1 Immunized BP2 mice developed an acute bronchoconstriction in viva and air
way muscle contraction in vitro in response to ovalbumin (OA) and these con
tractions were dose dependent.
2 Methysergide or atropine inhibited OA-induced bronchoconstriction in vivo
and airway muscle contraction in vitro.
3 Neostigmine potentiated the OA-induced bronchoconstriction in vivo and ai
rway muscle contraction in vitro of BP2 mice. This potentiation was markedl
y reduced by the administration of methysergide or atropine and when the tw
o antagonists were administered together, the responses were completely inh
ibited.
4 Neostigmine also potentiated the serotonin (5-HT)- and acetylcholine (ACh
)-induced bronchoconstriction and this potentiation was significantly rever
sed by atropine.
5 These results indicate that OA provokes a bronchoconstriction in immunize
d BP2 mice by stimulating the release of 5-HT, which in turn acts via the c
holinergic mediator, ACh.