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Aicariboside Inhibits Gluconeogenesis in Isolated Rat Hepatocytes

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Purine and Pyrimidine Metabolism in Man VII

Part of the book series: Advances in Experimental Medicine and Biology ((AEMB,volume 309B))

Abstract

AICAriboside (5-amino-4-imidazolecarboxamide riboside, Z-riboside) is the nucleoside corresponding to AICAribotide (AICAR or ZMP), an intermediate of the “de novo” biosynthesis of purines. AICAriboside is taken up and metabolized by various mammalian tissues, in which it is converted into ZMP by adenosine kinase (1,2). Development of AICAriboside for the treatment of human cardiovascular disease (3) led to the observation of reduction of blood glucose following large infusion (4). Investigations of the effects of AICAriboside on liver were therefore undertaken.

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References

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© 1991 Plenum Press, New York

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Vincent, M.F., Marangos, P., Gruber, H.E., Van den Berghe, G. (1991). Aicariboside Inhibits Gluconeogenesis in Isolated Rat Hepatocytes. In: Harkness, R.A., Elion, G.B., Zöllner, N. (eds) Purine and Pyrimidine Metabolism in Man VII. Advances in Experimental Medicine and Biology, vol 309B. Springer, New York, NY. https://doi.org/10.1007/978-1-4615-7703-4_81

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  • DOI: https://doi.org/10.1007/978-1-4615-7703-4_81

  • Publisher Name: Springer, New York, NY

  • Print ISBN: 978-1-4615-7705-8

  • Online ISBN: 978-1-4615-7703-4

  • eBook Packages: Springer Book Archive

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