BibTex RIS Cite

INHIBITION OF NITRIC OXIDE SYNTHESIS AMELIORATES BURN-INDUCED REMOTE ORGAN INJURY IN RATS: A LIGHT MICROSCOPIC STUDY

Year 2002, Volume: 15 Issue: 3, 155 - 160, 03.12.2016

Abstract

Objective: To investigate the role of endogenous nitric oxide (NO) on remote organ injury in the early phase of burn trauma.
Methods: Wistar albino rats (200-300 g) were exposed to 90°C (burn) or 25°C (sham) water bath for 10 sec.
Results: Microscopic score in the stomach was increased in the burn group compared to sham. Hemorrhage areas, epithelial desquamation and glandular cell degeneration were observed in the gastric mucosa of the burn group. NG-nitro-L- arginine methyl ester (L-NAME) treatment reduced the burn-induced damage score with an intact glandular architecture. In NG-nitro-D- arginine methyl ester (D-NAME) pretreated groups, histologic scores were not different than burn group, with desquamated and degenerated surface epithelium. L-arginine (L-arg) plus L- NAME pretreatment partially reversed this effect with prominent gastric mucosal damage. In the liver, the microscopic score was increased in the burn group compared to sham. Hepatocyte
vacuolar degeneration, sinusoidal congestion and increased number of Kupffer cells were observed in the burn group. Hepatic injury was slightly attenuated by L-NAME treatment whereas D-NAME or L-arg plus L-NAME pretreatment was ineffective.
Conclusion: In conclusion, inhibition of NO synthesis ameliorates gastric and hepatic damage, emphasizing the critical role of NO in the burn-induced remote organ injury.
Key Words: Burns, Nitric oxide, Remote organ injury, Myeloperoxidase activity

References

  • Moncrief JA. Effect of various fluid regimens and pharmacologic agents on the circulatory hemodynamics of the immediate postbum period. Ann Surg 1966; 164:723-752.
  • Martyn JAJ, Snider NT, Szyfelbein SH, Burke JF, Laver MB. Right ventricular dysfunction in acute thermal injury. Ann Surg 1980; 191:330- 335.
  • Bonate PL. Pathophysiology and pharmacokinetics following burn injury. Clin Pharmacokinet 1990; 18:118-130.
  • Demling Rfl, LaLonde C. Systemic lipid peroxidation and inflammation induced by thermal injury persists into the post resuscitation period. J Trauma 1990;30:69-71.
  • Jones II WQ, Minei JP, Barber AE, Pahey III TJ, Shires III GT, Shires GT. Splancnic vasoconstriction and bacterial translocation after thermal injury. Am J Physiol 1991 ;261 :H 1 190-PH 196.
  • Morris SE, Havaratnam H, Townsend CM, Herndon DPI. A comparison of the effect of thermal injury and smoke inhalation on bacterial translocation. J Trauma 1990;30:639-643.
  • Youn Y-H, LaLonde C, Demling R. The role of mediators in the response to thermal injury. World J Surg 1992; 16:30-36.
  • Eurchgott RE, Zawadzki JV. The obligatory role of endothelial cells in the relaxation of arterial smooth muscle by acetylcholine, nature 1980;288:373-376.
  • Moncada S, Palmer RMJ, Higgs EA. nitric
  • oxide: Physiology, pathophysiology and
  • pharmacology. Pharmacol Rev 1991:43:109- 142.
  • nussler AH, Billiar TR. Inflammation, immunoreguiation, and inducible nitric oxide synthase. J Leukocyte Biol I993;54:1 7l-l 78.
  • I I. Lloyd KC. Gut hormones in gastric function. Balliëres Clin Endocrinol Metab 1994;8: III- 136.
  • Alican /, Hubes P. A critical role for no in intestinal barrier function and dysfunction. Am J Physiol 1996;33:G225-G237.
  • Preiser JC, Reper P, Vlasselaer D, et at. nitric oxide production is increased in patients after burn injury. J Trauma 1996;40:368-371.
  • Chen LW, Hsu CM, Wang JS, Chen JS, Chen SC. Specific inhibition of inOS decreases the intestinal mucosal peroxynitrite level and improves the barrier function after thermal injury. Burns 1998;24:699-705.
  • Chen LW, Hsu CM, Cha MC, Chen JS, Chen SC. Changes in gut mucosal nitric oxide synthase (HOS) activity after thermal injury and its relation with barrier failure. Shock
  • ,1 1:104-1 10.
  • Demling R, LaLonde C, Hnox J, Youn Y, Zhu D, Daryani R. Fluid resuscitation with deferoxamine prevents systemic burn- induced oxidant injury. J Trauma 1991; 31: 538-544.
  • Hutcheson IR, Whittle BJR, Boughton-Smith HH. Role of nitric oxide in maintaining vascular integrity in endotoxin-induced acute intestinal damage in the rat. Br J Pharmacol 1990;101:815-820.
  • Boughton-Smith HH, Evans SM, Laszlo F, Whittle BJR, Moncada S. Br J Pharmacol 1993; I 10:1 189-1 195.
  • Ochoa JB, Udekwu AO, Billiar TR, et al. Hitrogen oxide levels in patients after trauma and during sepsis. Ann Surg 1991 ;214:621 - 626.
  • Gomez-Jimenez J, Salgado A, Mourelle M, et
  • al. L-Arginine: nitric oxide pathway
  • endotoxaemia and human septic shock. Crit Care Med 1995;23:253-258.
  • Gamelli RL, George M, Sharp-Pucci M, Dries DJ, Radisavljevic Z. Burn-induced nitric-oxide release in humans. J Trauma 1995,39:869- 877.
  • Harper R, Parkhouse H, Green C, Martin R. Hitric oxide production in burns: plasma nitrate levels are not increased in patients with minor thermal injuries. J Trauma 1997;43:467-474.
  • Wada H, Hamisaki Y, Ohkura T, et al. Direct measurement of nitric oxide release In gastric mucosa during ischemia-reperfusion in rats. Am J Physiol 1998:274:G465-G471.
Year 2002, Volume: 15 Issue: 3, 155 - 160, 03.12.2016

Abstract

References

  • Moncrief JA. Effect of various fluid regimens and pharmacologic agents on the circulatory hemodynamics of the immediate postbum period. Ann Surg 1966; 164:723-752.
  • Martyn JAJ, Snider NT, Szyfelbein SH, Burke JF, Laver MB. Right ventricular dysfunction in acute thermal injury. Ann Surg 1980; 191:330- 335.
  • Bonate PL. Pathophysiology and pharmacokinetics following burn injury. Clin Pharmacokinet 1990; 18:118-130.
  • Demling Rfl, LaLonde C. Systemic lipid peroxidation and inflammation induced by thermal injury persists into the post resuscitation period. J Trauma 1990;30:69-71.
  • Jones II WQ, Minei JP, Barber AE, Pahey III TJ, Shires III GT, Shires GT. Splancnic vasoconstriction and bacterial translocation after thermal injury. Am J Physiol 1991 ;261 :H 1 190-PH 196.
  • Morris SE, Havaratnam H, Townsend CM, Herndon DPI. A comparison of the effect of thermal injury and smoke inhalation on bacterial translocation. J Trauma 1990;30:639-643.
  • Youn Y-H, LaLonde C, Demling R. The role of mediators in the response to thermal injury. World J Surg 1992; 16:30-36.
  • Eurchgott RE, Zawadzki JV. The obligatory role of endothelial cells in the relaxation of arterial smooth muscle by acetylcholine, nature 1980;288:373-376.
  • Moncada S, Palmer RMJ, Higgs EA. nitric
  • oxide: Physiology, pathophysiology and
  • pharmacology. Pharmacol Rev 1991:43:109- 142.
  • nussler AH, Billiar TR. Inflammation, immunoreguiation, and inducible nitric oxide synthase. J Leukocyte Biol I993;54:1 7l-l 78.
  • I I. Lloyd KC. Gut hormones in gastric function. Balliëres Clin Endocrinol Metab 1994;8: III- 136.
  • Alican /, Hubes P. A critical role for no in intestinal barrier function and dysfunction. Am J Physiol 1996;33:G225-G237.
  • Preiser JC, Reper P, Vlasselaer D, et at. nitric oxide production is increased in patients after burn injury. J Trauma 1996;40:368-371.
  • Chen LW, Hsu CM, Wang JS, Chen JS, Chen SC. Specific inhibition of inOS decreases the intestinal mucosal peroxynitrite level and improves the barrier function after thermal injury. Burns 1998;24:699-705.
  • Chen LW, Hsu CM, Cha MC, Chen JS, Chen SC. Changes in gut mucosal nitric oxide synthase (HOS) activity after thermal injury and its relation with barrier failure. Shock
  • ,1 1:104-1 10.
  • Demling R, LaLonde C, Hnox J, Youn Y, Zhu D, Daryani R. Fluid resuscitation with deferoxamine prevents systemic burn- induced oxidant injury. J Trauma 1991; 31: 538-544.
  • Hutcheson IR, Whittle BJR, Boughton-Smith HH. Role of nitric oxide in maintaining vascular integrity in endotoxin-induced acute intestinal damage in the rat. Br J Pharmacol 1990;101:815-820.
  • Boughton-Smith HH, Evans SM, Laszlo F, Whittle BJR, Moncada S. Br J Pharmacol 1993; I 10:1 189-1 195.
  • Ochoa JB, Udekwu AO, Billiar TR, et al. Hitrogen oxide levels in patients after trauma and during sepsis. Ann Surg 1991 ;214:621 - 626.
  • Gomez-Jimenez J, Salgado A, Mourelle M, et
  • al. L-Arginine: nitric oxide pathway
  • endotoxaemia and human septic shock. Crit Care Med 1995;23:253-258.
  • Gamelli RL, George M, Sharp-Pucci M, Dries DJ, Radisavljevic Z. Burn-induced nitric-oxide release in humans. J Trauma 1995,39:869- 877.
  • Harper R, Parkhouse H, Green C, Martin R. Hitric oxide production in burns: plasma nitrate levels are not increased in patients with minor thermal injuries. J Trauma 1997;43:467-474.
  • Wada H, Hamisaki Y, Ohkura T, et al. Direct measurement of nitric oxide release In gastric mucosa during ischemia-reperfusion in rats. Am J Physiol 1998:274:G465-G471.
There are 28 citations in total.

Details

Journal Section Original Research
Authors

Özlem Güneysel This is me

Berna Oktar This is me

Berrak Yeğen This is me

Cumhur Yeğen This is me

Serap Arbak This is me

Publication Date December 3, 2016
Published in Issue Year 2002 Volume: 15 Issue: 3

Cite

APA Güneysel, Ö., Oktar, B., Yeğen, B., Yeğen, C., et al. (2016). INHIBITION OF NITRIC OXIDE SYNTHESIS AMELIORATES BURN-INDUCED REMOTE ORGAN INJURY IN RATS: A LIGHT MICROSCOPIC STUDY. Marmara Medical Journal, 15(3), 155-160.
AMA Güneysel Ö, Oktar B, Yeğen B, Yeğen C, Arbak S. INHIBITION OF NITRIC OXIDE SYNTHESIS AMELIORATES BURN-INDUCED REMOTE ORGAN INJURY IN RATS: A LIGHT MICROSCOPIC STUDY. Marmara Med J. March 2016;15(3):155-160.
Chicago Güneysel, Özlem, Berna Oktar, Berrak Yeğen, Cumhur Yeğen, and Serap Arbak. “INHIBITION OF NITRIC OXIDE SYNTHESIS AMELIORATES BURN-INDUCED REMOTE ORGAN INJURY IN RATS: A LIGHT MICROSCOPIC STUDY”. Marmara Medical Journal 15, no. 3 (March 2016): 155-60.
EndNote Güneysel Ö, Oktar B, Yeğen B, Yeğen C, Arbak S (March 1, 2016) INHIBITION OF NITRIC OXIDE SYNTHESIS AMELIORATES BURN-INDUCED REMOTE ORGAN INJURY IN RATS: A LIGHT MICROSCOPIC STUDY. Marmara Medical Journal 15 3 155–160.
IEEE Ö. Güneysel, B. Oktar, B. Yeğen, C. Yeğen, and S. Arbak, “INHIBITION OF NITRIC OXIDE SYNTHESIS AMELIORATES BURN-INDUCED REMOTE ORGAN INJURY IN RATS: A LIGHT MICROSCOPIC STUDY”, Marmara Med J, vol. 15, no. 3, pp. 155–160, 2016.
ISNAD Güneysel, Özlem et al. “INHIBITION OF NITRIC OXIDE SYNTHESIS AMELIORATES BURN-INDUCED REMOTE ORGAN INJURY IN RATS: A LIGHT MICROSCOPIC STUDY”. Marmara Medical Journal 15/3 (March 2016), 155-160.
JAMA Güneysel Ö, Oktar B, Yeğen B, Yeğen C, Arbak S. INHIBITION OF NITRIC OXIDE SYNTHESIS AMELIORATES BURN-INDUCED REMOTE ORGAN INJURY IN RATS: A LIGHT MICROSCOPIC STUDY. Marmara Med J. 2016;15:155–160.
MLA Güneysel, Özlem et al. “INHIBITION OF NITRIC OXIDE SYNTHESIS AMELIORATES BURN-INDUCED REMOTE ORGAN INJURY IN RATS: A LIGHT MICROSCOPIC STUDY”. Marmara Medical Journal, vol. 15, no. 3, 2016, pp. 155-60.
Vancouver Güneysel Ö, Oktar B, Yeğen B, Yeğen C, Arbak S. INHIBITION OF NITRIC OXIDE SYNTHESIS AMELIORATES BURN-INDUCED REMOTE ORGAN INJURY IN RATS: A LIGHT MICROSCOPIC STUDY. Marmara Med J. 2016;15(3):155-60.