Cargando…

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

BACKGROUND: 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 eval...

Descripción completa

Detalles Bibliográficos
Autores principales: Shimabukuro, Michio, Higa, Namio, Masuzaki, Hiroaki, Sata, Masataka, Ueda, Shinichiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4869187/
https://www.ncbi.nlm.nih.gov/pubmed/27188597
http://dx.doi.org/10.1186/s12933-016-0394-5
_version_ 1782432269368033280
author Shimabukuro, Michio
Higa, Namio
Masuzaki, Hiroaki
Sata, Masataka
Ueda, Shinichiro
author_facet Shimabukuro, Michio
Higa, Namio
Masuzaki, Hiroaki
Sata, Masataka
Ueda, Shinichiro
author_sort Shimabukuro, Michio
collection PubMed
description BACKGROUND: 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. METHODS: 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. RESULTS: (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. CONCLUSIONS: 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.
format Online
Article
Text
id pubmed-4869187
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-48691872016-05-18 Impact of individual metabolic risk components or its clustering on endothelial and smooth muscle cell function in men Shimabukuro, Michio Higa, Namio Masuzaki, Hiroaki Sata, Masataka Ueda, Shinichiro Cardiovasc Diabetol Original Investigation BACKGROUND: 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. METHODS: 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. RESULTS: (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. CONCLUSIONS: 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. BioMed Central 2016-05-17 /pmc/articles/PMC4869187/ /pubmed/27188597 http://dx.doi.org/10.1186/s12933-016-0394-5 Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Original Investigation
Shimabukuro, Michio
Higa, Namio
Masuzaki, Hiroaki
Sata, Masataka
Ueda, Shinichiro
Impact of individual metabolic risk components or its clustering on endothelial and smooth muscle cell function in men
title Impact of individual metabolic risk components or its clustering on endothelial and smooth muscle cell function in men
title_full Impact of individual metabolic risk components or its clustering on endothelial and smooth muscle cell function in men
title_fullStr Impact of individual metabolic risk components or its clustering on endothelial and smooth muscle cell function in men
title_full_unstemmed Impact of individual metabolic risk components or its clustering on endothelial and smooth muscle cell function in men
title_short Impact of individual metabolic risk components or its clustering on endothelial and smooth muscle cell function in men
title_sort impact of individual metabolic risk components or its clustering on endothelial and smooth muscle cell function in men
topic Original Investigation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4869187/
https://www.ncbi.nlm.nih.gov/pubmed/27188597
http://dx.doi.org/10.1186/s12933-016-0394-5
work_keys_str_mv AT shimabukuromichio impactofindividualmetabolicriskcomponentsoritsclusteringonendothelialandsmoothmusclecellfunctioninmen
AT higanamio impactofindividualmetabolicriskcomponentsoritsclusteringonendothelialandsmoothmusclecellfunctioninmen
AT masuzakihiroaki impactofindividualmetabolicriskcomponentsoritsclusteringonendothelialandsmoothmusclecellfunctioninmen
AT satamasataka impactofindividualmetabolicriskcomponentsoritsclusteringonendothelialandsmoothmusclecellfunctioninmen
AT uedashinichiro impactofindividualmetabolicriskcomponentsoritsclusteringonendothelialandsmoothmusclecellfunctioninmen