Our previous study showed that Evodiae fructus (the dried, unripe fruit of
Evodia rutaecarpa) has an inhibitory effect on the intestinal transit (anti
-transit effect) in mice. In the present study, a water extract of Evodiae
fructus was used to examine its effect on castor oil-induced diarrhea and t
o compare with its anti-transit effect in mice. The results indicated that
Evodiae fructus had both anti-transit and anti-diarrheal effects with compa
rable ID50 (the dose for 50% inhibition) values of 54 +/- 7 and 76 +/- 17 m
g/kg. The time-courses of Evodiae fructus pretreatment for both anti-transi
t and anti-diarrheal effects were very similar. Because no significant infl
uences of both nitric oxide (NO) precursor L-arginine (600 mg/kg, i.p.) and
NO synthase inhibitor N-G-nitro-L-arginine methyl ester (25 mg/kg, i.p.) p
retreatment, the NO system was not involved in both the anti-transit and an
ti-diarrheal effects of Evodiae fructus. Like Evodiae fructus, a muscarinic
acetylcholine receptor antagonist atropine inhibited castor oil-induced in
crease in fecal weight and loss of body weight. However, the potencies or t
ime-courses of atropine pretreatment for both anti-transit and anti-diarrhe
al effects were different. Furthermore, the anti-diarrheal effect of atropi
ne was independent of its anti-transit effect at the lower dose (0.5 mg/kg,
i.p.). Therefore, the action of Evodiae fructus appeared to be something d
ifferent from atropine, suggesting that an action other than the anti-musca
rinic action, as previously proposed for Evodiae fructus, may be involved.
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