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. 1977 Apr 15;164(1):33–39. doi: 10.1042/bj1640033

Guanylate cyclase activity and cyclic nucleotide concentrations during liver regeneration after experimental injury

Christo Goridis *,§, Jean Zwiller , Werner Reutter
PMCID: PMC1164755  PMID: 18146

Abstract

Cyclic nucleotide concentrations and guanylate cyclase activity were measured in regenerating rat liver. Previous work has shown that in livers of partially hepatectomized rats the activity of a membrane-bound guanylate cyclase increases considerably during the early replicative phase [Kimura & Murad (1975) Proc. Natl. Acad. Sci. U.S.A. 72, 1965–1969; Goridis & Reutter (1975) Nature (London) 257, 698–700]. Over the same time period after partial hepatectomy, increased tissue concentrations of cyclic GMP were found when the rats were killed under pentobarbital anaesthesia, but not when anaesthesia was omitted. The results obtained on hepatectomized livers were compared with the changes in guanylate cyclase activity and cyclic nucleotide concentrations during the response to galactosamine treatment. Here, a peak of guanylate cyclase activity and of cyclic GMP concentrations occurred at 8h, that is before the beginning of the proliferative response. Both parameters were normal at the time of increased DNA synthesis. There does not, therefore, seem to be a consistent correlation between changes in guanylate cyclase activity or concentrations of cyclic GMP and an increase in liver DNA synthesis. A modest rise in cyclic AMP concentrations was found, however, in livers of galactosamine-treated rats, which was coincident with the time of DNA synthesis.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. BUCHER N. L. REGENERATION OF MAMMALIAN LIVER. Int Rev Cytol. 1963;15:245–300. doi: 10.1016/s0074-7696(08)61119-5. [DOI] [PubMed] [Google Scholar]
  2. CERIOTTI G. A microchemical determination of desoxyribonucleic acid. J Biol Chem. 1952 Sep;198(1):297–303. [PubMed] [Google Scholar]
  3. Cailla H. L., Racine-Weisbuch M. S., Delaage M. A. Adenosine 3',5' cyclic monophosphate assay at 10-15 mole level. Anal Biochem. 1973 Dec;56(2):394–407. doi: 10.1016/0003-2697(73)90205-4. [DOI] [PubMed] [Google Scholar]
  4. Cailla H. L., Vannier C. J., Delaage M. A. Guanosine 3', 5'-cyclicmonophosphate assay at 10(-15)-mole level. Anal Biochem. 1976 Jan;70(1):195–202. doi: 10.1016/s0378-5173(83)90100-x. [DOI] [PubMed] [Google Scholar]
  5. EMMELOT P., BOS C. J., BENEDETTI E. L., RUEMKE P. STUDIES ON PLASMA MEMBRANES. I. CHEMICAL COMPOSITION AND ENZYME CONTENT OF PLASMA MEMBRANES ISOLATED FROM RAT LIVER. Biochim Biophys Acta. 1964 Jul 15;90:126–145. doi: 10.1016/0304-4165(64)90125-4. [DOI] [PubMed] [Google Scholar]
  6. Fausto N., Butcher F. R. Cyclic nucleotide levels in regenerating liver. Biochim Biophys Acta. 1976 May 28;428(3):702–706. doi: 10.1016/0304-4165(76)90200-2. [DOI] [PubMed] [Google Scholar]
  7. Goridis C., Reutter W. Plasma membrane-associated increase in guanylate cyclase activity in regenerating rat liver. Nature. 1975 Oct 23;257(5528):698–700. doi: 10.1038/257698a0. [DOI] [PubMed] [Google Scholar]
  8. Helwig J. J., Bollack C., Mandel P., Goridis C. Renal cortex guanylate cyclase. Preferential enrichment in glomerular membranes. Biochim Biophys Acta. 1975 Feb 19;377(2):463–472. doi: 10.1016/0005-2744(75)90326-5. [DOI] [PubMed] [Google Scholar]
  9. Keppler D., Lesch R., Reutter W., Decker K. Experimental hepatitis induced by D-galactosamine. Exp Mol Pathol. 1968 Oct;9(2):279–290. doi: 10.1016/0014-4800(68)90042-7. [DOI] [PubMed] [Google Scholar]
  10. Kimura H., Murad F. Increased particulate and decreased soluble guanylate cyclase activity in regenerating liver, fetal liver, and hepatoma. Proc Natl Acad Sci U S A. 1975 May;72(5):1965–1969. doi: 10.1073/pnas.72.5.1965. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Kimura H., Thomas E., Murad F. Effects of decapitation, ether and pentobarbital on guanosine 3',5'-phosphate and adenosine 3',5'-phosphate levels in rat tissues. Biochim Biophys Acta. 1974 May 24;343(3):519–528. doi: 10.1016/0304-4165(74)90269-4. [DOI] [PubMed] [Google Scholar]
  12. LOWRY O. H., ROSEBROUGH N. J., FARR A. L., RANDALL R. J. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951 Nov;193(1):265–275. [PubMed] [Google Scholar]
  13. Lesch R., Bachmann W., Reutter W. The alteration of the regenerative activity and the cell cycle of partially hepatectomized rat liver following administration of D-galactosamine. Cell Tissue Kinet. 1973 May;6(3):315–323. doi: 10.1111/j.1365-2184.1973.tb01620.x. [DOI] [PubMed] [Google Scholar]
  14. Lesch R., Reutter W., Keppler D., Decker K. Liver restitution after acute galactosamine hepatitis: autoradiographic and biochemical studies in rats. Exp Mol Pathol. 1970 Feb;12(1):58–69. doi: 10.1016/0014-4800(70)90075-4. [DOI] [PubMed] [Google Scholar]
  15. Macmanus J. P., Franks D. J., Youdale T., Braceland B. M. Increases in rat liver cyclic AMP concentrations prior to the initiation of DNA synthesis following partial hepatectomy or hormone infusion. Biochem Biophys Res Commun. 1972 Dec 4;49(5):1201–1207. doi: 10.1016/0006-291x(72)90596-7. [DOI] [PubMed] [Google Scholar]
  16. NEVILLE D. M., Jr The isolation of a cell membrane fraction from rat liver. J Biophys Biochem Cytol. 1960 Oct;8:413–422. doi: 10.1083/jcb.8.2.413. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Pastan I. H., Johnson G. S., Anderson W. B. Role of cyclic nucleotides in growth control. Annu Rev Biochem. 1975;44:491–522. doi: 10.1146/annurev.bi.44.070175.002423. [DOI] [PubMed] [Google Scholar]
  18. Reutter W., Lesch R., Keppler D., Decker K. Galactosamin-Hepatitis. Naturwissenschaften. 1968 Oct;55(10):497–497. doi: 10.1007/BF00599726. [DOI] [PubMed] [Google Scholar]
  19. Rudland P. S., Gospodarowicz D., Seifert W. Activation of guanyl cyclase and intracellular cyclic GMP by fibroblast growth factor. Nature. 1974 Aug 30;250(5469):741-2, 773-4. doi: 10.1038/250741a0. [DOI] [PubMed] [Google Scholar]
  20. Rudland P. S., Seeley M., Seifert W. Cyclic GMP and cyclic AMP levels in normal and transformed fibroblasts. Nature. 1974 Oct 4;251(5474):417–419. doi: 10.1038/251417a0. [DOI] [PubMed] [Google Scholar]
  21. Short J., Tsukada K., Rudert W. A., Lieberman I. Cyclic adenosine 3':5'-monophosphate and the induction of deoxyribonucleic acid synthesis in liver. J Biol Chem. 1975 May 25;250(10):3602–3606. [PubMed] [Google Scholar]
  22. Thrower S., Ord M. G. Hormonal control of liver regeneration. Biochem J. 1974 Nov;144(2):361–369. doi: 10.1042/bj1440361. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. WOLLENBERGER A., RISTAU O., SCHOFFA G. [A simple technic for extremely rapid freezing of large pieces of tissue]. Pflugers Arch Gesamte Physiol Menschen Tiere. 1960;270:399–412. [PubMed] [Google Scholar]
  24. Whitfield J. F., MacManus J. P., Rixon R. H., Boynton A. L., Youdale T., Swierenga S. The positive control of cell proliferation by the interplay on calcium ions and cyclic nucleotides. A review. In Vitro. 1976 Jan;12(1):1–18. doi: 10.1007/BF02832787. [DOI] [PubMed] [Google Scholar]

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