Literature DB >> 3368447

Cardiolipin from ethanol-fed rats confers tolerance to ethanol in liver mitochondrial membranes.

J S Ellingson1, T F Taraschi, A Wu, R Zimmerman, E Rubin.   

Abstract

In rats chronically consuming ethanol, the liver mitochondrial membranes develop resistance to the disordering effects of ethanol in vitro, so-called "membrane tolerance". To investigate the molecular basis of this tolerance in the inner mitochondrial membrane, multilamellar vesicles were produced by recombining the mitoplast phospholipids (quantitatively separated by preparative HPLC) from control and ethanol-fed animals in various combinations. The effect of in vitro ethanol on the physical properties of these vesicles was determined by electron spin resonance. Vesicles composed of all mitoplast phospholipids from control rats were disordered by 50-100 mM ethanol, whereas those made of the phospholipids from ethanol-fed animals were resistant. When phosphatidylcholine (46 mol %) or phosphatidylethanolamine (42 mol %) from ethanol-fed rats replaced the corresponding phospholipids of control rats, the vesicles were disordered by ethanol. By contrast, when as little as 2.5 mol % of cardiolipin (one-fourth the naturally occurring amount) from ethanol-fed rats replaced that phospholipid from control rats, vesicles were rendered entirely resistant to disordering by ethanol. The same amount of cardiolipin from ethanol-fed rats also conferred membrane tolerance to vesicles composed of bovine phospholipids, demonstrating that this effect is not restricted to rat mitoplast phospholipids. In vesicles composed of a single mitoplast-phospholipid class, only vesicles composed of cardiolipin from ethanol-fed rats resisted disordering. Phosphatidylinositol from liver microsomes of ethanol-fed rats also confers membrane tolerance and was the only microsomal phospholipid that formed tolerant vesicles. Thus, in livers of rats chronically fed ethanol, anionic phospholipids are selectively converted into potent promoters of membrane tolerance in both mitochondrial and microsomal membranes.

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Year:  1988        PMID: 3368447      PMCID: PMC280207          DOI: 10.1073/pnas.85.10.3353

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  26 in total

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Authors:  R A Demiel; W S Guerts van Kessel; L L van Deenen
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5.  Alcohol-induced hepatic injury in nonalcoholic volunteers.

Authors:  E Rubin; C S Lieber
Journal:  N Engl J Med       Date:  1968-04-18       Impact factor: 91.245

6.  Fatty liver, alcoholic hepatitis and cirrhosis produced by alcohol in primates.

Authors:  E Rubin; C S Lieber
Journal:  N Engl J Med       Date:  1974-01-17       Impact factor: 91.245

7.  Early fine structural changes in the human liver induced by alcohol.

Authors:  E Rubin; C S Lieber
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8.  Drug tolerance in biomembranes: a spin label study of the effects of ethanol.

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Authors:  C Schnaitman; J W Greenawalt
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  12 in total

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Review 2.  Uncoupler-resistant mutants of bacteria.

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4.  Relationship between lipid saturation and lipid-protein interaction in liver mitochondria modified by catalytic hydrogenation with reference to cardiolipin molecular species.

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5.  Maintenance of structural and functional characteristics of skeletal-muscle mitochondria and sarcoplasmic-reticular membranes after chronic ethanol treatment.

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6.  Changes in sensitivity of in vitro rat brain protein synthesis to the acute action of ethanol and isopropanol as a consequence of the long-term ingestion of isopropanol.

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9.  Chronic and acute ethanol treatment modifies fluidity and composition in plasma membranes of a human hepatic cell line (WRL-68).

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Journal:  Cell Biol Toxicol       Date:  1995-04       Impact factor: 6.691

Review 10.  The molecular basis of tolerance.

Authors:  Andrzej Z Pietrzykowski; Steven N Treistman
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