The antinociceptive actions of the steroid compounds isolated from the
leaves, stems, and roots of P. corcovadensis have been investigated i
n mice. Stigmasterol, stigmasterol acetate, beta-sitosterol, and aspir
in (3-100 mk/kg, i.p.) inhibited, in a dose-related manner, acetic aci
d-induced abdominal constriction in mice with ID(50)s of 16, 11, 9, an
d 24 mg/kg, respectively. In the formalin test, stigmasterol and stigm
asterol acetate (10-100 mg/kg, i.p.) caused graded inhibition of both
the neurogenic (first phase) and inflammatory phases (second phase) of
formalin-induced pain. However, both compounds were more effective in
relation of the second phase of the formalin test with ID50 values of
26 and 41 mg/kg, respectively. Furthermore, both steroids failed to a
ffect the edematogenic response of the formalin test. Given orally, st
igmasterol and stigmasterol acetate (50-200 mg/kg) also exhibited sign
ificant though less potent analgesic action against both acetic acid-
and formalin-induced nociception in mice. In addition, stigmasterol (u
p to 100 mg/kg, i.p.), in contrast to morphine (10 mg/kg, s.c.), had n
o analgesic effect in either tail-flick or hot-plate models. These fin
dings suggest that stigmasterol and beta-sitosterol may account, at le
ast in part, for the antinociceptive actions reported previously for t
he hydroalcoholic extract of Phyllanthus corcovadensis.