Literature DB >> 7298846

Sulfation of lithocholate as a possible modifier of chenodeoxycholic acid-induced elevations of serum transaminase in patients with gallstones.

J W Marks, S O Sue, B J Pearlman, G G Bonorris, P Varady, J M Lachin, L J Schoenfield.   

Abstract

Chenodeoxycholic acid (CDC), through its metabolite, lithocholic acid (LC), is hepatotoxic in certain species. The cause of elevations of serum transaminase in 25% of humans ingesting CDC, however, is unknown, but also may be due to LC. Because efficient hepatic sulfation of LC may protect against hepatic injury, the aim of this study was to determine if sulfation of LC might modify CDC-induced elevations of transaminase. Pretreatment sulfation fraction (SF) was estimated in 63 randomly selected patients with gallstones in a double-blind randomized trial of CDC, 750 mg/d, 375 mg/d, or placebo; in 27 of these, SF was repeated at 1 or 2 yr. In four other patients, the SF was measured at 2 yr only. Serum glutamic oxaloacetic transaminase and serum glutamic pyruvic transaminase were determined monthly for 3 mo and then every 3 or 4 mo; an elevation of transaminase was defined as > 150% of the normal upper limit in asymptomatic patients. 10 muCi of (3)H-glyco-LC (sp act 84 mCi/mol) was ingested 10-12 h before fasting duodenal biliary drainage. Bile acids in bile were separated by thin-layer chromatography. The SF was estimated as a percentage of total radioactivity (scintillation counting) in sulfated glyco-LC. The standard deviation for replicate SF determinations (n = 311) was 2.1% The pretreatment SF (mean 60.7+/-1.7 SEM) correlated inversely with age (r = 0.336, P < 0.005) and directly with the obesity index (r = 0.495, P > 0.001), but was independent of sex. The SF, remeasured at 1 or 2 yr, did not change significantly with time or CDC. Among CDC-treated patients, elevations of transaminase occurred in 75% of patients with a SF < 45% vs. 11% with a SF > 45% (P < 0.001). In conclusion, a SF < 45% occurred in patients with gallstones who had a high probability of developing elevated serum transaminase when treated with CDC. Thus, sulfation of lithocholate may modify CDC-induced elevations of serum transaminase.

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Year:  1981        PMID: 7298846      PMCID: PMC370913          DOI: 10.1172/jci110364

Source DB:  PubMed          Journal:  J Clin Invest        ISSN: 0021-9738            Impact factor:   14.808


  29 in total

1.  On the turnover and excretory products of cholic and chenodeoxycholic acid in man.

Authors:  H DANIELSSON; P ENEROTH; K HELLSTROM; S LINDSTEDT; J SJOVALL
Journal:  J Biol Chem       Date:  1963-07       Impact factor: 5.157

2.  Toxicity of chenodeoxycholic acid in the nonhuman primate.

Authors:  K P Morrissey; C K McSherry; R L Swarm; W H Nieman; J E Deitrick
Journal:  Surgery       Date:  1975-06       Impact factor: 3.982

3.  Letter: A simple calculation of the lithogenic index of bile: expressing biliary lipid composition on rectangular coordinates.

Authors:  P J Thomas; A F Hofmann
Journal:  Gastroenterology       Date:  1973-10       Impact factor: 22.682

4.  A physiological method for estimation of hepatic secretion of biliary lipids in man.

Authors:  S M Grundy; A L Metzger
Journal:  Gastroenterology       Date:  1972-06       Impact factor: 22.682

5.  Effects of sulfation of taurolithocholic and glycolithocholic acids on their intestinal transport.

Authors:  T S Low-Beer; M P Tyor; L Lack
Journal:  Gastroenterology       Date:  1969-04       Impact factor: 22.682

6.  Metabolism of lithocholate in healthy man. II. Enterohepatic circulation.

Authors:  A E Cowen; M G Korman; A F Hofmann; O W Cass; S B Coffin
Journal:  Gastroenterology       Date:  1975-07       Impact factor: 22.682

7.  Letter Prevention of chenodeoxycholic-acid toxicity with lincomycin.

Authors:  G Salen; H Dyrszka; T Chen; W H Saltzman; E H Mosbach
Journal:  Lancet       Date:  1975-05-10       Impact factor: 79.321

Review 8.  Bile acids, liver injury, and liver disease.

Authors:  R H Palmer
Journal:  Arch Intern Med       Date:  1972-10

9.  Influence of primary bile acid feeding on cholesterol metabolism and hepatic function in the rhesus monkey.

Authors:  K H Webster; M C Lancaster; A F Hofmann; D F Wease; A H Baggenstoss
Journal:  Mayo Clin Proc       Date:  1975-03       Impact factor: 7.616

10.  Bile acid sulfates. II. Formation, metabolism, and excretion of lithocholic acid sulfates in the rat.

Authors:  R H Palmer
Journal:  J Lipid Res       Date:  1971-11       Impact factor: 5.922

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  6 in total

1.  Separate transport systems for biliary secretion of sulfated and unsulfated bile acids in the rat.

Authors:  F Kuipers; M Enserink; R Havinga; A B van der Steen; M J Hardonk; J Fevery; R J Vonk
Journal:  J Clin Invest       Date:  1988-05       Impact factor: 14.808

2.  Hepatic and extrahepatic glucuronidation of bile acids in man. Characterization of bile acid uridine 5'-diphosphate-glucuronosyltransferase in hepatic, renal, and intestinal microsomes.

Authors:  S Matern; H Matern; E H Farthmann; W Gerok
Journal:  J Clin Invest       Date:  1984-08       Impact factor: 14.808

3.  Effect of taurolithocholate on in vivo sulfation and glucuronidation of acetaminophen in rats.

Authors:  R E Galinsky; B Chałasinska
Journal:  Pharm Res       Date:  1988-01       Impact factor: 4.200

4.  The effects of chenodiol on biliary lipids and their association with gallstone dissolution in the National Cooperative Gallstone Study (NCGS).

Authors:  S M Grundy; S P Lan; J Lachin
Journal:  J Clin Invest       Date:  1984-04       Impact factor: 14.808

5.  Lithocholate glucuronide is a cholestatic agent.

Authors:  D G Oelberg; M V Chari; J M Little; E W Adcock; R Lester
Journal:  J Clin Invest       Date:  1984-06       Impact factor: 14.808

6.  Drug and treatment efficacy of chenodeoxycholic acid in 97 patients with cholelithiasis and increased surgical risk.

Authors:  T Tangedahl; W D Carey; D R Ferguson; S Forsythe; M Williams; K Paradis; N C Hightower
Journal:  Dig Dis Sci       Date:  1983-06       Impact factor: 3.199

  6 in total

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