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Year 2011, Volume: 28 Issue: 1, 12 - 16, 15.02.2012

Abstract

References

  • Abu-Zidan, F.M., Bonham, M.J.D., Windsor, J.A. 2000. Severity of acute pancreatitis: a multivariate analysis of oxidative stress markers and modified Glasgow criteria. Br. J. Surg. 87, 1019-1023.
  • Bang, U.C., Semb, S., Nojgaard, C., Bendtsen, F. 2008. Pharmaclogical approach to acute pancreatitis. World J. Gastroenterol. 14, 2968- 2976.
  • Barnes, P.J. 1998. Anti-inflammatory actions of glucocorticoids: molecular mechanisms. Clin. Sci. 94, 557-572.
  • Dabrowski, A., Konturek, S.J., Konturek, J.W., Gabryelewicz, A. 1999. Role of oxidative stress in the pathogenesis of cerulean-induced acute pancreatitis. Europ. J. Pharmacol. 377, 1-11.
  • Dean, R.T., Fu, S., Stocker, R., Davies, M.J. 1997. Biochemistry and pathology of radical-mediated protein oxidation. Biochem. J. 324, 1-18. Denham, W., Fink, G., Yang, J., Ulrich, P., Tracey, K., Norman, J. 1997. Small molecule inhibition of tumor necrosis factor gene processing during acute pancreatitis prevents cytokine cascade progression and attenuates pancreatitis severity. Am. Surg. 63, 1045-1049.
  • Evans, P., Lyras, L., Halliwel, B. 1999. Measurement of protein carbonyls in human brain tissue. Methods Enzymol. 300, 145-156.
  • Genovese, T., Mazzon, E, Di Paola, R., Muia, C., Crisafulli, C., Menegazzi, M., 2006. Hypericum perforatum attenuates the development of cerulein-induced acute pancreatitis in mice. Shock. 25, 161-167.
  • Granell, S., Pereda, J., Gomez-Cambronero, L., Cassinello, N., Sabater, L., Closa, D., 2004. Circulating TNF-α and its soluble receptors dur ing experimental acute pancreatitis. Cytokine. 25,187-191.
  • Hughes, C.B., Gaber, L.W., Mohey el-Din, A.B., Grewal, H.P., Kotb, M., Mann, L.A.O.1996. Inhibition of TNF-α improves survival in an ex perimental model of acute pancreatitis. Am. Surg. 62, 8-13.
  • Kilic, E., Amanvermez, R., Kefeli, M., Polat, C., Gunay, M. 2010. Protective effects of etanercept and methylprednisolone on pancreatic dam agein cerulein-induced acute pancreatitis. Saudi Med. J. 31, 394-399.
  • Kimura, K., Shimosegawa, T., Sasano, H., Abe, R., Satoh, A., Masamune, A., 1998. Endogenous glucocorticoids decrease the acinar cell sensi tivity to apoptosis during cerulein pancreatitis in rats. Gastroenterology. 114, 372-381.
  • Kiziler, A.R., Aydemir, B., Gulyasar, T., Unal, E., Günes, P. 2008. Relationships among iron, protein oxidation and lipid peroxidation levels in rats with alcohol-induced acute pancreatitis. Biol. Trace Elem Res.124, 135-143.
  • Kyu Park, B., Chung, J.B., Lee, J.H., Hun Suh, J., Woo Park, S., Song, S.Y., 2003. Role of oxygen free radicals in patients with acute pancreati tis. World J. Gastroenterol. 9, 2266-2269.
  • Lowry, O.H., Rosebrough, N.J., Farr, A.L., Randal, R.J. 1951. Protein measurement with the folin phenol reagent. J. Biol. Chem. 193, 265- 275.
  • Malleo, G., Mazzon, E., Genovese, T., Paola, R.D., Muia, C., Centorrino, T., 2007. Etenarcept attenuates the development of cerulein-induced acute pancreatitis in mice: A comparison with TNF-α genetic deletion. Shock. 27, 542-551.
  • Pereda, J., Sabater, L., Aparisi, L., Escobar, J., Sandoval, J., Vina, J.2006. Interaction between cytokines and oxidative stress in acute pancrea- titis. Current Med. Chemistry 13, 2775-2787.
  • Pereda, J., Sabater, L., Cassinello, N., Gomez-Cambronero, L., Closa, D., Folch-Puy, E., 2004. Effect of simultaneous inhibition of TNF-α production and xanthine oxidase in experimental acute pancreatitis. Ann Surg. 240, 108-116.
  • Rakonczay, Z., Duda, E., Kaszaki, J., Ivanyi, B., Boros, I., Lanovics, J., 2003. The anti-inflammatory effect of methylprednisolone occurs down- stream of nuclear factor-ĸB DNA binding in acute pancreatitis. Eur. J. Pharmacol. 464, 217-227.
  • Reinhecke,l T., Nedelev, B., Prause, J., Augustin, W., Schulz, H.U., Lippert, H., 1998. Occurrence of oxidatively modified proteins: an early event in experimental acute pancreatitis. Free Rad. Biol. Med. 24, 393-400.
  • Rongione, A.J., Kusske, A.M., Kwan, K., Ashley, S.W., Reber, H.A., McFadden, D.W. 1997. Interleukin-10 reduces the severity of acute pan creatitis in rats. Gastroenterology. 112, 960-967.
  • Shi, C., Andersson, R., Zhao, X., Wang, X. 2005. Potential role of reactive oxygen species in pancreatitis-associated multiple organ dysfunc tion. Pancreatology. 5, 492-500.
  • Singh, R.P., Padmavathi, B., Rao, R. 2000. Modulatory influence of Adhatoda vesica leaf extract on the enzmes of xenobiotic metabolism, anti oxidant status and lipid peroxidation in mice. Mol. Cell Biochem. 213, 99-109.
  • Steer, M.L.2008. Exocrine pancreas. In: Tavsend CM, Beauchamp RD, Evers BM, Mattox KL (18th ed./eds). Sabiston textbook of surgery: the biological basis of modern surgical practice. Philadelphia: Saunders, Elsevier inc.1589 – 1623.
  • Takaoka, K., Kataoka, K., Sakagami, J. 2002. The effect of steroid pulse therapy in the development of acute pancreatitis induced by closed duodenal loop in rats. J. Gastroenterol. 37, 537-542.
  • Telek, G., Scoazec, J-Y, Chariot, J., Ducroc, R., Feldmann, G., Roze, C. 1999.Cerium-based histochemical demonstration of oxidative stress in taurocholate-induced acute pancreatitis in rats: a confocal laser scanning microscopic study. J. Histochem. Cytochem. 47, 1201-1212.
  • Yılmaz, M., Topsakal, S., Herek, O., Ozmen, O., Sahinduran, S., Buyukoglu, T., 2009. Effects of etanercept on sodium taurocholate-induced acute pancreatitis in rats. Translational Res. 154, 241-249.

The Combined Effects of Etanercept Plus Methylprednisolone on Pancreatic Oxidative Stress in Acute Pancreatitis Induced by Cerulein

Year 2011, Volume: 28 Issue: 1, 12 - 16, 15.02.2012

Abstract

ABSTRACT
Whether etanercept plus metylprednisolone reduce pancreatic oxidative stress and injury during pancreatitis is unknown well. The aim of this study was to examine the therapeutic effects of etanercept and methylprednisolone (MP) on acute pancreatitis and oxidative stress in acute pancreatitis (AP) induced by cerulein in a rat model. The study was performed with 48 rats divided into 6 groups (n = 8/group): 1-sham, 2-cerulein-induced pancreatitis (over 10 hours), 3- cerulein-pancreatitis (over 20 hours), 4-etanercept (5 mg/kg, i.p.), 5-methylprednisolone (10 mg/kg, i.m.), 6-etanercept plus methylprednisolone. Also, the rats in groups 4, 5, and 6 were cerulein-induced pancreatitis at 20 hours. After the treatment, the pancreas and blood were taken for histopathological and biochemical analysis. All cerulein-treated rats developed biochemical and pathological acute pancreatitis after 10-20 hours. The markers of oxidative stress such as protein carbonyls, lipid peroxidation, and myeloperoxidase (mpo) in the pancreas tissues were increased in the group 2 and 3, but these were lower in etanercept and MP-treated rats compared to groups 3. Pancreatic mpo activity was considerably reduced in pancreas tissues at 20 h after the administration of etanercept plus metylprednisolone in the group 6 compared to group 3. In AP induced by cerulein, the treatment of etanercept plus methylprednisolone may ameliorate pancreatic oxidative stress in rats. 

References

  • Abu-Zidan, F.M., Bonham, M.J.D., Windsor, J.A. 2000. Severity of acute pancreatitis: a multivariate analysis of oxidative stress markers and modified Glasgow criteria. Br. J. Surg. 87, 1019-1023.
  • Bang, U.C., Semb, S., Nojgaard, C., Bendtsen, F. 2008. Pharmaclogical approach to acute pancreatitis. World J. Gastroenterol. 14, 2968- 2976.
  • Barnes, P.J. 1998. Anti-inflammatory actions of glucocorticoids: molecular mechanisms. Clin. Sci. 94, 557-572.
  • Dabrowski, A., Konturek, S.J., Konturek, J.W., Gabryelewicz, A. 1999. Role of oxidative stress in the pathogenesis of cerulean-induced acute pancreatitis. Europ. J. Pharmacol. 377, 1-11.
  • Dean, R.T., Fu, S., Stocker, R., Davies, M.J. 1997. Biochemistry and pathology of radical-mediated protein oxidation. Biochem. J. 324, 1-18. Denham, W., Fink, G., Yang, J., Ulrich, P., Tracey, K., Norman, J. 1997. Small molecule inhibition of tumor necrosis factor gene processing during acute pancreatitis prevents cytokine cascade progression and attenuates pancreatitis severity. Am. Surg. 63, 1045-1049.
  • Evans, P., Lyras, L., Halliwel, B. 1999. Measurement of protein carbonyls in human brain tissue. Methods Enzymol. 300, 145-156.
  • Genovese, T., Mazzon, E, Di Paola, R., Muia, C., Crisafulli, C., Menegazzi, M., 2006. Hypericum perforatum attenuates the development of cerulein-induced acute pancreatitis in mice. Shock. 25, 161-167.
  • Granell, S., Pereda, J., Gomez-Cambronero, L., Cassinello, N., Sabater, L., Closa, D., 2004. Circulating TNF-α and its soluble receptors dur ing experimental acute pancreatitis. Cytokine. 25,187-191.
  • Hughes, C.B., Gaber, L.W., Mohey el-Din, A.B., Grewal, H.P., Kotb, M., Mann, L.A.O.1996. Inhibition of TNF-α improves survival in an ex perimental model of acute pancreatitis. Am. Surg. 62, 8-13.
  • Kilic, E., Amanvermez, R., Kefeli, M., Polat, C., Gunay, M. 2010. Protective effects of etanercept and methylprednisolone on pancreatic dam agein cerulein-induced acute pancreatitis. Saudi Med. J. 31, 394-399.
  • Kimura, K., Shimosegawa, T., Sasano, H., Abe, R., Satoh, A., Masamune, A., 1998. Endogenous glucocorticoids decrease the acinar cell sensi tivity to apoptosis during cerulein pancreatitis in rats. Gastroenterology. 114, 372-381.
  • Kiziler, A.R., Aydemir, B., Gulyasar, T., Unal, E., Günes, P. 2008. Relationships among iron, protein oxidation and lipid peroxidation levels in rats with alcohol-induced acute pancreatitis. Biol. Trace Elem Res.124, 135-143.
  • Kyu Park, B., Chung, J.B., Lee, J.H., Hun Suh, J., Woo Park, S., Song, S.Y., 2003. Role of oxygen free radicals in patients with acute pancreati tis. World J. Gastroenterol. 9, 2266-2269.
  • Lowry, O.H., Rosebrough, N.J., Farr, A.L., Randal, R.J. 1951. Protein measurement with the folin phenol reagent. J. Biol. Chem. 193, 265- 275.
  • Malleo, G., Mazzon, E., Genovese, T., Paola, R.D., Muia, C., Centorrino, T., 2007. Etenarcept attenuates the development of cerulein-induced acute pancreatitis in mice: A comparison with TNF-α genetic deletion. Shock. 27, 542-551.
  • Pereda, J., Sabater, L., Aparisi, L., Escobar, J., Sandoval, J., Vina, J.2006. Interaction between cytokines and oxidative stress in acute pancrea- titis. Current Med. Chemistry 13, 2775-2787.
  • Pereda, J., Sabater, L., Cassinello, N., Gomez-Cambronero, L., Closa, D., Folch-Puy, E., 2004. Effect of simultaneous inhibition of TNF-α production and xanthine oxidase in experimental acute pancreatitis. Ann Surg. 240, 108-116.
  • Rakonczay, Z., Duda, E., Kaszaki, J., Ivanyi, B., Boros, I., Lanovics, J., 2003. The anti-inflammatory effect of methylprednisolone occurs down- stream of nuclear factor-ĸB DNA binding in acute pancreatitis. Eur. J. Pharmacol. 464, 217-227.
  • Reinhecke,l T., Nedelev, B., Prause, J., Augustin, W., Schulz, H.U., Lippert, H., 1998. Occurrence of oxidatively modified proteins: an early event in experimental acute pancreatitis. Free Rad. Biol. Med. 24, 393-400.
  • Rongione, A.J., Kusske, A.M., Kwan, K., Ashley, S.W., Reber, H.A., McFadden, D.W. 1997. Interleukin-10 reduces the severity of acute pan creatitis in rats. Gastroenterology. 112, 960-967.
  • Shi, C., Andersson, R., Zhao, X., Wang, X. 2005. Potential role of reactive oxygen species in pancreatitis-associated multiple organ dysfunc tion. Pancreatology. 5, 492-500.
  • Singh, R.P., Padmavathi, B., Rao, R. 2000. Modulatory influence of Adhatoda vesica leaf extract on the enzmes of xenobiotic metabolism, anti oxidant status and lipid peroxidation in mice. Mol. Cell Biochem. 213, 99-109.
  • Steer, M.L.2008. Exocrine pancreas. In: Tavsend CM, Beauchamp RD, Evers BM, Mattox KL (18th ed./eds). Sabiston textbook of surgery: the biological basis of modern surgical practice. Philadelphia: Saunders, Elsevier inc.1589 – 1623.
  • Takaoka, K., Kataoka, K., Sakagami, J. 2002. The effect of steroid pulse therapy in the development of acute pancreatitis induced by closed duodenal loop in rats. J. Gastroenterol. 37, 537-542.
  • Telek, G., Scoazec, J-Y, Chariot, J., Ducroc, R., Feldmann, G., Roze, C. 1999.Cerium-based histochemical demonstration of oxidative stress in taurocholate-induced acute pancreatitis in rats: a confocal laser scanning microscopic study. J. Histochem. Cytochem. 47, 1201-1212.
  • Yılmaz, M., Topsakal, S., Herek, O., Ozmen, O., Sahinduran, S., Buyukoglu, T., 2009. Effects of etanercept on sodium taurocholate-induced acute pancreatitis in rats. Translational Res. 154, 241-249.
There are 26 citations in total.

Details

Primary Language English
Subjects Health Care Administration
Journal Section Basic Medical Sciences
Authors

Murat Günay

Erol Kılıç This is me

Ramazan Amanvermez This is me

Publication Date February 15, 2012
Submission Date March 4, 2011
Published in Issue Year 2011 Volume: 28 Issue: 1

Cite

APA Günay, M., Kılıç, E., & Amanvermez, R. (2012). The Combined Effects of Etanercept Plus Methylprednisolone on Pancreatic Oxidative Stress in Acute Pancreatitis Induced by Cerulein. Journal of Experimental and Clinical Medicine, 28(1), 12-16.
AMA Günay M, Kılıç E, Amanvermez R. The Combined Effects of Etanercept Plus Methylprednisolone on Pancreatic Oxidative Stress in Acute Pancreatitis Induced by Cerulein. J. Exp. Clin. Med. February 2012;28(1):12-16.
Chicago Günay, Murat, Erol Kılıç, and Ramazan Amanvermez. “The Combined Effects of Etanercept Plus Methylprednisolone on Pancreatic Oxidative Stress in Acute Pancreatitis Induced by Cerulein”. Journal of Experimental and Clinical Medicine 28, no. 1 (February 2012): 12-16.
EndNote Günay M, Kılıç E, Amanvermez R (February 1, 2012) The Combined Effects of Etanercept Plus Methylprednisolone on Pancreatic Oxidative Stress in Acute Pancreatitis Induced by Cerulein. Journal of Experimental and Clinical Medicine 28 1 12–16.
IEEE M. Günay, E. Kılıç, and R. Amanvermez, “The Combined Effects of Etanercept Plus Methylprednisolone on Pancreatic Oxidative Stress in Acute Pancreatitis Induced by Cerulein”, J. Exp. Clin. Med., vol. 28, no. 1, pp. 12–16, 2012.
ISNAD Günay, Murat et al. “The Combined Effects of Etanercept Plus Methylprednisolone on Pancreatic Oxidative Stress in Acute Pancreatitis Induced by Cerulein”. Journal of Experimental and Clinical Medicine 28/1 (February 2012), 12-16.
JAMA Günay M, Kılıç E, Amanvermez R. The Combined Effects of Etanercept Plus Methylprednisolone on Pancreatic Oxidative Stress in Acute Pancreatitis Induced by Cerulein. J. Exp. Clin. Med. 2012;28:12–16.
MLA Günay, Murat et al. “The Combined Effects of Etanercept Plus Methylprednisolone on Pancreatic Oxidative Stress in Acute Pancreatitis Induced by Cerulein”. Journal of Experimental and Clinical Medicine, vol. 28, no. 1, 2012, pp. 12-16.
Vancouver Günay M, Kılıç E, Amanvermez R. The Combined Effects of Etanercept Plus Methylprednisolone on Pancreatic Oxidative Stress in Acute Pancreatitis Induced by Cerulein. J. Exp. Clin. Med. 2012;28(1):12-6.