Glycosylceramides obtain from the starfish Asterias amurensis Lütken

Journal of Oleo Science

Volumn 57, Issue 9, 2008, Pages 477-484

  Shah, A K M Azad ^a   Kinoshita, Mikio ^b   Kurihara, Hideyuki ^a   Ohnishi, Masao ^b   Takahashi, Koretaro ^a  

^a HOKKAIDO UNIVERSITY   (Japan)

^b OBIHIRO UNIVERSITY OF AGRICULTURE AND VETERINARY MEDICINE   (Japan)

Author keywords

Asterias amurensis; Glycosylceramide; Sphingoid base

Indexed keywords

CERAMIDE HEXOSIDE; CEREBROSIDE; DRUG DERIVATIVE; GLUCOSYLCERAMIDE; ICOSAPENTAENOIC ACID; LIPID; SPHINGOSINE; TRIACYLGLYCEROL;

ANIMAL; APOPTOSIS; ARTICLE; ASTERIAS; CELL CULTURE; CELL STRAIN CACO 2; CHEMISTRY; COLON TUMOR; DRUG EFFECT; GONAD; HUMAN; ISOLATION AND PURIFICATION; MASS SPECTROMETRY; METABOLISM; PATHOLOGY; VISCERA;

ANIMALS; APOPTOSIS; ASTERIAS; CACO-2 CELLS; CEREBROSIDES; COLONIC NEOPLASMS; EICOSAPENTAENOIC ACID; GLUCOSYLCERAMIDES; GONADS; HUMANS; LIPIDS; MASS SPECTROMETRY; SPHINGOSINE; TRIGLYCERIDES; TUMOR CELLS, CULTURED; VISCERA;

EID: 55449110072     PISSN: 13458957     EISSN: 13473352     Source Type: Journal    
DOI: 10.5650/jos.57.477     Document Type: Article

References (41)

1. Goggin, C.L.; Bouland, C. The ciliate Orchitophrya df. stellarum and other parasites and commensals of the northern Pacific seastar Asterias amurensis from Japan. Int. J. Parasitol. 27, 1415-1418 (1997).
2. Sloan, N.A.; Aldrige, T.H. Observations on an aggregation of the starfish Asterias rubens L. in Morecambe Bay, Lancashire, England. J. Nat. Hist. 15, 407-418 (1981).
3. Dare, P.J. Notes on the swarming behaviour and population density of Asterias rubens L. (Echinodermata: Asteroidea) feeding on the mussel, Mytilus edulis L. J. Cons. Int. Explor. Mer. 40, 112-118 (1982).
4. Ito, H. Successful HOTAC method for developing scallop-sowing culture in the Nemuro district of east Hokkaido, northern Japan. Marine Ranching, Proceedings of the 17th US-Japan meeting on Aquaculture (Svrjcek, R.S. ed.). NOAA Tech. Rep. NMFS. pp.107-116 (1991).
5. Line, M.A. Recycling of seastar (Asterias amurensis) waste by composting. Bioresour. Technol. 49, 227-229 (1994).
6. Ishii, T.; Okino, T.; Mino, Y.; Tamiya, H.; Matsuda, F. Plant growth regulators from common starfish (Asterias amurensis Lütken) waste. Plant Growth Regulation 52, 131-139 (2007).
7. Hossain, Z.; Kurihara, H.; Hosokawa, M.; Takahashi, K. Docosahexaenoic and eicosahexaenoic acids-enriched Phosphatidylcholine liposomes enhance the permeability, transportation and uptake of phospholipids in Caco-2 cells. Mol. Cell. Biochem. 285, 155-163 (2006).
8. Sugita, M. Studies on the glycosphingolipids of the starfish, Asterina pectinifera. II. Isolation and characterization of a novel gangliosides with an internal sialic acid residue. J. Biochem. 86, 289-300 (1979).
9. Sugita, M. Studies on the glycosphingolipids of the starfish, Asterina pectinifera. III. Isolation and structural studies of two novel gangliosides internal sialic acid residues. J. Biochem. 86, 765-772 (1979).
10. Smirnova, G.P.; Kochetkov, N.K.; Sadovskaya, V.L. Gangliosides of the starfish Aphelasterias japonica, evidence for a new linkage between two N-glycolylneura minic acid residues through the hydroxyl group of the glycolic acid residue. Biochim. Biophys. Acta 920, 47-55 (1987).
11. Kawano, Y.; Higuchi, R.; Isobe, R.; Komori, T. Isolation and structure of six new cerebrosides. Liebigs Ann. Chem. 19-24 (1988).
12. Kawano, Y.; Higuchi, R.; Isobe, R.; Komori, T. Isolation and structure of two new ceramide lactosides. Liebigs Ann. Chem. 1181-1183 (1988).
13. Andersson, L.; Bohlin, L.; Iorizzi, M.; Riccio, R.; Minale, L.; Moreno-Lopez, W. Biological activity of saponins and saponin-like compounds from starfish and brittle-stars. Toxicon 27, 179-188 (1989).
14. Prokofèva, N.G.; Chaikina, E.L.; Kicha, A.A.; Ivanchina, N.V. Biological activities of steroid glycosides from starfish. Comp. Biochem. Physiol. B 134, 695-701 (2003).
15. Hannun, Y.A.; Bell, R.M. Functions of sphingolipids and sphingolipid breakdown products in cellular regulation. Science 243, 500-507 (1989).
16. Ahn, E.H.; Schroeder, J.J. Sphingoid bases and ceramide induce apoptosis in HT-29 and HCT-116 human colon cancer cells. Exp. Bio. Med. 227, 345-353 (2002).
17. Irie, A.; Kubo, H.; Hoshi, M. Glucosylceramide having a novel tri-unsaturated long chain base from the spermatozoa of the starfish, Asterias amurensis. J. Biochem. 107, 578-586 (1990).
18. Bligh, G.; Dyer, W.J. A rapid method of total lipid extraction and purification. Can. J. Biochem. Physiol. 37, 911-917 (1959).
19. Juaneda, P.; Rocquelin, G. Rapid and convenient separation of phospholipids and nonphospholipids from rat heart using silica cartridges. Lipids 20, 40-41 (1985).
20. Prevot, A.F.; Mordret, F.X. Utilisation des colonnes capillaries de verre pour l'analyse des corps gras par chromatographie en phase gazeuse. Rev Fse Corp Gras 23, 409-423 (1976).
21. Morrison, W.R.; Hay, J.D. Polar lipids in bovine milk II. Long-chain bases, normal and 2-hydroxy fatty acids, and isomers cis and trans monoenoic fatty acids in the sphingolipids. Biochim. Biophys. Acta 202, 460-467 (1970).
22. Ohnishi, M.; Ito, S.; Fujino, Y. Characterization of sphingolipids in spinach leaves. Biochim. Biophys. Acta 752, 416-422 (1983).
23. Karlsson, K.A.; Samuelsson, B.E.; Steen, G.O. Identification of hitherto unknown branched-chain bases in sulphatides of the salt (rectal) gland of spiny dogfish. Biochim. Biophys. Acta 306, 307-316 (1973).
24. Yasugi, E.; Kasama, T.; Seyama, Y. Branched long-chain bases in cerebrosides of the guinea pig Harderian gland. J. Biochem. 102, 1477-1482 (1987).
25. Harada-Shiba, M.; Kinoshita, M.; Kamido, H.; Shimokado, K. Oxidized low-density lipoprotein induces apoptosis in cultured human umbilical vein endothelial cells by common and unique mechanisms. J. Biol. Chem. 273, 9681-9687 (1998).
26. Dean, R.B.; Dixon, W.J. Simplified statistics for small numbers of observations. Anal. Chem. 23, 636-638 (1951).
27. Sugawara, T.; Zaima, N.; Yamamoto, A.; Sakai, S.; Noguchi, R.; Hirata, T. Isolation of sphingoid bases of sea cucumber cerebrosides and their cytotoxicity against human colon cancer cells. Biosci. Biotechnol. Biochem. 70, 2906-2912 (2006).
28. Sugawara, T.; Miyazawa, T. Separation and determination of glycolipids from edible plant sources by high-performance liquid chromatography and evaporative light-scattering detection. Lipids 34, 1231-1237 (1999).
29. Brett, M.T.; Muller-Navarra, D.C. The role of highly unsaturated fatty acids in aquatic foodweb processes. Freshwater Biology 38, 483-499 (1997).
30. Mullar-Navarra, D.C.; Brett, M.T.; Liston, A.M.; Goldman, C.R. A highly unsaturated fatty acid predicts carbon transfer between primary producers and consumers. Nature 403, 74-77 (2000).
31. Isay, S.V.; Busarova, N.G. Study on fatty acid composition of marine organisms-I. Unsaturated fatty acids of Japan sea invertebrates. Comp. Biochem. Physiol. B 77, 803-810 (1984).
32. Romashina, N.A. Marine invertebrates as a source of eicosapentaenoic and other polyenoic acids. Biologia Morya 2, 66-68 (1983).
33. Lynch, D.V. Sphingolipids in Lipid Metabolism in Plants. (Moore Jr., T.S. ed.). CRC Press Inc. Boca Raton, Florida, pp. 285-308 (1993).
34. Karlsson, K.A. On the chemistry and occurrence of sphingolipid long-chain bases. Chem. Phys. Lipids 5, 6-43 (1970).
35. Duran, R.; Zubia, E.; Ortega, M.J.; Naranjo, S.; Salva, J. Phallusides, new glucosphingolipids from the ascidian Phallusia fumigate. Tetrahedron 54, 14597-14602 (1998).
36. Diaz de Vivar, M.E.; Seldes, A.M.; Maier, M.S. Two novel glucosylceramides from gonads and body walls of the Patagonian starfish Allostichaster inaequalis. Lipids 37, 597-603 (2002).
37. Endo, M.; Nakagawa, M.; Hamamoto, Y.; Ishihara, M. Pharmacologically active substances from southern pacific marine invertebrates. Pure Appl. Chem. 58, 387-394 (1986).
38. Hirsch, S.; Kashman, Y. New glycosphingolipids from marine organisms. Tetrahedron 45, 3897-3906 (1989).
39. Cuvillier, O. Sphingosine in apoptosis signaling. Biochim. Biophys. Acta 1585, 153-162 (2002).
40. Aida, K.; Kinoshita, M.; Sugawara, T.; Ono, J.; Miyazawa, T.; Ohnishi, M. Apoptosis inducement by plant and fungus sphingoid bases in human colon cancer cells. J. Oleo Sci. 53, 503-510 (2004).
41. Sugawara, T.; Kinoshita, M.; Ohnishi, M.; Miyazawa, T. Apoptosis induction by wheat-flour sphingoid bases in DLD-1 human colon cancer cells. Biosci. Biotechnol. Biochem. 66, 2228-2231 (2002).