Abstract
1. Isolated hepatocytes were used to establish the reasons for the accumulation of aspartate, previously observed when the isolated rat liver was perfused with ethanol in the presence of alanine or ammonium lactate. 2. The isolated cells did not form aspartate when incubated with alanine and ethanol, but much aspartate was formed on incubation with ammonium lactate and ethanol. 3. Urea was the main nitrogenous product on incubation with alanine, in contrast with the perfused liver, where major quantities of NH4+ are also formed. When the formation of urea was nullified by the addition of urease, alanine plus ethanol caused aspartate formation, indicating that aspartate formation depends on the presence of critical concentrations of NH4+. 4. The accumulated aspartate was present in the cytosol. Ethanol halved the content of 2-oxoglutarate in the cytosol and more than trebled that of glutamate in the mitochondria. 5. The findings support the assumption that 2-oxoglutarate formed by the mitochondrial aspartate aminotransferase is not translocated to the cytosol in the presence of ethanol and NH4+, because it is rapidly converted into glutamate, the dehydrogenation of ethanol providing the required NADH. Aspartate, however, is translocated to the cytosol and accumulates there because of the lack of stoicheiometric amounts of oxoglutarate.
MeSH Terms
Alanine/metabolism
Ammonia/metabolism
Ammonium Chloride/metabolism
Animals
Aspartic Acid/biosynthesis
Cytosol/metabolism
Ethanol/pharmacology
Female
Gluconeogenesis/drug effects
Glutamates/metabolism
Ketoglutaric Acids/metabolism
Lactates/metabolism
Liver/drug effects,metabolism
Mitochondria, Liver/metabolism
Ornithine/pharmacology
Rats
Urea/biosynthesis
Chemicals
Glutamates
Ketoglutaric Acids
Lactates
Ammonium Chloride
Aspartic Acid
Ethanol
Ammonia
Urea
Ornithine
Alanine
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Stubbs M
Krebs H A
References (11)
11 references, click to expand
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