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Has the arginase inhibitory role in liver cell multiplicationin vivo?

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Research in Experimental Medicine

Summary

An increase of arginase activity was found in the liver 6 and 12 hrs after partial hepatectomy in saline-treated (11.9 and 20.3%, respectively) and in phenobarbital-treated animals (16.3 and 61.8%, respectively). In both groups the increase of arginase activity was achieved only after the removal of a “threshold” amount of liver tissue. For saline-treated rats the “threshold” amount was two thirds hepatectomy and in phenobarbital treated rats 34% hepatectomy. In both groups of animals the maximal response was obtained at two thirds hepatectomy, which at the same time provokes the maximal proliferative activation of the liver cells.

The existence of a positive correlation between the degree of increase of arginase activity during the first hours after partial hepatectomy and the degree of DNA synthesis and mitotic activiation of liver tissue, which followed 12 hrs later, excludes the arginase as a factor which inhibits cells multiplication during the regenerative growth of the liver.

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References

  1. Bakay, B., Sorof, S.: Soluble nuclear proteins of liver and tumor in azo dye carcinogenesis. Cancer Res.24, 1814 (1964).

    PubMed  Google Scholar 

  2. Bucher, N. L. R.: Regeneration of mammalian liver. Int. Rev. Cytol.15, 249 (1963).

    Google Scholar 

  3. Cohen, S., O'Malley, B. W., Stansly, M.: Estrogenic induction of ornithine decarboxylase in vivo and in vitro. Science170, 336 (1970).

    PubMed  Google Scholar 

  4. Freed, J. J., Sorof, S.: Reversible inhibition of cell multiplication by a small class of liver proteins. Biochem. biophys. Res. Commun.22, 1 (1966).

    PubMed  Google Scholar 

  5. Higgins, G. M., Anderson, R. M.: Experimental pathology of the liver. I.Restoration of the liver in the white rat following partial surgical removal. Arch. Path.12, 186 (1931).

    Google Scholar 

  6. Japundžić, M., Knežević, B., Djordjević-Čamba, V., Japundžić, I.: The influence of phenobarbital-Na on the mitotic activity of parenchymal liver cells during rat liver regeneration. Exp. Cell Res.48, 163 (1967).

    PubMed  Google Scholar 

  7. Liebermann, I., Ove, P.: Inhibition of growth of cultured mammalian cells by liver extracts. Biochim. biophys. Acta (Amst.)38, 153 (1960).

    Google Scholar 

  8. MacLean, O., Reid, E., Gurney, M. W.: Effect of azo-dye carcinogenesis on enzymes concerned with urea synthesis in rat liver. Biochem. J.91, 464 (1964).

    PubMed  Google Scholar 

  9. MacDonald, R. A., Rogers, A. E., Pechet, G.: Regeneration of liver. Relation of regenerative response to size of partial hepatectomy. Lab. Invest.11, 544 (1962).

    Google Scholar 

  10. Otsuka, H.: Differences of the inhibitor of DNA synthesis in liver extract from liver arginase. Cacer Res.29, 265 (1969).

    Google Scholar 

  11. Roger, S., Moore, M. J.: Studies of the mechanism of action of the shope rabbit papilloma virus. I. Concerning the nature of the induction of arginase in the infected cells. J. exp. Med.117, 521 (1963).

    PubMed  Google Scholar 

  12. Sorof, S., Cohen, P. P., Miller, E. C., Milles, J. A.: Electrophoretic studies on the soluble proteins from livers of rats fed aminoazo dyes. Cancer Res.11, 383 (1951).

    PubMed  Google Scholar 

  13. Sorof, S. E., Young, E. M., Fettermann, P. L.: Liver h2 protein(s) as a specific binding site for metabolites of two types of hepatocarcinogens. Proc. Amer. Ass. Cancer3, 269 (1961).

    Google Scholar 

  14. Sorof, S., Young, E. M., Luongo, L., Kish, V. M., Fred, J. J.: Inhibition of cell multiplication in vitro by liver arginase. Growth regulating substances for Animal cells in culture. In: The Wistar Symposium Monograph No. 7, p. 25. Philadelphia: The Wistar Press 1967.

    Google Scholar 

  15. Sorof, S., Kish, V. M.: On molecular size of rat liver arginase. Cancer Res.29, 261 (1969).

    PubMed  Google Scholar 

  16. Sorof, S.: Carcinogen-protein Conjugates in liver carcinogenesis. In: The Jerusalim Symp. on Quantum Chemistry and Biochemistry I. The Israel Academy of Sciences and Humanities, Jerusalem 208, 1969.

  17. Sidorova, V. F.: Mitotic activity of the rat liver subjected to various surgical interferences. Bul. Eksp. Biol. i. Med.59, 95 (1965).

    Google Scholar 

  18. Schrock, T. R., Oakman, N. J., Buches, N. L. R.: Ornithine decarboxylase in relation to liver growth. Fed. Proc.28, 599 (1969).

    Google Scholar 

  19. Van Slyke, D. D., Archibald, R. M.: Gasometric and photometric measurement of arginase activity. J. biol. Chem.165, 293 (1946).

    Google Scholar 

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Japundžić, I., Čupić, Ž., Mimić-Oka, J. et al. Has the arginase inhibitory role in liver cell multiplicationin vivo? . Res. Exp. Med. 157, 317–324 (1972). https://doi.org/10.1007/BF01852075

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  • DOI: https://doi.org/10.1007/BF01852075

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