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Dorsal Horn Gastrin-Releasing Peptide Expressing Neurons Transmit Spinal Itch But Not Pain Signals.
Albisetti, Gioele W; Pagani, Martina; Platonova, Evgenia; Hösli, Ladina; Johannssen, Helge C; Fritschy, Jean-Marc; Wildner, Hendrik; Zeilhofer, Hanns Ulrich.
Afiliação
  • Albisetti GW; Institute of Pharmacology and Toxicology, University of Zurich, CH-8057 Zurich, Switzerland.
  • Pagani M; Neuroscience Center Zurich, CH-8057 Zurich, Switzerland.
  • Platonova E; Institute of Pharmacology and Toxicology, University of Zurich, CH-8057 Zurich, Switzerland.
  • Hösli L; Neuroscience Center Zurich, CH-8057 Zurich, Switzerland.
  • Johannssen HC; Center for Microscopy and Image Analysis, University of Zurich, CH-8057 Zurich, Switzerland.
  • Fritschy JM; Institute of Pharmacology and Toxicology, University of Zurich, CH-8057 Zurich, Switzerland.
  • Wildner H; Neuroscience Center Zurich, CH-8057 Zurich, Switzerland.
  • Zeilhofer HU; Institute of Pharmacology and Toxicology, University of Zurich, CH-8057 Zurich, Switzerland.
J Neurosci ; 39(12): 2238-2250, 2019 03 20.
Article em En | MEDLINE | ID: mdl-30655357
Gastrin-releasing peptide (GRP) is a spinal itch transmitter expressed by a small population of dorsal horn interneurons (GRP neurons). The contribution of these neurons to spinal itch relay is still only incompletely understood, and their potential contribution to pain-related behaviors remains controversial. Here, we have addressed this question in a series of experiments performed in GRP::cre and GRP::eGFP transgenic male mice. We combined behavioral tests with neuronal circuit tracing, morphology, chemogenetics, optogenetics, and electrophysiology to obtain a more comprehensive picture. We found that GRP neurons form a rather homogeneous population of central cell-like excitatory neurons located in lamina II of the superficial dorsal horn. Multicolor high-resolution confocal microscopy and optogenetic experiments demonstrated that GRP neurons receive direct input from MrgprA3-positive pruritoceptors. Anterograde HSV-based neuronal tracing initiated from GRP neurons revealed ascending polysynaptic projections to distinct areas and nuclei in the brainstem, midbrain, thalamus, and the somatosensory cortex. Spinally restricted ablation of GRP neurons reduced itch-related behaviors to different pruritogens, whereas their chemogenetic excitation elicited itch-like behaviors and facilitated responses to several pruritogens. By contrast, responses to painful stimuli remained unaltered. These data confirm a critical role of dorsal horn GRP neurons in spinal itch transmission but do not support a role in pain.SIGNIFICANCE STATEMENT Dorsal horn gastrin-releasing peptide neurons serve a well-established function in the spinal transmission of pruritic (itch) signals. A potential role in the transmission of nociceptive (pain) signals has remained controversial. Our results provide further support for a critical role of dorsal horn gastrin-releasing peptide neurons in itch circuits, but we failed to find evidence supporting a role in pain.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Dor / Prurido / Peptídeo Liberador de Gastrina / Células do Corno Posterior / Nociceptividade Limite: Animals Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Dor / Prurido / Peptídeo Liberador de Gastrina / Células do Corno Posterior / Nociceptividade Limite: Animals Idioma: En Ano de publicação: 2019 Tipo de documento: Article