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http://purl.uniprot.org/citations/21114972http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/21114972http://www.w3.org/2000/01/rdf-schema#comment"We have used selective muscarinic receptor antagonists and M(2) and M(4) receptor knockout (KO) mouse tissue to define the functional muscarinic acetylcholine receptor populations in rodent striatum. [(3)H] NMS binding studies in rat and mouse striatum demonstrated that approximately 30% of muscarinic acetylcholine receptors expressed are M(1) receptors. Radioligand binding studies suggest that the remaining muscarinic acetylcholine receptor population is largely M(4) with small levels of M(2). In agreement, carbachol-induced GTPγS binding studies in M(2) and M(4) receptor KO mouse striatum implicated the M(4) receptor as the predominant functional receptor subtype. Based on these data we have developed a novel, native tissue M(4) receptor [(35)S] GTPγS binding assay. Pharmacological assessment of M(4) receptor agonist and positive 3modulators revealed clear differences in the potencies observed in a human recombinant CHO-M(4) receptor [(35)S] GTPγS binding assay as compared to the native tissue [(35)S] GTPγS binding assay. These differences are believed to reflect differences in receptor reserve between the assay systems as well as differences in compound pharmacology (relative contribution of compound affinity and efficacy to observed potency). These studies have demonstrated the importance of understanding the pharmacology of test compounds in a native environment when predicting in vivo response."xsd:string
http://purl.uniprot.org/citations/21114972http://purl.org/dc/terms/identifier"doi:10.1016/j.ejphar.2010.10.079"xsd:string
http://purl.uniprot.org/citations/21114972http://purl.uniprot.org/core/author"Kew J.N."xsd:string
http://purl.uniprot.org/citations/21114972http://purl.uniprot.org/core/author"Langmead C.J."xsd:string
http://purl.uniprot.org/citations/21114972http://purl.uniprot.org/core/author"Watson J.M."xsd:string
http://purl.uniprot.org/citations/21114972http://purl.uniprot.org/core/author"Chapman K.L."xsd:string
http://purl.uniprot.org/citations/21114972http://purl.uniprot.org/core/author"Vaswani D."xsd:string
http://purl.uniprot.org/citations/21114972http://purl.uniprot.org/core/author"Hendry N."xsd:string
http://purl.uniprot.org/citations/21114972http://purl.uniprot.org/core/date"2011"xsd:gYear
http://purl.uniprot.org/citations/21114972http://purl.uniprot.org/core/name"Eur J Pharmacol"xsd:string
http://purl.uniprot.org/citations/21114972http://purl.uniprot.org/core/pages"1-6"xsd:string
http://purl.uniprot.org/citations/21114972http://purl.uniprot.org/core/title"The muscarinic M(4) receptor is the functionally predominant subtype in rat and mouse striatum as demonstrated using [(35)S] GTPgammaS binding."xsd:string
http://purl.uniprot.org/citations/21114972http://purl.uniprot.org/core/volume"652"xsd:string
http://purl.uniprot.org/citations/21114972http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/21114972
http://purl.uniprot.org/citations/21114972http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/21114972
http://purl.uniprot.org/uniprot/#_Q0VBU3-mappedCitation-21114972http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/21114972
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http://purl.uniprot.org/uniprot/#_P32211-mappedCitation-21114972http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/21114972
http://purl.uniprot.org/uniprot/#_P10980-mappedCitation-21114972http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/21114972
http://purl.uniprot.org/uniprot/#_Q6PXP1-mappedCitation-21114972http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/21114972
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http://purl.uniprot.org/uniprot/P10980http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/21114972
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