Objectives: Lysophosphatidylcholine (LPC) in low-density lipoprotein (LDL)
comes into notice as an important atherogenic substance.
Methods: Since the effect of probucol, an antioxidative lipid-lowering drug
, on LPC molecular species has not been elucidated, two LPC molecular speci
es, stearoyl LPC (SLPC) and palmitoyl LPC (PLPC), were measured in LDL usin
g high-pressure liquid chromatography. LDL was obtained from 11 hyperlipide
mic patients, including 9 diabetic patients, in comparison with 11 age- and
gender-matched controls.
Results and conclusion: Hyperlipidemic patients showed nearly twofold highe
r levels of SLPC and PLPC per gram of LDL protein than those of controls. A
ll hyperlipidemic patients were treated with oral administration of 500 mg/
day of probucol for 3 months. Both LPCs in LDL were significantly reduced t
o control levels and were increased again up to the pretreatment levels 4 w
eeks after cessation of the treatment. Therefore, probucol has a potent eff
ect in reducing LPC and may contribute to decreasing the atherogenicity of
LDL.