Atorvastatin preferentially reduces LDL-associated platelet-activating factor acetylhydrolase activity in dyslipidemias of type IIA and type IIB

Arterioscler Thromb Vasc Biol. 2002 Feb 1;22(2):306-11. doi: 10.1161/hq0202.102918.

Abstract

Human plasma platelet-activating factor acetylhydrolase (PAF-AH) is a phospholipase A(2) that is primarily associated with low density lipoprotein (LDL). PAF-AH activity has also been found in high density lipoprotein (HDL), although it has recently been indicated that there is no PAF-AH protein in HDL. Plasma paraoxonase 1 (PON1) is an HDL-associated esterase, which also exhibits PAF-AH-like activity. The effect of atorvastatin (20 mg per day for 4 months) on PAF-AH and PON1 activities in patients with dyslipidemia of type IIA (n=55) or type IIB (n=21) was studied. In both patient groups, atorvastatin significantly reduced plasma PAF-AH activity because of the decrease in LDL plasma levels and the preferential decrease in PAF-AH activity on dense LDL subfractions (LDL-4 and LDL-5). Drug therapy did not affect HDL-associated PAF-AH activity or serum PON1 activities toward paraoxon and phenylacetate in either patient group. However, because of the reduction in LDL cholesterol levels, the ratios of HDL-associated PAF-AH and serum PON1 activities to LDL cholesterol levels were significantly increased after drug administration. The reduction of the LDL-associated PAF-AH activity and the elevation in the ratios of HDL-associated PAF-AH and PON1 activities to LDL plasma levels may represent a new dimension in the antiatherogenic effect of atorvastatin.

Publication types

  • Clinical Trial
  • Controlled Clinical Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • 1-Alkyl-2-acetylglycerophosphocholine Esterase
  • Anticholesteremic Agents / pharmacology*
  • Apolipoproteins B / blood
  • Apolipoproteins E / blood
  • Aryldialkylphosphatase
  • Atorvastatin
  • Cholesterol, LDL / metabolism
  • Esterases / blood
  • Heptanoic Acids / pharmacology*
  • Humans
  • Hyperlipidemias / drug therapy*
  • Hyperlipidemias / metabolism*
  • Lipoproteins, LDL / blood*
  • Macrophages / metabolism
  • Phospholipases A / drug effects*
  • Pyrroles / pharmacology*

Substances

  • Anticholesteremic Agents
  • Apolipoproteins B
  • Apolipoproteins E
  • Cholesterol, LDL
  • Heptanoic Acids
  • Lipoproteins, LDL
  • Pyrroles
  • Atorvastatin
  • Esterases
  • Phospholipases A
  • 1-Alkyl-2-acetylglycerophosphocholine Esterase
  • Aryldialkylphosphatase
  • PON1 protein, human