Effects of bile diversion in rats on intestinal sphingomyelinases and ceramidase

Biochimica et Biophysica Acta - Molecular and Cell Biology of Lipids

Volumn 1771, Issue 2, 2007, Pages 196-201

  Duan, R D ^a   Verkade, H J ^b   Cheng, Y ^a   Havinga, R ^b   Nilsson, A ^a  

^a LUND UNIVERSITY   (Sweden)

^b UNIVERSITY MEDICAL CENTER GRONINGEN   (Netherlands)

Author keywords

Bile diversion; Ceramidase; Colon; Rat; Small intestine; Sphingomyelinase

Indexed keywords

ACYLSPHINGOSINE DEACYLASE; SPHINGOMYELIN PHOSPHODIESTERASE;

ANIMAL CELL; ANIMAL TISSUE; ARTICLE; BILE; ENZYME ACTIVITY; HYDROLYSIS; INTESTINE MUCOSA; MALE; MICROVILLUS; NONHUMAN; PRIORITY JOURNAL; RAT; SMALL INTESTINE;

AMIDOHYDROLASES; ANIMALS; BILE; COLON; FECES; INTESTINAL MUCOSA; INTESTINE, SMALL; INTESTINES; MALE; RATS; RATS, WISTAR; SPHINGOMYELIN PHOSPHODIESTERASE;

RATTUS;

EID: 33846837412     PISSN: 13881981     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bbalip.2006.12.001     Document Type: Article

References (39)

1. Kolesnick R.N. Sphingomyelin and derivatives as cellular signals. Prog. Lipid Res. 30 (1991) 1-38
2. Hannun Y.A. The sphingomyelin cycle and the second messenger function of ceramide. J. Biol. Chem. 269 (1994) 3125-3128
3. Duan R.D., Bergman T., Xu N., Wu J., Cheng Y., Duan J., Nelander S., Palmberg C., and Nilsson A. Identification of human intestinal alkaline sphingomyelinase as a novel ecto-enzyme related to the nucleotide phosphodiesterase family. J. Biol. Chem. 278 (2003) 38528-38536
4. Wu J., Cheng Y., Palmberg C., Bergman T., Nilsson A., and Duan R.D. Cloning of alkaline sphingomyelinase from rat intestinal mucosa and adjusting of the hypothetical protein XP_221184 in GenBank. Biochim. Biophys. Acta 1687 (2005) 94-102
5. Olsson M., Duan R.D., Ohlsson L., and Nilsson A. Rat intestinal ceramidase: purification, properties, and physiological relevance. Am. J. Physiol.: Gastrointest. Liver Physiol. 287 (2004) G929-G937
6. Wu J., Hansen G.H., Nilsson A., and Duan R.D. Functional studies of human intestinal alkaline sphingomyelinase by deglycosylation and mutagenesis. Biochem. J. 386 (2005) 153-160
7. Nilsson Å. The presence of sphingomyelin- and ceramide-cleaving enzymes in the small intestinal tract. Biochim. Biophys. Acta 176 (1969) 339-347
8. Duan R.D., Cheng Y., Hansen G., Hertervig E., Liu J.J., Syk I., Sjostrom H., and Nilsson A. Purification, localization, and expression of human intestinal alkaline sphingomyelinase. J. Lipid Res. 44 (2003) 1241-1250
9. Hertervig E., Nilsson A., Nyberg L., and Duan R.D. Alkaline sphingomyelinase activity is decreased in human colorectal carcinoma. Cancer 79 (1997) 448-453
10. Sjöqvist U., Hertervig E., Nilsson A., Duan R.D., Ost A., Tribukait B., and Lofberg R. Chronic colitis is associated with a reduction of mucosal alkaline sphingomyelinase activity. Inflamm. Bowel Dis. 8 (2002) 258-263
11. Duan R.D. Alkaline sphingomyelinase: an old enzyme with novel implications. Biochim. Biophys. Acta 1761 (2006) 281-291
12. Cheng Y., Nilsson Å., Tömquist E., and Duan R.D. Purification, characterization and expression of rat intestinal alkaline sphingomyelinase. J. Lipid Res. 43 (2002) 316-324
13. Lundgren P., Nilsson Å., and Duan R.D. Distribution and properties of neutral ceramidase activity in rat intestinal tract. Dig. Dis. Sci. 46 (2001) 765-772
14. Duan R.D., Cheng Y., Tauschel H.D., and Nilsson A. Effects of ursodeoxycholate and other bile salts on levels of rat intestinal alkaline sphingomyelinase: a potential implication in tumorigenesis. Dig. Dis. Sci. 43 (1998) 26-32
15. Duan R.D., Nyberg L., and Nilsson A. Alkaline sphingomyelinase activity in rat gastrointestinal tract: distribution and characteristics. Biochim. Biophys. Acta 1259 (1995) 49-55
16. Cheng Y., Tauschel H.-T., Nilsson Å., and Duan R.-D. Administration of ursodeoxycholic acid increases the activities of alkaline sphingomyelinase and caspase-3 in rat colon. Scand J. Gastroenterol. 34 (1999) 915-920
17. Liu F., Cheng Y., Wu J., Tauschel H.D., and Duan R.D. Ursodeoxycholic acid differentially affects three types of sphingomyelinase in human colon cancer Caco 2 cells. Cancer Lett. 235 (2006) 141-146
18. Nyberg L., Duan R.D., Axelsson J., and Nilsson Å. Identification of an alkaline sphingomyelinase activity in human bile. Biochim. Biophys. Acta 1300 (1996) 42-48
19. Duan R.D., Hertervig E., Nyberg L., Hauge T., Sternby B., Lillienau J., Farooqi A., and Nilsson A. Distribution of alkaline sphingomyelinase activity in human beings and animals. Tissue and species differences. Dig. Dis. Sci. 41 (1996) 1801-1806
20. Nyberg L., Duan R.D., and Nilsson Å. A mutual inhibitory effect on absorption of sphingomyelin and cholesterol. J. Nutr. Biochem. 11 (2000) 244-249
21. Stoffel W. Chemical synthesis of choline-labeled lecithins and sphingomyelin. Methods Enzymol. 36 (1975) 533-541
22. Duan R.D., and Nilsson A. Sphingolipid hydrolyzing enzymes in the gastrointestinal tract. Methods Enzymol. 311 (2000) 276-286
23. Duan R.D., Cheng Y., Yang L., Ohlsson L., and Nilsson A. Evidence for specific ceramidase present in the intestinal contents of rats and humans. Lipids 36 (2001) 807-812
24. Amoscato A.A., Alexander J.W., and Babcock G.F. Surface aminopeptidase activity of human lymphocytes. I. Biochemical and biologic properties of intact cells. J. Immunol. 142 (1989) 1245-1252
25. Hannun Y.A., and Linardic C.M. Sphingolipid breakdown products: anti-proliferative and tumor-suppressor lipids. Biochim. Biophys. Acta 1154 (1993) 223-236
26. Roy C.C., Laurendeau G., Doyon G., Chartrand L., and Rivest M.R. The effect of bile and of sodium taurocholate on the epithelial cell dynamics of the rat small intestine. Proc. Soc. Exp. Biol. Med. 149 (1975) 1000-1004
27. Wu J., Cheng Y., Nilsson A., and Duan R.D. Identification of one exon deletion of intestinal alkaline sphingomyelinase in colon cancer HT-29 cells and a differentiation-related expression of the wild-type enzyme in Caco-2 cells. Carcinogenesis 25 (2004) 1327-1333
28. Shiozaki H., Yoshioka M., Miura S., Imaeda H., Morita A., Asakura H., Tsuchiya M., and Ishii H. Conjugated bile salts regulate turnover of rat intestinal brush border membrane hydrolases. Dig. Dis. Sci. 40 (1995) 1193-1198
29. Maroux S., Coudrier E., Feracci H., Gorvel J.P., and Louvard D. Molecular organization of the intestinal brush border. Biochimie 70 (1988) 1297-1306
30. Sonoyama K., Kiriyama S., and Niki R. Cholestyramine and bile diversion lower the aminopeptidase activity in the intestinal brush border membrane of rats. J. Nutr. Sci. Vitaminol. (Tokyo) 39 (1993) 617-625
31. Bossmann B., and Haschen R.J. De novo synthesis of brush border membrane enzymes during intestinal perfusion with bile salt in the rat. J. Clin. Chem. Clin. Biochem. 22 (1984) 449-451
32. Cheng Y., Ohlsson L., and Duan R.D. Psyllium and fat in diets differentially affect the activities and expressions of colonic sphingomyelinases and caspase in mice. Br. J. Nutr. 91 (2004) 715-723
33. Hertervig E., Nilsson Å., Björk J., Hultkrantz R., and Duan R.D. Familial adenomatous polyposis is associated with a marked decrease in alkaline sphingomyelinase activity; a key factor to the unrestrained cell proliferation. Br. J. Cancer 81 (1999) 232-236
34. Hertervig E., Nilsson A., Cheng Y., and Duan R.D. Purified intestinal alkaline sphingomyelinase inhibits proliferation without inducing apoptosis in HT-29 colon carcinoma cells. J. Cancer Res. Clin. Oncol. 129 (2003) 577-582
35. Williamson R.C., Bauer F.L., Ross J.S., Watkins J.B., and Malt R.A. Enhanced colonic carcinogenesis with azoxymethane in rats after pancreaticobiliary diversion to mid small bowel. Gastroenterology 76 (1979) 1386-1392
36. Chu M., Rehfeld J.F., and Borch K. Colonic mucosal proliferation after pancreaticobiliary diversion in the hamster. Dig. Dis. Sci. 38 (1993) 1978-1984
37. Eckhardt E.R., Wang D.Q., Donovan J.M., and Carey M.C. Dietary sphingomyelin suppresses intestinal cholesterol absorption by decreasing thermodynamic activity of cholesterol monomers. Gastroenterology 122 (2002) 948-956
38. Chen H., Born E., Mathur S.N., Johlin Jr. F.C., and Field F.J. Sphingomyelin content of intestinal cell membranes regulates cholesterol absorption. Evidence for pancreatic and intestinal cell sphingomyelinase activity. Biochem. J. 286 (1992) 771-777
39. Field F.J., Chen H., Born E., Dixon B., and Mathur S. Release of ceramide after membrane sphingomyelin hydrolysis decreases the basolateral secretion of triacylglycerol and apolipoprotein B in cultured human intestinal cells. J. Clin. Invest. 92 (1993) 2609-2619