Authors
George A Brooks, Hervé Dubouchaud, Marcia Brown, James P Sicurello, C Eric Butz
Publication date
1999/2/2
Journal
Proceedings of the National Academy of Sciences
Volume
96
Issue
3
Pages
1129-1134
Publisher
The National Academy of Sciences
Description
To evaluate the potential role of mitochondrial lactate dehydrogenase (LDH) in tissue lactate clearance and oxidation in vivo, isolated rat liver, cardiac, and skeletal muscle mitochondria were incubated with lactate, pyruvate, glutamate, and succinate. As well, α-cyano-4-hydroxycinnamate (CINN), a known monocarboxylate transport inhibitor, and oxamate, a known LDH inhibitor were used. Mitochondria readily oxidized pyruvate and lactate, with similar state 3 and 4 respiratory rates, respiratory control (state 3/state 4), and ADP/O ratios. With lactate or pyruvate as substrates, α-cyano-4-hydroxycinnamate blocked the respiratory response to added ADP, but the block was bypassed by addition of glutamate (complex I-linked) and succinate (complex II-linked) substrates. Oxamate increased pyruvate (≈10–40%), but blocked lactate oxidation. Gel electrophoresis and electron microscopy indicated LDH isoenzyme …
Total citations
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Scholar articles
GA Brooks, H Dubouchaud, M Brown, JP Sicurello… - Proceedings of the National Academy of Sciences, 1999