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Effect of Portacaval Anastomosis on Glutamine Synthetase Protein and Gene Expression in Brain, Liver and Skeletal Muscle

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Abstract

The effects of chronic liver insufficiency resulting from end-to-side portacaval anastomosis (PCA) on glutamine synthetase (GS) activities, protein and gene expression were studied in brain, liver and skeletal muscle of male adult rats. Four weeks following PCA, activities of GS in cerebral cortex and cerebellum were reduced by 32% and 37% (p<0.05) respectively whereas GS activities in muscle were increased by 52% (p<0.05). GS activities in liver were decreased by up to 90% (p<0.01), a finding which undoubtedly reflects the loss of GS-rich perivenous hepatocytes following portal-systemic shunting. Immunoblotting techniques revealed no change in GS protein content of brain regions or muscle but a significant loss in liver of PCA rats. GS mRNA determined by semi-quantitative RT-PCR was also significantly decreased in the livers of PCA rats compared to sham-operated controls. These findings demonstrate that PCA results in a loss of GS gene expression in the liver and that brain does not show a compensatory induction of enzyme activity, rendering it particularly sensitive to increases in ammonia in chronic liver failure. The finding of a post-translational increase of GS in muscle following portacaval shunting suggests that, in chronic liver failure, muscle becomes the major organ responsible for the removal of excess blood-borne ammonia.

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REFERENCES

  • Butterworth, R.F., Giguère, J.F., Michaud, J., Lavoie, J., and Pomier Layrargues, G. (1987). Ammonia: Key factor in the pathogenesis of hepatic encephalopathy. Neurochem. Pathol. 6:1–12.

    Google Scholar 

  • Butterworth, R.F., Girard, G. and Giguère, J. F. (1988). Regional differences in the capacity for ammonia removal by brain following portacaval anastomosis. J. Neurochem. 51:486–490.

    Google Scholar 

  • Butterworth, R.F. (1992). Evidence that hepatic encephalopathy results from a defect of glutamatergic synaptic regulation. Molec. Neuropharmacol. 2:229–232.

    Google Scholar 

  • Cooper, A.J.L., Mora, S.N., Cruz, N.F. and Gelbard, A.S. (1985). Cerebral ammonia metabolism in hyperammonemic rats. J. Neurochem. 4:1716–1723.

    Google Scholar 

  • Ganda, O.P. and Ruderman, N.B. (1976). Muscle nitrogen metabolism in chronic hepatic insufficiency. Metabolism 25:427–435.

    Google Scholar 

  • Gerbhardt, R, and Mecke, D. (1983). Heterogeneous distribution of glutamine synthetase among rat liver parenchymal cells in situ and in primary culture. EMBO J. 2:567–570.

    Google Scholar 

  • Giguère, J.F., Besnard, A.M., Lavoie, J., Pomier Layrargues, G., and Butterworth, R.F. (1989). Activities of glutamate-related enzymes in autopsied brain tissue from cirrhotic patients with hepatic encephalopathy. In (R.F. Butterworth and G. Pomier Layrargues, eds.) Hepatic Encephalopathy: Pathophysiology and Treatment, Humana Press, N.J., pp. 435–445.

    Google Scholar 

  • Girard, G., Giguère, J.-F. and Butterworth, R.F. (1993). Region-selective reductions in activities of glutamine synthetase in rat brain following portacaval anastomosis. Metab. Brain Dis. 8:207–215.

    Google Scholar 

  • Girard, G. and Butterworth, R.F. (1992). Effect of portacaval anastomosis on glutamine synthetase activities in liver, brain, and skeletal muscle. Dig. Dis. Sci. 37:1121–1126.

    Google Scholar 

  • Hansson, E. (1986). Primary cultures from defined brain areas III. Effects of seeding time on 3H-L-glutamate transport and glutamine synthetase activity. Dev. Brain Res. 24:203–209.

    Google Scholar 

  • Kaiser, S., Gerok, W., and Haussinger, D. (1988). Ammonia and glutamine metabolism in human liver slices: new aspects on the pathogenesis of hyperammonemia in chronic liver disease. Eur. J. Clin. Invest. 18:535–542.

    Google Scholar 

  • Kun, E. and Kearney, E.B. (1974). Ammonia. In (H.V. Berkmeyer, ed.) Methods of Enzymatic Analysis, Academy press, New York, pp. 1802–1806.

    Google Scholar 

  • Lavoie, J., Giguère, J.F., Pomier Layrargues G. and Butterworth, R.F. (1987). Activities of neuronal and astrocytic marker enzymes in autopsied brain tissue from patients with hepatic encephalopathy. MeTable Brain Dis. 2:283–290.

    Google Scholar 

  • Lee, S.H., and Fisher, B. (1961). Portocaval shunt in the rat. Surgery 50:668–672.

    Google Scholar 

  • Lockwood, A.H., McDonald, J.M., Reiman, R.E., Gelbard, A.S., Laughlin, J.S., Duffy, T.E. et al. (1979). The dynamics of ammonia metabolism in man. J. Clin. Invest. 63:449–460.

    Google Scholar 

  • Lowry, O.H., Rosebrough, N.J., Farr, A.L. and Randall, R.J. (1951). Protein measurement with the Folin phenol reagent. J. Biol. Chem. 193:265–275.

    Google Scholar 

  • Mill, J.F., Mearow K.M., Purohit, H.J., Haleem-Smith, H., King, R., and Freese, E. (1991). Cloning and functional characterization of the rat glutamine synthetase gene. Brain Res. Mol. Brain Res. 9:197–207.

    Google Scholar 

  • Moroni, F., Lombardi, G., Moneti, G., and Cortesini, C. (1983). The release and neosynthesis of glutamic acid are increased in experimental models of hepatic encephalopathy. J. Neurochem. 40:850–854.

    Google Scholar 

  • Norenberg, M.D. and Martinez-Hernandez, A. (1979). Fine structural localization of glutamine synthetase in astrocytes of rat brain. Brain Res. 161:631–635.

    Google Scholar 

  • Patel, A.J., Hunt, A., and Tahourdin, C.S.M. (1983). Regional development of glutamine synthetase activity in the rat brain and its association with the differentiation of astrocytes. Dev. Brain Res. 8:31–37.

    Google Scholar 

  • Ponte, P, Ng, S.Y., Engel, J., Gunning, P. And Kedes, L. (1984). Evolutionary conservation in the untranslated regions of actin mRNAs: DNA sequence of a human beta-actin cDNA. Nucleic Acids Res. 12:1687–1696.

    Google Scholar 

  • Qureshi, I.A., Ratnakumari, L. and Butterworth, R.F. (1995). Cerebral glutamate synthetase and glutamate dehydrogenase in congenitally hyperammonemic sparse-fur (spf/Y) mice: effect of acetyl-L-carnitine. Adv. Hepatic Enceph. and MeTable Nitrogen Exchange (CRC Press), pp. 154–158.

  • Tossman, U., Delin, A., Eriksson, L.S., and Ungerstedt, U. (1987). Brain cortical amino acids measured by intracerebral dialysis in portacaval shunted rats. Neurochem. Res. 12:265–269.

    Google Scholar 

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Correspondence to Roger F. Butterworth.

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Desjardins, P., Rao, K.R., Michalak, A. et al. Effect of Portacaval Anastomosis on Glutamine Synthetase Protein and Gene Expression in Brain, Liver and Skeletal Muscle. Metab Brain Dis 14, 273–280 (1999). https://doi.org/10.1023/A:1020741226752

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