The ability of several 5-HT3 receptor antagonists (MDL 72,222EF, the m
ethyl quaternary ammonium salt of MDL 72,222, dolasetron, tropisetron,
granisetron and ondansetron) to inhibit writhing induced in the mouse
by either 5-hydroxytryptamine (5-HT), acetylcholine or acetic acid wa
s examined. 2. All of the 5-HT3 receptor antagonists were able to inhi
bit writhing induced by acetylcholine. MDL 72,222EF and tropisetron we
re also able to inhibit writhing induced by 5-HT and acetic acid but h
igher doses were required to have the same effect as against acetylcho
line. Dolasetron inhibited writhes induced by 5-HT but failed to signi
ficantly affect writhes induced by acetic acid. 3. MDL 72,222EF and it
s quaternary salt were more potent and had a more rapid onset of actio
n after i.p. than after s.c, administration. 4. 2-Methyl-5-HT did not
induce writhing at doses up to 4 mg/kg i.p., whereas 5-HT dose-depende
ntly induced writhing over the range 0.5-2 mg/kg. 5. These results sho
w that 5-HT3 receptor antagonists can inhibit writhes induced by a var
iety of compounds and this appears to be a local action. However, the
inability of 2-methyl-5-HT to induce writhing and the high doses of an
tagonist required indicate that further studies are required to establ
ish a role for 5-HT3 receptors in this effect.