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Male obesity is associated with sperm telomere shortening and aberrant mRNA expression of autophagy-related genes

BACKGROUND: Obesity is regarded a global public health crisis. It has been implicated in a variety of health problems, but when it comes to male fertility, how and to what extent obesity affects it are poorly understood. Accordingly, semen samples from 32 individuals with obesity (body mass index (B...

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Autores principales: Raee, Pourya, Shams Mofarahe, Zahra, Nazarian, Hamid, Abdollahifar, Mohammad-Amin, Ghaffari Novin, Mahsa, Aghamiri, Shahin, Ghaffari Novin, Marefat
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10210264/
https://www.ncbi.nlm.nih.gov/pubmed/37226085
http://dx.doi.org/10.1186/s12610-023-00188-w
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author Raee, Pourya
Shams Mofarahe, Zahra
Nazarian, Hamid
Abdollahifar, Mohammad-Amin
Ghaffari Novin, Mahsa
Aghamiri, Shahin
Ghaffari Novin, Marefat
author_facet Raee, Pourya
Shams Mofarahe, Zahra
Nazarian, Hamid
Abdollahifar, Mohammad-Amin
Ghaffari Novin, Mahsa
Aghamiri, Shahin
Ghaffari Novin, Marefat
author_sort Raee, Pourya
collection PubMed
description BACKGROUND: Obesity is regarded a global public health crisis. It has been implicated in a variety of health problems, but when it comes to male fertility, how and to what extent obesity affects it are poorly understood. Accordingly, semen samples from 32 individuals with obesity (body mass index (BMI) ≥ 30 kg/m(2)) and 32 individuals with normal weight (BMI: 18.5-25 kg/m(2)) were obtained. Here, for the first time, we examined the association between obesity, relative sperm telomere length (STL) and autophagy-related mRNA levels such as Beclin1, AMPKa1, ULK1, BAX, and BCL2. Each group was also evaluated for conventional semen parameters, sperm apoptotic changes, DNA fragmentation index (DFI), sperm chromatin maturation, and reactive oxygen species (ROS) levels. RESULTS: Based on our findings, there was a marked reduction in relative STL in individuals with obesity as compared to the normal-weight group. We also found a significant negative correlation between relative STL and age, BMI, DFI, percentage of sperm with immature chromatin, and intracellular ROS levels in patients with obesity. In the normal-weight group, relative STL was only negatively correlated with DFI and intracellular ROS levels. Regarding mRNA expression, there was considerable upregulation of Beclin1, ULK1, and BCL2 in the group with obesity compared to the normal-weight group. Obesity was also found to be associated with a considerable decline in semen volume, total sperm count, progressive motility, and viability in comparison to normal-weight individuals. Furthermore, obesity was associated with considerably higher percentages of DFI, sperm with immature chromatin, late-stage apoptosis, and elevated ROS levels. CONCLUSION: According to our findings, obesity is associated with sperm telomere shortening and aberrant autophagy-related mRNA expression. It should be emphasized that telomere shortening in sperm may be an indirect consequence of obesity due to the oxidative stress associated with the condition. Nevertheless, further investigation is required for a more comprehensive understanding.
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spelling pubmed-102102642023-05-26 Male obesity is associated with sperm telomere shortening and aberrant mRNA expression of autophagy-related genes Raee, Pourya Shams Mofarahe, Zahra Nazarian, Hamid Abdollahifar, Mohammad-Amin Ghaffari Novin, Mahsa Aghamiri, Shahin Ghaffari Novin, Marefat Basic Clin Androl Research Article BACKGROUND: Obesity is regarded a global public health crisis. It has been implicated in a variety of health problems, but when it comes to male fertility, how and to what extent obesity affects it are poorly understood. Accordingly, semen samples from 32 individuals with obesity (body mass index (BMI) ≥ 30 kg/m(2)) and 32 individuals with normal weight (BMI: 18.5-25 kg/m(2)) were obtained. Here, for the first time, we examined the association between obesity, relative sperm telomere length (STL) and autophagy-related mRNA levels such as Beclin1, AMPKa1, ULK1, BAX, and BCL2. Each group was also evaluated for conventional semen parameters, sperm apoptotic changes, DNA fragmentation index (DFI), sperm chromatin maturation, and reactive oxygen species (ROS) levels. RESULTS: Based on our findings, there was a marked reduction in relative STL in individuals with obesity as compared to the normal-weight group. We also found a significant negative correlation between relative STL and age, BMI, DFI, percentage of sperm with immature chromatin, and intracellular ROS levels in patients with obesity. In the normal-weight group, relative STL was only negatively correlated with DFI and intracellular ROS levels. Regarding mRNA expression, there was considerable upregulation of Beclin1, ULK1, and BCL2 in the group with obesity compared to the normal-weight group. Obesity was also found to be associated with a considerable decline in semen volume, total sperm count, progressive motility, and viability in comparison to normal-weight individuals. Furthermore, obesity was associated with considerably higher percentages of DFI, sperm with immature chromatin, late-stage apoptosis, and elevated ROS levels. CONCLUSION: According to our findings, obesity is associated with sperm telomere shortening and aberrant autophagy-related mRNA expression. It should be emphasized that telomere shortening in sperm may be an indirect consequence of obesity due to the oxidative stress associated with the condition. Nevertheless, further investigation is required for a more comprehensive understanding. BioMed Central 2023-05-25 /pmc/articles/PMC10210264/ /pubmed/37226085 http://dx.doi.org/10.1186/s12610-023-00188-w Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Raee, Pourya
Shams Mofarahe, Zahra
Nazarian, Hamid
Abdollahifar, Mohammad-Amin
Ghaffari Novin, Mahsa
Aghamiri, Shahin
Ghaffari Novin, Marefat
Male obesity is associated with sperm telomere shortening and aberrant mRNA expression of autophagy-related genes
title Male obesity is associated with sperm telomere shortening and aberrant mRNA expression of autophagy-related genes
title_full Male obesity is associated with sperm telomere shortening and aberrant mRNA expression of autophagy-related genes
title_fullStr Male obesity is associated with sperm telomere shortening and aberrant mRNA expression of autophagy-related genes
title_full_unstemmed Male obesity is associated with sperm telomere shortening and aberrant mRNA expression of autophagy-related genes
title_short Male obesity is associated with sperm telomere shortening and aberrant mRNA expression of autophagy-related genes
title_sort male obesity is associated with sperm telomere shortening and aberrant mrna expression of autophagy-related genes
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10210264/
https://www.ncbi.nlm.nih.gov/pubmed/37226085
http://dx.doi.org/10.1186/s12610-023-00188-w
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