Literature DB >> 3593278

Solubilization of lipids from hamster bile-canalicular and contiguous membranes and from human erythrocyte membranes by conjugated bile salts.

J M Graham, T C Northfield.   

Abstract

We have demonstrated in vitro the efficacy of the taurine-conjugated dihydroxy bile salts deoxycholate and chenodeoxycholate in solubilizing both cholesterol and phospholipid from hamster liver bile-canalicular and contiguous membranes and from human erythrocyte membrane. On the other hand, the dihydroxy bile salt ursodeoxycholate and the trihydroxy bile salt cholate solubilize much less lipid. The lipid solubilization by the four bile salts correlated well with their hydrophobicity: glycochenodeoxycolate, which is more hydrophobic than the tauro derivative, also solubilized more lipid. All the dihydroxy bile salts have a threshold concentration above which lipid solubilization increases rapidly; this correlates approximately with the critical micellar concentration. The non-micelle-forming bile salt dehydrocholate solubilized no lipid at all up to 32 mM. All the dihydroxy bile acids are much more efficient at solubilizing phospholipid than cholesterol. Cholate does not show such a pronounced discrimination. Lipid solubilization by chenodeoxycholate was essentially complete within 1 min, whereas that by cholate was linear up to 5 min. Maximal lipid solubilization with chenodeoxycholate occurred at 8-12 mM; solubilization by cholate was linear up to 32 mM. Ursodeoxycholate was the only dihydroxy bile salt which was able to solubilize phospholipid (although not cholesterol) below the critical micellar concentration. This similarity between cholate and ursodeoxycholate may reflect their ability to form a more extensive liquid-crystal system. Membrane specificity was demonstrated only inasmuch as the lower the cholesterol/phospholipid ratio in the membrane, the greater the fractional solubilization of cholesterol by bile salts, i.e. the total amount of cholesterol solubilized depended only on the bile-salt concentration. On the other hand, the total amount of phospholipid solubilized decreased with increasing cholesterol/phospholipid ratio in the membrane.

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Year:  1987        PMID: 3593278      PMCID: PMC1147784          DOI: 10.1042/bj2420825

Source DB:  PubMed          Journal:  Biochem J        ISSN: 0264-6021            Impact factor:   3.857


  38 in total

1.  Protein measurement with the Folin phenol reagent.

Authors:  O H LOWRY; N J ROSEBROUGH; A L FARR; R J RANDALL
Journal:  J Biol Chem       Date:  1951-11       Impact factor: 5.157

2.  Biochemical evidence that Na+,K+-ATPase is located at the lateral region of the hepatocyte surface membrane.

Authors:  R E Poupon; W H Evans
Journal:  FEBS Lett       Date:  1979-12-15       Impact factor: 4.124

Review 3.  Cellular mechanisms of bile formation.

Authors:  B L Blitzer; J L Boyer
Journal:  Gastroenterology       Date:  1982-02       Impact factor: 22.682

4.  Oxidase determination of plasma cholesterol as cholest-4-en-3-one using iso-octane extraction.

Authors:  P Trinder
Journal:  Ann Clin Biochem       Date:  1981-03       Impact factor: 2.057

5.  Membrane lipid composition and susceptibility to bile salt damage.

Authors:  R Coleman; P J Lowe; D Billington
Journal:  Biochim Biophys Acta       Date:  1980-06-20

6.  Comparative aspects of the hepatobiliary transport of IgA.

Authors:  E Orlans; J V Peppard; A W Payne; B M Fitzharris; B M Mullock; R H Hinton; J G Hall
Journal:  Ann N Y Acad Sci       Date:  1983-06-30       Impact factor: 5.691

7.  The effects of colchicine on secretion into bile of bile salts, phospholipids, cholesterol and plasma membrane enzymes: bile salts are secreted unaccompanied by phospholipids and cholesterol.

Authors:  S G Barnwell; P J Lowe; R Coleman
Journal:  Biochem J       Date:  1984-06-15       Impact factor: 3.857

8.  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.

Authors:  M C Carey; J C Montet; M C Phillips; M J Armstrong; N A Mazer
Journal:  Biochemistry       Date:  1981-06-09       Impact factor: 3.162

9.  The influence of micelle formation on bile salt secretion.

Authors:  E R O'Máille
Journal:  J Physiol       Date:  1980-05       Impact factor: 5.182

10.  Cholesterol gallstone formation and prevention by chenodeoxycholic and ursodeoxycholic acids. A new hamster model.

Authors:  B J Pearlman; G G Bonorris; M J Phillips; A Chung; S Vimadalal; J W Marks; L J Schoenfield
Journal:  Gastroenterology       Date:  1979-10       Impact factor: 22.682

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  1 in total

Review 1.  Ursodeoxycholic acid in chronic liver disease.

Authors:  J S de Caestecker; R P Jazrawi; M L Petroni; T C Northfield
Journal:  Gut       Date:  1991-09       Impact factor: 23.059

  1 in total

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