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Decreased placental and muscular expression of the fibroblast growth factor 19 in gestational diabetes mellitus
AIMS/INTRODUCTION: Fibroblast growth factor (FGF)19 has been shown to improve glycemic homeostasis and lipid metabolism in animal models. In humans, decreased FGF19 level has been described in diabetes. The present study aimed to investigate the expression of FGF19 in gestational diabetes mellitus (...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6319613/ https://www.ncbi.nlm.nih.gov/pubmed/29734515 http://dx.doi.org/10.1111/jdi.12859 |
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author | Wang, Dongyu Xu, Shuqia Ding, Wenjing Zhu, Caixia Deng, Songqing Qiu, Xiwen Wang, Zilian |
author_facet | Wang, Dongyu Xu, Shuqia Ding, Wenjing Zhu, Caixia Deng, Songqing Qiu, Xiwen Wang, Zilian |
author_sort | Wang, Dongyu |
collection | PubMed |
description | AIMS/INTRODUCTION: Fibroblast growth factor (FGF)19 has been shown to improve glycemic homeostasis and lipid metabolism in animal models. In humans, decreased FGF19 level has been described in diabetes. The present study aimed to investigate the expression of FGF19 in gestational diabetes mellitus (GDM) patients. MATERIALS AND METHODS: Samples for measurement were obtained from 20 women with GDM and 25 healthy controls. The messenger ribonucleic acid (mRNA) and protein expression levels of FGF19, FGF21 and co‐receptor β‐klotho (KLB) in the placenta, rectus muscle and subcutaneous fat tissues were quantified by real‐time quantitative polymerase chain reaction, western blot and immunohistochemistry, respectively. RESULTS: Women with GDM had significantly lower mRNA and protein expressions of FGF19 than control women in the placenta (mRNA 0.33 ± 0.05 vs 0.72 ± 0.09; protein 0.34 ± 0.13 vs 0.85 ± 0.20) and rectus muscle (mRNA 0.83 ± 0.11 vs 1.28 ± 0.19; protein 0.78 ± 0.24 vs 1.23 ± 0.39). However, there were no significant differences between GDM women and controls with respect to the expression levels of FGF21 and β‐klotho in the placenta and rectus muscle. There were almost no detectable FGF19 and FGF21 expressions in subcutaneous fat tissue. Furthermore, β‐klotho expression levels were not different between the GDM and control group in subcutaneous fat. CONCLUSIONS: FGF19 expressions are decreased in the placenta and rectus muscle of women with GDM. This might contribute to the pathophysiology or development of GDM. |
format | Online Article Text |
id | pubmed-6319613 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-63196132019-01-08 Decreased placental and muscular expression of the fibroblast growth factor 19 in gestational diabetes mellitus Wang, Dongyu Xu, Shuqia Ding, Wenjing Zhu, Caixia Deng, Songqing Qiu, Xiwen Wang, Zilian J Diabetes Investig Articles AIMS/INTRODUCTION: Fibroblast growth factor (FGF)19 has been shown to improve glycemic homeostasis and lipid metabolism in animal models. In humans, decreased FGF19 level has been described in diabetes. The present study aimed to investigate the expression of FGF19 in gestational diabetes mellitus (GDM) patients. MATERIALS AND METHODS: Samples for measurement were obtained from 20 women with GDM and 25 healthy controls. The messenger ribonucleic acid (mRNA) and protein expression levels of FGF19, FGF21 and co‐receptor β‐klotho (KLB) in the placenta, rectus muscle and subcutaneous fat tissues were quantified by real‐time quantitative polymerase chain reaction, western blot and immunohistochemistry, respectively. RESULTS: Women with GDM had significantly lower mRNA and protein expressions of FGF19 than control women in the placenta (mRNA 0.33 ± 0.05 vs 0.72 ± 0.09; protein 0.34 ± 0.13 vs 0.85 ± 0.20) and rectus muscle (mRNA 0.83 ± 0.11 vs 1.28 ± 0.19; protein 0.78 ± 0.24 vs 1.23 ± 0.39). However, there were no significant differences between GDM women and controls with respect to the expression levels of FGF21 and β‐klotho in the placenta and rectus muscle. There were almost no detectable FGF19 and FGF21 expressions in subcutaneous fat tissue. Furthermore, β‐klotho expression levels were not different between the GDM and control group in subcutaneous fat. CONCLUSIONS: FGF19 expressions are decreased in the placenta and rectus muscle of women with GDM. This might contribute to the pathophysiology or development of GDM. John Wiley and Sons Inc. 2018-06-06 2019-01 /pmc/articles/PMC6319613/ /pubmed/29734515 http://dx.doi.org/10.1111/jdi.12859 Text en © 2018 The Authors. Journal of Diabetes Investigation published by Asian Association for the Study of Diabetes (AASD) and John Wiley & Sons Australia, Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Articles Wang, Dongyu Xu, Shuqia Ding, Wenjing Zhu, Caixia Deng, Songqing Qiu, Xiwen Wang, Zilian Decreased placental and muscular expression of the fibroblast growth factor 19 in gestational diabetes mellitus |
title | Decreased placental and muscular expression of the fibroblast growth factor 19 in gestational diabetes mellitus |
title_full | Decreased placental and muscular expression of the fibroblast growth factor 19 in gestational diabetes mellitus |
title_fullStr | Decreased placental and muscular expression of the fibroblast growth factor 19 in gestational diabetes mellitus |
title_full_unstemmed | Decreased placental and muscular expression of the fibroblast growth factor 19 in gestational diabetes mellitus |
title_short | Decreased placental and muscular expression of the fibroblast growth factor 19 in gestational diabetes mellitus |
title_sort | decreased placental and muscular expression of the fibroblast growth factor 19 in gestational diabetes mellitus |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6319613/ https://www.ncbi.nlm.nih.gov/pubmed/29734515 http://dx.doi.org/10.1111/jdi.12859 |
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