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Divergent Neural Pathways Emanating from the Lateral Parabrachial Nucleus Mediate Distinct Components of the Pain Response.
Chiang, Michael C; Nguyen, Eileen K; Canto-Bustos, Martha; Papale, Andrew E; Oswald, Anne-Marie M; Ross, Sarah E.
Afiliação
  • Chiang MC; Department of Neurobiology, University of Pittsburgh, Pittsburgh, PA 15213, USA; Pittsburgh Center for Pain Research, University of Pittsburgh, Pittsburgh, PA 15213, USA.
  • Nguyen EK; Department of Neurobiology, University of Pittsburgh, Pittsburgh, PA 15213, USA; Pittsburgh Center for Pain Research, University of Pittsburgh, Pittsburgh, PA 15213, USA.
  • Canto-Bustos M; Department of Neuroscience, University of Pittsburgh, Pittsburgh, PA 15213, USA.
  • Papale AE; Department of Neurobiology, University of Pittsburgh, Pittsburgh, PA 15213, USA.
  • Oswald AM; Department of Neuroscience, University of Pittsburgh, Pittsburgh, PA 15213, USA; Center for the Neural Basis of Cognition, Pittsburgh, PA, USA.
  • Ross SE; Department of Neurobiology, University of Pittsburgh, Pittsburgh, PA 15213, USA; Pittsburgh Center for Pain Research, University of Pittsburgh, Pittsburgh, PA 15213, USA; Center for the Neural Basis of Cognition, Pittsburgh, PA, USA. Electronic address: saross@pitt.edu.
Neuron ; 106(6): 927-939.e5, 2020 06 17.
Article em En | MEDLINE | ID: mdl-32289251
ABSTRACT
The lateral parabrachial nucleus (lPBN) is a major target of spinal projection neurons conveying nociceptive input into supraspinal structures. However, the functional role of distinct lPBN efferents in diverse nocifensive responses have remained largely uncharacterized. Here we show that that the lPBN is required for escape behaviors and aversive learning to noxious stimulation. In addition, we find that two populations of efferent neurons from different regions of the lPBN collateralize to distinct targets. Activation of efferent projections to the ventromedial hypothalamus (VMH) or lateral periaqueductal gray (lPAG) drives escape behaviors, whereas activation of lPBN efferents to the bed nucleus stria terminalis (BNST) or central amygdala (CEA) generates an aversive memory. Finally, we provide evidence that dynorphin-expressing neurons, which span cytoarchitecturally distinct domains of the lPBN, are required for aversive learning.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Aprendizagem da Esquiva / Reação de Fuga / Nociceptividade / Núcleos Parabraquiais Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Aprendizagem da Esquiva / Reação de Fuga / Nociceptividade / Núcleos Parabraquiais Idioma: En Ano de publicação: 2020 Tipo de documento: Article