Literature DB >> 8344502

Hepatic cholesterol and bile acid synthesis in Japanese patients with cholesterol gallstones.

A Honda1, T Yoshida, N Tanaka, Y Matsuzaki, B He, T Osuga, N Kobayashi, K Ozawa.   

Abstract

In Japan the composition of gallstones is changing rapidly from the once-predominant brown-pigment stones to cholesterol ones. The present work was undertaken to clarify the mechanism of cholesterol supersaturated bile production in Japanese patients with cholesterol gallstones. In 26 non-obese and normolipidemic patients (11 with cholesterol gallstones, 8 with black- or brown-pigment gallstones, 7 without gallstones) a liver biopsy and hepatic bile were surgically obtained under standardized conditions. The cholesterol saturation of hepatic bile was significantly higher in cholesterol gallstone patients than in gallstone-free controls (195 +/- 10 vs. 146 +/- 8%, respectively; P < 0.01). The microsomal activities of 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase, the rate-limiting enzyme for cholesterol synthesis, cholesterol 7 alpha-hydroxylase, the rate-limiting enzyme for bile acid synthesis, and 7 alpha-hydroxy-4-cholesten-3-one 12 alpha-hydroxylase (12 alpha-hydroxylase), the rate-limiting enzyme for cholic acid synthesis, were assayed simultaneously in the same subjects. There were positive correlations between HMG-CoA reductase and cholesterol 7 alpha-hydroxylase activities (Rs = 0.62, P < 0.005), and between cholesterol 7 alpha-hydroxylase and 12 alpha-hydroxylase activities (Rs = 0.44, P < 0.05) in all subjects, irrespective of the existence of gallstones. The activities of the three rate-limiting enzymes did not differ significantly among the three groups (cholesterol stone, pigment stone and stone-free). In conclusion, the cholesterol supersaturation of hepatic bile in nonobese and normolipidemic Japanese patients with cholesterol gallstones does not result from an increased hepatic cholesterol synthesis or a decreased bile acid synthesis.

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Year:  1993        PMID: 8344502     DOI: 10.1007/bf02776986

Source DB:  PubMed          Journal:  Gastroenterol Jpn        ISSN: 0435-1339


  53 in total

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  4 in total

1.  Upregulation of hepatic bile acid synthesis via fibroblast growth factor 19 is defective in gallstone disease but functional in overweight individuals.

Authors:  Olga Renner; Simone Harsch; Silke Matysik; Dieter Lütjohann; Gerd Schmitz; Eduard F Stange
Journal:  United European Gastroenterol J       Date:  2014-06       Impact factor: 4.623

2.  Plasma levels of mevalonate and 7 alpha-hydroxy-4-cholestene-3-one in cholesterol gallstone disease and their etiological significance.

Authors:  J Shoda; B F He; N Tanaka; Y Matzuzaki; T Osuga
Journal:  J Gastroenterol       Date:  1994-02       Impact factor: 7.527

3.  Increased bile acid concentration in liver tissue with cholesterol gallstone disease.

Authors:  A Honda; T Yoshida; N Tanaka; Y Matsuzaki; B He; J Shoda; T Osuga
Journal:  J Gastroenterol       Date:  1995-02       Impact factor: 7.527

4.  Accumulation of 7 alpha-hydroxycholesterol in liver tissue of patients with cholesterol gallstones.

Authors:  A Honda; T Yoshida; N Tanaka; Y Matsuzaki; B He; J Shoda; T Osuga
Journal:  J Gastroenterol       Date:  1995-10       Impact factor: 7.527

  4 in total

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