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Structure and origin of bile acids: An overview

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Summary

An overview of the structure and the origin of naturally occurring bile acids is given. Most naturally occurring bile acids belong to the 5β-series, with hydroxyl groups in the A, B, and C ring of the steroid system. Hydroxyl groups are mostly found at the C3, C6, C7, C12 and C23 positions and are α- rather than β-oriented. In most bile acids, the A/B ring junction iscis (5β-series). However, the A ring can be usually present in the more stable (chair) or less stable (boat) conformation. Both B/C and C/D ring junction aretrans. With respect to the angular C9-methyl group, the hydrogen atoms at C5 and C8 are m-oriented whereas those at C9 and C14 aretrans-oriented. The archetypal bile acid is 5β-cholanic acid (3) from which all other CM bile acids can be derived. In addition to the bile acids with 24 carbons, some naturally occurring C27 bile acids have been identified including di-, tri- and tetra-hydroxy derivatives of coprostanic acid isolated from bile of several reptile species. The most dominant bile acids and their natural sources are given and a selection of naturally occurring bile acids with unusual structures which have been mostly isolated from the bile of reptiles and amphibians is described.

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References

  1. Ali S.S., Kuksis A., Beveridge J.M.R. (1966):Can. J. Biochem. 44, 957.

    Article  CAS  PubMed  Google Scholar 

  2. Armstrong M.J., Corey M.C. (1982):J. Lipid Res. 23, 70.

    CAS  PubMed  Google Scholar 

  3. Wieland H., Weil F.J. (1912):Z Physiol. Chem. 80, 287.

    Google Scholar 

  4. Hammarsten O. (1908):Chem. Ber. 14, 71.

    Google Scholar 

  5. Wieland H., Boersch E. (1919):Z Physiol. Chem. 106, 190.

    CAS  Google Scholar 

  6. Windaus A. (1908):Arch. Pharm. 246, 117.

    Article  CAS  Google Scholar 

  7. Windaus A., Neukirchen K. (1919)Chem. Ber. 52, 1918.

    Google Scholar 

  8. Fischer H. (1911):Z Physiol. Chem. 73, 204.

    Google Scholar 

  9. Heusser H., Wuthier A. (1947):Helv. Chim. Acta 30, 2165.

    Article  CAS  PubMed  Google Scholar 

  10. Wieland H., Dane E., Scholz E. (1932):Z Physiol. Chem. 211, 261.

    CAS  Google Scholar 

  11. Fieser L.F., Ettorre R. (1953):J. Am. Chem. Soc. 75, 1700.

    Article  CAS  Google Scholar 

  12. Wells L.W. (1964):Ph. D. Thesis, University of St. Louis.

  13. Marsson T. (1849):Ann. Sci. Nat. 72, 317.

    Google Scholar 

  14. Wieland H., Revery G. (1924):Z Physiol. Chem. 140, 186.

    CAS  Google Scholar 

  15. Windaus H., Bohne A., Schwarzkopf E. (1924):Z Physiol. Chem. 140, 177.

    CAS  Google Scholar 

  16. Wieland H., Kishi S. (1933):Z Physiol. Chem. 214, 47.

    CAS  Google Scholar 

  17. Hammarsten O. (1902):Z Physiol. Chem. 36, 525.

    CAS  Google Scholar 

  18. Kanazawa T., Shimazaki A., Sato T., Hoshino T. (1954):Proc. Japan Acad. 30, 391.

    Article  CAS  Google Scholar 

  19. Haslewood G.A.D. (1962):Comparative Biochemistry, Academic Press, New York.

    Google Scholar 

  20. Eneroth P., Gordon B., Ryhage R., Sjövall J. (1966):J. Lipid Res. 7, 511.

    CAS  PubMed  Google Scholar 

  21. Danielsson H., Eneroth P., Hellström K., Sjövall J. (1962):J. Biol. Chem. 237, 3657.

    CAS  PubMed  Google Scholar 

  22. Gundelach C., Strecker A. (1847):Ann. Sci. Nat. 62, 205.

    Google Scholar 

  23. Jones D.N., Summers G.H.R. (1959): J. Chem. Soc., 2594.

  24. Kimura T. (1937):Z Physiol. Chem. 248, 280.

    CAS  Google Scholar 

  25. Moffett R.B., Hoehn W.M. (1947):J. Am. Chem. Soc. 69, 1995.

    Article  CAS  Google Scholar 

  26. Gallagher T.F., Xenos J.R. (1946):J. Biol. Chem. 165, 365.

    CAS  Google Scholar 

  27. Latschinoff P. (1885):Chem. Ber. 18, 3039, 1885.

    Article  Google Scholar 

  28. Mylius F. (1886):Chem. Ber. 19, 396.

    Google Scholar 

  29. Latschinoff P. (1887):Ber. Dtsch. Chem. Ges. 20, 1043.

    Article  Google Scholar 

  30. Lassar-Cohn (1893):Ber. Dtsch. Chem. Ges. 26, 146.

    Article  Google Scholar 

  31. Lassar-Cohn (1893):Z Physiol. Chem. 17, 607.

    Google Scholar 

  32. Wieland H., Sorge H. (1916):Z Physiol. Chem. 97, 1.

    CAS  Google Scholar 

  33. Cramer F. (1954): Einschlussverbindungen, Springer.

  34. Koechlin B., Reichstein T. (1942):Helv. Chim. Acta 25, 918.

    Article  CAS  Google Scholar 

  35. Chang F.C., Wood N.F., Holton W.G. (1965):Org. Chem. 30, 1718.

    Article  CAS  Google Scholar 

  36. Sobotka H. (1937):The Chemistry of the Steroids, Williams Wilkins Co., Baltimore.

    Google Scholar 

  37. Hirofuji S. (1965):J. Biochem. 58, 27.

    CAS  PubMed  Google Scholar 

  38. Hamilton J.G. (1963):Arch. Biochem. Biophys.101, 1.

    Article  Google Scholar 

  39. Eneroth P., Gordon B., Sjövall J. (1966):J. Lipid Res. 7, 524.

    CAS  PubMed  Google Scholar 

  40. Norman A., Sjövall J. (1958):J. Biol. Chem. 233, 872.

    CAS  PubMed  Google Scholar 

  41. Samelsson B. (1960):Acta Chem. Scand. 14, 17.

    Article  Google Scholar 

  42. Danielsson H., Eneroth P., Hellström K., Sjövall J. (1962):J. Biol. Chem. 237, 3657.

    CAS  PubMed  Google Scholar 

  43. Haslewood G.A.D., Sjövall J. (1954):Biochem. J. 57, 126.

    CAS  PubMed  Google Scholar 

  44. Hsia S.L., Matschiner J.T., Mahowald T.A., Elliott W.H., Doisy E.A., Jr., Thayer S.A., Doisy E.A. (1957):J. Biol. Chem. 225, 811.

    CAS  PubMed  Google Scholar 

  45. Matschiner J.T., Mahowald T.A., Elliott W.H., Doisy E.A., Jr., Hsia S.L., Doisy E.A. (1957):J. Biol. Chem. 225, 771.

    CAS  PubMed  Google Scholar 

  46. Hsia S.L., Matschiner J.T., Mahowald T.A., Elliott W.H., Doisy E.A., Jr., Thayer S.A., Doisy E.A. (1957):J. Biol. Chem. 226, 667

    CAS  Google Scholar 

  47. Hsia S.L., Matschiner J.T., Mahowald T.A., Elliott W.H., Doisy E.A. Jr., Thayer S.A., Doisy E.A. (1958):J. Biol. Chem. 230, 573.

    CAS  PubMed  Google Scholar 

  48. Haslewood G.A.D. (1951):Biochem. J. 29, 718.

    Google Scholar 

  49. Hammarsten O. (1909):Z Physiol. Chem. 61, 454.

    Google Scholar 

  50. Hammarsten O. (1910):Z Physiol. Chem. 68, 109.

    Google Scholar 

  51. Haslewood G.A.D. (1961):Biochem. J. 78, 352.

    CAS  PubMed  Google Scholar 

  52. Bergström S., Krabish L., Lindeberg U.G. (1959):Acta Soc. Med. Upsalien 64, 160.

    Google Scholar 

  53. Norman A., Sjövall J. (1958):J. Biol. Chem. 233, 872.

    CAS  PubMed  Google Scholar 

  54. Wiggins H.S., Wootton I.D.P. (1958):Biochem. 70, 349.

    CAS  Google Scholar 

  55. Kuroda M., Arata H. (1952):J. Biochem. 39, 225.

    CAS  Google Scholar 

  56. Haslewood G.A.D. (1967):Bile Salts, Methuen, London.

    Google Scholar 

  57. Kenzie B.F., Mattox V.R., Engel L.L., Kendall E.C. (1948):J. Biol Chem. 173, 211.

    Google Scholar 

  58. Fernholz E, (1935):Z Physiol. Chem. 232, 202.

    CAS  Google Scholar 

  59. Wieland H., Dane E. (1932):Z Physiol. Chem. 212, 41.

    CAS  Google Scholar 

  60. Imai I. (1937):Z Physiol. Chem. 248, 65.

    CAS  Google Scholar 

  61. Haslewood G.A.D. (1954):Biochem. J. 56, 581.

    CAS  PubMed  Google Scholar 

  62. Sihn T.S. (1938):J. Biochem. 27, 425.

    Google Scholar 

  63. Eneroth P., Gordon B., Sjövall J. (1966):J. Lipid Res. 7, 524.

    CAS  PubMed  Google Scholar 

  64. Wieland H., Kapitel W. (1932):Z Physiol. Chem. 212, 269.

    Google Scholar 

  65. Shimizu T., Oda T. (1936):Z Physiol. Chem. 239, 67.

    CAS  Google Scholar 

  66. Aigner A., Bauer A. (1988):Med. Monatschrift Pharm. 11, 369.

    CAS  Google Scholar 

  67. Une M., Hoshita T. (1994):Hiroshima J. Med. Sci. 43, 37.

    CAS  PubMed  Google Scholar 

  68. Anderson LG., Haslewood G.A.D. (1962):Biochem. J. 85, 236.

    CAS  PubMed  Google Scholar 

  69. Nair P.P., Kritchevsky D. (1971):The Bile Acids. Vol. 1. Plenum Press, New York-London.

    Google Scholar 

  70. Kuramoto T., Komeyama Y., Kaneda M., Shiro M., Hoshita T., Une M. (2000):Chem. Pharm. Bull. 48, 53.

    CAS  PubMed  Google Scholar 

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Kuhajda, K., Kandrac, J., Kevresan, S. et al. Structure and origin of bile acids: An overview. Eur. J. Drug Metab. Pharmacokinet. 31, 135–143 (2006). https://doi.org/10.1007/BF03190710

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