Source:http://linkedlifedata.com/resource/pubmed/id/16290260
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
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pubmed:dateCreated |
2006-5-29
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pubmed:abstractText |
Urotensin-II (U-II), a ligand for the G-protein-coupled receptor UT, has been characterized as the most potent mammalian vasoconstrictor identified to date. Although circulating levels of U-II are altered in lower species (e.g., fish) upon exposure to hypo-osmotic stress, little is known about the actions of this cyclic undecapeptide within the kidney, an organ that plays a pivotal role in the control of cardiovascular homeostasis, influencing both cardiac preload (plasma volume) and after load (peripheral resistance). The present study reports the identification of specific, high affinity [125I]hU-II binding sites in Sprague-Dawley rat kidney outer medulla by autoradiography and also through membrane radioligand binding (Kd 1.9 +/- 0.9 nM and Bmax 408 +/- 47 amol mm(-2) and Kd 1.4 +/- 0.3 nM and Bmax 51.3 +/- 7.8 fmol mg(-1) protein, respectively). Differences were observed in the binding characteristics within rat strains. Compared to the Sprague-Dawley, Wistar Kyoto (WKY) and spontaneously hypertensive (SHR) rat kidney outer medulla displayed low density < 20 fmol mg(-1) protein and low affinity (> 1 microM) [125I]hU-II binding sites. Thus, the relative contribution of specific U-II binding sites to the physiological actions of U-II in the control of cardiorenal homeostasis is worthy of further investigation.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Ligands,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, G-Protein-Coupled,
http://linkedlifedata.com/resource/pubmed/chemical/Urotensins,
http://linkedlifedata.com/resource/pubmed/chemical/Uts2r protein, rat,
http://linkedlifedata.com/resource/pubmed/chemical/urotensin II
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pubmed:status |
MEDLINE
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pubmed:month |
Jun
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pubmed:issn |
0196-9781
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
27
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1532-7
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pubmed:meshHeading |
pubmed-meshheading:16290260-Animals,
pubmed-meshheading:16290260-Autoradiography,
pubmed-meshheading:16290260-Binding, Competitive,
pubmed-meshheading:16290260-Binding Sites,
pubmed-meshheading:16290260-Humans,
pubmed-meshheading:16290260-Kidney Medulla,
pubmed-meshheading:16290260-Kinetics,
pubmed-meshheading:16290260-Ligands,
pubmed-meshheading:16290260-Protein Binding,
pubmed-meshheading:16290260-Rats,
pubmed-meshheading:16290260-Rats, Inbred SHR,
pubmed-meshheading:16290260-Rats, Inbred WKY,
pubmed-meshheading:16290260-Rats, Sprague-Dawley,
pubmed-meshheading:16290260-Receptors, G-Protein-Coupled,
pubmed-meshheading:16290260-Species Specificity,
pubmed-meshheading:16290260-Urotensins
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pubmed:year |
2006
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pubmed:articleTitle |
Identification and characterization of binding sites for human urotensin-II in Sprague-Dawley rat renal medulla using quantitative receptor autoradiography.
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pubmed:affiliation |
Department of Vascular Biology and Thrombosis, Cardiovascular and Urogenital Center of Excellence for Drug Discovery, GlaxoSmithKline, 709 Swedeland Road, King of Prussia, PA 19406, USA.
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pubmed:publicationType |
Journal Article
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