Effect of oxidants on small intestinal brush border membranes and colonic apical membranes - A comparative study

Comparative Biochemistry and Physiology - C Toxicology and Pharmacology

Volumn 134, Issue 3, 2003, Pages 329-339

  Prabhu, R ^a   Balasubramanian, K A ^a  

^a CHRISTIAN MEDICAL COLLEGE   (India)

Author keywords

Brush border membrane; Colonic apical membrane; Lipid peroxidation; Phospholipids; Superoxide

Indexed keywords

ALKADIENE; ALKALINE PHOSPHATASE; ALLOPURINOL; CARBONYL DERIVATIVE; CHOLESTEROL; GLUCOSE; HYDROGEN PEROXIDE; MALONALDEHYDE; OXIDIZING AGENT; PEROXIDE; PHOSPHOLIPID; SUPEROXIDE; SUPEROXIDE DISMUTASE; TERTIARY BUTYL HYDROPEROXIDE; UNCLASSIFIED DRUG; XANTHINE; XANTHINE OXIDASE;

ANIMAL TISSUE; ANTIOXIDANT ACTIVITY; APICAL MEMBRANE; ARTICLE; COLON; CONTROLLED STUDY; ENZYME ACTIVITY; GASTROINTESTINAL MUCOSA; INTESTINE BRUSH BORDER MEMBRANE; LIPID COMPOSITION; LIPID PEROXIDATION; NONHUMAN; OXIDATIVE STRESS; PRIORITY JOURNAL; RAT;

EID: 0037338666     PISSN: 15320456     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1532-0456(02)00250-8     Document Type: Article

References (49)

1. Anup R., Madesh M., Balasubramanian K.A. Entrocyte mitochondrial dysfunction due to oxidative stress. Indian J. Biochem. Biophys. 36:1999;266-271.
2. Babbs C.F. Oxygen radicals in ulcerative colitis. Free Radical Biol. Med. 46:1992;2402-2406.
3. Babbs C.F. Free radical and etiology of colon cancer. Free Radical Biol. Med. 8:1990;191-200.
4. Bartlett G.R. Phosphorous assays in column chromatography. J. Biol. Chem. 234:1959;466-468.
5. Baskar L., Balasubramanian K.A. Effect of oxidant exposure on isolated tat colonocytes. Scand. J. Gastroenterol. 30:1995;332-336.
6. 2 in uterine stromal cells. Biochem. Biophys. Res. Commun. 276:2000;613-618.
7. Blakeborough M.H., Owen R.W., Bilton R.F. Free radical generating mechanisms in the colon: their role in the induction and promotion of colorectal cancer? Free Radical Biol. Med. 6:1989;359-367.
8. Bligh E.G., Dyer W.J. A rapid method of total lipid extraction and purification. Can. J. Biochem. Physiol. 37:1959;911-917.
9. 2 in microsomal lipid peroxidation induced with tertiary butyl hydroperoxide. Biochem. Biophys. Res. Commun. 158:1989;1021-1028.
10. Chan H.W., Levett G. Auto oxidation of methyl linoleate. Separation and analysis of isomeric mixtures of methyl linoleate hydroperoxides and methyl hydroxy linoleates. Lipids. 12:1972;99-104.
11. Courjault-Gautier F., Le Grimellec C., Giocondi M.C., Toutain H.J. Modulation of sodium-coupled uptake and membrane fluidity by cisplatin in renal proximal tubular cells in primary culture and brush-border membrane vesicles. Kidney Int. 47:1995;1048-1056.
12. Cuzzocrea S., Mazzon E., Dugo L., Caputi A.P., Riley D.P., Savemini D. Protective effects of M40403, a superoxide dismutase mimetic, in a rodent model of colitis. Eur. J. Pharmacol. 432:2001;79-89.
13. Dipolk A.T., Balasubramanian K.A., Manohar M., Mathan V.I., Ashton D. Purification and chemical characterisation of the inhibitor of lipid peroxidation from intestinal mucosa. Biochim. Biophys. Acta. 962:1988;42-50.
14. Djurdjic V., Mandic L. A spectrophotometric method of simultaneous determination of protein-bound hexoses and fucose with a mixture of L-cysteine and phenol. Anal. Biochem. 188:1990;222-227.
15. Dudeja P.K., Brasitus T.A. Inactivation of rat small intestinal brush-border membrane alkaline phosphatase by oxygen free radicals. Gastroentrology. 105:1993;357-366.
16. 2. FEBS Lett. 309:1992;190-192.
17. Habeeb A.F.S. A Reaction of protein sulfhydryl groups with Ellmans's reagent. Methods Enzymol. 25:1972;457-464.
18. Huycke M.M., Abrams V., Moore D.R. Enterococcus faecalis produces extracellular superoxide and hydrogen peroxide that damages colonic epithelial cell DNA. Carcinogenesis. 23:2002;529-536.
19. Koch T.R., Yuan L.X., Stryker S.J., Ratliff P., Telford G.L., Opara E.C. Total antioxidant capacity of colon in patients with chronic ulcerative colitis. Digest. Dis. Sci. 45:2000;1814-1819.
20. Lambert G.P., Gisolfi C.V., Berg D.J., Mosley P.C., Oberley L.W., Kerga K.C. Selected contribution: hyperthermia-induced permeability and the role of oxidative and nitrosative stress. J. Appl. Physiol. 92:2002;1750-1761.
21. Lowry O.H., Rosebrough N.J., Farr A.L., Randall R.J. Protein measurement with the Folin phenol reagent. J. Biol. Chem. 193:1970;265-275.
22. MacDonald T.T., Murch S.H., Nicholls S.W., Breese E.J. Diarrhoeal disease: current concepts and future challenges. Intestinal cytokines in inflammatory bowel disease and invasive diarrhoea. Trans. R. Soc. Trop. Med. Hyg. 87:1993;23-26.
23. Madesh M., Balasubramanian K.A. Activation of liver mitochondrial phospholipase A2 by superoxide. Arch. Biochem. Biophys. 346:1997;187-192.
24. Mezes M., Surai P., Sulyi G., Speake B.K., Goal T., Maldjian. Nutritional metabolic diseases of poultry and disorders of the biological antioxidant defence system. Acta Veg. Hung. 45:1997;349-360.
25. Nalini S., Ahamed S., Balasubramanian K.A. Effect of oxidant exposure on monkey intestinal brush-border membrane. Biochim. Biophys. Acta. 1147:1993;169-176.
26. Nalini S., Balasubramanian K.A. Effect of luminal exposure of oxidants intestinal mucosal lipid peroxidation and absorptive function. Scand. J. Gastroenterol. 28:1993;281-284.
27. Nigam S., Schewe T. Phospholipase A(2)s and lipid peroxidation. Biochim. Biophys. Acta. 1488:2000;167-181.
28. Ohkawn J.P., Ohishi N., Yagi K. Assay for lipid peroxides in animal tissues by thiobarbituric acid reaction. Anal. Biochem. 95:1979;351-358.
29. Ohyashiki T., Kumanda Y., Hafanaka N., Mafsui K. Oxygen free radical-induced inhibition of alkaline phosphatase activity in reconstituted membranes. Arch. Biochem. Biophys. 313:1994;310-317.
30. 2 and decreased lyso phospholipase activity in the small intestinal mucosa after ischemia and revascularisation. Gut. 28:1987;1445-1453.
31. 2 inhibition prevents mucosal damage associated with small intestinal ischemia in rats. Gut. 29:1988;489-494.
32. Otamiri T. Oxygen radicals, lipid peroxidation and neutrophil infiltration after small intestinal ischemia and reperfusion. Surgery. 105:1989;593-597.
33. Parks D.A. Oxygen radicals: mediators of gastrointestinal pathophysiology. Gut. 30:1989;293-298.
34. Pavlick K.P., Laroux F.S., Fuseler J., et al. Role of reactive metabolites of oxygen and nitrogen in inflammatory bowel disease. Free Radical Biol. Med. 33:2002;311-322.
35. Plaa G.L., Witschi. Chemicals, drugs and lipid peroxidation. Annu. Rev. Pharmacol. Toxicol. 16:1976;125-141.
36. Pons L., Droy-Leferix M.T., Barquet P., Buero L. Role of free radicals and platelet-activating factor in the genesis of intestinal motor disturbances induced by Escherihia coli endotoxins in rats. Gastroenterology. 100:1991;946-953.
37. Prabhu R., Balasubramanian K.A. A novel method of preparation of small intestinal brush border membrane vesicles by poly ethylene glycol precipitation. Anal. Biochem. 289:2001;157-161.
38. Prabhu R., Anup R., Balasubramanian K.A. Surgical stress induces phospholipid degradation in the intestinal brush border membrane. J. Surg. Res. 94:2000;178-184.
39. Ribeiro C.M. Oxygen free radicals in medicine. Acta Med. Port. 2:1987;93-102.
40. Roediger W.E.W., True love S.C. Method of preparing isolated colonic epithelial cells (colonocytes) for metabolic studies. Gut. 20:1979;484-488.
41. Serifer A., Gerstenfeld S. Photometric determination of sialic acid I serum and cerebrospinal fluid with thiobarbituric acid method. Clin. Chem. Acta. 7:1962;467-475.
42. Sohal R.S., Agarwal S., Dubey A., Orr W.S. Protein oxidative damage is associated with life expectancy of houseflies. Proc. Natl. Acad. Sci. USA. 90:1993;7255-7259.
43. Synder F., Stephen N. A simplified spectrophotometric determination of ester groups in lipids. Biochim. Biophys. Acta. 34:1959;244-245.
44. Thambidurai D., Bachawat B.K. Purification and properties of brain alkaline phosphatase. J. Neurochem. 29:1977;503-512.
45. Williams J.G. Phagocytes, toxic oxygen metabolites and inflammatory bowel disease: implication for treatment. Ann. R. Coll. Surg. Engl. 72:1990;253-262.
46. Williams J.G. Toxic oxygen metabolite production by circulating phagocytic cells in inflammatory bowel disease. Gut. 31:1990;187-193.
47. Wolfgang F.C. Physiology and pathophysiology of intestinal absorption. Am. J. Clin. Nutr. 55:1992;299S-308S.
48. Yoshikowa T., Kondo M. Free radicals in digestive diseases. Nippon Ronan Igakkai Zasshi. 27:1990;150-160.
49. Zaltkis A., Zak B., Boyle A.J. A new method for the determination of serum cholesterol. J. Lab. Clin. Med. 41:1953;486-492.