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Phrenic motor neuron survival below cervical spinal cord hemisection.
Allen, Latoya L; Nichols, Nicole L; Asa, Zachary A; Emery, Anna T; Ciesla, Marissa C; Santiago, Juliet V; Holland, Ashley E; Mitchell, Gordon S; Gonzalez-Rothi, Elisa J.
Afiliação
  • Allen LL; Breathing Research and Therapeutics Center, Department of Physical Therapy and McKnight Brain Institute, University of Florida, Gainesville, FL 32610, USA.
  • Nichols NL; Department of Biomedical Sciences and Dalton Cardiovascular Research Center, University of Missouri, Columbia, MO 65211, USA.
  • Asa ZA; Breathing Research and Therapeutics Center, Department of Physical Therapy and McKnight Brain Institute, University of Florida, Gainesville, FL 32610, USA.
  • Emery AT; MNGI Digestive Health, Woodbury, MN 55125, USA.
  • Ciesla MC; Breathing Research and Therapeutics Center, Department of Physical Therapy and McKnight Brain Institute, University of Florida, Gainesville, FL 32610, USA.
  • Santiago JV; Breathing Research and Therapeutics Center, Department of Physical Therapy and McKnight Brain Institute, University of Florida, Gainesville, FL 32610, USA.
  • Holland AE; Breathing Research and Therapeutics Center, Department of Physical Therapy and McKnight Brain Institute, University of Florida, Gainesville, FL 32610, USA.
  • Mitchell GS; Breathing Research and Therapeutics Center, Department of Physical Therapy and McKnight Brain Institute, University of Florida, Gainesville, FL 32610, USA.
  • Gonzalez-Rothi EJ; Breathing Research and Therapeutics Center, Department of Physical Therapy and McKnight Brain Institute, University of Florida, Gainesville, FL 32610, USA. Electronic address: elisagon@phhp.ufl.edu.
Exp Neurol ; 346: 113832, 2021 12.
Article em En | MEDLINE | ID: mdl-34363808
ABSTRACT
Cervical spinal cord injury (cSCI) severs bulbospinal projections to respiratory motor neurons, paralyzing respiratory muscles below the injury. C2 spinal hemisection (C2Hx) is a model of cSCI often used to study spontaneous and induced plasticity and breathing recovery post-injury. One key assumption is that C2Hx dennervates motor neurons below the injury, but does not affect their survival. However, a recent study reported substantial bilateral motor neuron death caudal to C2Hx. Since phrenic motor neuron (PMN) death following C2Hx would have profound implications for therapeutic strategies designed to target spared neural circuits, we tested the hypothesis that C2Hx minimally impacts PMN survival. Using improved retrograde tracing methods, we observed no loss of PMNs at 2- or 8-weeks post-C2Hx. We also observed no injury-related differences in ChAT or NeuN immunolabeling within labelled PMNs. Although we found no evidence of PMN loss following C2Hx, we cannot rule out neuronal loss in other motor pools. These findings address an essential prerequisite for studies that utilize C2Hx as a model to explore strategies for inducing plasticity and/or regeneration within the phrenic motor system, as they provide important insights into the viability of phrenic motor neurons as therapeutic targets after high cervical injury.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Nervo Frênico / Traumatismos da Medula Espinal / Medula Cervical / Neurônios Motores Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Revista: Exp Neurol Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Nervo Frênico / Traumatismos da Medula Espinal / Medula Cervical / Neurônios Motores Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Revista: Exp Neurol Ano de publicação: 2021 Tipo de documento: Article