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Corticotropin-releasing hormone neurons control trigeminal neuralgia-induced anxiodepression via a hippocampus-to-prefrontal circuit. | LitMetric

Corticotropin-releasing hormone neurons control trigeminal neuralgia-induced anxiodepression via a hippocampus-to-prefrontal circuit.

Sci Adv

Department of Translational Neuroscience, Jing'an District Centre Hospital of Shanghai, State Key Laboratory of Medical Neurobiology and MOE Frontiers Center for Brain Science, Institutes of Brain Science, Fudan University, Shanghai 200032, China.

Published: January 2024

AI Article Synopsis

  • Anxiety and depression are common in patients with trigeminal neuralgia (TN), but the underlying neural mechanisms are not well understood.
  • Research found a specific neural circuit connecting the ventral hippocampus (vHPC) to the medial prefrontal cortex (mPFC) that influences TN-related anxiety and depression.
  • Activation of this circuit increases excitatory signals that lead to depressive-like behaviors, suggesting potential targets for treating anxiety and depression associated with pain.

Article Abstract

Anxiety and depression are frequently observed in patients suffering from trigeminal neuralgia (TN), but neural circuits and mechanisms underlying this association are poorly understood. Here, we identified a dedicated neural circuit from the ventral hippocampus (vHPC) to the medial prefrontal cortex (mPFC) that mediates TN-related anxiodepression. We found that TN caused an increase in excitatory synaptic transmission from vHPC neurons to mPFC inhibitory neurons marked by the expression of corticotropin-releasing hormone (CRH). Activation of CRH neurons subsequently led to feed-forward inhibition of layer V pyramidal neurons in the mPFC via activation of the CRH receptor 1 (CRHR1). Inhibition of the vHPC-mPFC circuit ameliorated TN-induced anxiodepression, whereas activating this pathway sufficiently produced anxiodepressive-like behaviors. Thus, our studies identified a neural pathway driving pain-related anxiodepression and a molecular target for treating pain-related psychiatric disorders.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10798562PMC
http://dx.doi.org/10.1126/sciadv.adj4196DOI Listing

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