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2-adrenoceptors on
cholinergic and adrenergic nerve endings of the guinea pig trachea
Department of Molecular Pharmacology, University of Groningen, 9713 AV Groningen, The Netherlands
Using electrical field stimulation of
epithelium-denuded intact guinea pig tracheal tube preparations, we
studied the presence and role of prejunctional
2-adrenoceptors by
measuring evoked endogenous acetylcholine (ACh) and norepinephrine (NE)
release directly. Analysis of ACh and NE was through two HPLC systems with electrochemical detection. Electrical field stimulation (150 mA,
0.8 ms, 16 Hz, 5 min, biphasic pulses) released 29.1 ± 2.5 pmol
ACh/g tissue and 70.2 ± 6.2 pmol NE/g tissue. Preincubation for 15 min with the selective
2-adrenoceptor agonist
fenoterol (1 µM) increased both ACh and NE overflow to 178 ± 28 (P < 0.01) and 165 ± 12%
(P < 0.01), respectively, of control
values, increases that were abolished completely by the selective
2-adrenoceptor antagonist
ICI-118551 (1 µM). Further experiments with increasing fenoterol
concentrations (0.1-100 µM) and different preincubation periods
(1, 5, and 15 min) showed a strong and concentration-dependent facilitation of NE release, with maximum response levels decreasing (from nearly 5-fold to only 2.5-fold of control value) with increasing agonist contact time. In contrast, sensitivity of facilitatory
2-adrenoceptors on cholinergic
nerves to fenoterol gradually increased when the incubation period was
prolonged; in addition, a bell-shaped concentration-response
relationship was found at 15 min of preincubation. Fenoterol
concentration-response relationships (15-min agonist preincubation) in
the presence of atropine and yohimbine (1 µM each) were similar in
the case of NE release, but in the case of ACh release, the bell shape
was lost. The results indicate a differential capacity and response
time profile of facilitatory prejunctional
2-adrenoceptors on adrenergic
and cholinergic nerve terminals in the guinea pig trachea and suggest that the receptors on adrenergic nerves are more susceptible to desensitization.
facilitatory prejunctional
2-adrenoceptors; acetylcholine
release; norepinephrine release
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