Antioxidative effect of epigallocatechin gallate against D-galactosamine-induced injury in primary culture of rat hepatocytes
Jazyk angličtina Země Česko Médium print
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
25006656
DOI
10.14712/18059694.2014.1
Knihovny.cz E-zdroje
- Klíčová slova
- D-galactosamine, Epigallocatechin gallate, Hepatocytes, Oxidative stress,
- MeSH
- antioxidancia farmakologie MeSH
- buněčné kultury MeSH
- galaktosamin farmakologie MeSH
- glutathion farmakologie MeSH
- hepatocyty účinky léků patologie MeSH
- katechin analogy a deriváty farmakologie MeSH
- krysa rodu Rattus MeSH
- zvířata MeSH
- Check Tag
- krysa rodu Rattus MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- antioxidancia MeSH
- epigallocatechin gallate MeSH Prohlížeč
- galaktosamin MeSH
- glutathion MeSH
- katechin MeSH
Literature data support that green tea and its major component epigallocatechin gallate (EGCG) have powerful antioxidant effects. Contrary, hepatotoxicity can be induced by high-dose EGCG. The timing of exposure to green tea in relation to administration of hepatotoxic agent plays an import role too. The aim of our work was a verification of antioxidative effect of EGCG on D-galactosamine-induced injury in primary culture of rat hepatocytes. Hepatocytes were incubated with EGCG at concentrations of 1.25-10 μM and toxic D-galactosamine (GalN) for 24 hrs. Alternatively, hepatocytes were pretreated with EGCG for 24 hrs, and then incubated with EGCG and GalN for further 24 hrs. Cytotoxicity was analysed by lactate dehydrogenase activity, functional capacity by albumin production. Oxidative stress was evaluated from a production of malondialdehyde and glutathione content in the cells. EGCG protected hepatocytes against GalN-induced cytotoxicity but preventive treatment of intact hepatocytes with EGCG was required to diminish the development of hepatocyte injury. Oxidative stress induced in our study seems to overcome the ability of hepatocytes to improve GSH depletion and albumin production. Prolongation of the pretreatment with EGCG could be a promising strategy leading to amelioration of its hepatoprotective effect.
Citace poskytuje Crossref.org
In vitro toxicity of epigallocatechin gallate in rat liver mitochondria and hepatocytes