Articles |
-Tocopherol Oxidative Lability and Ascorbic Acid Sparing Effects in Buoyant and Dense LDL
Presented in part at the 67th Scientific Sessions of the American Heart Association, Dallas, Tex, November 14-17, 1994, and published in abstract form in Circulation (1994;90[pt 2]:I-409).
From the Department of Molecular and Nuclear Medicine (D.L.T., P.M.T., R.M.K.), Life Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, Calif, and Children's Hospital Oakland (Calif) Research Institute (J.J.M.v.d.B.).
Correspondence to Dr Diane L. Tribble, Lawrence Berkeley National Laboratory, Donner Laboratory, Room 465, University of California, Berkeley, CA 94720.
Abstract The enhanced oxidizability of smaller, more dense
LDL is explained in part by a lower content of antioxidants, including
ubiquinol-10 and
-tocopherol. In the present
studies, we also observed greater rates of depletion of
-tocopherol (mole per mole LDL per minute) in dense
(d=1.040 to 1.054 g/mL) compared with buoyant
(d=1.026 to 1.032 g/mL) LDL in the presence of either
Cu2+ or the radical-generating agent
2,2'-azobis(2-amidinopropane)dihydrochloride. Differences were
particularly pronounced at the lowest Cu2+ concentration
tested (0.25 µmol/L), with a fivefold greater rate in dense LDL. At
higher concentrations (1.0 and 2.5 µmol/L Cu2+), there
was a greater dependence of depletion rate on initial amount of
-tocopherol, which was reduced in dense LDL, thus
resulting in smaller subfraction-dependent differences in depletion
rates. Inclusion of ascorbic acid (15 µmol/L), an aqueous antioxidant
capable of recycling
-tocopherol by hydrogen
donation, was found to extend the course of Cu2+-induced
-tocopherol depletion in both buoyant and dense LDL,
but this effect was more pronounced in dense LDL (time to
half-maximal
-tocopherol depletion was extended
15.6-fold and 21.2-fold in buoyant and dense LDL, respectively, at 2.5
µmol/L Cu2+; P<.05). Thus, dense LDL exhibits
more rapid
-tocopherol depletion and conjugated
diene formation than buoyant LDL when oxidation is performed in the
absence of ascorbic acid, but these differences are reversed in the
presence of ascorbic acid. These results suggest that differences in
oxidative behavior among LDL density subfractions may involve
differences in antioxidant activity and thus that the efficacy of
antioxidant regimens designed to inhibit LDL oxidation in vivo may vary
in relation to interindividual variations in LDL particle distribution
profiles.
Key Words: lipoproteins, low-density
-tocopherol antioxidants ascorbic acid atherosclerosis
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