Amphibolic role of the Krebs cycle in the insulin-stimulated protein synthesis
It has been a generally held view that insulin does not significantly affect the incorporation of amino acids into liver protein. This interpretation was based on data obtained from studies using the branched chain amino acids, which are poorly metabolized by the hepatic tissue. The effect of insuli...
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Published in | Archives of biochemistry and biophysics Vol. 289; no. 1; pp. 83 - 89 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
San Diego, CA
Elsevier Inc
15.08.1991
Elsevier |
Subjects | |
Online Access | Get full text |
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Summary: | It has been a generally held view that insulin does not significantly affect the incorporation of amino acids into liver protein. This interpretation was based on data obtained from studies using the branched chain amino acids, which are poorly metabolized by the hepatic tissue. The effect of insulin on
14CO
2 formation and protein incorporation of several 1-
14C-labeled or U-
14C-labeled amino acids was studied in isolated rat hepatocytes and diaphragm pieces. It was shown that insulin enhanced
14CO
2 formation and protein incorporation primarily of those carbons of amino acids which are metabolized through the mitochondrial Krebs cycle. Using aminooxyacetic acid (0.5 m
m), a potent inhibitor of the transamination reaction, it was shown that there exists an “insulin-sensitive” pool of glutamate which is preferentially utilized for protein synthesis in the presence of insulin. The insulin effect on protein incorporation of
14C-labeled glutamate generated in the Krebs cycle was abolished in the presence of aminooxyacetic acid. We interpret these results to signify that mitochondrial transamination of α-ketoglutarate to glutamate is essential for insulin stimulation of
14C incorporation into hepatocyte protein. |
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Bibliography: | S20 9156208 L50 ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0003-9861 1096-0384 |
DOI: | 10.1016/0003-9861(91)90445-O |