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Effects of Ursodeoxycholate and Other Bile Salts on Levels of Rat Intestinal Alkaline Sphingomyelinase (A Potential Implication in Tumorigenesis)

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Abstract

Previous studies showed that bile salts had apromoting effect on colon cancer development and thiseffect was inhibited by ursodeoxycholate (UDC). Werecently found that both human colorectal adenomas and carcinomas were associated with a specificdecrease in alkaline sphingomyelinase activity. In thiswork, we compared the effects of ursodeoxycholate andother bile salts on the levels of rat intestinal alkaline sphingomyelinase both in theintestinal loops and after oral administration. Bilesalts at different concentrations were injected intointestinal loops and the dissociation of alkalinesphingomyelinase from the mucosa was assayed. We found that bilesalts, including taurocholate, taurodeoxycholate,glycocholate, glycochenodeoxycholate, and3-(3-cholamidopropyl dimethylammonio)-1-propanesulonate(CHAPS), dose dependently dissociated alkalinesphingomyelinase from the intestinal mucosa. UDC alonedid not dissociate the enzyme but significantlyinhibited the dissociation caused by other bile saltsand CHAPS. Feeding rats with 0.3% (w/w) taurocholate forfour days decreased peak activity of intestinal alkalinesphingomyelinase by 39% and total activity in theintestine by 20% and increased the output of the enzyme in the feces. In contrast, feeding 0.3%(w/w) UDC for four days increased the peak activity ofalkaline sphingomyelinase in the small intestine by 87%and the activity in the colon by 187% . The total activity of alkaline sphingomyelinase wasincreased by 80% and the output of the enzyme in thefeceswas only slightly increased by UDC administration.The changes in alkaline phosphatase after feeding taurocholate and UDC were much smaller. Ourresults indicate that UDC and other bile salts havedifferent effects on the levels of alkalinesphingomyelinase, which may be implicated in theirdifferent influences on cancer development reportedpreviously.

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REFERENCES

  1. Narisawa T, Magadia NE, Weisburger JH, Wynder EL: Promoting effect of bile salts on colon cancinogenesis after intrarectal instillation of N-me thyl-N-nitrosoguanidine in rats. J Natl Cancer Inst 53: 1093–1097, 1974

    Google Scholar 

  2. Reddy BS, Narisawa T, Weisburger JH, Wynder EL: Promoting effect of sodium deoxycholate on colon adenocarcinomas in germ-free rats. J Natl Cancer Inst 56: 441–442, 1976

    Google Scholar 

  3. Cohen BI, Raicht RF, De schner EE, Takahashi M, Sarwal AN, Fazzini E: Effect of cholic acid feeding on N-me thyl-N-nitrosourea induced colon tumors and cell kinetics in rats. J Natl Cancer Inst 64: 573–578, 1980

    Google Scholar 

  4. Koga S, Kaibara N, Takeda R: Effect of bile acids on 1,2-dime thylhydrazine-induced colon cancer in rats. Cancer 50: 543–547, 1982

    Google Scholar 

  5. Mower HF, Ray RM, Shoff R, Stemmermann GN, Nomura A, Glober GA, Kamiyama S, Shimada A, Yamakawa H: Fe cal bile acids in two Japanese populations with different colon cancer risks. Can Re s 39: 328–331, 1979

    Google Scholar 

  6. Johansen C, Chow W-H, Jorgensen T, Mellemkjaer L, Engholm G, Olsen JH: Risk of colorectal cancer and other cancers in patients with gall stones. Gut 39: 439–443, 1996

    Google Scholar 

  7. Weiss NS, Daling JR, Chow W-H: Cholecystectomy and the incidence of cancer of the large bowel. Cancer 49: 1713–1715, 1982

    Google Scholar 

  8. Alley PG, Lee SP: The increased risk of proximal colonic cancer after cholecystectomy. Dis Colon Rectum 26: 522–524, 1983

    Google Scholar 

  9. Broome U, Lofberg R, Verse s B, Eriksson LS: Primary scle rosing cholangitis and ulcerative colitis: Evidence for increase d neoplastic potential. Hepatology 22: 1404–1408, 1995

    Google Scholar 

  10. Earnest DL, Holubec H, Wali RK, Jolley CS, Bissonette M, Bhattacharyya AK, Roy H, Khare S, Brasitus TA: Chemopre vention of azoxymethane-induced colonic carcinogene sis by supplemental dietary ursodeoxycholic acid. Can Res 54: 5071–5074, 1994

    Google Scholar 

  11. Merrill AH, Schmelz EM, Wang E, Schroeder JJ, Dillehay DL, Riley RT: Role of dietary sphingolipids and inhibitors of sphingolipids metabolism in cancer and other diseases. J Nutr 125: 16775–16825, 1995

    Google Scholar 

  12. Gelderblom WCA, Kriek NPJ, Marasas WFO, Thiel PG: Toxicity and carcinoge nicity of the fusarium moniliforme metabolism, fumonisin B1, in rats. Carcinogenesis 12: 1247–1251, 1991

    Google Scholar 

  13. Dude ja PK, Dahiya R, Brasitus TA: The role of sphingomyel in and sphingomye linase in 1,2-dime thylhydrazine-induced lipid alterations of rat colonic plasma membrane. Biochim Biophys Acta 863: 309–312, 1986

    Google Scholar 

  14. Dillehay DL, Webb SK, Schmelz EM, Merrill AH: Dietary sphingomyelin inhibits 1,2-dimethylhydrazine-induced colon cancer in CF1 mice. J Nutr 124: 615–620, 1994

    Google Scholar 

  15. Hertervig E, Nilsson Å, Nyberg L, Duan R-D: Alkaline sphingomyelinase activity is decreased in human colorectal Cancer. Cancer 79: 448–453, 1997

    Google Scholar 

  16. Duan R-D, Hertervig E, Hauge T, Nyberg L, Nilsson Å: Specific decrease in alkaline sphingomyelinase activity in human colorectal Cancer and adenomas. Gastroenterology 110(suppl): A509, 1996

    Google Scholar 

  17. Nilsson Å: The presence of sphingomyelin-and ceramide-cleaving enzyme in the small intestinal tract. Biochim Biophys Acta 176: 339–347, 1969

    Google Scholar 

  18. Duan R-D, Nyberg L, Nilsson Å: Alkaline sphingomyelinase activity in rat gastrointe stinal tract: Distribution and characteristics. Biochim Biophys Acta 1259: 1060–1065, 1995

    Google Scholar 

  19. Spence MW: Sphingomye linase. Adv Lipid Res 26: 3–23, 1993

    Google Scholar 

  20. Chatterjee S: Neutral sphingomyelinase. Adv Lipid Res 26: 25–57, 1993

    Google Scholar 

  21. Duan R-D, Hertervig E, Nyberg L, Hauge T, Sternby B, Lillienau J, Farooqi A, Nilsson Å: Distribution of alkaline sphingomyelinase activity in human beings and animals, tissue and species differences. Dig Dis Sci 41: 1801–1806, 1996

    Google Scholar 

  22. Nyberg L, Duan R-D, Axelson J, Nilsson Å: Identification of an alkaline sphingomyelinase activity in human bile. Biochim Biophys Acta 1300: 42–48, 1996

    Google Scholar 

  23. Kolesnick RN: Sphingomyelin and derivative s as cellular signals. Prog Lipid Res 30: 1–38, 1991

    Google Scholar 

  24. Hannun YA, Obeid LM: Ceramide: an intracellular signal for apoptosis. TIBS 20: 73–77, 1995

    Google Scholar 

  25. Shiozaki H, Yoshioka M, Miura S, Imaeda H, Morita A, Asakura H, Tsuchiya M, Ishii H: Conjugated bile salts regulate turnover of rat intestinal brush border membrane hydrolases. Dig Dis Sci 40: 1193–1198, 1995

    Google Scholar 

  26. Accatino L, Pizarro M, Solis N, Koenig CS: Association of canalicular membrane enzyme s with bile acid micelles and lipid aggregate s in human and rat bile. Biochim Biophys Acta 1243: 33–42, 1995

    Google Scholar 

  27. Nyberg L, Burling H: Methods for extracting sphingomyelin, SE-patent 9300454-7, Patent & Registreringsverket, Stockholm, 1993

    Google Scholar 

  28. Stoffel W: Chemical synthesis of choline-labeled lacithins and sphingomyelin. Methods Enzymol 36: 533–541, 1975

    Google Scholar 

  29. Bowman BB, Rosenberg IH: Biotin absorption by distal rat intestine. J Nutr 117: 2121–2126, 1987

    Google Scholar 

  30. Hofmann AF: Bile acids. InThe Live r, Biology and Pathology. IM Arias, WB Jakoby, H Popper, D Schachter, DA Shafritz (eds). New York, Raven Press, 1988, pp 553–572

    Google Scholar 

  31. Lillienau J, Grombie DL, Munoz J, Longmire-Cook SJ, Hagey LR, Hofmann AF: Negative feedback regulation of the ileal bile acid transport system in rodents. Gastroenterology 104: 38–46, 1993

    Google Scholar 

  32. Billington D, Evans CE, Godfrey PP, Coleman R: Effects of bile salts on the plasma membrane of isolated rat hepatocytes. Biochem J 188: 321–327, 1980

    Google Scholar 

  33. Barnwell SG, Lowe PJ, Coleman R: Effect of taurochenodeoxycholate or tauroursodeoxycholate upon biliary output of phospholipids and plasma-membrane enzymes, and the extent of cell damage, in isolated perfused rat livers. Biochim J 216: 107–111, 1983

    Google Scholar 

  34. Kitani K, Ohta M, Kanai S: Tauroursodeoxycholate prevents biliary protein excre tion induced by other bile salts in the rat. Am J Physiol 248: G407–G417, 1985

    Google Scholar 

  35. Galle PR, Theilmann L, Raedsch R, Otto G, Stiehl A: Ursode-oxycholate reduces hepatoxicity of bile salts in primary human hepatocytes. Hepatology 12: 486–491, 1990

    Google Scholar 

  36. Chadwick VS, Gaginella TS, Carlson GL, Debongnie J-C, Phillips SF, Hofmann AF: Effect of molecular structure on bile acid-induced alterations in absorptive function, permeability, and morphology in the perfused rat colon. J Lab Clin Invest 94: 661–674, 1979

    Google Scholar 

  37. Koga Y: Anti-cholestatic and cytoprote ctive properties of ursodeoxycholic acid. Studies in vivoand in vitro .Acta Hepatol Jpn 28: 1597–1604, 1987

    Google Scholar 

  38. Bedi A, Pasricha PJ, Akhtar AJ, Barber JP, Bedi GC, Giardiello FM, Zehnbauer BA, Homilton SR, Jones RJ: Inhibition of apoptosis during deve lopment of colorectal cancer. Can Res 55: 1811–1816, 1995

    Google Scholar 

  39. Rigas B, Tsioulias GJ, Allan C, Wali R, Brasitus TA: Ursode-oxycholic acid and piroxicam up-regulate MHC antigen expression in rat colonocytes during colon cancer development. Gastroente rology 106: A433, 1994

    Google Scholar 

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Duan, RD., Cheng, Y., Tauschel, HD. et al. Effects of Ursodeoxycholate and Other Bile Salts on Levels of Rat Intestinal Alkaline Sphingomyelinase (A Potential Implication in Tumorigenesis). Dig Dis Sci 43, 26–32 (1998). https://doi.org/10.1023/A:1018807600683

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