Hypoxia-induced long-term increase of dopamine and tyrosine hydroxylase mRNA levels
Jazyk angličtina Země Česko Médium print
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
15782555
Knihovny.cz E-zdroje
- MeSH
- DNA vazebné proteiny metabolismus MeSH
- dopamin genetika metabolismus MeSH
- exprese genu MeSH
- faktor 1 indukovatelný hypoxií - podjednotka alfa MeSH
- faktor 1 indukovatelný hypoxií MeSH
- hypoxie metabolismus MeSH
- jaderné proteiny metabolismus MeSH
- krysa rodu Rattus MeSH
- kultivované buňky MeSH
- messenger RNA metabolismus MeSH
- mezencefalon metabolismus MeSH
- potkani Wistar MeSH
- transkripční faktory metabolismus MeSH
- tyrosin-3-monooxygenasa genetika metabolismus MeSH
- zvířata MeSH
- Check Tag
- krysa rodu Rattus MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- DNA vazebné proteiny MeSH
- dopamin MeSH
- faktor 1 indukovatelný hypoxií - podjednotka alfa MeSH
- faktor 1 indukovatelný hypoxií MeSH
- Hif1a protein, rat MeSH Prohlížeč
- jaderné proteiny MeSH
- messenger RNA MeSH
- transkripční faktory MeSH
- tyrosin-3-monooxygenasa MeSH
The aim of the present study was to determine hypoxia-induced changes in the long-term expression of tyrosine hydroxylase (TH) mRNA and the steady-state dopamine (DA) levels in rat mesencephalic cell cultures. The cultures were exposed to hypoxia during the early developmental period, and DA content and TH mRNA expression were determined on day in vitro (DIV) 14. Hypoxic exposure of 5-day-old cultures resulted in increased DA (control 89.9+/-8.9, hypoxia 135.8+/-23.7 pg/microg protein) and TH mRNA (control 37.3+/-4.7, hypoxia 143.1+/-49.4 pg/microg RNA) levels. To analyze the involvement of hypoxia-inducible factor-1 (HIF-1) in these changes, we studied its activation using reporter gene. Hypoxia caused a 3-fold increase in HIF-1 activity. Our data suggest that hypoxia/ischemia during the putative critical developmental period of neurons may determine the tyrosine hydroxylase gene expression and, consequently, the development of the dopaminergic system.