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A pharmacological analysis of receptors mediating the excitatory response to 5‐hydroxytryptamine in the guinea‐pig isolated trachea
Author(s) -
Lucchelli Adele,
SantagostinoBarbone Maria Grazia,
Barbieri Annalisa,
Tonini Marcello
Publication year - 1994
Publication title -
british journal of pharmacology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.432
H-Index - 211
eISSN - 1476-5381
pISSN - 0007-1188
DOI - 10.1111/j.1476-5381.1994.tb13144.x
Subject(s) - ketanserin , agonist , endocrinology , medicine , receptor antagonist , chemistry , 5 ht receptor , acetylcholine , serotonin , antagonist , muscarinic acetylcholine receptor , pharmacology , cholinergic , methysergide , receptor , biology
1 Experiments were carried out to characterize the receptors mediating the indirect excitatory response to 5‐hydroxytryptamine (5‐HT) in the guinea‐pig isolated trachea. 2 5‐HT caused concentration‐dependent contractions of tracheal strips, and the resulting concentration‐response curve was biphasic in nature. The first phase was obtained with agonist concentrations in the range of 0.01–3 n m and achieved a maximum which was 30% of the total 5‐HT response, while the second phase was in the range 10 n m –1 μ m . 3 Atropine (0.1 μ m ) and tetrodotoxin (TTX: 0.3 μ m ) significantly reduced both phases of the 5‐HT curve. Morphine (10 μ m ), which can act to inhibit neuronal acetylcholine release, abolished the first phase and reduced the second phase. This suggests that the first phase is mainly neurogenic (cholinergic) in nature, while the second phase is in part neurogenic and in part due to direct activation of the effector cells. 4 The 5‐HT 2A receptor antagonist, ketanserin (0.01, 0.1 μ m ) markedly depressed the first phase and shifted the second phase to the right in a parallel manner, with some depression of the 5‐HT response maximum. The less selective (5‐HT 1 /5‐HT 2A ) antagonist, methiothepin (0.1 μ m ) mimicked the action of ketanserin, albeit with less potency. Concomitant administration of ketanserin and methiothepin (each at 0.1 μ m ) produced an antagonism similar to that caused by ketanserin (0.1 μ m ) alone. 5 The 5‐HT3 receptor antagonists, ondansetron (0.1 μ m ) and granisetron (0.01 μ m ) slightly but significantly inhibited the first phase of the 5‐HT curve without altering the second phase. SDZ 205,557 (0.3 μ m ), a 5‐HT 4 receptor antagonist, was ineffective. 6 Our results suggest that neural 5‐HT 2A and, to a lesser extent, 5‐HT 3 receptor subtypes mediate the first phase of the 5‐HT curve in the guinea‐pig trachea. The second phase is mediated by 5‐HT 2A receptors, which are probably located at both the neural and muscular level. No evidence for the participation of 5‐HT 1 receptors in the 5‐HT response has been obtained.