Sirt1 mediates improvement in cognitive defects induced by focal cerebral ischemia following hyperbaric oxygen preconditioning in rats
Language English Country Czech Republic Media print-electronic
Document type Journal Article
PubMed
28937253
DOI
10.33549/physiolres.933544
PII: 933544
Knihovny.cz E-resources
- MeSH
- Time Factors MeSH
- Behavior, Animal * MeSH
- Doublecortin Domain Proteins MeSH
- Phosphorylation MeSH
- Hippocampus enzymology physiopathology MeSH
- Hyperbaric Oxygenation * MeSH
- Infarction, Middle Cerebral Artery enzymology physiopathology psychology therapy MeSH
- Cognition * MeSH
- Cognition Disorders enzymology physiopathology prevention & control psychology MeSH
- Disease Models, Animal MeSH
- Neurofilament Proteins metabolism MeSH
- Neuropeptides metabolism MeSH
- Rats, Sprague-Dawley MeSH
- Doublecortin Protein MeSH
- Microtubule-Associated Proteins metabolism MeSH
- RNA Interference MeSH
- Sirtuin 1 genetics metabolism MeSH
- Animals MeSH
- Check Tag
- Male MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Dcx protein, rat MeSH Browser
- Doublecortin Domain Proteins MeSH
- neurofilament protein H MeSH Browser
- Neurofilament Proteins MeSH
- Neuropeptides MeSH
- Doublecortin Protein MeSH
- Microtubule-Associated Proteins MeSH
- Sirt1 protein, rat MeSH Browser
- Sirtuin 1 MeSH
Hyperbaric oxygen preconditioning (HBO-PC) has been proposed as a safe and practical approach for neuroprotection in ischemic stroke. However, it is not known whether HPO-PC can improve cognitive deficits induced by cerebral ischemia, and the mechanistic basis for any beneficial effects remains unclear. We addressed this in the present study using rats subjected to middle cerebral artery occlusion (MCAO) as an ischemic stroke model following HBO-PC. Cognitive function and expression of phosphorylated neurofilament heavy polypeptide (pNF-H) and doublecortin (DCX) in the hippocampus were evaluated 14 days after reperfusion and after short interfering RNA-mediated knockdown of sirtuin1 (Sirt1). HBO-PC increased pNF-H and DCX expression and mitigated cognitive deficits in MCAO rats. However, these effects were abolished by Sirt1 knockdown. Our results suggest that HBO-PC can protect the brain from injury caused by ischemia-reperfusion and that Sirt1 is a potential molecular target for therapeutic approaches designed to minimize cognitive deficits caused by cerebral ischemia.
References provided by Crossref.org
Impact of prenatal hypoxia on the development and behavior of the rat offspring
Impact of perinatal hypoxia on the developing brain
