It was demonstrated that incubation of blood platelets with sodium selenite
(1-100 mu M) resulted in a dose- and time-dependent loss of platelet thiol
s (both glutathione and protein -SH groups). The effects of sodium selenite
on platelet membrane lipid fluidity by the EPR spin-labelling method was a
lso investigated. We showed there were no alterations in membrane fluidity
at the deeper regions (12-DOXYL-Ste) in lipid bilayer, a slight increase (a
pprox. 7%, p < 0.03) of h(+1)/h(0) for spin probe 5-DOXYL-Ste was monitored
. The amount of Triton-insoluble protein fraction isolated from platelets a
fter incubation (60 min) with selenite was significantly elevated (p < 0.00
6). It has been suggested that limited increase in lipid fluidity at the su
rface regions in the lipid bilayer of the platelet membrane in selenite-tre
ated platelets may be the result of alteration in lipid-protein interaction
s caused by protein conformational changes.