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Volume 176, Issue 1, Pages 57-62 (September 2004)


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Effects of intravenous apolipoprotein A-I/phosphatidylcholine discs on paraoxonase and platelet-activating factor acetylhydrolase in human plasma and tissue fluid

Takeshi Kujiraokaa, Hiroaki HattoriaCorresponding Author Informationemail address, Mayumi Itoa, M.Nazeem Nanjeeb, Mitsuaki Ishiharaa, Makoto Naganoa, Tadao Iwasakia, C.Justin Cookeb, Waldemar L Olszewskic, Irina P Stepanovab, Tohru Egashiraa, Norman E Millerb

Received 1 December 2003; received in revised form 1 March 2004; accepted 19 March 2004.

Abstract 

We have previously shown that intravenous apolipoprotein (apo) A-I/phosphatidylcholine (apo A-I/PC) discs increase plasma high-density lipoprotein (HDL) concentration in humans. We have now studied the associated changes in two enzymes, paraoxonase (PON) and platelet-activating factor acetylhydrolase (PAF-AH) that are carried in whole or in part by HDLs, and are thought to influence atherogenesis by hydrolyzing oxidized phospholipids in lipoproteins. Apo A-I/PC discs (40mg/kg over 4h) were infused into eight healthy males. Although plasma apo A-I and HDL cholesterol increased on average by 178 and 158%, respectively, plasma total PON and total PAF-AH concentrations did not rise. By the end of the infusion, HDL-associated PAF-AH had increased by 0.56 ± 0.14μg/mL (mean ± S.D., P < 0.01), and nonHDL-associated PAF-AH had decreased by 0.84 ± 0.11μg/mL (P < 0.05). These changes were accompanied by an increase in the HDL-associated PAF-AH/apo A-I ratio from 0.19 to 0.35 (P < 0.05), and by a decrease in the nonHDL-associated PAF-AH/apo B ratio from 2.1 to 1.4 (P < 0.05). No changes in PON or PAF-AH concentrations were detected in prenodal lymph (tissue fluid), collected continuously from the leg. Our results show that the total concentrations of PON and PAF-AH in plasma are uninfluenced by plasma HDL concentration. PAF-AH transfers readily between HDLs and LDLs in vivo, and its distribution between them is determined partly by their relative concentrations and partly by HDL composition.

a Department of Advanced Medical Technology and Development, BML Inc, 1361-1 Matoba, Kawagoe, Saitama 350-1101, Japan

b Department of Cardiovascular Biochemistry, St. Bartholomew’s and the Royal London School of Medicine and Dentistry, London, UK

c Medical Research Center, Polish Academy of Sciences, Warsaw, Poland

Corresponding Author InformationCorresponding author. Tel.: +81 49 232 0440; fax: +81 49 232 5480.

PII: S0021-9150(04)00244-8

doi:10.1016/j.atherosclerosis.2004.03.026


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