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The effects of diabetes on male fertility and epigenetic regulation during spermatogenesis
The effects of diabetes mellitus include long-term damages, dysfunctions, and failures of various organs. An important complication of diabetes is the disturbance in the male reproductive system. Glucose metabolism is an important event in spermatogenesis. Moreover, glucose metabolism is also import...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4814953/ https://www.ncbi.nlm.nih.gov/pubmed/25814158 http://dx.doi.org/10.4103/1008-682X.150844 |
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author | Ding, Guo-Lian Liu, Ye Liu, Miao-E Pan, Jie-Xue Guo, Meng-Xi Sheng, Jian-Zhong Huang, He-Feng |
author_facet | Ding, Guo-Lian Liu, Ye Liu, Miao-E Pan, Jie-Xue Guo, Meng-Xi Sheng, Jian-Zhong Huang, He-Feng |
author_sort | Ding, Guo-Lian |
collection | PubMed |
description | The effects of diabetes mellitus include long-term damages, dysfunctions, and failures of various organs. An important complication of diabetes is the disturbance in the male reproductive system. Glucose metabolism is an important event in spermatogenesis. Moreover, glucose metabolism is also important for maintaining basic cell activity, as well as specific functions, such as motility and fertilization ability in mature sperm. Diabetic disease and experimentally induced diabetes both demonstrated that either type 1 diabetes or type 2 diabetes could have detrimental effects on male fertility, especially on sperm quality, such as sperm motility, sperm DNA integrity, and ingredients of seminal plasma. Epigenetic modifications are essential during spermatogenesis. The epigenetic regulation represents chromatin modifications including DNA methylation, histone modifications, remodeling of nucleosomes and the higher-order chromatin reorganization and noncoding RNAs. If spermatogenesis is affected during the critical developmental window, embryonic gonadal development, and germline differentiation, environmentally-induced epigenetic modifications may become permanent in the germ line epigenome and have a potential impact on subsequent generations through epigenetic transgenerational inheritance. Diabetes may influence the epigenetic modification during sperm spermatogenesis and that these epigenetic dysregulation may be inherited through the male germ line and passed onto more than one generation, which in turn may increase the risk of diabetes in offspring. |
format | Online Article Text |
id | pubmed-4814953 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-48149532016-04-19 The effects of diabetes on male fertility and epigenetic regulation during spermatogenesis Ding, Guo-Lian Liu, Ye Liu, Miao-E Pan, Jie-Xue Guo, Meng-Xi Sheng, Jian-Zhong Huang, He-Feng Asian J Androl Invited Review The effects of diabetes mellitus include long-term damages, dysfunctions, and failures of various organs. An important complication of diabetes is the disturbance in the male reproductive system. Glucose metabolism is an important event in spermatogenesis. Moreover, glucose metabolism is also important for maintaining basic cell activity, as well as specific functions, such as motility and fertilization ability in mature sperm. Diabetic disease and experimentally induced diabetes both demonstrated that either type 1 diabetes or type 2 diabetes could have detrimental effects on male fertility, especially on sperm quality, such as sperm motility, sperm DNA integrity, and ingredients of seminal plasma. Epigenetic modifications are essential during spermatogenesis. The epigenetic regulation represents chromatin modifications including DNA methylation, histone modifications, remodeling of nucleosomes and the higher-order chromatin reorganization and noncoding RNAs. If spermatogenesis is affected during the critical developmental window, embryonic gonadal development, and germline differentiation, environmentally-induced epigenetic modifications may become permanent in the germ line epigenome and have a potential impact on subsequent generations through epigenetic transgenerational inheritance. Diabetes may influence the epigenetic modification during sperm spermatogenesis and that these epigenetic dysregulation may be inherited through the male germ line and passed onto more than one generation, which in turn may increase the risk of diabetes in offspring. Medknow Publications & Media Pvt Ltd 2015 2015-03-24 /pmc/articles/PMC4814953/ /pubmed/25814158 http://dx.doi.org/10.4103/1008-682X.150844 Text en Copyright: © Asian Journal of Andrology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms. |
spellingShingle | Invited Review Ding, Guo-Lian Liu, Ye Liu, Miao-E Pan, Jie-Xue Guo, Meng-Xi Sheng, Jian-Zhong Huang, He-Feng The effects of diabetes on male fertility and epigenetic regulation during spermatogenesis |
title | The effects of diabetes on male fertility and epigenetic regulation during spermatogenesis |
title_full | The effects of diabetes on male fertility and epigenetic regulation during spermatogenesis |
title_fullStr | The effects of diabetes on male fertility and epigenetic regulation during spermatogenesis |
title_full_unstemmed | The effects of diabetes on male fertility and epigenetic regulation during spermatogenesis |
title_short | The effects of diabetes on male fertility and epigenetic regulation during spermatogenesis |
title_sort | effects of diabetes on male fertility and epigenetic regulation during spermatogenesis |
topic | Invited Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4814953/ https://www.ncbi.nlm.nih.gov/pubmed/25814158 http://dx.doi.org/10.4103/1008-682X.150844 |
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