Literature DB >> 8157945

Influence of cholesterol lowering on plasma membrane lipids and cationic transport systems.

P Lijnen1, H Celis, R Fagard, J Staessen, A Amery.   

Abstract

BACKGROUND: In order to determine whether alterations in membrane lipids affect transmembrane cationic transport systems in erythrocytes and platelets, cationic fluxes and intracellular cationic concentrations were measured in hypercholesterolaemic patients before and during administration of an inhibitor of 3-hydroxy-3-methlglutaryl coenzyme A reductase.
METHODS: After a 1-month run-in placebo period on a lipid-lowering diet the patients were treated, in a double-blind manner, with either placebo (n = 25) or pravastatin (n = 25) for 6 months. Placebo or pravastatin (10 mg during the first month, 20 mg during the second month and 40 mg during the remaining 4 months) was administered once a day in the evening.
RESULTS: Compared with the placebo group, the erythrocyte and platelet membrane cholesterol content was reduced in the patients treated with pravastatin. The intra-erythrocyte and intraplatelet Na+ concentration was reduced during pravastatin administration, whereas the activity of the erythrocyte and platelet Na(+)-K+ pump was increased. However, the intra-erythrocyte and intraplatelet K+, Mg2+ and cytosolic Ca2+ concentrations, and water content, as well as the activities of the erythrocyte Na(+)-Li+ countertransporter and Na+,K+ cotransporter, and Na+ and K+ leakage, were not changed during pravastatin treatment.
CONCLUSIONS: The present data show that cholesterol lowering in hypercholesterolaemic patients may result in a significant decrease in erythrocyte and platelet membrane cholesterol content. These changes in membrane cholesterol are accompanied by an increase in activity of the Na(+)-K+ pump and a decrease in intra-erythrocyte and intraplatelet Na+ concentrations.

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Year:  1994        PMID: 8157945

Source DB:  PubMed          Journal:  J Hypertens        ISSN: 0263-6352            Impact factor:   4.844


  8 in total

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3.  Influence of the use of statin on the stability of erythrocyte membranes in multiple sclerosis.

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4.  Therapeutic levels of the hydroxmethylglutaryl-coenzyme A reductase inhibitor lovastatin activate ras signaling via phospholipase D2.

Authors:  Kwang-Jin Cho; Michelle M Hill; Sravanthi Chigurupati; Guangwei Du; Robert G Parton; John F Hancock
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Review 5.  Effects of HMG-CoA reductase inhibitors on skeletal muscle: are all statins the same?

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Review 6.  Alterations in sodium metabolism as an etiological model for hypertension.

Authors:  P Lijnen
Journal:  Cardiovasc Drugs Ther       Date:  1995-06       Impact factor: 3.727

7.  Pravastatin has no direct effect on transmembrane cationic transport systems in human erythrocytes and platelets.

Authors:  P Lijnen; V Petrov; A Amery
Journal:  Eur J Clin Pharmacol       Date:  1994       Impact factor: 2.953

Review 8.  Benefits and risks of simvastatin in patients with familial hypercholesterolaemia.

Authors:  Pedro Mata; Rodrigo Alonso; Juan Badimón
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  8 in total

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