Serum plant sterols and biliary cholesterol secretion in humans: studies with ursodeoxycholic acid

被引:10
作者
Lindenthal, B
Sudhop, T
Schiedermaier, P
Agnan, M
Sauerbruch, T
von Bergmann, K [1 ]
机构
[1] Univ Bonn, Dept Clin Pharmacol, D-5300 Bonn, Germany
[2] Univ Bonn, Dept Internal Med, D-5300 Bonn, Germany
关键词
cholestanol; sitosterol; campesterol; non-cholesterol sterols;
D O I
10.1194/jlr.M100438-JLR200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Ratios of cholestanol, campesterol, and sitosterol to cholesterol in serum are known to reflect cholesterol absorption efficiency. Here, a possible link between these ratios and biliary secretion rates of cholesterol was investigated. Biliary lipid secretion rates and serum sterols were determined in 13 patients with gallstones. Seven were treated with ursodeoxycholic acid (UDCA) (1,000 mg/d). Serum cholesterol and non-cholesterol sterols were also measured in a cross over study in 20 healthy volunteers, who received either placebo or UDCA (750 mg/d). Biliary cholesterol secretion was significantly lower, whereas the non-cholesterol sterols and their ratio to cholesterol were higher in patients with gallstones treated with UDCA. A highly significant negative linear correlation between the ratios of non-cholesterol sterols to cholesterol and biliary cholesterol secretion was observed. In volunteers, administration of UDCA for 4 weeks was followed by a significant increase in non-cholesterol sterols and their ratios. Even 4 weeks after discontinuing UDCA administration, campesterol and sitosterol were still significantly higher than pretreatment levels, which was also true for the campesterol-cholesterol ratio after 8 weeks. The results suggest that the ratios of cholestanol, campesterol, and sitosterol to cholesterol can be used as indicators of changes in biliary cholesterol secretion rates. Serum plant sterols and biliary cholesterol secretion in man: studies with ursodeoxycholic acid.
引用
收藏
页码:1072 / 1077
页数:6
相关论文
共 33 条
  • [1] Accumulation of dietary cholesterol in sitosterolemia caused by mutations in adjacent ABC transporters
    Berge, KE
    Tian, H
    Graf, GA
    Yu, LQ
    Grishin, NV
    Schultz, J
    Kwiterovich, P
    Shan, B
    Barnes, R
    Hobbs, HH
    [J]. SCIENCE, 2000, 290 (5497) : 1771 - 1775
  • [2] BOBERG KM, 1990, J LIPID RES, V31, P1083
  • [3] THERMODYNAMIC AND MOLECULAR-BASIS FOR DISSIMILAR CHOLESTEROL-SOLUBILIZING CAPACITIES BY MICELLAR SOLUTIONS OF BILE-SALTS - CASES OF SODIUM CHENODEOXYCHOLATE AND SODIUM URSODEOXYCHOLATE AND THEIR GLYCINE AND TAURINE CONJUGATES
    CAREY, MC
    MONTET, JC
    PHILLIPS, MC
    ARMSTRONG, MJ
    MAZER, NA
    [J]. BIOCHEMISTRY, 1981, 20 (12) : 3637 - 3648
  • [4] DELEON MP, 1980, GASTROENTEROLOGY, V78, P214
  • [5] FRANCO-BELGIAN COOPERATIVE STUDY OF URSODEOXYCHOLIC ACID IN THE MEDICAL DISSOLUTION OF GALLSTONES - A DOUBLE-BLIND, RANDOMIZED, DOSE-RESPONSE STUDY, AND COMPARISON WITH CHENODEOXYCHOLIC ACID
    ERLINGER, S
    LEGO, A
    HUSSON, JM
    FEVERY, J
    [J]. HEPATOLOGY, 1984, 4 (02) : 308 - 314
  • [6] FEDOROWSKI T, 1977, GASTROENTEROLOGY, V73, P1131
  • [7] THE EFFECTS OF CHENODIOL ON BILIARY LIPIDS AND THEIR ASSOCIATION WITH GALLSTONE DISSOLUTION IN THE NATIONAL COOPERATIVE GALLSTONE STUDY (NCGS)
    GRUNDY, SM
    LAN, SP
    LACHIN, J
    BAUM, RA
    HABIG, RL
    HANSON, RF
    HERSH, T
    HIGHTOWER, NC
    HOFMANN, AF
    LASSER, EC
    MARKS, JW
    MEKHJIAN, H
    OKUN, R
    SCHAEFER, RA
    SCHOENFIELD, LJ
    SHAW, L
    SOLOWAY, RD
    THISTLE, JL
    THOMAS, FP
    TYOR, MP
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1984, 73 (04) : 1156 - 1166
  • [8] GRUNDY SM, 1972, GASTROENTEROLOGY, V62, P1200
  • [9] SERUM NONCHOLESTEROL STEROLS RELATED TO CHOLESTEROL-METABOLISM IN FAMILIAL HYPERCHOLESTEROLEMIA
    GYLLING, H
    MIETTINEN, TA
    [J]. CLINICA CHIMICA ACTA, 1988, 178 (01) : 41 - 49
  • [10] HARDISON WGM, 1984, GASTROENTEROLOGY, V87, P130