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1000 Titel
  • Neuroprotective and antioxidative effects of pioglitazone in brain tissue adjacent to the ischemic core are mediated by PI3K/Akt and Nrf2/ARE pathways
1000 Autor/in
  1. Zhao, Yi |
  2. Lützen, Ulf |
  3. Gohlke, Peter |
  4. Jiang, Ping |
  5. Herdegen, Thomas |
  6. Culman, Juraj |
1000 Erscheinungsjahr 2021
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2021-04-16
1000 Erschienen in
1000 Quellenangabe
  • 99(8):1073-1083
1000 Copyrightjahr
  • 2021
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1007/s00109-021-02065-3 |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8313471/ |
1000 Publikationsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • The present study elucidates the neuroprotective mechanisms of the PPARγ (peroxisome proliferator-activated receptor γ) agonist pioglitazone in survival of ischemic neurons following middle cerebral artery occlusion with reperfusion (MCAO). Intracerebroventricular infusion of pioglitazone over 5 days before and 24 or 48 h after MCAO alleviated neurological impairments, inhibited apoptosis 24 h, and activated the PI3K/Akt pathway along with increased phosphorylation of Akt (ser473) and GSK-3β (ser9) in the peri-infarct cortical areas 48 h after MCAO. In primary cortical neurons, pioglitazone suppressed the glutamate-induced release of lactate dehydrogenase by a PPARγ-dependent mechanism. This protective effect was reversed after co-treatment with PI3K and Akt inhibitors, LY294002 and SH-6, respectively. Pioglitazone enhanced the expression of the antioxidative transcription factor Nrf2 and its target gene protein, heme oxidase-1, in the peri-infarct area. Pioglitazone also increased activation of the antioxidant response element (ARE) in neuronal PC12 cells transfected with the pNQO1-rARE plasmid. We demonstrate in primary cortical neurons from Nrf2 knockout mice that the lack of Nrf2 completely abolished the neuroprotective effects of pioglitazone against oxidative and excitotoxic damage. Our results strongly suggest that the neuroprotective effects of PPARγ in peri-infarct brain tissues comprise the concomitant activation of the PI3K/Akt and Nrf2/ARE pathways. KEY MESSAGES: Pioglitazone inhibits apoptosis in ischemic brain tissue.  Pioglitazone acting on PPARγ activates PI3K/Akt pathway in ischemic brain tissue. Pioglitazone activates via Nrf2 the antioxidant defense pathway in injured neurons. Pioglitazone activates the antioxidant response element in neuronal PC12 cells. Pioglitazone fails to protect primary neurons lacking Nrf2 against oxidative damage. Activation of PPARγ supports the survival of viable neurons in peri-infarct regions.
1000 Sacherschließung
lokal Nrf2
lokal PC12 Cells [MeSH]
lokal Phosphorylation [MeSH]
lokal Brain Ischemia/etiology [MeSH]
lokal Pioglitazone
lokal Brain Ischemia/metabolism [MeSH]
lokal Gene Expression [MeSH]
lokal NF-E2-Related Factor 2/metabolism [MeSH]
lokal Pioglitazone/pharmacology [MeSH]
lokal Original Article
lokal Male [MeSH]
lokal Neuroprotection/drug effects [MeSH]
lokal Signal Transduction/drug effects [MeSH]
lokal Cerebrovascular Circulation/drug effects [MeSH]
lokal Disease Models, Animal [MeSH]
lokal PPARγ
lokal Antioxidants/pharmacology [MeSH]
lokal Apoptosis/drug effects [MeSH]
lokal Rats [MeSH]
lokal Animals [MeSH]
lokal Disease Susceptibility [MeSH]
lokal PI3K/Akt
lokal Cerebral ischemia
lokal Neuroprotective Agents/pharmacology [MeSH]
lokal Proto-Oncogene Proteins c-akt/metabolism [MeSH]
lokal Brain Ischemia/drug therapy [MeSH]
lokal Phosphatidylinositol 3-Kinases/metabolism [MeSH]
lokal Neuroprotection
lokal Biomarkers [MeSH]
lokal Brain Ischemia/pathology [MeSH]
1000 Liste der Beteiligten
  1. https://frl.publisso.de/adhoc/uri/WmhhbywgWWk=|https://frl.publisso.de/adhoc/uri/TMO8dHplbiwgVWxm|https://frl.publisso.de/adhoc/uri/R29obGtlLCBQZXRlcg==|https://frl.publisso.de/adhoc/uri/SmlhbmcsIFBpbmc=|https://frl.publisso.de/adhoc/uri/SGVyZGVnZW4sIFRob21hcw==|https://orcid.org/0000-0002-9220-7652
1000 Hinweis
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1000 Erstellt am 2023-05-03T18:03:37.847+0200
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1000 Zuletzt bearbeitet 2023-10-20T22:24:23.102+0200
1000 Objekt bearb. Fri Oct 20 22:24:23 CEST 2023
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