Dibutyryl cyclic AMP stimulated the activity of phosphoenolpyruvate carboxykinase in perfused livers of rats, fed on a low-protein diet, linearly over a 6h period. The enzyme activity was also significantly elevated by dexamethasone, the effect being considerably lower than that of the cyclic nucleotide. Since the time-course of phosphoenolpyruvate carboxykinase activity in response to dibutyryl cyclic AMP resembled that observed after dibutyryl cyclic AMP injection into intact animals, it is suggested that induction of the enzyme in vivo is due to a direct action of the cyclic nucleotide on the liver. Combined administration of dibutyryl cyclic AMP and glucocorticoids did not lead to an additive increase of liver phosphoenolpyruvate carboxykinase activity, either in vivo or in the perfused organ.
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September 1974
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Research Article|
September 01 1974
Stimulation by 6-N,2′-O-dibutyryladenosine 3′:5′-cyclic monophosphate and glucocorticoids of phosphoenolpyruvate carboxykinase in the isolated perfused rat liver (Short Communication) Available to Purchase
Wieland B. Huttner;
Wieland B. Huttner
1Physiologisch-Chemisches Institut der Universität, 2 Hamburg 20, Martinistrasse 52, German Federal Republic
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Wilhelm Krone;
Wilhelm Krone
1Physiologisch-Chemisches Institut der Universität, 2 Hamburg 20, Martinistrasse 52, German Federal Republic
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Hans J. Seitz;
Hans J. Seitz
1Physiologisch-Chemisches Institut der Universität, 2 Hamburg 20, Martinistrasse 52, German Federal Republic
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Wolfgang Tarnowski
Wolfgang Tarnowski
1Physiologisch-Chemisches Institut der Universität, 2 Hamburg 20, Martinistrasse 52, German Federal Republic
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Publisher: Portland Press Ltd
Online ISSN: 1470-8728
Print ISSN: 0264-6021
© 1974 London: The Biochemical Society
1974
Biochem J (1974) 142 (3): 691–693.
Citation
Wieland B. Huttner, Wilhelm Krone, Hans J. Seitz, Wolfgang Tarnowski; Stimulation by 6-N,2′-O-dibutyryladenosine 3′:5′-cyclic monophosphate and glucocorticoids of phosphoenolpyruvate carboxykinase in the isolated perfused rat liver (Short Communication). Biochem J 1 September 1974; 142 (3): 691–693. doi: https://doi.org/10.1042/bj1420691
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