Ischaemic accumulation of succinate controls reperfusion injury through mitochondrial ROS

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Summary

It is shown that selective accumulation of the citric acid cycle intermediate succinate is a universal metabolic signature of ischaemia in a range of tissues and is responsible for mitochondrial ROS production during reperfusion, and a new pathway for metabolic control of ROS production in vivo is revealed.

Type
article
Published
2014-11-05
Cited by
2,631
References
56

Keywords

Reactive oxygen species, Mitochondrial ROS, Reperfusion injury, Mitochondrion, Ischemia

References

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