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Pharmacologic rescue of motor and sensory function by the neuroprotective compound P7C3 following neonatal nerve injury.
Kemp, S W P; Szynkaruk, M; Stanoulis, K N; Wood, M D; Liu, E H; Willand, M P; Morlock, L; Naidoo, J; Williams, N S; Ready, J M; Mangano, T J; Beggs, S; Salter, M W; Gordon, T; Pieper, A A; Borschel, G H.
Affiliation
  • Kemp SWP; Department of Surgery, Division of Plastic and Reconstructive Surgery, The Hospital for Sick Children, Toronto, ON, Canada; The Hospital for Sick Children Research Institute, Program in Neuroscience and Mental Health, Toronto, ON, Canada. Electronic address: stevekemp.phd@gmail.com.
  • Szynkaruk M; Department of Surgery, Division of Plastic and Reconstructive Surgery, The Hospital for Sick Children, Toronto, ON, Canada.
  • Stanoulis KN; Department of Surgery, Division of Plastic and Reconstructive Surgery, The Hospital for Sick Children, Toronto, ON, Canada.
  • Wood MD; Department of Surgery, Division of Plastic and Reconstructive Surgery, The Hospital for Sick Children, Toronto, ON, Canada; The Hospital for Sick Children Research Institute, Program in Neuroscience and Mental Health, Toronto, ON, Canada.
  • Liu EH; Department of Surgery, Division of Plastic and Reconstructive Surgery, The Hospital for Sick Children, Toronto, ON, Canada.
  • Willand MP; Department of Surgery, Division of Plastic and Reconstructive Surgery, The Hospital for Sick Children, Toronto, ON, Canada; The Hospital for Sick Children Research Institute, Program in Neuroscience and Mental Health, Toronto, ON, Canada.
  • Morlock L; Department of Biochemistry, UT Southwestern Medical Center, Dallas, TX, USA.
  • Naidoo J; Department of Biochemistry, UT Southwestern Medical Center, Dallas, TX, USA.
  • Williams NS; Department of Biochemistry, UT Southwestern Medical Center, Dallas, TX, USA.
  • Ready JM; Department of Biochemistry, UT Southwestern Medical Center, Dallas, TX, USA.
  • Mangano TJ; Psychoactive Drug Screening Program, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.
  • Beggs S; The Hospital for Sick Children Research Institute, Program in Neuroscience and Mental Health, Toronto, ON, Canada.
  • Salter MW; The Hospital for Sick Children Research Institute, Program in Neuroscience and Mental Health, Toronto, ON, Canada.
  • Gordon T; Department of Surgery, Division of Plastic and Reconstructive Surgery, The Hospital for Sick Children, Toronto, ON, Canada; The Hospital for Sick Children Research Institute, Program in Neuroscience and Mental Health, Toronto, ON, Canada.
  • Pieper AA; Departments of Psychiatry, Neurology and Veterans Affairs, Carver College of Medicine, University of Iowa, Iowa City, IA 52242, USA. Electronic address: andrew-pieper@uiowa.edu.
  • Borschel GH; Department of Surgery, Division of Plastic and Reconstructive Surgery, The Hospital for Sick Children, Toronto, ON, Canada; The Hospital for Sick Children Research Institute, Program in Neuroscience and Mental Health, Toronto, ON, Canada; University of Toronto, Department of Surgery and Institute of
Neuroscience ; 284: 202-216, 2015 Jan 22.
Article in En | MEDLINE | ID: mdl-25313000
ABSTRACT
Nerve injuries cause pain, paralysis and numbness that can lead to major disability, and newborns often sustain nerve injuries during delivery that result in lifelong impairment. Without a pharmacologic agent to enhance functional recovery from these injuries, clinicians rely solely on surgery and rehabilitation to treat patients. Unfortunately, patient outcomes remain poor despite application of the most advanced microsurgical and rehabilitative techniques. We hypothesized that the detrimental effects of traumatic neonatal nerve injury could be mitigated with pharmacologic neuroprotection, and tested whether the novel neuroprotective agent P7C3 would block peripheral neuron cell death and enhance functional recovery in a rat neonatal nerve injury model. Administration of P7C3 after sciatic nerve crush injury doubled motor and sensory neuron survival, and also promoted axon regeneration in a dose-dependent manner. Treatment with P7C3 also enhanced behavioral and muscle functional recovery, and reversed pathological mobilization of spinal microglia after injury. Our findings suggest that the P7C3 family of neuroprotective compounds may provide a basis for the development of a new neuroprotective drug to enhance recovery following peripheral nerve injury.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Sensation / Carbazoles / Neuroprotective Agents / Sciatic Neuropathy / Peripheral Nerve Injuries / Movement Disorders Type of study: Etiology_studies / Prognostic_studies Limits: Animals Language: En Journal: Neuroscience Year: 2015 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Sensation / Carbazoles / Neuroprotective Agents / Sciatic Neuropathy / Peripheral Nerve Injuries / Movement Disorders Type of study: Etiology_studies / Prognostic_studies Limits: Animals Language: En Journal: Neuroscience Year: 2015 Document type: Article