Abstract
1. N-Ethylmaleimide inhibited the influx and efflux of P(i) in rat liver mitochondria. 2. The efflux was stimulated by either succinate or malate in the presence of N-ethylmaleimide, and this stimulation was reversed by 2-n-butylmalonate. 2-Oxoglutarate and citrate, even in the presence of low concentrations of malate, were relatively ineffective in stimulating efflux of P(i) under these conditions, as was glutamate. 3. By using radioactively labelled P(i) and dicarboxylate ions an exchange was demonstrated, the stoicheiometry of which was 1.3+/-0.5 dicarboxylate ions:1 P(i) (n=10). 4. An exchange between unlabelled and labelled P(i) in the presence of N-ethylmaleimide was found which was sensitive to 2-n-butylmalonate. 5. It is concluded that the mitochondrial dicarboxylate carrier can transport phosphate by an exchange diffusion with certain penetrant dicarboxylic acids or with phosphate itself. The exchange mechanism is sensitive to 2-n-butylmalonate but is unaffected by N-ethylmaleimide; the action of mersalyl in this context is commented on.
MeSH Terms
Animals
Biological Transport, Active/drug effects
Butanes/pharmacology
Carbon Radioisotopes
Dicarboxylic Acids/metabolism
Ethylmaleimide/pharmacology
In Vitro Techniques
Ketoglutaric Acids/pharmacology
Malates/pharmacology
Malonates/pharmacology
Mitochondria, Liver/metabolism
Phosphates/metabolism
Phosphorus Radioisotopes
Rats
Succinates/pharmacology
Chemicals
Butanes
Carbon Radioisotopes
Dicarboxylic Acids
Ketoglutaric Acids
Malates
Malonates
Phosphates
Phosphorus Radioisotopes
Succinates
Ethylmaleimide
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Johnson R N
Chappell J B
References (14)
14 references, click to expand
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