Fenofibrate induces HDL-associated PAF-AH but attenuates enzyme activity associated with apoB-containing lipoproteins

被引:95
作者
Tsimihodimos, V
Kakafika, A
Tambaki, AP
Bairaktari, E
Chapman, MJ
Elisaf, M
Tselepis, AD [1 ]
机构
[1] Univ Ioannina, Dept Internal Med, GR-45110 Ioannina, Greece
[2] Univ Ioannina, Sch Med, Biol Chem Lab, GR-45110 Ioannina, Greece
[3] Univ Ioannina, Biochem Lab, GR-45110 Ioannina, Greece
[4] Univ Ioannina, Dept Chem, GR-45110 Ioannina, Greece
[5] Hop Pitie, Unite 551, F-75651 Paris 13, France
[6] INSERM, F-75651 Paris 13, France
关键词
hyperlipidemia; platelet-activating factor-acetylhydrolase; paraoxonase;
D O I
10.1194/jlr.M200452-JLR200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Human plasma platelet-activating factor acetylhydrolase (PAF-AH) is an enzyme associated mainly with the apolipoprotein B (apoB)-containing lipoproteins and primarily with LDL. A small proportion of enzymatic activity is also associated with HDL. Plasma paraoxonase 1 (PON1) Is an esterase exclusively associated with HDL. The effect of fenofibrate on PAF-AH and PON1 activities in patients with dyslipidemias of Types IIA, IIB, and IV were studied. Fenofibrate reduced plasma PAF-AH activity in all patient groups. In Type IIA patients, this reduction was mainly due to a fall in enzyme activity associated with the dense LDL subspecies, whereas in Type IIB and Type IV patients, it was due to the decrease in PAF-AH activity associated with both the VLDL+IDL and dense LDL subspecies. Drug therapy in Type IIB and Type IV patients significantly increased the HDL-associated PAF-AH activity due to the increase in enzyme activity associated with the HDL-3c subfraction. Fenofibrate did not affect serum PON1 activities toward paraoxon and phenylacetate in either patient group. The fenofibrate-induced elevation of HDL-associated PAF-AH activity in dyslipidemic patients of Type IIB and Type IV, as well as the reduction in enzyme activity associated with atherogenic apoB-containing lipoproteins in all patient groups, may represent a new and important antiatherogenic effect of this potent lipid-modulating agent.
引用
收藏
页码:927 / 934
页数:8
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