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Research Article Free access | 10.1172/JCI107489

Alkaline Phosphatase. POSSIBLE INDUCTION BY CYCLIC AMP AFTER CHOLERA ENTEROTOXIN ADMINISTRATION

Alfred Baker, Marshall Kaplan, and Daniel V. Kimberg

Gastroenterology Section of the Department of Medicine, Tufts-New England Medical Center, Boston, Massachusetts 02111

Department of Medicine, Harvard Medical School and the Gastrointestinal Unit of the Beth Israel Hospital, Boston, Massachusetts 02215

Find articles by Baker, A. in: PubMed | Google Scholar

Gastroenterology Section of the Department of Medicine, Tufts-New England Medical Center, Boston, Massachusetts 02111

Department of Medicine, Harvard Medical School and the Gastrointestinal Unit of the Beth Israel Hospital, Boston, Massachusetts 02215

Find articles by Kaplan, M. in: PubMed | Google Scholar

Gastroenterology Section of the Department of Medicine, Tufts-New England Medical Center, Boston, Massachusetts 02111

Department of Medicine, Harvard Medical School and the Gastrointestinal Unit of the Beth Israel Hospital, Boston, Massachusetts 02215

Find articles by Kimberg, D. in: PubMed | Google Scholar

Published November 1, 1973 - More info

Published in Volume 52, Issue 11 on November 1, 1973
J Clin Invest. 1973;52(11):2928–2934. https://doi.org/10.1172/JCI107489.
© 1973 The American Society for Clinical Investigation
Published November 1, 1973 - Version history
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Abstract

The present studies were undertaken to determine the role, if any, of cyclic 3′,5′-adenosine monophosphate (cyclic AMP) as a chemical inducer of rat liver alkaline phosphatase. Cholera enterotoxin, given intravenously to rats, led to a rapid rise in the activity of hepatic adenyl cyclase that was 7½ times greater than control values in 6 h. Cyclic AMP levels were also significantly increased above control values while the activity of cyclic nucleotide phosphodiesterase was unchanged. Hepatic alkaline phosphatase activity was increased 5½ times above control in 12 h, but its rise followed that of adenyl cyclase and cyclic AMP by several hours. Cycloheximide inhibited the rise of hepatic alkaline phosphatase but not that of adenyl cyclase. The administration of glucagon, a known stimulator of hepatic adenyl cyclase, and of dibutyryl cyclic AMP, led to similar striking increases in hepatic alkaline phosphatase activity. This alkaline phosphatase increase was blocked by the prior administration of cycloheximide. Bile duct ligation, a known stimulator of hepatic alkaline phosphatase activity, failed to produce any significant changes in adenyl cyclase or cyclic AMP. Concomitant treatment of rats with bile duct ligation and cholera enterotoxin or bile duct ligation and glucagon, had no additive effect on the increase in hepatic alkaline phosphatase activity, although the increase occurred earlier. These results suggest that: (a) cyclic AMP may act as an inducer of hepatic alkaline phosphatase: (b) the stimulation of hepatic alkaline phosphatase by cholera enterotoxin is mediated by cyclic AMP; (c) the rise in hepatic alkaline phosphatase following bile duct ligation is not mediated by cyclic AMP; (d) the same alkaline phosphatase in rat liver may be induced by two (or more) mechanisms, only one of which requires cyclic AMP.

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