Dilinoleoylphosphatidylcholine protects human low density lipoproteins against oxidation

Citation
Kp. Navder et al., Dilinoleoylphosphatidylcholine protects human low density lipoproteins against oxidation, ATHEROSCLER, 152(1), 2000, pp. 89-95
Citations number
32
Categorie Soggetti
Cardiovascular & Respiratory Systems","Cardiovascular & Hematology Research
Journal title
ATHEROSCLEROSIS
ISSN journal
00219150 → ACNP
Volume
152
Issue
1
Year of publication
2000
Pages
89 - 95
Database
ISI
SICI code
0021-9150(200009)152:1<89:DPHLDL>2.0.ZU;2-N
Abstract
LDL oxidation may promote atherosclerosis. We found that polyenyphosphatidy lcholine (PPC), a mixture of polyunsaturated phospholipids extracted from s oybeans, has antioxidant effects in in vivo models of oxidative stress. To assess whether components of PPC affect the in vitro oxidizability of LDL, plasma from 15 healthy volunteers was incubated with 10 mu M of either dili noleoyl-, palmitoyl-linoleoyl-, linoleoyl-palmitoyl- or distearoyl-phosphat idylcholine as well as 10 mu M and 1 mM alpha-tocopherol. LDL oxidation was initiated with 5 mu M Cu2+ sulfate and monitored by conjugated diene produ ction, or with 2,2'-azobis (2-amidinopropane) dihydrochloride. a free radic al generator, and monitored by O-2 consumption. After addition of Cu2+, the lag phase (indicative of resistance of LDL to oxidation) was longer (140% of controls; P < 0.001) for LDL incubated with dilinoleoyl-. but not with t he other phosphatidylcholine species. This effect was similar to that of 1 mM alpha-tocopherol (135%,). After addition of 2,2'-azobis (2-amidinopropan e) dihydrochloride, the inhibition time (also reflecting the antioxidant co ntent of LDL) was prolonged (P<0.001) for alpha-tocopherol (206%) and dilin oleoyl-( 188%), but not for distearoyl-phosphatidyl-choline. Thus, dilinole oyl-phosphatidylcholine (the main component of PPC) protects against LDL ox idation, a possible mechanism for its reported anti-atherosclerosis effects . (C) 2000 Elsevier Science Ireland Ltd. All rights reserved.