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Walking Training Increases microRNA-126 Expression and Muscle Capillarization in Patients with Peripheral Artery Disease
Patients with peripheral artery disease (PAD) have reduced muscle capillary density. Walking training (WT) is recommended for PAD patients. The goal of the study was to verify whether WT promotes angiogenesis in PAD-affected muscle and to investigate the possible role of miRNA-126 and the vascular e...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9858623/ https://www.ncbi.nlm.nih.gov/pubmed/36672843 http://dx.doi.org/10.3390/genes14010101 |
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author | da Silva, Natan D. Andrade-Lima, Aluisio Chehuen, Marcel R. Leicht, Anthony S. Brum, Patricia C. Oliveira, Edilamar M. Wolosker, Nelson Pelozin, Bruno R. A. Fernandes, Tiago Forjaz, Cláudia L. M. |
author_facet | da Silva, Natan D. Andrade-Lima, Aluisio Chehuen, Marcel R. Leicht, Anthony S. Brum, Patricia C. Oliveira, Edilamar M. Wolosker, Nelson Pelozin, Bruno R. A. Fernandes, Tiago Forjaz, Cláudia L. M. |
author_sort | da Silva, Natan D. |
collection | PubMed |
description | Patients with peripheral artery disease (PAD) have reduced muscle capillary density. Walking training (WT) is recommended for PAD patients. The goal of the study was to verify whether WT promotes angiogenesis in PAD-affected muscle and to investigate the possible role of miRNA-126 and the vascular endothelium growth factor (VEGF) angiogenic pathways on this adaptation. Thirty-two men with PAD were randomly allocated to two groups: WT (n = 16, 2 sessions/week) and control (CO, n = 16). Maximal treadmill tests and gastrocnemius biopsies were performed at baseline and after 12 weeks. Histological and molecular analyses were performed by blinded researchers. Maximal walking capacity increased by 65% with WT. WT increased the gastrocnemius capillary-fiber ratio (WT = 109 ± 13 vs. 164 ± 21 and CO = 100 ± 8 vs. 106 ± 6%, p < 0.001). Muscular expression of miRNA-126 and VEGF increased with WT (WT = 101 ± 13 vs. 130 ± 5 and CO = 100 ± 14 vs. 77 ± 20%, p < 0.001; WT = 103 ± 28 vs. 153 ± 59 and CO = 100 ± 36 vs. 84 ± 41%, p = 0.001, respectively), while expression of PI3KR2 decreased (WT = 97 ± 23 vs. 75 ± 21 and CO = 100 ± 29 vs. 105 ± 39%, p = 0.021). WT promoted angiogenesis in the muscle affected by PAD, and miRNA-126 may have a role in this adaptation by inhibiting PI3KR2, enabling the progression of the VEGF signaling pathway. |
format | Online Article Text |
id | pubmed-9858623 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-98586232023-01-21 Walking Training Increases microRNA-126 Expression and Muscle Capillarization in Patients with Peripheral Artery Disease da Silva, Natan D. Andrade-Lima, Aluisio Chehuen, Marcel R. Leicht, Anthony S. Brum, Patricia C. Oliveira, Edilamar M. Wolosker, Nelson Pelozin, Bruno R. A. Fernandes, Tiago Forjaz, Cláudia L. M. Genes (Basel) Article Patients with peripheral artery disease (PAD) have reduced muscle capillary density. Walking training (WT) is recommended for PAD patients. The goal of the study was to verify whether WT promotes angiogenesis in PAD-affected muscle and to investigate the possible role of miRNA-126 and the vascular endothelium growth factor (VEGF) angiogenic pathways on this adaptation. Thirty-two men with PAD were randomly allocated to two groups: WT (n = 16, 2 sessions/week) and control (CO, n = 16). Maximal treadmill tests and gastrocnemius biopsies were performed at baseline and after 12 weeks. Histological and molecular analyses were performed by blinded researchers. Maximal walking capacity increased by 65% with WT. WT increased the gastrocnemius capillary-fiber ratio (WT = 109 ± 13 vs. 164 ± 21 and CO = 100 ± 8 vs. 106 ± 6%, p < 0.001). Muscular expression of miRNA-126 and VEGF increased with WT (WT = 101 ± 13 vs. 130 ± 5 and CO = 100 ± 14 vs. 77 ± 20%, p < 0.001; WT = 103 ± 28 vs. 153 ± 59 and CO = 100 ± 36 vs. 84 ± 41%, p = 0.001, respectively), while expression of PI3KR2 decreased (WT = 97 ± 23 vs. 75 ± 21 and CO = 100 ± 29 vs. 105 ± 39%, p = 0.021). WT promoted angiogenesis in the muscle affected by PAD, and miRNA-126 may have a role in this adaptation by inhibiting PI3KR2, enabling the progression of the VEGF signaling pathway. MDPI 2022-12-29 /pmc/articles/PMC9858623/ /pubmed/36672843 http://dx.doi.org/10.3390/genes14010101 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article da Silva, Natan D. Andrade-Lima, Aluisio Chehuen, Marcel R. Leicht, Anthony S. Brum, Patricia C. Oliveira, Edilamar M. Wolosker, Nelson Pelozin, Bruno R. A. Fernandes, Tiago Forjaz, Cláudia L. M. Walking Training Increases microRNA-126 Expression and Muscle Capillarization in Patients with Peripheral Artery Disease |
title | Walking Training Increases microRNA-126 Expression and Muscle Capillarization in Patients with Peripheral Artery Disease |
title_full | Walking Training Increases microRNA-126 Expression and Muscle Capillarization in Patients with Peripheral Artery Disease |
title_fullStr | Walking Training Increases microRNA-126 Expression and Muscle Capillarization in Patients with Peripheral Artery Disease |
title_full_unstemmed | Walking Training Increases microRNA-126 Expression and Muscle Capillarization in Patients with Peripheral Artery Disease |
title_short | Walking Training Increases microRNA-126 Expression and Muscle Capillarization in Patients with Peripheral Artery Disease |
title_sort | walking training increases microrna-126 expression and muscle capillarization in patients with peripheral artery disease |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9858623/ https://www.ncbi.nlm.nih.gov/pubmed/36672843 http://dx.doi.org/10.3390/genes14010101 |
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