Sirt1 mediates improvement in cognitive defects induced by focal cerebral ischemia following hyperbaric oxygen preconditioning in rats
Jazyk angličtina Země Česko Médium print-electronic
Typ dokumentu časopisecké články
PubMed
28937253
DOI
10.33549/physiolres.933544
PII: 933544
Knihovny.cz E-zdroje
- MeSH
- časové faktory MeSH
- chování zvířat * MeSH
- doménové proteiny doublecortinu MeSH
- fosforylace MeSH
- hipokampus enzymologie patofyziologie MeSH
- hyperbarická oxygenace * MeSH
- infarkt arteria cerebri media enzymologie patofyziologie psychologie terapie MeSH
- kognice * MeSH
- kognitivní poruchy enzymologie patofyziologie prevence a kontrola psychologie MeSH
- modely nemocí na zvířatech MeSH
- neurofilamentové proteiny metabolismus MeSH
- neuropeptidy metabolismus MeSH
- potkani Sprague-Dawley MeSH
- protein doublecortin MeSH
- proteiny asociované s mikrotubuly metabolismus MeSH
- RNA interference MeSH
- sirtuin 1 genetika metabolismus MeSH
- zvířata MeSH
- Check Tag
- mužské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- Dcx protein, rat MeSH Prohlížeč
- doménové proteiny doublecortinu MeSH
- neurofilament protein H MeSH Prohlížeč
- neurofilamentové proteiny MeSH
- neuropeptidy MeSH
- protein doublecortin MeSH
- proteiny asociované s mikrotubuly MeSH
- Sirt1 protein, rat MeSH Prohlížeč
- 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.
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