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Simvastatin protects high glucose-induced H9c2 cells from injury by inducing autophagy
CONTEXT: Simvastatin is the first line therapeutic drug for coronary heart disease and atherosclerosis. The protective effect mechanism of simvastatin on cardiomyocytes is unclear. OBJECTIVE: This study explores the effect of simvastatin on high glucose induced cardiomyocyte injury and the role of a...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7655079/ https://www.ncbi.nlm.nih.gov/pubmed/33164619 http://dx.doi.org/10.1080/13880209.2020.1839512 |
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author | E, Lusha Jiang, Hong |
author_facet | E, Lusha Jiang, Hong |
author_sort | E, Lusha |
collection | PubMed |
description | CONTEXT: Simvastatin is the first line therapeutic drug for coronary heart disease and atherosclerosis. The protective effect mechanism of simvastatin on cardiomyocytes is unclear. OBJECTIVE: This study explores the effect of simvastatin on high glucose induced cardiomyocyte injury and the role of autophagy during the process. MATERIALS AND METHODS: H9c2 cells were incubated with different doses of glucose (0, 50, 100, 200 mM) for 24 h to verify the glucose induced injury. The H9c2 cells were pre-treated with simvastatin at different dosages (0, 0.1, 0.5, 1 μM) for 30 min to rescue the injury followed by the autophagy evaluation. 3-MA was used as an autophagy inhibitor to confirm the role of autophagy in simvastatin treated process. CCK-8 assay, FACS assay, confocal microscopy, western blotting and immunofluorescence analysis were conducted to evaluate the high glucose induced injury or protective effects of simvastatin in H9c2 cell line. RESULTS: High glucose dramatically decreased H9c2 cell viability (0 mM, 0.58 ± 0.09%; vs. 50 mM, 8.67 ± 0.43%; 100 mM, 16.1 ± 3.56%; 200 mM, 32.9 ± 2.63%), induced significant cell apoptosis (0 mM, 0.96 ± 0.16%, vs. 50 mM, 7.00 ± 0.63%; 100 mM, 12.9 ± 0.78%; 200 mM, 21.8 ± 1.17%) and suppressed cell autophagy. Simvastatin decreased apoptosis and attenuate injury by decreasing cell apoptosis ratio, elevating Bcl-2 expression while decreasing Bax and caspase-3 protein expressions. Meanwhile, simvastatin restored the autophagy depicted by western blotting with increased ATG-5, Beclin1 and LC3II/LC3I protein expression and decreased p62 expression, as well as immunofluorescence with elevated LC3 fluorescence density. DISCUSSION AND CONCLUSIONS: The myocardial protective effect mediated by autophagy activated by simvastatin to some extent elucidated the mechanism of the protective effect of simvastatin on H9c2 cell injury, which provided a certain theoretical basis for the clinical application of simvastatin in the treatment of cardiovascular diseases. In addition, we speculate that simvastatin may be used for diabetes associated cardiovascular diseases. |
format | Online Article Text |
id | pubmed-7655079 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-76550792020-11-19 Simvastatin protects high glucose-induced H9c2 cells from injury by inducing autophagy E, Lusha Jiang, Hong Pharm Biol Original Article CONTEXT: Simvastatin is the first line therapeutic drug for coronary heart disease and atherosclerosis. The protective effect mechanism of simvastatin on cardiomyocytes is unclear. OBJECTIVE: This study explores the effect of simvastatin on high glucose induced cardiomyocyte injury and the role of autophagy during the process. MATERIALS AND METHODS: H9c2 cells were incubated with different doses of glucose (0, 50, 100, 200 mM) for 24 h to verify the glucose induced injury. The H9c2 cells were pre-treated with simvastatin at different dosages (0, 0.1, 0.5, 1 μM) for 30 min to rescue the injury followed by the autophagy evaluation. 3-MA was used as an autophagy inhibitor to confirm the role of autophagy in simvastatin treated process. CCK-8 assay, FACS assay, confocal microscopy, western blotting and immunofluorescence analysis were conducted to evaluate the high glucose induced injury or protective effects of simvastatin in H9c2 cell line. RESULTS: High glucose dramatically decreased H9c2 cell viability (0 mM, 0.58 ± 0.09%; vs. 50 mM, 8.67 ± 0.43%; 100 mM, 16.1 ± 3.56%; 200 mM, 32.9 ± 2.63%), induced significant cell apoptosis (0 mM, 0.96 ± 0.16%, vs. 50 mM, 7.00 ± 0.63%; 100 mM, 12.9 ± 0.78%; 200 mM, 21.8 ± 1.17%) and suppressed cell autophagy. Simvastatin decreased apoptosis and attenuate injury by decreasing cell apoptosis ratio, elevating Bcl-2 expression while decreasing Bax and caspase-3 protein expressions. Meanwhile, simvastatin restored the autophagy depicted by western blotting with increased ATG-5, Beclin1 and LC3II/LC3I protein expression and decreased p62 expression, as well as immunofluorescence with elevated LC3 fluorescence density. DISCUSSION AND CONCLUSIONS: The myocardial protective effect mediated by autophagy activated by simvastatin to some extent elucidated the mechanism of the protective effect of simvastatin on H9c2 cell injury, which provided a certain theoretical basis for the clinical application of simvastatin in the treatment of cardiovascular diseases. In addition, we speculate that simvastatin may be used for diabetes associated cardiovascular diseases. Taylor & Francis 2020-11-09 /pmc/articles/PMC7655079/ /pubmed/33164619 http://dx.doi.org/10.1080/13880209.2020.1839512 Text en © 2020 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article E, Lusha Jiang, Hong Simvastatin protects high glucose-induced H9c2 cells from injury by inducing autophagy |
title | Simvastatin protects high glucose-induced H9c2 cells from injury by inducing autophagy |
title_full | Simvastatin protects high glucose-induced H9c2 cells from injury by inducing autophagy |
title_fullStr | Simvastatin protects high glucose-induced H9c2 cells from injury by inducing autophagy |
title_full_unstemmed | Simvastatin protects high glucose-induced H9c2 cells from injury by inducing autophagy |
title_short | Simvastatin protects high glucose-induced H9c2 cells from injury by inducing autophagy |
title_sort | simvastatin protects high glucose-induced h9c2 cells from injury by inducing autophagy |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7655079/ https://www.ncbi.nlm.nih.gov/pubmed/33164619 http://dx.doi.org/10.1080/13880209.2020.1839512 |
work_keys_str_mv | AT elusha simvastatinprotectshighglucoseinducedh9c2cellsfrominjurybyinducingautophagy AT jianghong simvastatinprotectshighglucoseinducedh9c2cellsfrominjurybyinducingautophagy |