THE study was undertaken to evaluate the role of nitric oxide (NO) in
pretectal (PTN)-induced analgesia in rats. Microinjection of varying c
oncentrations of L-arginine (1 nM to 1 muM) produced a quick, long-las
ting and concentration-dependent analgesic response, whereas similar c
oncentrations Of D-arginine failed to produce analgesia. Moreover pret
reatment with N-nitro-L-arginine methyl ester (L-NAME, 1 muM) signific
antly prevented L-arginine induced analgesia. Further, pretreatment of
animals with methylene blue, a known guanylate cyclase inhibitor also
prevented the development of analgesia. Our study suggests that L-arg
inine caused production of NO, which in turn activates pretectal analg
esic system involving cyclic GMP.