Anti-diarrheal effect of water extract of Evodiae fructus in mice

Citation
Ll. Yu et al., Anti-diarrheal effect of water extract of Evodiae fructus in mice, J ETHNOPHAR, 73(1-2), 2000, pp. 39-45
Citations number
11
Categorie Soggetti
Pharmacology & Toxicology
Journal title
JOURNAL OF ETHNOPHARMACOLOGY
ISSN journal
03788741 → ACNP
Volume
73
Issue
1-2
Year of publication
2000
Pages
39 - 45
Database
ISI
SICI code
0378-8741(200011)73:1-2<39:AEOWEO>2.0.ZU;2-I
Abstract
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. (C) 2000 Elsevier Science Ireland Ltd. All rights reserved.