The effect of allosteric antagonists in modulating muscarinic M2-receptor function in guinea-pig isolated trachea.

Article Details

Citation

Copy to clipboard

Spina D, Minshall E, Goldie RG, Page CP

The effect of allosteric antagonists in modulating muscarinic M2-receptor function in guinea-pig isolated trachea.

Br J Pharmacol. 1994 Jul;112(3):901-5.

PubMed ID

7522861 [View in PubMed

]

Abstract

1. We have assessed the influence of a range of synthetic cationic polypeptides with putative inhibitory actions at prejunctional muscarinic M2-receptors on electrical field stimulation-induced contraction of guinea-pig isolated tracheal preparations. Electrical field stimulation of epithelium-denuded guinea-pig trachea resulted in frequency-dependent contractile responses. As expected, tracheal smooth muscle sensitivity to electrical field stimulation was increased in tissues pretreated with the muscarinic M2-receptor antagonist, gallamine. In contrast, gallamine did not significantly alter the contractile potency to acetylcholine. 2. Unlike gallamine, the synthetic cationic polypeptides, poly-L-arginine, poly-L-lysine, poly-D-lysine, the cationic dye ruthenium red and the anionic polysaccharide, heparin, failed to increase significantly tracheal smooth muscle sensitivity to electrical field stimulation. 3. Poly-L-arginine, ruthenium red and heparin had no effect on the contractile response to exogenously applied methacholine. 4. These data are consistent with the concept that in guinea-pig tracheal smooth muscle, gallamine is an allosteric antagonist of guinea-pig tracheal muscarinic M2-receptors, whereas the various cationic polypeptides and the polyanion, heparin, are not.

DrugBank Data that Cites this Article

Drug Targets

Drug	Target	Kind	Organism	Ph值armacological Action	Actions
Gallamine triethiodide	Muscarinic acetylcholine receptor M2	Protein	Humans	Yes	Antagonist	Details