pubmed-article:10215647 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:10215647 | lifeskim:mentions | umls-concept:C0014653 | lld:lifeskim |
pubmed-article:10215647 | lifeskim:mentions | umls-concept:C0019010 | lld:lifeskim |
pubmed-article:10215647 | lifeskim:mentions | umls-concept:C0013725 | lld:lifeskim |
pubmed-article:10215647 | lifeskim:mentions | umls-concept:C0037473 | lld:lifeskim |
pubmed-article:10215647 | lifeskim:mentions | umls-concept:C0387583 | lld:lifeskim |
pubmed-article:10215647 | lifeskim:mentions | umls-concept:C0021467 | lld:lifeskim |
pubmed-article:10215647 | lifeskim:mentions | umls-concept:C1280500 | lld:lifeskim |
pubmed-article:10215647 | lifeskim:mentions | umls-concept:C0205369 | lld:lifeskim |
pubmed-article:10215647 | lifeskim:mentions | umls-concept:C1980011 | lld:lifeskim |
pubmed-article:10215647 | lifeskim:mentions | umls-concept:C0021469 | lld:lifeskim |
pubmed-article:10215647 | pubmed:issue | 2 | lld:pubmed |
pubmed-article:10215647 | pubmed:dateCreated | 1999-5-20 | lld:pubmed |
pubmed-article:10215647 | pubmed:abstractText | Conventional nonsteroidal anti-inflammatory drugs inhibit both cyclooxygenase (Cox) isoforms (Cox-1 and Cox-2) and may be associated with nephrotoxicity. The present study was undertaken to assess the renal effects of the specific Cox-2 inhibitor, MK-966. Healthy older adults (n = 36) were admitted to a clinical research unit, placed on a fixed sodium intake, and randomized under double-blind conditions to receive the specific Cox-2 inhibitor, MK-966 (50 mg every day), a nonspecific Cox-1/Cox-2 inhibitor, indomethacin (50 mg t.i.d.), or placebo for 2 weeks. All treatments were well tolerated. Both active regimens were associated with a transient but significant decline in urinary sodium excretion during the first 72 h of treatment. Blood pressure and body weight did not change significantly in any group. The glomerular filtration rate (GFR) was decreased by indomethacin but was not changed significantly by MK-966 treatment. Thromboxane biosynthesis by platelets was inhibited by indomethacin only. The urinary excretion of the prostacyclin metabolite 2,3-dinor-6-keto prostaglandin F1alpha was decreased by both MK-966 and indomethacin and was unchanged by placebo. Cox-2 may play a role in the systemic biosynthesis of prostacyclin in healthy humans. Selective inhibition of Cox-2 by MK-966 caused a clinically insignificant and transient retention of sodium, but no depression of GFR. Inhibition of both Cox isoforms by indomethacin caused transient sodium retention and a decline in GFR. Our data suggest that acute sodium retention by nonsteroidal anti-inflammatory drugs in healthy elderly subjects is mediated by the inhibition of Cox-2, whereas depression of GFR is due to inhibition of Cox-1. | lld:pubmed |
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pubmed-article:10215647 | pubmed:language | eng | lld:pubmed |
pubmed-article:10215647 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:10215647 | pubmed:citationSubset | IM | lld:pubmed |
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pubmed-article:10215647 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:10215647 | pubmed:month | May | lld:pubmed |
pubmed-article:10215647 | pubmed:issn | 0022-3565 | lld:pubmed |
pubmed-article:10215647 | pubmed:author | pubmed-author:LasseterK CKC | lld:pubmed |
pubmed-article:10215647 | pubmed:author | pubmed-author:FitzGeraldG... | lld:pubmed |
pubmed-article:10215647 | pubmed:author | pubmed-author:KapoorSS | lld:pubmed |
pubmed-article:10215647 | pubmed:author | pubmed-author:GertzB JBJ | lld:pubmed |
pubmed-article:10215647 | pubmed:author | pubmed-author:QuanHH | lld:pubmed |
pubmed-article:10215647 | pubmed:author | pubmed-author:MorrisonB WBW | lld:pubmed |
pubmed-article:10215647 | pubmed:author | pubmed-author:AntesLL | lld:pubmed |
pubmed-article:10215647 | pubmed:author | pubmed-author:McAdamBB | lld:pubmed |
pubmed-article:10215647 | pubmed:author | pubmed-author:Catella-Lawso... | lld:pubmed |
pubmed-article:10215647 | pubmed:author | pubmed-author:KujubuDD | lld:pubmed |
pubmed-article:10215647 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:10215647 | pubmed:volume | 289 | lld:pubmed |
pubmed-article:10215647 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:10215647 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:10215647 | pubmed:pagination | 735-41 | lld:pubmed |
pubmed-article:10215647 | pubmed:dateRevised | 2007-11-15 | lld:pubmed |
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pubmed-article:10215647 | pubmed:year | 1999 | lld:pubmed |
pubmed-article:10215647 | pubmed:articleTitle | Effects of specific inhibition of cyclooxygenase-2 on sodium balance, hemodynamics, and vasoactive eicosanoids. | lld:pubmed |
pubmed-article:10215647 | pubmed:affiliation | University of Pennsylvania, School of Medicine, Philadelphia, Pennsylvania, USA. francesca@spirit.GCRC.upenn.edu | lld:pubmed |
pubmed-article:10215647 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:10215647 | pubmed:publicationType | Clinical Trial | lld:pubmed |
pubmed-article:10215647 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
pubmed-article:10215647 | pubmed:publicationType | Randomized Controlled Trial | lld:pubmed |
pubmed-article:10215647 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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