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A Neural Circuit for the Suppression of Pain by a Competing Need State.
Alhadeff, Amber L; Su, Zhenwei; Hernandez, Elen; Klima, Michelle L; Phillips, Sophie Z; Holland, Ruby A; Guo, Caiying; Hantman, Adam W; De Jonghe, Bart C; Betley, J Nicholas.
Afiliação
  • Alhadeff AL; Department of Biology, University of Pennsylvania, Philadelphia, PA 19104, USA.
  • Su Z; Department of Biology, University of Pennsylvania, Philadelphia, PA 19104, USA.
  • Hernandez E; Department of Biology, University of Pennsylvania, Philadelphia, PA 19104, USA.
  • Klima ML; Department of Biology, University of Pennsylvania, Philadelphia, PA 19104, USA.
  • Phillips SZ; Department of Biology, University of Pennsylvania, Philadelphia, PA 19104, USA.
  • Holland RA; Department of Biobehavioral Health Sciences, University of Pennsylvania, Philadelphia, PA 19104, USA.
  • Guo C; Janelia Research Campus, Howard Hughes Medical Institute, Ashburn, VA 20147, USA.
  • Hantman AW; Janelia Research Campus, Howard Hughes Medical Institute, Ashburn, VA 20147, USA.
  • De Jonghe BC; Department of Biobehavioral Health Sciences, University of Pennsylvania, Philadelphia, PA 19104, USA.
  • Betley JN; Department of Biology, University of Pennsylvania, Philadelphia, PA 19104, USA. Electronic address: jnbetley@sas.upenn.edu.
Cell ; 173(1): 140-152.e15, 2018 03 22.
Article em En | MEDLINE | ID: mdl-29570993
ABSTRACT
Hunger and pain are two competing signals that individuals must resolve to ensure survival. However, the neural processes that prioritize conflicting survival needs are poorly understood. We discovered that hunger attenuates behavioral responses and affective properties of inflammatory pain without altering acute nociceptive responses. This effect is centrally controlled, as activity in hunger-sensitive agouti-related protein (AgRP)-expressing neurons abrogates inflammatory pain. Systematic analysis of AgRP projection subpopulations revealed that the neural processing of hunger and inflammatory pain converge in the hindbrain parabrachial nucleus (PBN). Strikingly, activity in AgRP → PBN neurons blocked the behavioral response to inflammatory pain as effectively as hunger or analgesics. The anti-nociceptive effect of hunger is mediated by neuropeptide Y (NPY) signaling in the PBN. By investigating the intersection between hunger and pain, we have identified a neural circuit that mediates competing survival needs and uncovered NPY Y1 receptor signaling in the PBN as a target for pain suppression.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Dor / Neurônios Tipo de estudo: Etiology_studies Limite: Animals Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Dor / Neurônios Tipo de estudo: Etiology_studies Limite: Animals Idioma: En Ano de publicação: 2018 Tipo de documento: Article