The most common complication in the lethal cases of ophidian bites in Brazi
l is acute renal failure, but its pathogenesis is obscure. The effects of B
othrops jararacussu venom (3, 10 and 30 mug/ml) were examined using the iso
lated perfused kidney from Wistar rats. Dexamethasone, and WEB 2086, a tria
zolobenzodiazepine substance, which is a platelet activating factor recepto
r antagonist, were tested for a possible blockade of the renal effects in t
he presence of 10 mug/ml of venom. The most intense effects of the venom we
re noticed at 120 min after using 30 mug/ml. We observed a decrease in the
perfusion pressure and in the renal vascular resistance. However, the glome
rular filtration rate (GFR) and the urinary flow (UF) increased significant
ly. The percent of sodium (%Na-tot(+)) and potassium (%K-tot(+)) tubular tr
ansport were also decreased. Dexamethasone to to was unable to block the ef
fects of B. jararacussu in the kidney, while WEB 2086 blocked its effect in
glomerular filtration rate, urinary flow and in the percentage of total tu
bular potassium reabsorption. We suggest that this venom promotes diuresis
independently of perfusion pressure drop. The alterations in GFR, UF and %K
-tot(+), are probably mediated by platelet activating to factor. Dexamethas
one did not block the renal effects maybe because of the concentration used
in this work or maybe the renal effects are promoted by the myotoxin, whic
h does not have PLA, activity. (C) 2001 Elsevier Science Ltd. All rights re
served.