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Pharmacological properties of nicotinic acetylcholine receptors in isolated Locusta migratoria neurones

✍ Scribed by Charles Jackson; Isabel Bermudez; David J. Beadle


Publisher
John Wiley and Sons
Year
2002
Tongue
English
Weight
362 KB
Volume
56
Category
Article
ISSN
1059-910X

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✦ Synopsis


Abstract

Mechanically dissociated neuronal cell bodies from the thoracic ganglia of Locusta migratoria were viable in culture conditions for up to 2 days and were voltage‐clamped to record the effects of GABAergic drugs and physostigmine on the membrane conductance and ACh responses of the dissociated cells. Bicuculline, hydrastine, and gabazine inhibited the EC~50~ ACh responses of the cells. Both bicuculline and hydrastine were full inhibitors of the ACh responses but gabazine behaved as a partial inhibitor. Bicuculline, hydrastine, and gabazine inhibited the ACh responses in a non‐competitive and voltage‐independent fashion, suggesting that they are allosteric inhibitors of locust nicotinic ACh receptors. Physostigmine activated currents when applied onto isolated locust neurones. The responses activated by physostigmine were inhibited competitively by tubocurarine, which indicates that physostigmine interacts with the ACh site of locust nicotinic ACh receptors. However, maximal concentrations of physostigmine elicited currents of smaller amplitudes to those evoked by maximal ACh concentrations. Single‐channel recordings suggest that the partial efficacy of physostigmine may reflect the low frequency of opening of physostigmine‐induced single currents relative to that of ACh‐single currents. Microsc. Res. Tech. 56:249–255, 2002. © 2002 Wiley‐Liss, Inc.


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