Development of oxidative stress and cell damage in the liver of rats with water-immersion restraint stress

REFERENCES

• Yoshikawa T, Miyagawa H, Yoshida N, Sugino S, Kondo M. Increase in lipid peroxidation in rat gastric mucosal lesions induced by water-immersion restraint stress. J Clin Biochem Nutr 1986; 1: 271–277.
   Google Scholar
• Hirota M, Inoue M, Ando Yet al. Inhibition of stress-induced gastric injury in the rat by glutathione. Gastroenterology 1989; 97: 853–859.
   PubMed Web of Science ®Google Scholar
• Nishida K, Ohta Y, Kobayashi T, Ishiguro I. Involvement of the xanthine-xanthine oxidase system and neutrophils in the development of acute gastric mucosal lesions in rats with water immersion restraint stress. Digestion 1997; 58: 340–351.
   PubMed Web of Science ®Google Scholar
• Nishida K, Ohta Y, Ishiguro I. Changes in nitric oxide production with lesion development in the gastric mucosa of rats with water immersion restraint stress. Res Commun Mol Pathol Pharmacol 1998; 100: 201–212.
   PubMed Web of Science ®Google Scholar
• Shin WM, Sasaki I, Kamiyama Y, Naito H, Matsugo S, Miyazawa T. The role of lipid peroxidation on gastric mucosal lesions induced by water-immersion-restraint stress in rats. Surg Today 2000; 30: 49–53.
   PubMed Web of Science ®Google Scholar
• Iwai K, Onodera A, Matsue H. Antioxidant activity and inhibitory effect of Gamazumi (Viburnum dilatatum THUB.) on oxidative damage induced by water immersion restraint stress in rats. Int J Food Sci Nutr 2001; 52: 443–451.
   PubMed Web of Science ®Google Scholar
• Iwai K, Onodera A, Matsue H. Mechanism of preventive action of Viburnum dilatatum Thunb (gamazumi) crude extract on oxidative damage in rats subjected to stress. J Sci Food Agric 2003; 83: 1593–1599.
   Web of Science ®Google Scholar
• Yasukawa K, Kasazaki K, Hyodo F, Utsumi H. Non-invasive analysis of reactive oxygen species generated in rats with water immersion restraint-induced gastric mucosal lesions using in vivo electron spin resonance spectroscopy. Free Radic Res 2004; 38: 147–155.
   PubMed Web of Science ®Google Scholar
• Ohta Y, Kamiya Y, Imai Y, Arisawa T, Nakano H. Role of gastric mucosal ascorbic acid in gastric mucosal lesion development in rats with water immersion restraint stress. Inflammopharmacology 2005; 13: 249–259.
   PubMedGoogle Scholar
• Alpekin N, Seykin S, Dogru-Abbasoglu S, Koyak-Toker N, cevikbas U, Uysai M. Effect of vitamin C on glutathione and lipid peroxide levels in rats exposed to water-immersion restraint stress. Med Sci Res 1998; 26: 595–597.
   Google Scholar
• Schierwagen C, Blyund-Fellenous A-C, Lundberg C. Improved method for quantification of tissue PMN accumulation measured by myeloperoxidase. J Pharmacol Methods 1990; 23: 179–186.
   PubMedGoogle Scholar
• Komatsu H, Koo A, Ghadishah E et al. Neutrophil accumulation in ischemic reperfused rat liver: evidence for a role for superoxide free radicals. Am J Physiol 1992; 262: G669–G676.
   PubMed Web of Science ®Google Scholar
• Takagi K, Okabe S. The effects of drugs on the stress ulcer in rats. Jpn J Pharmacol 1968; 18: 9–18.
   PubMedGoogle Scholar
• Yagi K. A simple fluorometric assay for lipoperoxides in blood sample. Biochem Med 1976; 15: 212–216.
   PubMed Web of Science ®Google Scholar
• Green LC, Wagner DA, Glogowski J, Skipper PL, Eishnok JS, Tannenbaum SR. Analysis of nitrate, nitrite, and [15N]nitrate in biological fluid. Anal Biochem 1982; 126: 131–138.
   PubMed Web of Science ®Google Scholar
• Zannoi V, Lynch M, Goldstein S, Sato P. A rapid micromethod for the determination of ascorbic acid in plasma and tissues. Biochem Med 1974; 11: 41–48.
   PubMed Web of Science ®Google Scholar
• Sedlak J, Lindsay RH. Estimation of total, protein-bound, and nonprotein sulfhydryl groups in tissue with Ellman's reagent. Anal Biochem 1958; 25: 192–205.
   Web of Science ®Google Scholar
• Kamiya Y, Ohta Y, Imai Y, Arisawa T, Nakano H. A critical role of gastric mucosal ascorbic acid in the progression of acute gastric mucosal lesions induced by compound 48/80 in rats. World J Gastroenterol 2005; 11: 1324–1332.
   PubMed 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: 351–358.
   PubMed Web of Science ®Google Scholar
• Oyanagui Y. Reevaluation of assay methods and establishment of kit for superoxide dismutase activity. Anal Biochem 1984; 142: 290–296.
   PubMed Web of Science ®Google Scholar
• Suzuki K, Ota H, Sasagawa S, Sakatani T, Fujikura T. Assay method for myeloperoxidase in human polymorphonuclear leukocytes. Anal Biochem 1983; 132: 345–353.
   PubMed Web of Science ®Google Scholar
• Hashimoto S. A new spectrophotometric assay method of xanthine oxidase in crude tissue homogenate. Anal Biochem 1974; 62: 426–433.
   PubMed Web of Science ®Google Scholar
• Lowry OH, Rosebrough NH, Farr AD, Randal RJ. Protein measurement with the Folin phenol reagent. J Biol Chem 1951; 193: 265–273.
   PubMed Web of Science ®Google Scholar
• Alpekin N, Seykin S, Dogru-Abbasoglu S et al. Lipid peroxidation, glutathione, y-glutamylcysteine synthetase and 7-glutamyltranspeptidase activities in several tissues of ratsfollowing water-immersion stress. Pharmacol Res 1996; 34: 167–169.
   PubMed Web of Science ®Google Scholar
• Winkler BS, Orselli SM, Rex TS. The redox couple between glutathione and ascorbic acid: a chemical and physiological perspective. Free Radic Biol Med 1994; 17: 333–349.
   PubMed Web of Science ®Google Scholar
• Beyer RR. The role of ascorbate in antioxidant protection of biomembranes: interaction with vitamin E and coenzyme Q. J Bioenerg Biomembranes 1994; 26: 349–358.
   PubMed Web of Science ®Google Scholar
• Bredt D. Endogenous nitric oxide synthesis: biological functions and pathophysiology. Free Radic Res 1999; 31: 577–596.
   PubMed Web of Science ®Google Scholar
• Dwenger A, Funk M, Lueken B, Schweitwer G, Lehmann U. Effect of ascorbic acid on neutrophil functions and hypoxanthine/xanthine oxidase-generated, oxygen-derived radicals. Eur J Clin Chem Clin Biochem 1992; 30: 187–191.
   PubMedGoogle Scholar
• Ross D, Cotgreave I, Moldeus P. The interaction of reduced glutathione with active oxygen species generated by xanthine-oxidase-catalyzed metabolism of xanthine. Biochim Biophys Ada 1985; 841: 278–282.
   PubMed Web of Science ®Google Scholar
• Hemild H., Roberts P, Wikstrom M. Activated polymorphonuclear leucocytes consume vitamin C. FEBS Lett 1984; 178: 25–30.
   PubMedGoogle Scholar
• Halliwell B, Wasil M, Grootveld M. Biologically significant scavenging of the myeloperoxidase-derived oxidant hypochlorous acid by ascorbic acid. FEBS Lett 1987; 213: 15–17.
   PubMed Web of Science ®Google Scholar
• Hata T, Kita T, Kwabata A, Itoh E, Nishimura Y. Changes of tissue blood flow in mice with SART (repeated cold) stress or restraint and water immersion stress and the effect of administered neurotropin. Jpn J Pharmacol 1986; 41: 69–79.
   PubMedGoogle Scholar
• Matsui N, Satsuki I, Morita Y et al. Xanthine oxidase-derived reactive oxygen species activate nuclear factor kappa B during hepatic ischemia in rats. Jpn J Pharmacol 2000; 84: 363–366.
   PubMedGoogle Scholar
• Amould T, Thibaut-Vercruyseen R, Bouaziz N, Dieu M, Remade J, Michiels C. PGF2, a proposed released by endothelial cells activated by hypoxia, is a chemoattractant candidate for neutrophil recruitment. Am J Pathol 2001; 159: 345–357.
   PubMed Web of Science ®Google Scholar
• Zimmerman JJ, Ciesielski W, Lewandoski J. Neutrophil-mediated phospholipid peroxidation assessed by gas chromatography-mass spectroscopy. Am J Physiol 1997; 273: C653–C661.
   PubMed Web of Science ®Google Scholar
• Stelmaszynska T, Kukovetz E, Egger G, Schaur RJ. Possible involvement of myeloperoxidase in lipid peroxidation. Int J Biochem 1992; 24: 121–128.
   PubMedGoogle Scholar
• Kolls J, Xie J, LeBlanc R et al. Rapid induction of messenger RNA for nitric oxide synthase II in rats neutrophils in vivo by endotoxin and its suppression by prednisolone. Proc Soc Exp Biol Med 1994; 205: 220–225.
   PubMed Web of Science ®Google Scholar
• Huie RE, Padmaja S. The reaction of NO with superoxide. Free Radic Res Commun 1993; 18: 195–199.
   PubMed Web of Science ®Google Scholar
• Hogg N, Kalyanaraman B. Nitric oxide and lipid peroxidation. Biochim Biophys Acta 1999; 1411: 378–384.
   PubMed Web of Science ®Google Scholar
• MacMillan-Crow LA, Crow JP, Thompson JA. Peroxynitrite-mediated inactivation of manganese superoxide dismutase involves nitration and oxidation of critical tyrosine residue. Biochemistry 1998; 37: 1613–1622.
   PubMed Web of Science ®Google Scholar