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Please use this identifier to cite or link to this item: http://hdl.handle.net/2381/8080

Title: Pharmacological Assessment of M1 Muscarinic Acetylcholine Receptor-Gq/11 Protein Coupling in Membranes Prepared from Postmortem Human Brain Tissue
Authors: Salah-Uddin, Hasib
Thomas, David R.
Davies, Ceri H.
Hagan, Jim J.
Wood, Martyn D.
Watson, Jeannette M.
Challiss, R.A. John
Issue Date: 1-Jun-2008
Publisher: American Society for Pharmacology and Experimental Therapeutics (ASPET)
Citation: Journal of Pharmacology and Experimental Therapeutics, 2008, 325 (3), pp. 869-874.
Abstract: Using a selective Gαq/11 protein antibody capture guanosine 5′-O-(3-[35S]thio)triphosphate ([35S]GTPγS) binding approach, it has been possible to perform a quantitative pharmacological examination of the functional activity of the M1 muscarinic acetylcholine receptor (mAChR) in membranes prepared from human postmortem cerebral cortex. Oxotremorine-M caused a ≥2-fold increase in [35S]GTPγS-Gαq/11 binding with a pEC50 of 6.06 ± 0.16 in Brodmann's areas 23 and 25 that was almost completely inhibited by preincubation of membranes with the M1 mAChR subtype-selective antagonist muscarinic toxin-7. In addition, the orthosteric and allosteric agonists, xanomeline [3(3-hexyloxy-1,2,5-thiadiazol-4-yl)-1,2,5,6-tetrahydro-1-methylpyridine] and AC-42 (4-n-butyl-1-[4-(2-methylphenyl)-4-oxo-1-butyl]-piperidine hydrogen chloride), increased [35S]-GTPγS-Gαq/11 binding, but with reduced intrinsic activities, inducing maximal responses that were 42 ± 1 and 44 ± 2% of the oxotremorine-M-induced response, respectively. These data indicate that the M1 receptor is the predominant mAChR subtype coupling to the Gαq/11 G protein in these brain regions and that it is possible to quantify the potency and intrinsic activity of full and partial M1 mAChR receptor agonists in postmortem human brain using a selective Gαq/11 protein antibody capture [35S]GTPγS binding assay.
ISSN: 0022-3565
Links: http://dx.doi.org/10.1124/jpet.108.137968
Type: Article
Description: This paper was published as Journal of Pharmacology and Experimental Therapeutics, 2008, 325 (3), pp. 869-874. It is available from http://jpet.aspetjournals.org/content/325/3/869.abstract. Doi: 10.1124/jpet.108.137968
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Appears in Collections:Published Articles, Dept. of Cell Physiology and Pharmacology

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