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Role of nitric oxide synthase activity in experimental ischemic acute renal failure in rats

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Guanidino Compounds in Biology and Medicine

Abstract

To determine the role of nitric oxide (NO) in acute renal failure (ARF), we have studied the time course change activities to activity of nitric oxide synthase (NOS) isoform activities, both calcium dependent and independent NOS, in experimental ischemic ARF. We have also analyzed change activities to activity of the NOS activities in both renal cortex and medulla. Male SD rats (n = 5) were inducted to ARF by ischemia-reperfusion injury and divided into the following groups; Control group (sham operation), Day 0 group, (measurement performed on that day of operation), Day 1 group, (measurement performed one day after induction of ARF), Day 3 group and Day 7 group. Measurement of NOS activity was based on the following principles; NO is synthesized from arginine by nitric oxide synthase (NOS) and NO is converted to NO2 -/NO3 -(NOx) by oxidation. Detection of the final metabolite of NO, NOx was done using flow injection method (Griess reaction). The results were, (1) calcium dependent NOS activity in the cortex and medulla decreased, however it increased in the recovery period in the renal cortex (Cortex; Control, 0.941 ± 0.765, DO, 0.382 ± 0.271, D1, 0.118 ± 0.353, D3, 2.030 ± 0.235, D7, 3.588 ± 2.706, Medulla; Control, 1.469 ± 0.531, DO, 0.766 ± 0.156, D1, 0.828 ± 0.187, D3, 2.078 ± 0.094, D7, 1.289 ± 0.313 µmol NOx produced/mg protein/30 min). (2) On the other hand, iNOS activity increased in the early phase of ARF, both in the cortex and medulla, but returned to control values during the recovery phase in cortex and was maintained at higher levels in the medulla (Cortex; Control, 0.333 ± 0.250, DO, 0.583 ± 0.428, D1, 1.167 ± 0.262, D3, 0.250 ± 0.077, D7, 0.452 ± 0.292, Medulla; Control, 0.139 ± 0.169, DO, 0.279 ± 0.070, D1, 1.140 ± 0.226, D3, 0.452 ± 0.048, D7, 0.625 ± 0.048 µcool NOx produced/mg protein/30 min) These findings suggest that the role of NOS in ARF are different for the different NOS isoforms and have anatomic heterogeneity. (Mol Cell Biochem244:129-133, 2003)

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References

  1. Shah SV: Role of reactive oxygen metabolism in experimental glomerular disease. Kidney Int 35: 1093–1106, 1989

    Article  PubMed  CAS  Google Scholar 

  2. Diamond JR: The role of reactive oxygen species in animal model of glomerular disease. Am J Kidney Dis 19: 292–300, 1992

    PubMed  CAS  Google Scholar 

  3. Kone BC: Nitric oxide in renal health and disease. Am J Kidney Dis 30: 311–333, 1997

    Article  PubMed  CAS  Google Scholar 

  4. Lieberthal W: Biology of ischemic and toxic renal tubular cell injury: Role of nitric oxide and the inflammatory response. Curr Opin Nephrol Hypertens 7: 289–295, 1998

    Article  PubMed  CAS  Google Scholar 

  5. Schramm L, Heidbreder E, Schmitt A, Kartenbender K, Zimmermann J, Ling H, Heidland A: Role of L-arginine derived NO in ischemic acute renal failure in the rat. Renal Failure 16: 555–569, 1994

    Article  PubMed  CAS  Google Scholar 

  6. Jerkic M, Varagic J, Javovic D, Radujkovic-Kuburovic G, NasticMiric D, Adanja-Grujic G, Markovic-Lipkovski J, Dimitrijevic J, Miloradovic Z, Vojvodic SB: L-arginine reduces tubular cell injury in acute post-ischemic renal failure. Nephrol Dial Transplant 14: 1398–1407, 1999

    Article  PubMed  CAS  Google Scholar 

  7. Peresleni T, Noiri E, Bahou W, Goligorsky M: Antisense oligodeoxynucleotides to inducible NO synthase rescue epithelial cells from oxidative stress injury. Am J Physiol 270: F971–F977, 1996

    PubMed  CAS  Google Scholar 

  8. Noiri E, Peresleni T, Miller F, Goligorsky MSL:In-vivotargeting of inducible NO synthase with oligodeoxynucleotides protects rat kidney against ischemia. J Clin Invest 97: 2377–2383, 1996

    Article  PubMed  CAS  Google Scholar 

  9. Yokoi I, Habu H, Kabuto H, Mori A: Analysis of nitrite, nitrate, and nitric oxide synthase activity in brain tissue by automated flow injection technique. Meth Enzymol 268: 152–159, 1996

    Article  PubMed  CAS  Google Scholar 

  10. Higuchi K, Motomizu S: Flow-injection spectrophotometric determination of nitrite and nitrate in biological samples. Anal Sci 15: 129–134, 1999

    Article  CAS  Google Scholar 

  11. Leach M, Frank S, Olbrich A, Pfeilschiter J, Thiemermann C: Decline in the expression of copper/zinc superoxide dismutase in the kidney of rats with endotoxic shock: Effects of the superoxide anion radical scavenger, tempol, on organ injury. Br J Pharm 125: 817–825, 1998

    Article  CAS  Google Scholar 

  12. Zager RA: Hypoperfusion-induced acute renal failure in the rat: An evaluation of oxidant tissue injury. Circ Res 62: 430–435, 1988

    Article  PubMed  CAS  Google Scholar 

  13. Zager RA, Fuerstenberg SM, Baehr PH, Myerson D, Torok-Storb B: An evaluation of antioxidant effects on recovery from postischemic acute renal failure. J Am Soc Nephrol 4: 1588–1597, 1994

    PubMed  CAS  Google Scholar 

  14. Fischereder M, Trick W, Nath KA: Therapeutic strategies in the prevention of acute renal failure. Semin Nephrol 14: 41–52, 1994

    PubMed  CAS  Google Scholar 

  15. Beckman JS, Beckman TW, Chen J, Marshall PA, Freeman BA: Apparent hydroxyl radical production by peroxynitrite — implications for endothelial injury from nitric oxide and superoxide. Proc Acad Sci USA 87: 1620–1624, 1990

    Article  CAS  Google Scholar 

  16. McKee M, Scavone C, Nathanson JA: Nitric oxide, cGMP and hormone regulation of active sodium transport. Proc Natl Acad Sci USA 91: 12056–12060, 1994

    Article  PubMed  CAS  Google Scholar 

  17. Guzman NJ, Fang MZ, Tang SS, Ingelginger JR, Garg LC: Autocrine inhibition of Na/K-ATPase by nitric oxide in mouse proximal tubule epithelial cells. J Clin Invest 95: 2083–2088, 1995

    Article  PubMed  CAS  Google Scholar 

  18. Yaqoob M, Edelstein C, Weider E, Alkhunaizi A, Gengaro P, Nemenoff R, Schrier R: Nitric oxide kinetics during hypoxia in proximal tubules: Effects of acidosis and glycine. Kidney Int 49: 1314–1319, 1996

    Article  PubMed  CAS  Google Scholar 

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Komurai, M. et al. (2003). Role of nitric oxide synthase activity in experimental ischemic acute renal failure in rats. In: Clark, J.F. (eds) Guanidino Compounds in Biology and Medicine. Molecular and Cellular Biochemistry, vol 40. Springer, Boston, MA. https://doi.org/10.1007/978-1-4615-0247-0_19

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  • DOI: https://doi.org/10.1007/978-1-4615-0247-0_19

  • Publisher Name: Springer, Boston, MA

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