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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
8973
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pubmed:dateCreated |
1995-9-14
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pubmed:abstractText |
To study whether vascular dysfunction in hypercholesterolaemia is reversible, we investigated patients without overt arterial disease who were taking maintenance treatment for hypercholesterolaemia. Medication was stopped for 2 weeks, reinstituted for 12 weeks, and again stopped for 6 weeks. During both maintenance treatment and the 12 weeks of step-up medication the lipid profile was improved but did not return to normal. Dose-response curves for serotonin-induced vasodilatation, an index of nitric oxide-dependent vasodilatation, showed a comparable and significant rightward shift after a medication-free period of 2 and 6 weeks compared with control subjects, indicating endothelial dysfunction, which was already maximum after 2 weeks. After 12 weeks of lipid-lowering medication, the difference in endothelial function between controls and patients had disappeared. Co-infusion of L-arginine, the substrate for nitric oxide synthase, returned the impaired serotonin response during hypercholesterolaemia to normal, but had no effect on this response in controls or in patients while on lipid-lowering medication. Neither endothelium-independent vasorelaxation, assessed by sodium nitroprusside infusion, nor vasoconstriction induced by the nitric oxide blocker L-NMMA, were different between controls and patients, whether the latter were on or off lipid-lowering medication. Our results show an L-arginine-sensitive, impaired nitric-oxide-mediated vascular relaxation of forearm resistance vessels in hypercholesterolaemia which is reproducible, and reversible after short-term lipid-lowering therapy. Demonstration of such changes in this readily accessible vascular bed will allow larger trials assessing vascular function during lipid-lowering therapy to be done.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Arginine,
http://linkedlifedata.com/resource/pubmed/chemical/Cholesterol,
http://linkedlifedata.com/resource/pubmed/chemical/Cholestyramine Resin,
http://linkedlifedata.com/resource/pubmed/chemical/Hypolipidemic Agents,
http://linkedlifedata.com/resource/pubmed/chemical/Lovastatin,
http://linkedlifedata.com/resource/pubmed/chemical/Nitroprusside,
http://linkedlifedata.com/resource/pubmed/chemical/Serotonin,
http://linkedlifedata.com/resource/pubmed/chemical/Simvastatin,
http://linkedlifedata.com/resource/pubmed/chemical/omega-N-Methylarginine
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pubmed:status |
MEDLINE
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pubmed:month |
Aug
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pubmed:issn |
0140-6736
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
19
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pubmed:volume |
346
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
467-71
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pubmed:dateRevised |
2010-11-18
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pubmed:meshHeading |
pubmed-meshheading:7637480-Adult,
pubmed-meshheading:7637480-Arginine,
pubmed-meshheading:7637480-Blood Pressure,
pubmed-meshheading:7637480-Cholesterol,
pubmed-meshheading:7637480-Cholestyramine Resin,
pubmed-meshheading:7637480-Dose-Response Relationship, Drug,
pubmed-meshheading:7637480-Drug Therapy, Combination,
pubmed-meshheading:7637480-Female,
pubmed-meshheading:7637480-Forearm,
pubmed-meshheading:7637480-Humans,
pubmed-meshheading:7637480-Hyperlipoproteinemia Type II,
pubmed-meshheading:7637480-Hypolipidemic Agents,
pubmed-meshheading:7637480-Infusions, Intravenous,
pubmed-meshheading:7637480-Lovastatin,
pubmed-meshheading:7637480-Male,
pubmed-meshheading:7637480-Nitroprusside,
pubmed-meshheading:7637480-Regional Blood Flow,
pubmed-meshheading:7637480-Serotonin,
pubmed-meshheading:7637480-Simvastatin,
pubmed-meshheading:7637480-Vasodilation,
pubmed-meshheading:7637480-omega-N-Methylarginine
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pubmed:year |
1995
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pubmed:articleTitle |
Vascular function in the forearm of hypercholesterolaemic patients off and on lipid-lowering medication.
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pubmed:affiliation |
Department of Nephrology, University Hospital Utrecht, The Netherlands.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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