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http://purl.uniprot.org/citations/12697744http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/12697744http://www.w3.org/2000/01/rdf-schema#comment"The gamma-melanocyte-stimulating hormone (gamma-MSH) is a natriuretic peptide derived from the N-terminal region of proopiomelanocortin (POMC). Evidence suggests that it may be part of the coordinated response to a low-sodium diet (LSD). We tested the effect of the HSD (8% NaCl) compared with LSD (0.07%) on mean arterial pressure (MAP) in mice with targeted disruption of the PC2 gene (PC2(-/-)), necessary for processing of POMC into gamma-MSH, or the melanocortin receptor 3 gene (Mc3r(-/-); the receptor for MSH). In wild-type mice, HSD for 1 week did not alter MAP versus LSD mice, but plasma gamma-MSH immunoreactivity was more than double the LSD value. In contrast, in PC2(-/-) mice, MAP on the LSD was not greater than in wild-type mice, but plasma gamma-MSH was reduced to one-seventh the wild-type value. On the HSD, MAP rose to a markedly hypertensive level while plasma gamma-MSH concentration remained severely depressed. Intravenous infusion of gamma-MSH (0.2 pmol/min) for 30 min to PC2(-/-) mice after 1 week of HSD lowered MAP from hypertensive levels to normal; infusion of alpha-MSH at the same rate had no effect. Injection of 60 fmol of gamma-MSH into the lateral cerebral ventricle of hypertensive mice also lowered MAP to normal. Administration of a stable analogue of gamma-MSH intra-abdominally by microosmotic pump to PC2(-/-) mice prevented the development of hypertension when ingesting the HSD. In mice with targeted disruption of the Mc3r gene, the HSD also led to marked hypertension accompanied by elevated plasma levels of gamma-MSH; infusion of exogenous gamma-MSH to these mice had no effect on MAP. These results strongly suggest that PC2-dependent processing of POMC into gamma-MSH is necessary for the normal response to the HSD. gamma-MSH deficiency results in marked salt-sensitive hypertension that is rapidly improved with exogenous gamma-MSH through a central site of action. alpha-MSH infused at the same rate had no effect on MAP, indicating that the hypertension is a specific consequence of impaired POMC processing into gamma-MSH. Absence of Mc3r produces gamma-MSH resistance and hypertension on the HSD. These findings demonstrate a novel pathway mediating salt-sensitivity of blood pressure."xsd:string
http://purl.uniprot.org/citations/12697744http://purl.org/dc/terms/identifier"doi:10.1172/jci16993"xsd:string
http://purl.uniprot.org/citations/12697744http://purl.uniprot.org/core/author"Cone R.D."xsd:string
http://purl.uniprot.org/citations/12697744http://purl.uniprot.org/core/author"Humphreys M.H."xsd:string
http://purl.uniprot.org/citations/12697744http://purl.uniprot.org/core/author"Pearce D."xsd:string
http://purl.uniprot.org/citations/12697744http://purl.uniprot.org/core/author"Butler A.A."xsd:string
http://purl.uniprot.org/citations/12697744http://purl.uniprot.org/core/author"Ni X.P."xsd:string
http://purl.uniprot.org/citations/12697744http://purl.uniprot.org/core/date"2003"xsd:gYear
http://purl.uniprot.org/citations/12697744http://purl.uniprot.org/core/name"J Clin Invest"xsd:string
http://purl.uniprot.org/citations/12697744http://purl.uniprot.org/core/pages"1251-1258"xsd:string
http://purl.uniprot.org/citations/12697744http://purl.uniprot.org/core/title"Genetic disruption of gamma-melanocyte-stimulating hormone signaling leads to salt-sensitive hypertension in the mouse."xsd:string
http://purl.uniprot.org/citations/12697744http://purl.uniprot.org/core/volume"111"xsd:string
http://purl.uniprot.org/citations/12697744http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/12697744
http://purl.uniprot.org/citations/12697744http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/12697744
http://purl.uniprot.org/uniprot/#_P21661-mappedCitation-12697744http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/12697744
http://purl.uniprot.org/uniprot/#_Q3UZV3-mappedCitation-12697744http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/12697744
http://purl.uniprot.org/uniprot/#_Q3ZAT4-mappedCitation-12697744http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/12697744
http://purl.uniprot.org/uniprot/#_P33033-mappedCitation-12697744http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/12697744
http://purl.uniprot.org/uniprot/#_Q3TYM6-mappedCitation-12697744http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/12697744
http://purl.uniprot.org/uniprot/#_Q3TT48-mappedCitation-12697744http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/12697744
http://purl.uniprot.org/uniprot/#_Q544G7-mappedCitation-12697744http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/12697744
http://purl.uniprot.org/uniprot/#_Q547J8-mappedCitation-12697744http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/12697744
http://purl.uniprot.org/uniprot/#_Q9D3A4-mappedCitation-12697744http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/12697744
http://purl.uniprot.org/uniprot/P33033http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/12697744