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Reducing effect of insulin resistance on alpha-synuclein gene expression in skeletal muscle
BACKGROUND: Alpha-synuclein (SNCA) as the presynaptic protein is expressed in different tissues and prevents insulin-resistance (IR) through increasing glucose-uptake by adipocytes and muscles. However, the effect of insulin metabolism on SNCA expression has scarcely elucidated. In present study we...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6889442/ https://www.ncbi.nlm.nih.gov/pubmed/31827624 http://dx.doi.org/10.1186/s13098-019-0499-6 |
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author | Khoshi, Amirhosein Goodarzi, Golnaz Mohammadi, Rezvan Arezumand, Roghaye Moghbeli, Meysam Najariyan, Mahnaz |
author_facet | Khoshi, Amirhosein Goodarzi, Golnaz Mohammadi, Rezvan Arezumand, Roghaye Moghbeli, Meysam Najariyan, Mahnaz |
author_sort | Khoshi, Amirhosein |
collection | PubMed |
description | BACKGROUND: Alpha-synuclein (SNCA) as the presynaptic protein is expressed in different tissues and prevents insulin-resistance (IR) through increasing glucose-uptake by adipocytes and muscles. However, the effect of insulin metabolism on SNCA expression has scarcely elucidated. In present study we assessed the probable effect of insulin resistance on SNCA expression in muscle C2C12 cells and also skeletal muscle tissues of type 2 diabetic mice. MATERIALS AND METHODS: Sixteen male C57BL/6 mice were divided into two experimental groups, including control and type 2 diabetic mice with IR (induced by high-fat diet + low-dose streptozotocin). The animals of the study involved the measurements of fasting blood glucose, oral-glucose-tolerance-test, as well as fasting plasma insulin. Moreover, insulin-resistant and insulin-sensitive muscle C2C12 cells were prepared. The insulin-resistance was confirmed by the glucose-uptake assay. Comparative quantitative real time PCR was used to assess the SNCA expression. RESULTS: The obtained results have showed a significant ~ 27% decrease in SNCA expression level in muscle tissue of diabetic mice (P = 0.022). Moreover, there was a significant change of SNCA expression in insulin-resistant C2C12 cells (P < 0.001). CONCLUSION: Type 2 diabetes due to insulin-resistance can decrease SNCA gene expression in muscles. In addition to the role of SNCA in cell susceptibility to insulin and glucose uptake, the SNCA expression can also be affected by insulin metabolism. |
format | Online Article Text |
id | pubmed-6889442 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-68894422019-12-11 Reducing effect of insulin resistance on alpha-synuclein gene expression in skeletal muscle Khoshi, Amirhosein Goodarzi, Golnaz Mohammadi, Rezvan Arezumand, Roghaye Moghbeli, Meysam Najariyan, Mahnaz Diabetol Metab Syndr Research BACKGROUND: Alpha-synuclein (SNCA) as the presynaptic protein is expressed in different tissues and prevents insulin-resistance (IR) through increasing glucose-uptake by adipocytes and muscles. However, the effect of insulin metabolism on SNCA expression has scarcely elucidated. In present study we assessed the probable effect of insulin resistance on SNCA expression in muscle C2C12 cells and also skeletal muscle tissues of type 2 diabetic mice. MATERIALS AND METHODS: Sixteen male C57BL/6 mice were divided into two experimental groups, including control and type 2 diabetic mice with IR (induced by high-fat diet + low-dose streptozotocin). The animals of the study involved the measurements of fasting blood glucose, oral-glucose-tolerance-test, as well as fasting plasma insulin. Moreover, insulin-resistant and insulin-sensitive muscle C2C12 cells were prepared. The insulin-resistance was confirmed by the glucose-uptake assay. Comparative quantitative real time PCR was used to assess the SNCA expression. RESULTS: The obtained results have showed a significant ~ 27% decrease in SNCA expression level in muscle tissue of diabetic mice (P = 0.022). Moreover, there was a significant change of SNCA expression in insulin-resistant C2C12 cells (P < 0.001). CONCLUSION: Type 2 diabetes due to insulin-resistance can decrease SNCA gene expression in muscles. In addition to the role of SNCA in cell susceptibility to insulin and glucose uptake, the SNCA expression can also be affected by insulin metabolism. BioMed Central 2019-12-02 /pmc/articles/PMC6889442/ /pubmed/31827624 http://dx.doi.org/10.1186/s13098-019-0499-6 Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Khoshi, Amirhosein Goodarzi, Golnaz Mohammadi, Rezvan Arezumand, Roghaye Moghbeli, Meysam Najariyan, Mahnaz Reducing effect of insulin resistance on alpha-synuclein gene expression in skeletal muscle |
title | Reducing effect of insulin resistance on alpha-synuclein gene expression in skeletal muscle |
title_full | Reducing effect of insulin resistance on alpha-synuclein gene expression in skeletal muscle |
title_fullStr | Reducing effect of insulin resistance on alpha-synuclein gene expression in skeletal muscle |
title_full_unstemmed | Reducing effect of insulin resistance on alpha-synuclein gene expression in skeletal muscle |
title_short | Reducing effect of insulin resistance on alpha-synuclein gene expression in skeletal muscle |
title_sort | reducing effect of insulin resistance on alpha-synuclein gene expression in skeletal muscle |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6889442/ https://www.ncbi.nlm.nih.gov/pubmed/31827624 http://dx.doi.org/10.1186/s13098-019-0499-6 |
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