Pyruvate is a well-known scavenger of hydrogen peroxide (H2O2). Ln add
ition, it scavenges superoxide radical (O-2(.-)). However, evidence on
its intracellular antioxidant function is meager at present Hence, we
have examined the effectiveness of this metabolite and its ethyl este
r against intracellular oxidative damage to the lens under organ cultu
re. Menadione, a redoxcycling quinone, was used to generate the reacti
ve oxygen species (ROS). It was found to inhibit lens metabolism as ev
idenced by a decrease of Am. Additionally, tissue oxidation was appare
nt by loss of glutathione (GSH), and increase in the level of oxidized
glutathione (GSSG), coupled with increase of the urea soluble protein
s (water insoluble). The overall physiological damage was apparent by
the inhibition of the Na+-K+-ATPase dependent cation pump, as evidence
d by a decreased rubidium transport. These deleterious effects were at
tenuated by pyruvate and ethyl-pyruvate. The later was found to be mor
e effective.