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Autonomic function may not modulate irisin release in healthy adults: findings from a randomized cross-over study
OBJECTIVE: Autonomic nervous system, especially the sympathetic nervous system, may stimulate the expression of peroxisome proliferator-activated receptor γ coactivator-1α, which regulates irisin. This study aimed to explore whether there was any association between autonomic function as assessed by...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Sociedade Brasileira de Endocrinologia e Metabologia
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10522212/ https://www.ncbi.nlm.nih.gov/pubmed/32555986 http://dx.doi.org/10.20945/2359-3997000000243 |
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author | Qiu, Shanhu Bosnyák, Edit Zügel, Martina Steinacker, Jürgen Michael Schumann, Uwe |
author_facet | Qiu, Shanhu Bosnyák, Edit Zügel, Martina Steinacker, Jürgen Michael Schumann, Uwe |
author_sort | Qiu, Shanhu |
collection | PubMed |
description | OBJECTIVE: Autonomic nervous system, especially the sympathetic nervous system, may stimulate the expression of peroxisome proliferator-activated receptor γ coactivator-1α, which regulates irisin. This study aimed to explore whether there was any association between autonomic function as assessed by heart rate related indices and irisin release following acute exercise. SUBJECTS AND METHODS: Seventeen healthy adults were asked to perform an incremental exhaustive cycling as well as an incremental exhaustive running separately on different days. Heart rate was monitored, and blood samples were collected before, immediately, 10-, and 60-minutes post-exercise. Serum irisin was measured using ELISA kit. RESULTS: Markers for autonomic function, such as heart rate at rest, peak, or recovery, heart rate reserve, heart rate recovery, and chronotropic index, were comparable between cycling and running (all P > 0.10). Irisin was increased immediately following both exercise. No significant association was observed between heart rate at rest, peak, or recovery and irisin level at the corresponding time-point, as well as between heart rate reserve, heart rate recovery, or chronotropic index and exercise induced irisin release, with or without controlling for age, body mass index, and glucose (all P > 0.10). CONCLUSIONS: Autonomic function might not be associated with irisin release in healthy adults. Arch Endocrinol Metab. 2020;64(3):201-4 |
format | Online Article Text |
id | pubmed-10522212 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Sociedade Brasileira de Endocrinologia e Metabologia |
record_format | MEDLINE/PubMed |
spelling | pubmed-105222122023-09-27 Autonomic function may not modulate irisin release in healthy adults: findings from a randomized cross-over study Qiu, Shanhu Bosnyák, Edit Zügel, Martina Steinacker, Jürgen Michael Schumann, Uwe Arch Endocrinol Metab Brief Report OBJECTIVE: Autonomic nervous system, especially the sympathetic nervous system, may stimulate the expression of peroxisome proliferator-activated receptor γ coactivator-1α, which regulates irisin. This study aimed to explore whether there was any association between autonomic function as assessed by heart rate related indices and irisin release following acute exercise. SUBJECTS AND METHODS: Seventeen healthy adults were asked to perform an incremental exhaustive cycling as well as an incremental exhaustive running separately on different days. Heart rate was monitored, and blood samples were collected before, immediately, 10-, and 60-minutes post-exercise. Serum irisin was measured using ELISA kit. RESULTS: Markers for autonomic function, such as heart rate at rest, peak, or recovery, heart rate reserve, heart rate recovery, and chronotropic index, were comparable between cycling and running (all P > 0.10). Irisin was increased immediately following both exercise. No significant association was observed between heart rate at rest, peak, or recovery and irisin level at the corresponding time-point, as well as between heart rate reserve, heart rate recovery, or chronotropic index and exercise induced irisin release, with or without controlling for age, body mass index, and glucose (all P > 0.10). CONCLUSIONS: Autonomic function might not be associated with irisin release in healthy adults. Arch Endocrinol Metab. 2020;64(3):201-4 Sociedade Brasileira de Endocrinologia e Metabologia 2020-06-05 /pmc/articles/PMC10522212/ /pubmed/32555986 http://dx.doi.org/10.20945/2359-3997000000243 Text en https://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Brief Report Qiu, Shanhu Bosnyák, Edit Zügel, Martina Steinacker, Jürgen Michael Schumann, Uwe Autonomic function may not modulate irisin release in healthy adults: findings from a randomized cross-over study |
title | Autonomic function may not modulate irisin release in healthy adults: findings from a randomized cross-over study |
title_full | Autonomic function may not modulate irisin release in healthy adults: findings from a randomized cross-over study |
title_fullStr | Autonomic function may not modulate irisin release in healthy adults: findings from a randomized cross-over study |
title_full_unstemmed | Autonomic function may not modulate irisin release in healthy adults: findings from a randomized cross-over study |
title_short | Autonomic function may not modulate irisin release in healthy adults: findings from a randomized cross-over study |
title_sort | autonomic function may not modulate irisin release in healthy adults: findings from a randomized cross-over study |
topic | Brief Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10522212/ https://www.ncbi.nlm.nih.gov/pubmed/32555986 http://dx.doi.org/10.20945/2359-3997000000243 |
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