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http://purl.uniprot.org/citations/8138923http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/8138923http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/8138923http://www.w3.org/2000/01/rdf-schema#comment"Exposure of HeLa cells stably expressing cloned human 5-hydroxytryptamine (5-HT)1A receptors (HA7 cells) to the agonist 8-hydroxy-2-(di-N-propylamino)-tetralin (8-OH-DPAT) results in a loss of high-affinity binding sites and a desensitization of receptor-adenylate cyclase coupling, as measured by 5-HT1A-mediated inhibition of forskolin-stimulated adenylate cyclase activity. These responses can also be observed after exposure to forskolin, which activates cyclic AMP-dependent protein kinase A or after treatment with known activators of protein kinase C (PKC) such as phorbol-12-myristate 13-acetate (PMA). The responses elicited by exposure to 8-OH-DPAT or PMA can be blocked completely by inhibitors of PKC and also by 24-hr exposure to PMA. Preincubation of HA7 cells with 8-OH-DPAT also stimulates hydrolysis of inositol phospholipids and the production of arachidonic acid. Inhibition of phospholipase A2 with quinacrine or by removal of extracellular Ca++ blocks the agonist-mediated loss of 5-HT1A receptor binding sites. These data demonstrate that agonist-induced down regulation of the 5-HT1A receptor occurs after stimulation of both the PKC and phospholipase A2 signaling pathways, both of which may activate PKC. The subsequent response is a loss of high-affinity ligand binding sites and functional receptor coupling to adenylate cyclase."xsd:string
http://purl.uniprot.org/citations/8138923http://purl.uniprot.org/core/author"Ciaranello R.D."xsd:string
http://purl.uniprot.org/citations/8138923http://purl.uniprot.org/core/author"Ciaranello R.D."xsd:string
http://purl.uniprot.org/citations/8138923http://purl.uniprot.org/core/author"Harrington M.A."xsd:string
http://purl.uniprot.org/citations/8138923http://purl.uniprot.org/core/author"Harrington M.A."xsd:string
http://purl.uniprot.org/citations/8138923http://purl.uniprot.org/core/author"Shaw K."xsd:string
http://purl.uniprot.org/citations/8138923http://purl.uniprot.org/core/author"Shaw K."xsd:string
http://purl.uniprot.org/citations/8138923http://purl.uniprot.org/core/author"Zhong P."xsd:string
http://purl.uniprot.org/citations/8138923http://purl.uniprot.org/core/author"Zhong P."xsd:string
http://purl.uniprot.org/citations/8138923http://purl.uniprot.org/core/date"1994"xsd:gYear
http://purl.uniprot.org/citations/8138923http://purl.uniprot.org/core/date"1994"xsd:gYear
http://purl.uniprot.org/citations/8138923http://purl.uniprot.org/core/name"J. Pharmacol. Exp. Ther."xsd:string
http://purl.uniprot.org/citations/8138923http://purl.uniprot.org/core/name"J. Pharmacol. Exp. Ther."xsd:string
http://purl.uniprot.org/citations/8138923http://purl.uniprot.org/core/pages"1098-1106"xsd:string
http://purl.uniprot.org/citations/8138923http://purl.uniprot.org/core/pages"1098-1106"xsd:string
http://purl.uniprot.org/citations/8138923http://purl.uniprot.org/core/title"Agonist-induced desensitization and loss of high-affinity binding sites of stably expressed human 5-HT1A receptors."xsd:string
http://purl.uniprot.org/citations/8138923http://purl.uniprot.org/core/title"Agonist-induced desensitization and loss of high-affinity binding sites of stably expressed human 5-HT1A receptors."xsd:string
http://purl.uniprot.org/citations/8138923http://purl.uniprot.org/core/volume"268"xsd:string
http://purl.uniprot.org/citations/8138923http://purl.uniprot.org/core/volume"268"xsd:string
http://purl.uniprot.org/citations/8138923http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/8138923
http://purl.uniprot.org/citations/8138923http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/8138923
http://purl.uniprot.org/citations/8138923http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/8138923
http://purl.uniprot.org/citations/8138923http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/8138923