Chondroitin 4-sulphate (C4S), a basic component of the extracellular m
atrix of the artery wail, inhibited copper-induced low density lipopro
tein (LDL) oxidation by prolonging the lag time and reducing the rate
of propagation, LDL oxidation was assessed by monitoring conjugated di
enes and low level chemiluminescence, A possible initial key reaction
in LDL oxidation, the reduction of copper(II) to copper(I) by LDL, was
decreased in the presence of C4S. Moreover, C4S protected tryptophan
residues of C4S in the early stage of LDL oxidation and during the sub
sequent propagation phase, The presence of the sulphate group in posit
ion 4 of N-acetylgalactosaminyl residues of C4S is crucial for protect
ive activity, In Fact, the structurally related chondroitin 6-sulphate
, also present in tissues, had no effect an LDH. oxidation. These data
suggest that C4S mag contribute to protest LDL against oxidation in a
rterial intima. (C) 1997 Federation of European Biochemical Societies.