rdf:type |
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lifeskim:mentions |
umls-concept:C0009813,
umls-concept:C0018036,
umls-concept:C0021467,
umls-concept:C0021469,
umls-concept:C0205178,
umls-concept:C0205191,
umls-concept:C0205263,
umls-concept:C0599946,
umls-concept:C1261287,
umls-concept:C1760025,
umls-concept:C2684089
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pubmed:issue |
3
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pubmed:dateCreated |
2009-11-17
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pubmed:abstractText |
We explored the role of 20-hydroxy-5Z, 8Z, 11Z, 14Z-eicosatetraenoic acid (20-HETE) in oxygen-induced vasoconstriction in a normal renin form of hypertension [the 1 kidney-1 clip Goldblatt hypertensive rat (1K1C)] and a high renin form of hypertension [the 2 kidney-1 clip Goldblatt hypertensive rat (2K1C)]. A silver clip was placed around the left renal artery of adult Sprague-Dawley males. The right kidney was removed in the 1K1C group and left intact in the 2K1C group. Arteriolar responses to elevation of O(2) concentration in the superfusion solution from 0% O(2) to 21% O(2) were determined in the in situ cremaster muscle before and after inhibition of cytochrome P450 4A omega-hydroxylase (CYP450 4A) with N-methyl-sulfonyl-12, 12-dibromododec-11-enamide (DDMS). Arteriolar constriction to elevated PO(2) was enhanced in the chronic 1K1C but not the acute 1K1C or 2K1C. DDMS eliminated O(2)-induced arteriolar constriction in the 9-week 1K1C, but had no effect in the 2-week 1K1C, and only partially inhibited O(2)-induced constriction of arterioles in the 4-week 2K1C rat. These findings indicate that although the CYP4A/20-HETE system contributes to arteriolar constriction in response to elevated PO(2) in the established stage of 1K1C renovascular hypertension, physiological alterations in other mechanisms are the primary determinants of O(2)-induced constriction of arterioles in the early and developing stages of 1K1C and 2K1C hypertension.
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pubmed:grant |
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/20-hydroxy-5,8,11,14-eicosatetraenoi...,
http://linkedlifedata.com/resource/pubmed/chemical/Amides,
http://linkedlifedata.com/resource/pubmed/chemical/Cytochrome P-450 Enzyme System,
http://linkedlifedata.com/resource/pubmed/chemical/DDMS,
http://linkedlifedata.com/resource/pubmed/chemical/Enzyme Inhibitors,
http://linkedlifedata.com/resource/pubmed/chemical/Hydroxyeicosatetraenoic Acids,
http://linkedlifedata.com/resource/pubmed/chemical/Oxygen,
http://linkedlifedata.com/resource/pubmed/chemical/Sulfones,
http://linkedlifedata.com/resource/pubmed/chemical/cytochrome P-450 omega-hydroxylase
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pubmed:status |
MEDLINE
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pubmed:month |
Dec
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pubmed:issn |
1095-9319
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pubmed:author |
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pubmed:issnType |
Electronic
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pubmed:volume |
78
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
442-6
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pubmed:dateRevised |
2011-3-3
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pubmed:meshHeading |
pubmed-meshheading:19761780-Amides,
pubmed-meshheading:19761780-Animals,
pubmed-meshheading:19761780-Arterioles,
pubmed-meshheading:19761780-Chronic Disease,
pubmed-meshheading:19761780-Cytochrome P-450 Enzyme System,
pubmed-meshheading:19761780-Disease Models, Animal,
pubmed-meshheading:19761780-Enzyme Inhibitors,
pubmed-meshheading:19761780-Hydroxyeicosatetraenoic Acids,
pubmed-meshheading:19761780-Hypertension, Renovascular,
pubmed-meshheading:19761780-Male,
pubmed-meshheading:19761780-Muscle, Skeletal,
pubmed-meshheading:19761780-Nephrectomy,
pubmed-meshheading:19761780-Oxygen,
pubmed-meshheading:19761780-Rats,
pubmed-meshheading:19761780-Rats, Sprague-Dawley,
pubmed-meshheading:19761780-Sulfones,
pubmed-meshheading:19761780-Vasoconstriction
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pubmed:year |
2009
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pubmed:articleTitle |
CYP450 4A inhibition attenuates O2 induced arteriolar constriction in chronic but not acute Goldblatt hypertension.
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pubmed:affiliation |
Medical College of Wisconsin; Milwaukee, WI 53226, USA. mpkunert@uwm.edu
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pubmed:publicationType |
Journal Article,
Research Support, N.I.H., Extramural
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