First-pass extracted concept

vmPFC to DRN excitatory input pathway

Candidate: concept label1 source documents5 linked claims
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Aliases

ventromedial prefrontal cortex inputs to the dorsal raphe nucleus, vmPFC-DRN pathway

Evidence Snippets

Here we examined the organization and plasticity of microcircuits implicated in top-down control of 5-HT neurons in the dorsal raphe nucleus (DRN) by excitatory inputs from the ventromedial prefrontal cortex (vmPFC).
Evidence 1Source 1DOIPubMedprovenance

Supporting Sources

Linked Claims

Claim 1anatomical localizationsupports2014Source 1DOIPubMed

Excitatory vmPFC projections in the DRN primarily localize to GABA-rich areas rather than serotonergic subregions.

Quoted textsource-backed
found that excitatory vmPFC projections primarily localized to GABA-rich areas of the DRN
Claim 2behavioral effectsupports2014Source 1DOIPubMed

Optogenetically increasing excitatory vmPFC input to the DRN during sensory exposure to aggressor cues enhances avoidance bias, whereas decreasing that input diminishes avoidance bias.

Quoted textsource-backed
optogenetically increasing or decreasing excitatory vmPFC input to the DRN during sensory exposure to an aggressor's cues enhances or diminishes avoidance bias, respectively
Claim 3circuit interpretationsupports2014Source 1DOIPubMed

DRN GABAergic neurons act as a key cellular element filtering top-down vmPFC influences on affect-regulating 5-HT output.

Quoted textsource-backed
identify GABAergic neurons as a key cellular element filtering top-down vmPFC influences on affect-regulating 5-HT output
Claim 4mechanismsupports2014Source 1DOIPubMed

vmPFC axons drive synaptic activity and immediate early gene expression in genetically identified DRN GABA neurons through an AMPA receptor-dependent mechanism.

Quoted textsource-backed
vmPFC axons drive synaptic activity and immediate early gene expression in genetically identified DRN GABA neurons through an AMPA receptor-dependent mechanism
Claim 5negative mechanistic observationsupports2014Source 1DOIPubMed

The authors did not detect vmPFC-driven synaptic activity in 5-HT neurons and observed only limited cFos induction in 5-HT neurons.

Quoted textsource-backed
we did not detect vmPFC-driven synaptic activity in 5-HT neurons and cFos induction in 5-HT neurons was limited