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Identification of a convergent spinal neuron population that encodes itch.
Sheahan, Tayler D; Warwick, Charles A; Cui, Abby Y; Baranger, David A A; Perry, Vijay J; Smith, Kelly M; Manalo, Allison P; Nguyen, Eileen K; Koerber, H Richard; Ross, Sarah E.
Afiliação
  • Sheahan TD; Pittsburgh Center for Pain Research and Department of Neurobiology, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
  • Warwick CA; Co-first authors.
  • Cui AY; Pittsburgh Center for Pain Research and Department of Neurobiology, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
  • Baranger DAA; Co-first authors.
  • Perry VJ; Pittsburgh Center for Pain Research and Department of Neurobiology, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
  • Smith KM; Department of Psychological and Brain Sciences, Washington University in St. Louis, St. Louis Missouri, USA.
  • Manalo AP; Pittsburgh Center for Pain Research and Department of Neurobiology, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
  • Nguyen EK; Pittsburgh Center for Pain Research and Department of Neurobiology, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
  • Koerber HR; Current Address: Biohaven Pharmaceuticals, LTD, Pittsburgh, Pennsylvania, USA.
  • Ross SE; Pittsburgh Center for Pain Research and Department of Neurobiology, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
bioRxiv ; 2023 Nov 08.
Article em En | MEDLINE | ID: mdl-37873278
Itch is a protective sensation that drives scratching. Although specific cell types have been proposed to underlie itch, the neural circuit basis for itch remains unclear. Here, we used two-photon Ca2+ imaging of the dorsal horn to visualize the neuronal populations that are activated by itch-inducing agents. We identify a convergent population of spinal neurons that is defined by the expression of GRPR. Moreover, we discover that itch is conveyed to the brain via GRPR-expressing spinal output neurons that target the lateral parabrachial nucleus. Further, we show that nalfurafine, a clinically effective kappa opioid receptor agonist, relieves itch by inhibiting GRPR spinoparabrachial neurons. Finally, we demonstrate that a subset of GRPR spinal neurons show persistent, cell-intrinsic Ca2+ oscillations. These experiments provide the first population-level view of the spinal neurons that respond to pruritic stimuli, pinpoint the output neurons that convey itch to the brain, and identify the cellular target of kappa opioid receptor agonists for the inhibition of itch.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article