Protective Effects of Curcumin on Intestinal Damage in Cholestatic Rats

REFERENCES

• Yang R, Martin-Hawver L, Woodall C, et al. Administration of glutamine after hemorrhagic shock restores cellular energy, reduces cell apoptosis and damage, and increases survival. Parenter Enteral Nutr. 2007;31:94–100.
   PubMed Web of Science ®Google Scholar
• Deitch EA, Sitting K, Li M, et al. Obstructive jaundice promotes bacterial translocation from the gut. Am J Surg. 1990;159:79–84.
   PubMed Web of Science ®Google Scholar
• Scopa CD, Koureleas S, Tsamandas AC, et al. Beneficial effects of growth hormone and insulin-like growth factor 1 on intestinal bacterial translocation, endotoxemia, and apoptosis in experimentally jaundiced rats. J Am Coll Surg. 1990;190:423–431.
   Web of Science ®Google Scholar
• Parks RW, Clements WD, Smye MG, et al. Intestinal barrier dysfunction in clinical and experimental obstructive jaundice and its reversal by internal biliary drainage. Br J Surg. 1996;83:1345–1349.
   PubMed Web of Science ®Google Scholar
• Clements WD, Parks R, Erwin P, et al. Role of the gut in the pathophysiology of extrahepatic biliary obstruction. Gut. 1996;39:587–593.
   PubMed Web of Science ®Google Scholar
• Parks RW, Stuart Cameron CH, Gannon CD, et al. Changes in gastrointestinal morphology associated with obstructive jaundice. J Pathol. 2000;192:526–532.
   PubMed Web of Science ®Google Scholar
• Scopa CD, Koureleas S, Tsamandas AC, et al. Beneficial effects of growth hormone and insulin-like growth factor 1 on intestinal bacterial translocation, endotoxemia, and apoptosis in experimentally jaundiced rats. J Am Coll Surg. 2000;190:423–431.
   PubMed Web of Science ®Google Scholar
• Assimakopoulos SF, Scopa CD, Charonis A, et al. Experimental obstructive jaundice disrupts intestinal mucosal barrier by altering occludin expression: beneficial effect of bombesin and neurotensin. J Am Coll Surg 2004a;198(5):748–757.
   PubMed Web of Science ®Google Scholar
• Thompson CB. Apoptosis in the pathogenesis and treatment of disease. Science. 1995;267:1456–1462.
   PubMed Web of Science ®Google Scholar
• Chai J, Du C, Wu JW, et al. Structural and biochemical basis of apoptotic activation by Smac/DIABLO. Nature. 2000;406:855–862.
   PubMed Web of Science ®Google Scholar
• Kalpana C, Menon VP. Curcumin ameliorates oxidative stress during nicotine induced lung toxicity in Wistar rats. Ital J Biochem. 2004;53:82–86.
   PubMedGoogle Scholar
• Polas K, Naidu NA, Ravindranath I, et al. Inhibition of B(a)P induced strand breaks in presence of curcumin. Mutat Res. 2004;557:203–213.
   PubMed Web of Science ®Google Scholar
• Erenoglu C, Kanter M, Aksu B, et al. Protective effect of curcumin on liver damage induced by biliary obstruction in rats. Balkan Med J. 2011;28:352–335.
   Web of Science ®Google Scholar
• Ohkawa H, Ohishi N, Yagi K. Assay for lipid peroxides in animal tissues by thiobarbituric acid reaction. Anal Biochem. 1979;95:358.
   Web of Science ®Google Scholar
• Lowry OH, Rosenbrough NJ, Farr AC, et al. Protein measurement with the folin phenol regent. J Biol Chem. 1951;193:265–275.
   PubMed Web of Science ®Google Scholar
• Ellman GL. Tissue sulfhydryl groups. Arch Biochem Biophys. 1959;82:70–77.
   PubMed Web of Science ®Google Scholar
• Wei H, Frenkel K. Relationship of oxidative events and DNA oxidation in SENCAR mice to in vivo promoting activity of phorbol ester-type tumor promoters. Carcinogenesis. 1993;14:1195–1201.
   PubMed Web of Science ®Google Scholar
• Chiu CJ, McArdle AH, Brown R, et al. Intestinal mucosal lesion in low-flow states. I. A morphological, hemodynamic, and metabolic reappraisal. Arch Surg. 1970;101:478–483.
   PubMedGoogle Scholar
• Hsu SM, Raine L, Fanger H. Use of Avidin-Biotin-Peroxidase complex (ABC) in immunoperoxidase techniques: a comparison between ABC and unlabeled antibody (PAP) procedures. J Histochem Cytochem. 1981;29:577–580.
   PubMed Web of Science ®Google Scholar
• Guicciardi ME, Gores GJ. Bile acid-mediated hepatocyte apoptosis and cholestatic liver disease. Dig Liver Dis. 2002;34:387–392
   PubMedGoogle Scholar
• Sokol RJ, Devereaux MW, Khandwala R. Effect of oxypurinol, a xanthine oxidase inhibitor, on hepatic injury in the bile duct-ligated rat. Pediatr Res. 1998;44:397–401.
   PubMed Web of Science ®Google Scholar
• Pastor A, Collado PS, Almar M, et al. Antioxidant enzyme status in biliary obstructed rats: effects of N-acetylcysteine. J Hepatol. 1997;27(2): 363–370.
   PubMed Web of Science ®Google Scholar
• Kimura H, Sawada T, Oshima S, et al. Toxicity and roles of reactive oxygen species. Curr Drug Targets Inflamm Allergy. 2005;4:489–495.
   PubMedGoogle Scholar
• Oguz S, Kanter M, Erboga M, et al. Protective effects of thymoquinone against cholestatic oxidative stress and hepatic damage after biliary obstruction in rats. J Mol Histol. 2012;43:151–159.
   PubMed Web of Science ®Google Scholar
• Gurleyik Emin, Coskun O, Ustundag N, et al. Prostaglandin E1 maintains structural integrity of intestinal mucosa and prevents bacterial translocation during experimental obstructive jaundice. Investigative Surgery 2006;19(5):283–289.
   PubMed Web of Science ®Google Scholar
• Aller M A, Nava MP, Arias JL, et al. Microsurgical extrahepatic cholestasis in the rat: a long-term study. Investigative Surgery. 2004;17(2):99–104.
   PubMed Web of Science ®Google Scholar
• Krahenbuhl S, Talos C, Lauterburg BH, et al. Reduced antioxidative capacity in liver mitochondria from bile duct ligated rats. Hepatology. 1995;22:607–612.
   PubMed Web of Science ®Google Scholar
• Portincasa P, Grattagliano I, Testini M, et al. Parallel intestinal and liver injury during early cholestasis in the rat: Modulation by bile salts and antioxidants. Free Radical Bio Med. 2007;42:1381–1391.
   PubMed Web of Science ®Google Scholar
• Wang XD, Ar'Rajab A, Andersson R, et al. The influence of surgically induced acute liver failure on the intestine in the rat. Scand J Gastroenterol. 1993;28:31–40.
   PubMed Web of Science ®Google Scholar
• Levi AC, Borghi F, Petrino R, et al. Modifications of the trophism of intestinal mucosa after intestinal and bilio-pancreatic diversion in the rat. Ital J Gastroenterol. 1991;23:202–207.
   PubMedGoogle Scholar
• Assimakopoulos SF, Vagianos CE, Patsoukis N, et al. Evidence for intestinal oxidative stress in tructive jaundice-induced gut barrier dysfunction in rats. Acta Physiol Scand. 2004b;180:177–185.
   PubMedGoogle Scholar
• Sheen-Chen SM, Ho HT, Chen WJ, Eng HL. Obstructive jaundice alters proliferating cell nuclear antigen expression in rat small intestine. World J Surg. 2003;27(10): 1161–1164.
   PubMed Web of Science ®Google Scholar
• Kruidenier L, Verspaget HW. Review article: oxidative stress as a pathogenic factor in inflammatory bowel disease—radicals or ridiculous? Aliment Pharmacol Ther. 2002;16:1997–2015.
   PubMed Web of Science ®Google Scholar
• Schimpl G, Pesendorfer P, Steinwender G, et al. Allopurinol and glutamine attenuate bacterial translocation in chronic portal Hypertensive and common bile duct ligated growing rats. Gut. 1996a;39:48–53.
   PubMed Web of Science ®Google Scholar
• Schimpl G, Pesendorfer P, Steinwender G, et al. Allopurinol reduces bacterial translocation, intestinal mucosal lipid peroxidation, and neutrophilderived myeloperoxidase activity in chronic portal hypertensive and common bile duct-ligated growing rats. Pediatr Res 1996b;40:422–428.
   PubMed Web of Science ®Google Scholar
• Reddy ACP, Lokesh BR. Studies on the inhibitory effect of curcumin and euganol on the formation of reactive species and the oxidation of ferrous iron. Mol Cell Biochem. 1994;137:1–8.
   PubMed Web of Science ®Google Scholar
• Sreejayan N, Rao MN. Free radical scavenging activity of curcuminoids. Arzneimittelforschung. 1996;46: 169–171.
   PubMed Web of Science ®Google Scholar
• El-Demerdash FM, Yousef MI, Radwan FM. Ameliorating effect of curcumin on sodium arsenite-induced oxidative damage and lipid peroxidation in different rat organs. Food Chem Toxicol. 2009;47:249–254.
   PubMed Web of Science ®Google Scholar
• Yucel AF, Kanter M, Pergel A, et al. The role of curcumin on intestinal oxidative stress, cell proliferation and apoptosis after ischemia/reperfusion injury in rats. J Mol Hist. 2011;42:579–587.
   PubMed Web of Science ®Google Scholar