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Exercise combined with trimetazidine improves anti-fatal stress capacity through enhancing autophagy and heat shock protein 70 of myocardium in mice

Background: Anti-stress capacity is important to resist the occurrence of adverse events. To observe the effects of exercise, trimetazidine alone or combined on the anti-stress capacity of mice, and further explore its potential mechanism. Methods: Forty-four C57BL/6 male mice aged 8 weeks were rand...

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Autores principales: Jiang, Lingjun, Shen, Xuanlin, Dun, Yaoshan, Xie, Murong, Fu, Siqian, Zhang, Wenliang, Qiu, Ling, Ripley-Gonzalez, Jeffrey W., Liu, Suixin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7976563/
https://www.ncbi.nlm.nih.gov/pubmed/33746584
http://dx.doi.org/10.7150/ijms.53899
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author Jiang, Lingjun
Shen, Xuanlin
Dun, Yaoshan
Xie, Murong
Fu, Siqian
Zhang, Wenliang
Qiu, Ling
Ripley-Gonzalez, Jeffrey W.
Liu, Suixin
author_facet Jiang, Lingjun
Shen, Xuanlin
Dun, Yaoshan
Xie, Murong
Fu, Siqian
Zhang, Wenliang
Qiu, Ling
Ripley-Gonzalez, Jeffrey W.
Liu, Suixin
author_sort Jiang, Lingjun
collection PubMed
description Background: Anti-stress capacity is important to resist the occurrence of adverse events. To observe the effects of exercise, trimetazidine alone or combined on the anti-stress capacity of mice, and further explore its potential mechanism. Methods: Forty-four C57BL/6 male mice aged 8 weeks were randomly divided into four groups (n=11 for each group): control group (group C), exercise group (group E), trimetazidine group (group T), exercise combined with trimetazidine group (group TE). After the intervention, each group was randomly subdivided into the exhaustive exercise (EE, n=6) and the non-EE (n=5) subgroups. The mice in the EE-subgroup underwent EE. Mice were sacrificed 12 hours later after EE. The myocardial ultrastructure and autophagosomes were observed under an electron microscope. The expression of autophagy-related proteins: BNIP3, LC3-II, and P62 were analyzed and the heat shock protein 70 mRNA transcription and protein expression were also investigated. Results: Exercise or trimetazidine increased the expression of BNIP3, LC3-II, and heat shock protein 70, decreased the expression of P62 pre- and post-EE while the combination has the synergistic effect. Conclusion: Exercise and trimetazidine, alone or combined enhanced the anti-stress capacity of mice significantly. The underlying mechanism may be associated with the promotion of autography and the expression of heat shock protein 70.
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spelling pubmed-79765632021-03-19 Exercise combined with trimetazidine improves anti-fatal stress capacity through enhancing autophagy and heat shock protein 70 of myocardium in mice Jiang, Lingjun Shen, Xuanlin Dun, Yaoshan Xie, Murong Fu, Siqian Zhang, Wenliang Qiu, Ling Ripley-Gonzalez, Jeffrey W. Liu, Suixin Int J Med Sci Research Paper Background: Anti-stress capacity is important to resist the occurrence of adverse events. To observe the effects of exercise, trimetazidine alone or combined on the anti-stress capacity of mice, and further explore its potential mechanism. Methods: Forty-four C57BL/6 male mice aged 8 weeks were randomly divided into four groups (n=11 for each group): control group (group C), exercise group (group E), trimetazidine group (group T), exercise combined with trimetazidine group (group TE). After the intervention, each group was randomly subdivided into the exhaustive exercise (EE, n=6) and the non-EE (n=5) subgroups. The mice in the EE-subgroup underwent EE. Mice were sacrificed 12 hours later after EE. The myocardial ultrastructure and autophagosomes were observed under an electron microscope. The expression of autophagy-related proteins: BNIP3, LC3-II, and P62 were analyzed and the heat shock protein 70 mRNA transcription and protein expression were also investigated. Results: Exercise or trimetazidine increased the expression of BNIP3, LC3-II, and heat shock protein 70, decreased the expression of P62 pre- and post-EE while the combination has the synergistic effect. Conclusion: Exercise and trimetazidine, alone or combined enhanced the anti-stress capacity of mice significantly. The underlying mechanism may be associated with the promotion of autography and the expression of heat shock protein 70. Ivyspring International Publisher 2021-02-06 /pmc/articles/PMC7976563/ /pubmed/33746584 http://dx.doi.org/10.7150/ijms.53899 Text en © The author(s) This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/). See http://ivyspring.com/terms for full terms and conditions.
spellingShingle Research Paper
Jiang, Lingjun
Shen, Xuanlin
Dun, Yaoshan
Xie, Murong
Fu, Siqian
Zhang, Wenliang
Qiu, Ling
Ripley-Gonzalez, Jeffrey W.
Liu, Suixin
Exercise combined with trimetazidine improves anti-fatal stress capacity through enhancing autophagy and heat shock protein 70 of myocardium in mice
title Exercise combined with trimetazidine improves anti-fatal stress capacity through enhancing autophagy and heat shock protein 70 of myocardium in mice
title_full Exercise combined with trimetazidine improves anti-fatal stress capacity through enhancing autophagy and heat shock protein 70 of myocardium in mice
title_fullStr Exercise combined with trimetazidine improves anti-fatal stress capacity through enhancing autophagy and heat shock protein 70 of myocardium in mice
title_full_unstemmed Exercise combined with trimetazidine improves anti-fatal stress capacity through enhancing autophagy and heat shock protein 70 of myocardium in mice
title_short Exercise combined with trimetazidine improves anti-fatal stress capacity through enhancing autophagy and heat shock protein 70 of myocardium in mice
title_sort exercise combined with trimetazidine improves anti-fatal stress capacity through enhancing autophagy and heat shock protein 70 of myocardium in mice
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7976563/
https://www.ncbi.nlm.nih.gov/pubmed/33746584
http://dx.doi.org/10.7150/ijms.53899
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