Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Query: EC:3.6.3.14 (
ATP synthase
)
7,042
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
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.
...
PMID:Flavonoid diosmetin increases ATP levels in kidney cells and relieves ATP depleting effect of ochratoxin A. 2455 81