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著作: [島袋 充生]/Higa N/Masuzaki H/[佐田 政隆]/Ueda S/Impact of individual metabolic risk components or its clustering on endothelial and smooth muscle cell function in men./[Cardiovascular Diabetology]

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EID
312429
EOID
835920
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0
LastModified
2016年9月6日(火) 21:02:24
Operator
大家 隆弘
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TRUE
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Owner
佐田 政隆
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種別 必須 学術論文(審査論文)
言語 必須 英語
招待 推奨
審査 推奨
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著者 必須
  1. 島袋 充生
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    学籍番号 推奨
  2. (英) Higa N
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  3. (英) Masuzaki H
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  4. 佐田 政隆([徳島大学.大学院医歯薬学研究部.医学域.医科学部門.内科系.循環器内科学])
    役割 任意
    貢献度 任意
    学籍番号 推奨
  5. (英) Ueda S
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    貢献度 任意
    学籍番号 推奨
題名 必須

(英) Impact of individual metabolic risk components or its clustering on endothelial and smooth muscle cell function in men.

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(英) Impaired vasoreactivity is often observed in subjects with metabolic syndrome, a condition that includes the presence of a specific cluster of risk factors for obesity and cardiovascular disease. However, hierarchical causes in the impaired vasoreactivity have not been clarified. We evaluated the impact of individual metabolic risk components or its clustering under the condition of insulin resistance on endothelial and smooth muscle cell function. Vascular reactivity to acetylcholine (Ach), with or without nitric oxide synthase (NOS) inhibitor N (G)-monomethyl-L-arginine (L-NMMA), or sodium nitroprusside (SNP) by forearm venous occlusion plethysmography and insulin sensitivity index (M mg/kg/min) in euglycemic clamp were measured in men without (n = 18, control group) or with (n = 19, metabolic syndrome group) metabolic syndrome. (1) Ach-induced maximal forearm blood flow (maxFBF) was impaired in subjects with metabolic syndrome. In particular, the NOS-dependent component of Ach-induced maxFBF was selectively decreased, while the NOS-independent component remained relatively unchanged. (2) Ach-induced maxFBF and ∆Ach-induced maxFBF with L-NMMA were correlated with waist circumference, glucose, and triglycerides, and most strongly correlated with visceral fat area, adiponectin, and M. (3) Multivariate regression analysis indicated that individual metabolic risk components explained Ach-induced maxFBF by 4-21 %. Clustering of all metabolic risk components increased this to 35 %, and the presence of metabolic syndrome explained 30 %, indicating that defining metabolic syndrome can effectively predict impairment of endothelial dysfunction. Endothelial dysfunction was correlated with individual metabolic risk components, but more strongly with clustering of the components under a condition with low insulin sensitivity. We suggest that in subjects with metabolic syndrome, endothelial function is impaired by multiple cardiovascular risk factors exclusively when under the condition of insulin insensitivity and also that defining metabolic syndrome can effectively predict impairment of endothelial dysfunction.

キーワード 推奨
発行所 推奨 BioMed Central Ltd.
誌名 必須 Cardiovascular Diabetology([BioMed Central Ltd.])
(eISSN: 1475-2840)
ISSN 任意 1475-2840
ISSN: 1475-2840 (eISSN: 1475-2840)
Title: Cardiovascular diabetology
Title(ISO): Cardiovasc Diabetol
Publisher: BioMed Central
 (NLM Catalog  (Scopus  (CrossRef (Scopus information is found. [need login])
必須 15
必須 1
必須 77 77
都市 任意
年月日 必須 2016年 5月 17日
URL 任意
DOI 任意 10.1186/s12933-016-0394-5    (→Scopusで検索)
PMID 任意 27188597    (→Scopusで検索)
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  1. (英) Article.ELocationID: 10.1186/s12933-016-0394-5

  2. (英) Article.PublicationTypeList.PublicationType: Journal Article

  3. (英) Article.PublicationTypeList.PublicationType: Research Support, Non-U.S. Gov't

  4. (英) OtherID: PMC4869187

  5. (英) KeywordList.Keyword: Endothelial function

  6. (英) KeywordList.Keyword: Insulin resistance

  7. (英) KeywordList.Keyword: Metabolic syndrome

  8. (英) KeywordList.Keyword: Obesity