Oxidized low-density lipoprotein (ox-LDL) is well known to play an importan
t role in atherogenesis through the recruitment of monocytes into vessel wa
lls and the deposition of cholesterol ester in the macrophages, which leads
to the formation of lipid-rich plaque. It was assumed that only trace amou
nts of ox-LDL were present in plasma because the half-life of ox-LDL was on
ly a few minutes. Recently, through the use of a monoclonal antibody agains
t ox-LDL, a quantitative method to measure serum ox-LDL concentration has b
een developed. Metabolites of doxazosin, an alpha (1)-adrenergic antihypert
ensive agent, have been reported to inhibit oxidation of LDL in vitro. In t
his study, we investigated the in vivo effect of doxazosin on LDL oxidation
using this new method to measure serum ox-LDL concentration. After the adm
inistration of doxazosin for 1 to 2 months, serum concentration of ox-LDL d
ecreased significantly (P < .05). Although the reduction of ox-LDL concentr
ation does not strictly indicate doxazosin's antiatherosclerotic effect, it
may constitute one of doxazosin's additional weapons beside lowering blood
pressure and serum lipid values in the prevention of atherosclerosis. (C)
2001 American Journal of Hypertension, Ltd.