Ce. Teixeira et al., Nonadrenergic, noncholinergic relaxation of human isolated corpus cavernosum induced by scorpion venom, UROLOGY, 57(4), 2001, pp. 816-820
Objectives, To examine the effects of Tityus serrulatus scorpion venom (TSV
) on human corpus cavernosum (HCC) using a bioassay cascade. Priapism is oc
casionally observed in scorpion envenomation, mostly in children.
Methods. HCC strips were suspended in a cascade system and superfused with
aerated and warmed Krebs' solution at 5 mL/min. Noradrenaline (5 mu mol/L)
was infused to induce a submaximal contraction of the HCC strips. The relea
se of cyclooxygenase products was prevented by infusing indomethacin (6 mu
mol/L).
Results. N-omega-nitro-L-arginine methyl ester (10 mu mol/L; n = 10) increa
sed the tone of the preparations and significantly reduced (P <0.01)the ace
tylcholine (ACh) and TSV-induced relaxations. Subsequent infusion of L-argi
nine (300 <mu>mol/L) partially reversed the increased tone and significantl
y restored the relaxations induced by TSV and ACh (P <0.01). The soluble gu
anylyl cyclase inhibitor ODQ (10 <mu>mol/L; n = 8) markedly reduced (P <0.0
1) the relaxations induced by TSV, ACh, glyceryl trinitrate, and bradykinin
. 7-Nitroindazole (10 <mu>mol/L; n = 8) inhibited the relaxations induced b
y TSV by 84% (P <0.01) and also caused small, but significant, reductions i
n the ACh and bradykinin-induced HCC relaxations (P <0.05). Atropine (1 mu
mol/L; n = 6) abolished the relaxations evoked by ACh (P <0.01), but had no
effect on those elicited by TSV. Tetrodotoxin (1 <mu>mol/L; n = 6) abolish
ed the relaxations induced by TSV (P <0.01) and also reversed the establish
ed TSV-induced relaxation (n = 4).
Conclusions, Our results indicate that TSV relaxes HCC through the release
of nitric oxide from nonadrenergic, noncholinergic (NANC) nerves. The eluci
dation of the mechanism responsible for the TSV-induced relaxations might b
e useful for a better understanding of the development of priapism in cases
of scorpion envenomation. UROLOGY 57: 816-820, 2001. (C) 2001, Elsevier Sc
ience Inc.