Flavonoid diosmetin increases ATP levels in kidney cells and relieves ATP depleting effect of ochratoxin A

•Diosmetin (DIOS) increases ATP levels both in kidney and in liver cells.•Inhibition of glycolysis or citric acid cycle does not decrease the observed effect.•DIOS-induced elevation of ATP levels is abolished by the inhibition of ATP synthase.•DIOS is able to completely reverse the ATP-depleting eff...

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Veröffentlicht in:Journal of photochemistry and photobiology. B, Biology Biology, 2014-03, Vol.132, p.1-9
Hauptverfasser: Poór, Miklós, Veres, Balázs, Jakus, Péter B., Antus, Csenge, Montskó, Gergely, Zrínyi, Zita, Vladimir-Knežević, Sanda, Petrik, József, Kőszegi, Tamás
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Sprache:eng
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Zusammenfassung:•Diosmetin (DIOS) increases ATP levels both in kidney and in liver cells.•Inhibition of glycolysis or citric acid cycle does not decrease the observed effect.•DIOS-induced elevation of ATP levels is abolished by the inhibition of ATP synthase.•DIOS is able to completely reverse the ATP-depleting effect of ochratoxin A.•DIOS-induced impact on ATP does not originate from its antioxidant property. Diosmetin (DIOS) is a flavone aglycone commonly occurring in citrus species and olive leaves, in addition it is one of the active ingredients of some medications. Based on both in vitro and in vivo studies several beneficial effects are attributed to DIOS but the biochemical background of its action seems to be complex and it has not been completely explored yet. Previous investigations suggest that most of the flavonoid aglycones have negative effect on ATP synthesis in a dose dependent manner. In our study 17 flavonoids were tested and interestingly DIOS caused a significant elevation of intracellular ATP levels after 6- and 12-h incubation in MDCK kidney cells. In order to understand the mechanism of action, intracellular ATP and protein levels, ATP/ADP ratio, cell viability and ROS levels were determined after DIOS treatment. In addition, impacts of different enzyme inhibitors and effect of DIOS on isolated rat liver mitochondria were also tested. Finally, the influence of DIOS on the ATP depleting effect of the mycotoxin, ochratoxin A was also investigated. Our major conclusions are the followings: DIOS increases intracellular ATP levels both in kidney and in liver cells. Inhibition of glycolysis or citric acid cycle does not decrease the observed effect. DIOS-induced elevation of ATP levels is completely abolished by the inhibition of ATP synthase. DIOS is able to completely reverse the ATP-depleting effect of the mycotoxin, ochratoxin A. Most probably the DIOS-induced impact on ATP system does not originate from the antioxidant property of DIOS. Based on our findings DIOS may be promising agent to positively influence ATP depletion caused by some metabolic poisons.
ISSN:1011-1344
1873-2682
DOI:10.1016/j.jphotobiol.2014.01.016