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dc.contributor.author Szijártó István András
dc.contributor.author Molnár Gergő Attila
dc.contributor.author Mikolás Esztella Zsóka
dc.contributor.author Fisi Viktória
dc.contributor.author Cseh Judit
dc.contributor.author Laczy Boglárka
dc.contributor.author Kovács Tibor
dc.contributor.author Böddi Katalin
dc.contributor.author Takátsy Anikó
dc.contributor.author Maik Gollasch
dc.contributor.author Koller Ákos
dc.contributor.author Wittmann István
dc.date.accessioned 2015-02-04T08:29:14Z
dc.date.available 2015-02-04T08:29:14Z
dc.date.issued 2014
dc.identifier.citation pagination=749-752;journalVolume=46;journalIssueNumber=11;journalTitle=HORMONE AND METABOLIC RESEARCH; hu
dc.identifier.uri http://repo.lib.semmelweis.hu//handle/123456789/1317
dc.identifier.uri doi:10.1055/s-0034-1387701
dc.description.abstract Previous studies have shown that in diabetes mellitus, insulin-induced relaxation of arteries is impaired and the level of ortho-tyrosine (o-Tyr), an oxidized amino acid is increased. Thus, we hypothesized that elevated vascular level of o-Tyr contributes to the impairment of insulin-induced vascular relaxation. Rats were fed with o-Tyr for 4 weeks. Insulin-induced vasomotor responses of isolated femoral artery were studied using wire myography. Vascular o-Tyr content was measured by HPLC, whereas immunoblot analyses were preformed to detect eNOS phosphorylation. Sustained oral supplementation of rats with o-Tyr increased the content of o-Tyr in the arterial wall and significantly reduced the relaxations to insulin. Sustained supplementation of cultured endothelial cells with o-Tyr increased the incorporation of o-Tyr and mitigated eNOS Ser (1 177) phosphorylation to insulin. Increasing arterial wall o-Tyr level attenuates insulin-induced relaxation - at least in part - by decreasing eNOS activation. Elevated level of o-Tyr could be an underlying mechanism for vasomotor dysfunction in diabetes mellitus. hu
dc.relation.ispartof urn:issn:0018-5043
dc.title Elevated Vascular Level of ortho-Tyrosine Contributes to the Impairment of Insulin-Induced Arterial Relaxation. hu
dc.type Journal Article hu
dc.date.updated 2015-02-04T08:26:49Z
dc.language.rfc3066 en hu
dc.identifier.mtmt 2743437
dc.identifier.wos 000343583200001
dc.identifier.pubmed 25208272
dc.contributor.department PTE/Szentágothai János Kutatóközpont
dc.contributor.department SE/AOK/I/Kórélettani Intézet
dc.contributor.institution Pécsi Tudományegyetem
dc.contributor.institution Semmelweis Egyetem


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