Cargando…
Insulin-induced changes in skeletal muscle microvascular perfusion are dependent upon perivascular adipose tissue in women
AIMS/HYPOTHESIS: Obesity increases the risk of cardiovascular disease and type 2 diabetes, partly through reduced insulin-induced microvascular vasodilation, which causes impairment of glucose delivery and uptake. We studied whether perivascular adipose tissue (PVAT) controls insulin-induced vasodil...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4499111/ https://www.ncbi.nlm.nih.gov/pubmed/26003324 http://dx.doi.org/10.1007/s00125-015-3606-8 |
_version_ | 1782380726800351232 |
---|---|
author | Meijer, Rick I. Serné, Erik H. Korkmaz, H. Ibrahim van der Peet, Donald L. de Boer, Michiel P. Niessen, Hans W. M. van Hinsbergh, Victor W. M. Yudkin, John S. Smulders, Yvo M. Eringa, Etto C. |
author_facet | Meijer, Rick I. Serné, Erik H. Korkmaz, H. Ibrahim van der Peet, Donald L. de Boer, Michiel P. Niessen, Hans W. M. van Hinsbergh, Victor W. M. Yudkin, John S. Smulders, Yvo M. Eringa, Etto C. |
author_sort | Meijer, Rick I. |
collection | PubMed |
description | AIMS/HYPOTHESIS: Obesity increases the risk of cardiovascular disease and type 2 diabetes, partly through reduced insulin-induced microvascular vasodilation, which causes impairment of glucose delivery and uptake. We studied whether perivascular adipose tissue (PVAT) controls insulin-induced vasodilation in human muscle, and whether altered properties of PVAT relate to reduced insulin-induced vasodilation in obesity. METHODS: Insulin-induced microvascular recruitment was measured using contrast enhanced ultrasound (CEU), before and during a hyperinsulinaemic–euglycaemic clamp in 15 lean and 18 obese healthy women (18–55 years). Surgical skeletal muscle biopsies were taken on a separate day to study perivascular adipocyte size in histological slices, as well as to study ex vivo insulin-induced vasoreactivity in microvessels in the absence and presence of PVAT in the pressure myograph. Statistical mediation of the relation between BMI and microvascular recruitment by PVAT was studied in a mediation model. RESULTS: Obese women showed impaired insulin-induced microvascular recruitment and lower metabolic insulin sensitivity compared with lean women. Microvascular recruitment was a mediator in the association between obesity and insulin sensitivity. Perivascular adipocyte size, determined in skeletal muscle biopsies, was larger in obese than in lean women, and statistically explained the difference in microvascular recruitment between obese and lean women. PVAT from lean women enhanced insulin-induced vasodilation in isolated skeletal muscle resistance arteries, while PVAT from obese women revealed insulin-induced vasoconstriction. CONCLUSIONS/INTERPRETATION: PVAT from lean women enhances insulin-induced vasodilation and microvascular recruitment whereas PVAT from obese women does not. PVAT adipocyte size partly explains the difference in insulin-induced microvascular recruitment between lean and obese women. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00125-015-3606-8) contains peer-reviewed but unedited supplementary material, which is available to authorised users. |
format | Online Article Text |
id | pubmed-4499111 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-44991112015-07-16 Insulin-induced changes in skeletal muscle microvascular perfusion are dependent upon perivascular adipose tissue in women Meijer, Rick I. Serné, Erik H. Korkmaz, H. Ibrahim van der Peet, Donald L. de Boer, Michiel P. Niessen, Hans W. M. van Hinsbergh, Victor W. M. Yudkin, John S. Smulders, Yvo M. Eringa, Etto C. Diabetologia Article AIMS/HYPOTHESIS: Obesity increases the risk of cardiovascular disease and type 2 diabetes, partly through reduced insulin-induced microvascular vasodilation, which causes impairment of glucose delivery and uptake. We studied whether perivascular adipose tissue (PVAT) controls insulin-induced vasodilation in human muscle, and whether altered properties of PVAT relate to reduced insulin-induced vasodilation in obesity. METHODS: Insulin-induced microvascular recruitment was measured using contrast enhanced ultrasound (CEU), before and during a hyperinsulinaemic–euglycaemic clamp in 15 lean and 18 obese healthy women (18–55 years). Surgical skeletal muscle biopsies were taken on a separate day to study perivascular adipocyte size in histological slices, as well as to study ex vivo insulin-induced vasoreactivity in microvessels in the absence and presence of PVAT in the pressure myograph. Statistical mediation of the relation between BMI and microvascular recruitment by PVAT was studied in a mediation model. RESULTS: Obese women showed impaired insulin-induced microvascular recruitment and lower metabolic insulin sensitivity compared with lean women. Microvascular recruitment was a mediator in the association between obesity and insulin sensitivity. Perivascular adipocyte size, determined in skeletal muscle biopsies, was larger in obese than in lean women, and statistically explained the difference in microvascular recruitment between obese and lean women. PVAT from lean women enhanced insulin-induced vasodilation in isolated skeletal muscle resistance arteries, while PVAT from obese women revealed insulin-induced vasoconstriction. CONCLUSIONS/INTERPRETATION: PVAT from lean women enhances insulin-induced vasodilation and microvascular recruitment whereas PVAT from obese women does not. PVAT adipocyte size partly explains the difference in insulin-induced microvascular recruitment between lean and obese women. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00125-015-3606-8) contains peer-reviewed but unedited supplementary material, which is available to authorised users. Springer Berlin Heidelberg 2015-05-24 2015 /pmc/articles/PMC4499111/ /pubmed/26003324 http://dx.doi.org/10.1007/s00125-015-3606-8 Text en © The Author(s) 2015 Open Access This 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. |
spellingShingle | Article Meijer, Rick I. Serné, Erik H. Korkmaz, H. Ibrahim van der Peet, Donald L. de Boer, Michiel P. Niessen, Hans W. M. van Hinsbergh, Victor W. M. Yudkin, John S. Smulders, Yvo M. Eringa, Etto C. Insulin-induced changes in skeletal muscle microvascular perfusion are dependent upon perivascular adipose tissue in women |
title | Insulin-induced changes in skeletal muscle microvascular perfusion are dependent upon perivascular adipose tissue in women |
title_full | Insulin-induced changes in skeletal muscle microvascular perfusion are dependent upon perivascular adipose tissue in women |
title_fullStr | Insulin-induced changes in skeletal muscle microvascular perfusion are dependent upon perivascular adipose tissue in women |
title_full_unstemmed | Insulin-induced changes in skeletal muscle microvascular perfusion are dependent upon perivascular adipose tissue in women |
title_short | Insulin-induced changes in skeletal muscle microvascular perfusion are dependent upon perivascular adipose tissue in women |
title_sort | insulin-induced changes in skeletal muscle microvascular perfusion are dependent upon perivascular adipose tissue in women |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4499111/ https://www.ncbi.nlm.nih.gov/pubmed/26003324 http://dx.doi.org/10.1007/s00125-015-3606-8 |
work_keys_str_mv | AT meijerricki insulininducedchangesinskeletalmusclemicrovascularperfusionaredependentuponperivascularadiposetissueinwomen AT serneerikh insulininducedchangesinskeletalmusclemicrovascularperfusionaredependentuponperivascularadiposetissueinwomen AT korkmazhibrahim insulininducedchangesinskeletalmusclemicrovascularperfusionaredependentuponperivascularadiposetissueinwomen AT vanderpeetdonaldl insulininducedchangesinskeletalmusclemicrovascularperfusionaredependentuponperivascularadiposetissueinwomen AT deboermichielp insulininducedchangesinskeletalmusclemicrovascularperfusionaredependentuponperivascularadiposetissueinwomen AT niessenhanswm insulininducedchangesinskeletalmusclemicrovascularperfusionaredependentuponperivascularadiposetissueinwomen AT vanhinsberghvictorwm insulininducedchangesinskeletalmusclemicrovascularperfusionaredependentuponperivascularadiposetissueinwomen AT yudkinjohns insulininducedchangesinskeletalmusclemicrovascularperfusionaredependentuponperivascularadiposetissueinwomen AT smuldersyvom insulininducedchangesinskeletalmusclemicrovascularperfusionaredependentuponperivascularadiposetissueinwomen AT eringaettoc insulininducedchangesinskeletalmusclemicrovascularperfusionaredependentuponperivascularadiposetissueinwomen |