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Plasma carnitine and lipid-lowering drugs
Atherosclerosis
|June 1, 1985
Summary
Oral carnitine supplementation can lower lipids, but high carnitine levels were observed with probucol and clofibrate therapy, independent of high-density lipoprotein cholesterol changes. Carnitine levels normalized after discontinuing clofibrate.
Area of Science:
- Biochemistry
- Pharmacology
- Lipid Metabolism
Background:
- Oral carnitine is known to reduce lipids and increase high-density lipoprotein cholesterol (HDL-C).
- Carnitine levels may be affected by lipid-lowering drug combinations.
Purpose of the Study:
- To investigate the effect of a probucol and clofibrate combination on plasma carnitine levels and HDL-C.
- To determine the relationship between carnitine levels and clofibrate therapy.
Main Methods:
- Observational study of subjects receiving probucol and clofibrate.
- Measurement of plasma carnitine and HDL-C levels.
- Analysis of carnitine level changes with drug cessation.
Main Results:
- Subjects on combination therapy showed unexpectedly high basal carnitine concentrations.
- Elevated carnitine levels correlated with clofibrate administration.
- Carnitine levels decreased upon cessation of clofibrate therapy.
- Increased carnitine levels were not associated with increased HDL-C.
Conclusions:
- Clofibrate therapy, in combination with probucol, can lead to elevated plasma carnitine levels.
- The observed increase in carnitine is reversible and not linked to HDL-C elevation.
- Carnitine metabolism may be influenced by clofibrate.