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Succinate in ischemia: Where does it come from?
被引:39
|作者:
Chinopoulos, Christos
[1
]
机构:
[1] Semmelweis Univ, Dept Med Biochem, Tuzolto St 37-47, H-1094 Budapest, Hungary
来源:
关键词:
Fumarate;
Hypoxia;
Anoxia;
Substrate-level phosphorylation;
TCA cycle;
Succinate dehydrogenase;
SUBSTRATE-LEVEL PHOSPHORYLATION;
CITRIC-ACID CYCLE;
MITOCHONDRIAL ENERGY-METABOLISM;
CATALYTIC ELECTRON-TRANSPORT;
FUMARATE REDUCTASE-ACTIVITY;
ANAEROBIC RAT-HEART;
COMPLEX II;
NUCLEOSIDE DIPHOSPHOKINASE;
UBIQUINONE REDUCTASE;
REPERFUSION INJURY;
D O I:
10.1016/j.biocel.2019.105580
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
During tissue ischemia succinate accumulates. Herein, literature spanning the past nine decades is reviewed leaning towards the far greater role of Krebs cycle's canonical activity yielding succinate through alpha-ketoglutarate - > succinyl-CoA - > succinate even in hypoxia, as opposed to reversal of succinate dehydrogenase. Furthermore, the concepts of i) a diode-like property of succinate dehydrogenase rendering it difficult to reverse, and ii) the absence of mammalian mitochondrial quinones exhibiting redox potentials in the [-60, -80] mV range needed for fumarate reduction, are discussed. Finally, it is emphasized that a "fumarate reductase" enzyme entity reducing fumarate to succinate found in some bacteria and lower eukaryotes remains to be discovered in mammalian mitochondria.
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页数:6
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