Elimination of cholesterol from arterial tissue, crucial in limiting a
therogenesis, may be achieved via high-density lipoprotein (HDL)-media
ted reverse cholesterol transport (RCT); components of this pathway ca
n be modulated by oxidative stress. Here we have examined the relation
s between cholesterol efflux, esterification and transfer in human pla
sma treated with the powerfully reactive nitrogen species, peroxynitri
te. Cellular cholesterol efflux to whole plasma, or to peroxynitrite-m
odified HDL3, was relatively insensitive to peroxynitrite, as,vas the
transfer of esterified cholesterol. However, plasma cholesterol esteri
fication, via lecithin:cholesterol acyltransferase (LCAT), was markedl
y inhibited, both directly and indirectly, by peroxynitrite treatment,
implying inefficient RCT follows HDL sequestration of cellular choles
terol. (C) 1998 Federation of European Biochemical Societies.