Abstract
Endomorphin-1 and -2 (μ-opioid receptor agonists) produced a concentration-dependent and naloxone-sensitive inhibition of cholinergic contractile responses in guinea-pig trachea (at 10 μM, 46.1±8.0% and 33.8±8.6%, respectively). Endomorphin-1 and -2 also inhibited electrically-evoked acetylcholine release from cholinergic nerves innervating guinea-pig (at 0.1 μM, 41.8±10.9%; at 1 μM 60.1±6.3%, respectively) and human trachea (at 10 μM, 76.2±18.1%, and 77.7±14.3%, respectively). Naloxone prevented the inhibition by endomorphin-1 and -2 in both guinea-pig and human trachea, suggesting that these peptides can inhibit cholinergic, parasympathetic neurotransmission to the airways via the activation of classical opioid receptors.
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