Skip to main content

Advertisement

Log in

The differential induction of two immediate early genes,c-fos andc-jun, after systemic hypovolemic shock/resuscitation in the rat liver and kidney

  • Original Articles
  • Published:
Surgery Today Aims and scope Submit manuscript

Abstract

The aim of this study was to investigate the expression of the immediate early genes (IEGs),c-fos andc-jun, in the rat kidney and liver in two types of hemorrhage shock/ resuscitation models. In the first group, hemorrhagic shock was induced by the withdrawal of blood through the carotid artery. A mean arterial blood pressure (MAP) of 40mmHg was maintained for 1h before blood was reperfused. In the second group, the MAP was maintained at the same level for 2 h. Animals were resuscitated with Ringer’s lactate solution. In the first group, a rapid and transient induction ofc-fos andc-jun mRNAs in both the liver and kidney was observed, peaking 0 to 2h after reperfusion. In the second group, a more protracted pattern of induction was evident in both organs. In both models, the induction ofc-fos mRNA was distinctly different in the liver and kidney. These results indicated, first, that with respect to IEG expression, organs respond differently to a systemic shock/resuscitation stimuli, and second, that alterations in the pattern of IEG expression might represent an indication of the degree of organ damage or the repair processes subsequent to hypotension/reperfusion.

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. Baue AE (1983) Multiple, progressive or sequential systems failure: a syndrome of the 1970s. Arch Surg 110:779–781

    Google Scholar 

  2. Faist E, Baue AE, Dittmer M, Hebere G (1983) Multiple organ failure in polytrauma patients. J Trauma 23:775–787

    Article  PubMed  CAS  Google Scholar 

  3. Ozawa K, Aoyama H, Yasuda K, Shimahara Y, Nakatani T, Tanaka J, Yamamoto M, Kamiyama Y, Tobe T (1983) Metabolic abnormalities associated with postoperative organ failure: a redox theory. Arch Surg 118:1245–1251

    PubMed  CAS  Google Scholar 

  4. Bellamy RF, Pedersen DC, DeGuzman LR (1984) Organ blood flow and the cause of death following massive hemorrhage. Circ Shock 14:113–127

    PubMed  CAS  Google Scholar 

  5. Guyton AC (1981) Textbook of Medical Physiology. Saunders, Philadelphia, pp 332–419

    Google Scholar 

  6. Wang P, Hauptman JG, Chaudry IH (1990) Hepatocellular dysfunction occurs early after hemorrhage and persists despite fluid resuscitation. J Surg Res 48:464–470

    Article  PubMed  CAS  Google Scholar 

  7. DePalma RG, Levey S, Holden WD (1970) Ultrastructure and oxidative phosphorylation of liver mitochondria in experimental hemorrhagic shock. J Trauma 10:122–134

    Article  PubMed  CAS  Google Scholar 

  8. Iwata S, Tanaka A, Ozawa K (1992) Alterations in the proton ATPase activity of rat liver mitochondria after hemorrhagic shock. J Lab Clin Med 120:420–427

    PubMed  CAS  Google Scholar 

  9. Rasmussen HH, Ibels LS (1982) Acute renal failure. Multivariate analysis of causes and risk factors. Am J Med 73:211–218

    Article  PubMed  CAS  Google Scholar 

  10. Ratcliffe PJ, Mooden CTW, Holloway PAH, Ledingham JGG, Radda GK (1986) Acute renal failure in haemorrhagic hypotension: cellular energetics and renal function. Kidney Int 30:355–360

    Article  PubMed  CAS  Google Scholar 

  11. Dobyan DC, Nagle RB, Bulger RE (1977) Acute tubular necrosis in the rat kidney following sustained hypotension. Lab Invest 37:411–422

    PubMed  CAS  Google Scholar 

  12. Morgan JI, Curran T (1991) Stimulus-transcription coupling in the nervous system: involvement of the inducible protooncogenes fos and jun. Annu Rev Neurosci 14:421–451

    Article  PubMed  CAS  Google Scholar 

  13. Curran T, Franza BR (1988) Fos and Jun. The AP-1 connection. Cell 55:395–397

    CAS  Google Scholar 

  14. Franza BR, Rauscher FJ, Josephs SF, Curran T (1988) The fos complex and fos related antigen recognize sequence elements that contain AP-1 sites. Science 239:1150–1153

    Article  PubMed  CAS  Google Scholar 

  15. Smeyne RJ, Vendrell M, Hayward M, Baker SJ, Miao GG, Schilling K, Robertson LM, Curran T, Morgan JI (1993) Continuousc-fos expression precedes programmed cell death in vivo. Nature 363:166–169

    Article  PubMed  CAS  Google Scholar 

  16. Maki A, Berezesky IK, Fragnoli J, HolbrooK NJ, Trump BF (1992) Role of [Ca2+]i in induction ofc-fos, c-jun and c-myc mRNA in rat PTE after oxidative stress. FASEB J 6:919–924

    PubMed  CAS  Google Scholar 

  17. Le F, Wilce PA, Cassady I, Hume DA, Shanley BC (1990) Acute administration of ethanol supresses pentylenetetrazole-induced c-fos expression in rat brain. Neurosci Lett 120:271–274

    Article  PubMed  CAS  Google Scholar 

  18. Le F, Wilce PA, Hume DA, Shanley BC (1992) Involvement of r-aminobutyric acid and N-methyl-D-aspartate receptors in the inhibitory effects of ethanol on pentylenetetrazole-inducedc-fos expression in rat brain. J Neurochem 59:1309–1315

    Article  PubMed  CAS  Google Scholar 

  19. Matsumoto I, Leah J, Shanley B, Wilce P (1993) Immediate early gene expression in the rat brain during ethanol withdrawal. Mol Cell Neurosci 4:485–491

    Article  PubMed  CAS  Google Scholar 

  20. Cowley BD, Chadwick LJ, Grantham JJ, Calvet JP (1989) Sequential protooncogene expression in regenerating kidney following acute renal injury. J Biol Chem 264:8389–8393

    PubMed  CAS  Google Scholar 

  21. Rosenberg ME, Paller MS (1991) Differential gene expression in the recovery from ischemic renal injury. Kidney Int 39:1156–1161

    Article  PubMed  CAS  Google Scholar 

  22. Safirstein R, Price PM, Saggi SJ, Harris RC (1990) Changes in gene expression after temporary renal ischemia. Kidney Int 37:1515–1521

    Article  PubMed  CAS  Google Scholar 

  23. Schiaffonati L, Rappocciolo E, Tacchini L, Cairo G, Bernelli-Zazzera (1990) Reprogramming of gene expression in postischemic rat liver: induction of protooncogenes and hsp 70 gene family. J Cell Physiol 143:79–87

    Article  PubMed  CAS  Google Scholar 

  24. Marterre WF, Kindy MS, Carney M, Landrum RW, Strodel WE (1991) Induction of the protooncogenec-fos and recovery of cytosolic adenosine triphosphate in reperfused liver after transient warm ischemia: effect of nitrone free-radical spin-trap agents. Surgery 110:184–191

    PubMed  Google Scholar 

  25. Herbst H, Milani H, Schuppan D, Stein H (1991) Temporal and spatial patterns of proto-oncogene expression at early stages of toxic liver injury in the rat. Lab Invest 65:324–333

    PubMed  CAS  Google Scholar 

  26. Thompson NL, Mead JE, Goyette M, Shank PR, Fausto N (1986) Sequential proto-oncogene expression during rat liver regeneration. Cancer Res 46:3111–3117

    PubMed  CAS  Google Scholar 

  27. Dragnow M, Young D, Hughes P, MacGibbon G, Lawlor P, Singleton K, Sirimanne E, Beilarnz E, Gluckman P (1993) Isc-jun involved in nerve cell death following status epilepticus and hypoxic-ischaemic brain injury? Mol Brain Res 18:347–352

    Article  Google Scholar 

  28. Goto S, Matsumoto I, Kamada N, An Bui, Saito T, Findlay M, Pujic Z, Wilce P (1994) The induction of immediate early genes in postischemic and transplanted livers in rats; its relation to organ survival. Transplantation 58:840–845

    PubMed  CAS  Google Scholar 

  29. Werle JM, Cosby RS, Wiggers J (1942) Observations on haemorrhagic hypotension and haemorrhagic shock. Am J Physiol 136:401–420

    Google Scholar 

  30. Wang P, Chaudry IH (1991) Crystalloid resuscitation restores but does not maintain cardiac output following severe hemorrhage. J Surg Res 50:163–169

    Article  PubMed  CAS  Google Scholar 

  31. Hsu SM, Raine L, Fanger H (1981) Use of avidin-biotinperoxidase complex (ABC) in immunoperoxidase techniques. J Histochem Cytochem 29:577–580

    Article  PubMed  CAS  Google Scholar 

  32. Vogt PK, Bos TJ (1990) JUN: oncogene and transcription factor. Adv Cancer Res 55:2–36

    Google Scholar 

  33. Kovary K, Bravo R (1991) Expression of different Jun and Fos proteins during the G0-to-G1 transition in mouse fibroblasts: In vitro and in vivo associations. Mol Cell Biol 13:2451–2459

    Google Scholar 

  34. Sonnenberg JL, Macgregor-Leon, Curran T, Morgan JL (1989) Dynamic alterations occur in the level and composition of transcription factor AP-1 complex after seizure. Neuron 3:359–365

    Article  PubMed  CAS  Google Scholar 

  35. Cole AJ, Saffen JM, Baraban JM, Worley PF (1989) Rapid increase in immediate early gene mRNA in hippocampal neurons by synaptic NMDA receptor activation. Nature 340:474–476

    Article  PubMed  CAS  Google Scholar 

  36. Rogue P, Vicendon (1992) Dopamine D2 receptor antagonists induced immediate early genes in the rat striatum. Brain Res Bull 29:469–472

    Article  PubMed  CAS  Google Scholar 

  37. Gass P, Herdegen T, Bravo R, Kiessling M (1992) Induction of immediate early gene encoded proteins in the rat hippocampus after bicuculline-induced seizures. Differential expression of KROX-24, FOS and JUN. Neuroscience 48:315–324

    Article  PubMed  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Saito, T., Matsumoto, I., Goto, S. et al. The differential induction of two immediate early genes,c-fos andc-jun, after systemic hypovolemic shock/resuscitation in the rat liver and kidney. Surg Today 28, 608–617 (1998). https://doi.org/10.1007/s005950050193

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s005950050193

Key Words

Navigation