS
DOI: 10.1016/j.neuron.2020.04.024

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Funding

  1. Intramural Research Program (IRP) of the National Institute on Drug Abuse (IRP/NIDA/NIH)
  2. NIDA K99/R00 pathway to independence award [DA043572]
  3. NATIONAL INSTITUTE ON DRUG ABUSE [ZIADA000543] Funding Source: NIH RePORTER

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The ventral tegmental area (VTA) has dopamine, GABA, and glutamate neurons, which have been implicated in reward and aversion. Here, we determined whether VTA-glutamate or -GABA neurons play a role in innate defensive behavior. By VTA cell-type-specific genetic ablation, we found that ablation of glutamate, but not GABA, neurons abolishes escape behavior in response to threatening stimuli. We found that escape behavior is also decreased by chemogenetic inhibition of VTA-glutamate neurons and detected increases in activity in VTA-glutamate neurons in response to the threatening stimuli. By ultrastructural and electrophysiological analysis, we established that VTA-glutamate neurons receive a major monosynaptic glutamatergic input from the lateral hypothalamic area (LHA) and found that photoinhibition of this input decreases escape responses to threatening stimuli. These findings indicate that VTA-glutamate neurons are activated by and required for innate defensive responses and that information on threatening stimuli to VTA-glutamate neurons is relayed by LHA-glutamate neurons.

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