4.7 Article

Preclinical neurorehabilitation with environmental enrichment confers cognitive and histological benefits in a model of pediatric asphyxial cardiac arrest

Journal

EXPERIMENTAL NEUROLOGY
Volume 335, Issue -, Pages -

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.expneurol.2020.113522

Keywords

Cardiac arrest; Pediatric; Environmental enrichment; Cognitive; Motor; Anxiety-like behavior; Recovery

Categories

Funding

  1. National Institutes of Health [HD075760, NS117000, NS107785, NS060005, HD069620, NS084967, NS094950, NS099683, NS110609]
  2. Children's Neuroscience Institute Award
  3. Children's Hospital of Pittsburgh
  4. University of Pittsburgh Physicians/UPMC Academic Foundation
  5. Children's Hospital of Pittsburgh Research Advisory Committee Award

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The study suggests that rehabilitation with environmental enrichment can reduce histopathology and improve motor and cognitive abilities in children following pediatric asphyxial cardiac arrest. This rehabilitation intervention shows positive effects on the outcomes of pediatric asphyxial cardiac arrest.
Pediatric asphyxial cardiac arrest (ACA) often leaves children with physical, cognitive, and emotional disabilities that affect overall quality of life, yet rehabilitation is neither routinely nor systematically provided. Environmental enrichment (EE) is considered a preclinical model of neurorehabilitation and thus we sought to investigate its efficacy in our established model of pediatric ACA. Male Sprague-Dawley rat pups (post-natal day 16-18) were randomly assigned to ACA (9.5 min) or Sham injury. After resuscitation, the rats were assigned to 21 days of EE or standard (STD) housing during which time motor, cognitive, and anxiety-like (i.e., affective) outcomes were assessed. Hippocampal CA(1) cells were quantified on post-operative day-22. Both ACA + STD and ACA + EE performed worse on beam-balance vs. Sham controls (p < 0.05) and did not differ from one another overall (p > 0.05); however, a single day analysis on the last day of testing revealed that the ACA + EE group performed better than the ACA + STD group (p < 0.05) and did not differ from the Sham controls (p > 0.05). Both Sham groups performed better than ACA + STD (p < 0.05) but did not differ from ACA + EE (p > 0.05) in the open field test. Spatial learning and declarative memory were improved and CA1 neuronal loss was attenuated in the ACA + EE vs. ACA + STD group (p < 0.05). Collectively, the data suggest that providing rehabilitation after pediatric ACA can reduce histopathology and improve motor and cognitive ability.

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