| http://purl.uniprot.org/citations/19474191 | http://www.w3.org/1999/02/22-rdf-syntax-ns#type | http://purl.uniprot.org/core/Journal_Citation |
| http://purl.uniprot.org/citations/19474191 | http://www.w3.org/2000/01/rdf-schema#comment | "1Alpha,25(OH)(2) vitamin D(3) [1,25(OH)(2)D(3)] increases serum Ca(2+) concentration in vivo, an action counteracted by activation of the Ca(2+)-sensing receptor (CaSR), which decreases parathyroid hormone (PTH) secretion and increases renal Ca(2+) excretion. Relatively little is known of the role the CaSR plays in this response through its potentially direct actions in kidney, gut, and bone independently of PTH. We report PTH-independent roles of the CaSR in modulating the response to exogenous 1,25(OH)(2)D(3) in mice with targeted disruption of both the CaSR and PTH genes (C(-)P(-)) compared with that in mice with disruption of the PTH gene alone (C(+)P(-)) or wild-type mice (C(+)P(+)). After intraperitoneal injection of 0.5 ng/g body wt 1,25(OH)(2)D(3), peak calcemic responses were observed at 24 h in all three genotypes in association with 1) a greater increase in serum Ca(2+) in C(-)P(-) mice than in the other genotypes on a Ca(2+)-replete diet that was attenuated by a Ca(2+)-deficient diet and pamidronate, 2) increased urinary Ca(2+)-to-creatinine ratios (UCa/Cr) in the C(+)P(-) and C(+)P(+) mice but a lowered ratio in the C(-)P(-) mice on a Ca(2+)-replete diet, and 3) no increase in calcitonin (CT) secretion in the C(+)P(+) and C(+)P(-) mice and a small increase in the C(-)P(-) mice. PTH deficiency had the anticipated effects on the expression of key genes involved in Ca(2+) transport at baseline in the duodenum and kidney, and injection of 1,25(OH)(2)D(3) increased gene expression 8 h later. However, the changes in the genes evaluated did not fully explain the differences in serum Ca(2+) seen among the genotypes. In conclusion, mice lacking the full-length CaSR have increased sensitivity to the calcemic action of 1,25(OH)(2)D(3) in the setting of PTH deficiency. This is principally from enhanced 1,25(OH)(2)D(3)-mediated gut Ca(2+) absorption and decreased renal Ca(2+) excretion, without any differences in bone-related release of Ca(2+) or CT secretion among the three genotypes that could explain the differences in their calcemic responses."xsd:string |
| http://purl.uniprot.org/citations/19474191 | http://purl.org/dc/terms/identifier | "doi:10.1152/ajprenal.00164.2009"xsd:string |
| http://purl.uniprot.org/citations/19474191 | http://purl.uniprot.org/core/author | "Brown E."xsd:string |
| http://purl.uniprot.org/citations/19474191 | http://purl.uniprot.org/core/author | "Kantham L."xsd:string |
| http://purl.uniprot.org/citations/19474191 | http://purl.uniprot.org/core/author | "Butters R."xsd:string |
| http://purl.uniprot.org/citations/19474191 | http://purl.uniprot.org/core/author | "Goltzman D."xsd:string |
| http://purl.uniprot.org/citations/19474191 | http://purl.uniprot.org/core/author | "Quinn S."xsd:string |
| http://purl.uniprot.org/citations/19474191 | http://purl.uniprot.org/core/author | "Pang J."xsd:string |
| http://purl.uniprot.org/citations/19474191 | http://purl.uniprot.org/core/author | "Pollak M."xsd:string |
| http://purl.uniprot.org/citations/19474191 | http://purl.uniprot.org/core/author | "Egbuna O."xsd:string |
| http://purl.uniprot.org/citations/19474191 | http://purl.uniprot.org/core/date | "2009"xsd:gYear |
| http://purl.uniprot.org/citations/19474191 | http://purl.uniprot.org/core/name | "Am J Physiol Renal Physiol"xsd:string |
| http://purl.uniprot.org/citations/19474191 | http://purl.uniprot.org/core/pages | "F720-8"xsd:string |
| http://purl.uniprot.org/citations/19474191 | http://purl.uniprot.org/core/title | "The full-length calcium-sensing receptor dampens the calcemic response to 1alpha,25(OH)2 vitamin D3 in vivo independently of parathyroid hormone."xsd:string |
| http://purl.uniprot.org/citations/19474191 | http://purl.uniprot.org/core/volume | "297"xsd:string |
| http://purl.uniprot.org/citations/19474191 | http://www.w3.org/2004/02/skos/core#exactMatch | http://purl.uniprot.org/pubmed/19474191 |
| http://purl.uniprot.org/citations/19474191 | http://xmlns.com/foaf/0.1/primaryTopicOf | https://pubmed.ncbi.nlm.nih.gov/19474191 |
| http://purl.uniprot.org/uniprot/#_Q540C1-mappedCitation-19474191 | http://www.w3.org/1999/02/22-rdf-syntax-ns#object | http://purl.uniprot.org/citations/19474191 |
| http://purl.uniprot.org/uniprot/#_P22858-mappedCitation-19474191 | http://www.w3.org/1999/02/22-rdf-syntax-ns#object | http://purl.uniprot.org/citations/19474191 |
| http://purl.uniprot.org/uniprot/#_Q8CDP3-mappedCitation-19474191 | http://www.w3.org/1999/02/22-rdf-syntax-ns#object | http://purl.uniprot.org/citations/19474191 |
| http://purl.uniprot.org/uniprot/#_O88982-mappedCitation-19474191 | http://www.w3.org/1999/02/22-rdf-syntax-ns#object | http://purl.uniprot.org/citations/19474191 |
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| http://purl.uniprot.org/uniprot/#_Q9QY96-mappedCitation-19474191 | http://www.w3.org/1999/02/22-rdf-syntax-ns#object | http://purl.uniprot.org/citations/19474191 |
| http://purl.uniprot.org/uniprot/#_Q924X4-mappedCitation-19474191 | http://www.w3.org/1999/02/22-rdf-syntax-ns#object | http://purl.uniprot.org/citations/19474191 |