Impaired Circulating Angiogenic Cells Mobilization and Metalloproteinase-9 Activity after Dynamic Exercise in Early Metabolic Syndrome

Increased levels of adhesion molecules or metalloproteinases (MMPs) may indicate endothelial dysfunction. Exercise mobilizes circulating angiogenic cells (CACs) from bone marrow in healthy subjects, improving vascular function. However, it is unclear whether this mechanism is preserved in the early...

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Main Authors: Natalia G. Rocha, Allan R. K. Sales, Leticia A. Penedo, Felipe S. Pereira, Mayra S. Silva, Renan L. Miranda, Jemima F. R. Silva, Bruno M. Silva, Aline A. Santos, Antonio C. L. Nobrega
Format: Article
Language:English
Published: Hindawi Limited 2015-01-01
Series:BioMed Research International
Online Access:http://dx.doi.org/10.1155/2015/920356
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spelling doaj-54cafbf12a1c43fdb649d134d65be7322020-11-24T23:37:45ZengHindawi LimitedBioMed Research International2314-61332314-61412015-01-01201510.1155/2015/920356920356Impaired Circulating Angiogenic Cells Mobilization and Metalloproteinase-9 Activity after Dynamic Exercise in Early Metabolic SyndromeNatalia G. Rocha0Allan R. K. Sales1Leticia A. Penedo2Felipe S. Pereira3Mayra S. Silva4Renan L. Miranda5Jemima F. R. Silva6Bruno M. Silva7Aline A. Santos8Antonio C. L. Nobrega9Laboratory of Exercise Sciences, Department of Physiology and Pharmacology, Fluminense Federal University, 24210-130 Niterói, RJ, BrazilLaboratory of Exercise Sciences, Department of Physiology and Pharmacology, Fluminense Federal University, 24210-130 Niterói, RJ, BrazilLaboratory of Exercise Sciences, Department of Physiology and Pharmacology, Fluminense Federal University, 24210-130 Niterói, RJ, BrazilLaboratory of Exercise Sciences, Department of Physiology and Pharmacology, Fluminense Federal University, 24210-130 Niterói, RJ, BrazilLaboratory of Exercise Sciences, Department of Physiology and Pharmacology, Fluminense Federal University, 24210-130 Niterói, RJ, BrazilLaboratory of Exercise Sciences, Department of Physiology and Pharmacology, Fluminense Federal University, 24210-130 Niterói, RJ, BrazilLaboratory of Exercise Sciences, Department of Physiology and Pharmacology, Fluminense Federal University, 24210-130 Niterói, RJ, BrazilDepartment of Physiology, Section of Exercise Physiology, Federal University of São Paulo, 04023-062 São Paulo, SP, BrazilLaboratory of Exercise Sciences, Department of Physiology and Pharmacology, Fluminense Federal University, 24210-130 Niterói, RJ, BrazilLaboratory of Exercise Sciences, Department of Physiology and Pharmacology, Fluminense Federal University, 24210-130 Niterói, RJ, BrazilIncreased levels of adhesion molecules or metalloproteinases (MMPs) may indicate endothelial dysfunction. Exercise mobilizes circulating angiogenic cells (CACs) from bone marrow in healthy subjects, improving vascular function. However, it is unclear whether this mechanism is preserved in the early stages of metabolic syndrome (early MetS). We aimed to evaluate the acute effects of exercise on adhesion molecules, angiogenic factors, MMPs, and CACs in early MetS. Fifteen subjects with early MetS and nine healthy controls underwent an exercise session and a nonexercise session, randomly. Adhesion molecules, angiogenic factors, CACs, and MMPs were evaluated before and after exercise or nonexercise sessions. At baseline, levels of sE-selectin, sICAM-1, and MMP-9 were higher in early MetS than in controls (P≤0.03). After exercise, sE-selectin, sICAM-1, and MMP-9 levels were still higher in early MetS (P<0.05). Subjects with early MetS presented less CACs (P=0.02) and higher MMP-9 activity (P≤0.04), while healthy controls presented higher MMP-2 activity after exercise. There was no difference between moments in nonexercise session (P>0.05). In conclusion, subjects with early MetS already presented impaired endothelial function at rest along with a decrease in CACs and an increase in MMP-9 activity in response to exercise.http://dx.doi.org/10.1155/2015/920356
collection DOAJ
language English
format Article
sources DOAJ
author Natalia G. Rocha
Allan R. K. Sales
Leticia A. Penedo
Felipe S. Pereira
Mayra S. Silva
Renan L. Miranda
Jemima F. R. Silva
Bruno M. Silva
Aline A. Santos
Antonio C. L. Nobrega
spellingShingle Natalia G. Rocha
Allan R. K. Sales
Leticia A. Penedo
Felipe S. Pereira
Mayra S. Silva
Renan L. Miranda
Jemima F. R. Silva
Bruno M. Silva
Aline A. Santos
Antonio C. L. Nobrega
Impaired Circulating Angiogenic Cells Mobilization and Metalloproteinase-9 Activity after Dynamic Exercise in Early Metabolic Syndrome
BioMed Research International
author_facet Natalia G. Rocha
Allan R. K. Sales
Leticia A. Penedo
Felipe S. Pereira
Mayra S. Silva
Renan L. Miranda
Jemima F. R. Silva
Bruno M. Silva
Aline A. Santos
Antonio C. L. Nobrega
author_sort Natalia G. Rocha
title Impaired Circulating Angiogenic Cells Mobilization and Metalloproteinase-9 Activity after Dynamic Exercise in Early Metabolic Syndrome
title_short Impaired Circulating Angiogenic Cells Mobilization and Metalloproteinase-9 Activity after Dynamic Exercise in Early Metabolic Syndrome
title_full Impaired Circulating Angiogenic Cells Mobilization and Metalloproteinase-9 Activity after Dynamic Exercise in Early Metabolic Syndrome
title_fullStr Impaired Circulating Angiogenic Cells Mobilization and Metalloproteinase-9 Activity after Dynamic Exercise in Early Metabolic Syndrome
title_full_unstemmed Impaired Circulating Angiogenic Cells Mobilization and Metalloproteinase-9 Activity after Dynamic Exercise in Early Metabolic Syndrome
title_sort impaired circulating angiogenic cells mobilization and metalloproteinase-9 activity after dynamic exercise in early metabolic syndrome
publisher Hindawi Limited
series BioMed Research International
issn 2314-6133
2314-6141
publishDate 2015-01-01
description Increased levels of adhesion molecules or metalloproteinases (MMPs) may indicate endothelial dysfunction. Exercise mobilizes circulating angiogenic cells (CACs) from bone marrow in healthy subjects, improving vascular function. However, it is unclear whether this mechanism is preserved in the early stages of metabolic syndrome (early MetS). We aimed to evaluate the acute effects of exercise on adhesion molecules, angiogenic factors, MMPs, and CACs in early MetS. Fifteen subjects with early MetS and nine healthy controls underwent an exercise session and a nonexercise session, randomly. Adhesion molecules, angiogenic factors, CACs, and MMPs were evaluated before and after exercise or nonexercise sessions. At baseline, levels of sE-selectin, sICAM-1, and MMP-9 were higher in early MetS than in controls (P≤0.03). After exercise, sE-selectin, sICAM-1, and MMP-9 levels were still higher in early MetS (P<0.05). Subjects with early MetS presented less CACs (P=0.02) and higher MMP-9 activity (P≤0.04), while healthy controls presented higher MMP-2 activity after exercise. There was no difference between moments in nonexercise session (P>0.05). In conclusion, subjects with early MetS already presented impaired endothelial function at rest along with a decrease in CACs and an increase in MMP-9 activity in response to exercise.
url http://dx.doi.org/10.1155/2015/920356
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