Carnosine and taurine have been suggested to protect excitable tissues agai
nst oxidative stress. We have investigated the protection of cerebellar gra
nule cells (neurons) by these compounds against free radicals generated by
kainic acid (KA), and 3-morpholinosydnonimine hydrochloride (SIN-1) treatme
nt. Carnosine decreased free radical levels in KA and SIN-1 treated cells,
and increased cell viability. The KA effect, but not that of SIN-I, was dep
endent on the presence of external Ca2+ ions. Taurine increased cell viabil
ity, but did not decrease free radical levers. These results suggest that t
here are multiple pathways leading to cell death, not all of which involve
decreases in intracellular free radical levels, and also indicate that mult
iple mechanisms of cellular defense exist against oxidative stress. (C) 199
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