Skip to main content
Log in

Effect of Ischemia-Reperfusion on Heat Shock Protein 70 and 90 Gene Expression in Rat Liver: Relation to Nutritional Status

  • Published:
Digestive Diseases and Sciences Aims and scope Submit manuscript

Abstract

Heat shock proteins are intracellular proteinsassociated with a generalized response of cells tostress. The purpose of this study was to assess RNAlevels of heat shock protein 70 and 90 in fed or fasted rat livers during ischemia-reperfusion.Northern blot analysis of heat shock proteins wasperformed. Adenosine triphosphate and glutathione wereassessed. In baseline conditions, livers of fasted ratsshowed a twofold increase in mRNA for both heat shockproteins and 38% and 43% reductions in adenosinetriphosphate and glutathione, respectively, whencompared with organs from fed rats. After ischemia,livers of fasted rats presented a twofold decrease inheat shock protein mRNA, while no changes were observedin livers of fed rats; reduced glutathione and adenosinetriphosphate decreased 55% and 50% in fasted livers and 25% and 20% in fed organs,respectively. After 120 min of reperfusion, heat shockprotein mRNA rose threefold in fasted livers, while aslight decrease was observed in the fed group; reduced glutathione and adenosine triphosphate returnedto 65% and 70% of baseline values in fasted livers and85% and 90% in fed organs, respectively. In conclusion,the nutritional status affects heat shock protein expression determined by reperfusion. Thereduced antioxidant status leading to increasedoxidative stress could be the mechanism underlying thephenomenon.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

REFERENCES

  1. Rymsa B, Wang JF, De Groot H: O2 release by activated Kuppfer cells upon hypoxia-reoxygenation. Am J Physiol 261:G602-G607, 1991

    Google Scholar 

  2. Broughan TA, Jin GF, Papacostantinou J: Early gene response to hepatic ischemia/reperfusion. J Surg Res 63:98 -104, 1996

    Google Scholar 

  3. Schoeniger LO, Reilly P, Bulkley GB, Buchman TG: Molecular biology of circulatory shock. V. Heat shock gene expression exclude s hepatic acute phase gene expression following resuscitation from hemorragic shock. Surgery 112:355-363, 1992

    Google Scholar 

  4. Schoeniger LO, Andreoni KA, Ott GR, Risby TH, Bulkley GB, Udelsman R, Burdick JF, et al: Induction of heat-shock gene expression in postischemic pig liver depends on superoxide generation. Gastroenterology 106:177-184, 1994 (zaq;2

    Google Scholar 

  5. Schiaffonati L, Rappocciolo E, Tacchini L, Cairo G, Bernelli-Zazzera A: Reprogramming of gene expression in postischemic rat liver: Induction of proto-oncogenes and hsp 70 gene family. J Cell Physiol 143:79 -87, 1990

    Google Scholar 

  6. Li GC: Induction of thermotolerance and enhanced heat shock protein synthesis in Chinese hamster fibroblast by sodium arsenite and by ethanol. J Cell Physiol 115:116 -122, 1983

    Google Scholar 

  7. Watowich SS, Morimoto RI: Complex regulation of heat shock and glucose responsive genes in human cells. Mol Cell Biol 8:393-405, 1988

    Google Scholar 

  8. Hightower LE: Heat shock, stress protein, chaperones, and proteotoxicity. Cell 66:191-197, 1991

    Google Scholar 

  9. Schiaffonati L, Tacchini L, Pappalardo C: Heat shock response in the liver: Expression and regulation of the HSP70 gene family and early response genes after in vivohyperthermia. Hepatology 20:975-983, 1994

    Google Scholar 

  10. Chomczynsky P, Sacchi N: Single step method of RNA extraction by acid guanidinium thiocyanate -phenol-chloroform extraction. Anal Biochem 162:156 -159, 1979

    Google Scholar 

  11. Cairo G, Bardella L, Schiaffonati L, Arosio P, Levi S, Bernelli-Zazzera A: Multiple mechanisms of iron-induced ferritin synthesis in He La cells. Biochem Biophys Res Commun 133:314 - 321, 1985

    Google Scholar 

  12. Tietze F: Enzymatic method for quantitative determination of nanogram amounts of total and oxidated glutathione: Applications to mammalian blood and other tissue. Anal Biochem 27:502-522, 1969

    Google Scholar 

  13. Donne lly TJ, Sievers RE, Vissern FLJ, Welch WJ, Wolfe CL: Heat shock protein induction in rat hearts: a role for improved myocardial salvage after ischemia and reperfusion? Circulation 85:769 -778, 1982

    Google Scholar 

  14. Perdrizet GA, Kaneko H, Buckley TM, Fishman MS, Pleau M, Bow L, Schweizer RT: Heat shock and recovery protects renal allografts from warm ischemic injury and enhances HSP 72 production. Transplant Proc 25:1670 -1673, 1993

    Google Scholar 

  15. Van Why SK, Hildebrandt F, Ardito T, Mann AS, Siegel NJ, Kashgarian M: Induction and intracellular location of HSP 72 after renal ischemia. Am J Physiol 263:F769 -F775, 1992

    Google Scholar 

  16. Currie RW, Tanguay RM, Kingma JG: He at shock response and limitation of tissue necrosis during occlusion/reperfusion in rabbit hearts. Circulation 87:963-971, 1993

    Google Scholar 

  17. De Groot H, Brecht M: Reoxygenation injury in rat hepatocytes: medication by O2/H2O2 liberated by sources other than xanthine oxidase. Biol Chem Hoppe Seyler 372:35-41, 1991

    Google Scholar 

  18. Buchman TG, Cabin DE, Vickers S, Deutschman CS, Delgado E, Sussman MM, Bulkley GB: Molecular biology of circulatory shock. Expression of four groups of hepatic genes is enhanced following re suscitation from cardiogenic shock. Surgery 108:559 -566, 1990

    Google Scholar 

  19. Blake MJ, Gershon D, Fargnoli J, Holbrook NJ: Discordant expression of heat shock protein mRNAs in tissue of heat-stressed rats. J Biol Chem 25:15275-15279, 1990

    Google Scholar 

  20. Xia E, Rao G, Van Remmen H, Heydari AR, Richardson A: Activities of antioxidant enzymes in various tissues of male Fischer 344 rats are altearted by food restriction. J Nutr 125:195-201, 1995

    Google Scholar 

  21. Gasbarrini A, Borle AB, Fargharli H, Bender C, Francavilla A, Van Thiel DH: Effect of anoxia on intracellular ATP, Na+, Ca++ and cytotoxicity in rat hepatocytes. J. Biol Chem 267(10):6654 -6663, 1992

    Google Scholar 

  22. Gasbarrini A, Borle AB, Fargharli H, Caracini P, Francavilla A, Van Thiel DH: Fasting enhances the effects of anoxia on ATP, Ca+ and cell injury in isolated rat hepatocytes. Biochim Biophys Acta 1178:9 -19, 1993

    Google Scholar 

  23. Gasbarrini A, Colantoni A, Di Campli C, De Notariis S, Masetti M, Iovine E, Mazziotti A, Massari I, Gasbarrini G, Pola P, Bernardi M: Intermittent anoxia reduce s oxygen free radicals formation during reoxygenation in rat hepatocytes. Free Radic Biol Med 23:1067-1072, 1997

    Google Scholar 

  24. Gasbarrini A, Caraceni P, Colantoni A, De Notariis S, Facchini A, Roda E, Van Thiel DH, Gasbarrini G, Bernardi M: Nutritional status affects the sensitivity to anoxia/reoxyge nation in hepatocytes. Transplant Proc 26:3408 -3409, 1994

    Google Scholar 

Download references

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Gasbarrini, A., Esposti, S.D., Di Campli, C. et al. Effect of Ischemia-Reperfusion on Heat Shock Protein 70 and 90 Gene Expression in Rat Liver: Relation to Nutritional Status. Dig Dis Sci 43, 2601–2605 (1998). https://doi.org/10.1023/A:1026630706426

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1023/A:1026630706426

Navigation