Abstract

Benzodiazepines are an effective treatment of anxiety disorders for years, but misgiving over side effects have led to prescribe some antidepressant drugs even though they present a delayed onset of action. Here, we seek to evaluate whether serotonin type 4 receptor (5-HT4R) activation and targeting glutamatergic axon terminals arising from the medial prefrontal cortex (mPFC) in the dorsal raphe nucleus (DRN) may constitute a new way to induce fast anxiolytic effects.

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