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Distinct circuits and molecular targets of the paraventricular hypothalamus decode visceral and somatic pain. | LitMetric

Distinct circuits and molecular targets of the paraventricular hypothalamus decode visceral and somatic pain.

Neuron

Clinical Research Center of Neurological Disease, The Second Affiliated Hospital of Soochow University, Jiangsu Key Laboratory of Neuropsychiatric Diseases and Institute of Neuroscience, Soochow University, Suzhou 215123, Jiangsu, P.R. China. Electronic address:

Published: November 2024

AI Article Synopsis

  • Visceral and somatic pain are protective mechanisms, and the paraventricular hypothalamus (PVH) is key in processing these pain types.
  • Researchers found separate neuronal groups in the PVH that handle visceral and somatic pain, with different receptors (P2X3R for visceral and VIPR2 for somatic).
  • These PVH groups send pain signals to different brain areas, indicating that the PVH acts like a sorting center for pain, which could lead to new ways of understanding and treating pain.

Article Abstract

Visceral and somatic pain serve as protective mechanisms against external threats. Accumulated evidence has confirmed that the paraventricular hypothalamus (PVH) plays an important role in the perception of visceral and somatic pain, whereas the exact neural pathways and molecules distinguishing them remain unclear. Here, we report distinct neuronal ensembles within the PVH dedicated to processing visceral and somatic pain signals. An essential discovery is the distinct expression of P2X3R and VIPR2 in visceral and somatic pain-activated PVH neuronal ensembles. Furthermore, visceral pain- and somatic pain-responsive PVH neuronal ensembles project to specific downstream regions, the ventral part of the lateral septal nucleus (LSV) and the caudal part of the zona incerta (ZIC), respectively. These findings unveil that the PVH acts as a pain sorting center that distinctly processes visceral and somatic pain, identifying potential molecular targets for specific pain processing and providing a new framework for comprehending how the brain processes nociceptive information.

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Source
http://dx.doi.org/10.1016/j.neuron.2024.08.024DOI Listing

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