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Effects of experimentally-induced diabetes on sperm parameters and chromatin quality in mice
Background: Diabetes mellitus (DM), primary or idiopathic is a chronic disorder of the carbohydrate, lipid and protein metabolism. DM may impact male reproductive function at several levels. It is shown that DM has detrimental effects on sperm parameters in human and experimental animals. Objective:...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Research and Clinical Center for Infertility
2013
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3941382/ https://www.ncbi.nlm.nih.gov/pubmed/24639693 |
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author | Mangoli, Esmat Talebi, Ali Reza Anvari, Morteza Pourentezari, Majid |
author_facet | Mangoli, Esmat Talebi, Ali Reza Anvari, Morteza Pourentezari, Majid |
author_sort | Mangoli, Esmat |
collection | PubMed |
description | Background: Diabetes mellitus (DM), primary or idiopathic is a chronic disorder of the carbohydrate, lipid and protein metabolism. DM may impact male reproductive function at several levels. It is shown that DM has detrimental effects on sperm parameters in human and experimental animals. Objective: The aim of this study was to observe the effects of diabetes on sperm parameters (viability, count, morphology and motility) and evaluation of sperm chromatin quality in mice. Materials and Methods: Totally twenty adult male Syrian mice were divided randomly into 2 groups (n=10). The animals of group A were considered as controls while group B mice were diabetic that received a single dose (200 mg/kg) streptozotocin (STZ) intra peritoneally. After 35 days, the cauda epididymis of each diabetic mouse was dissected and placed in culture medium for 30 min. The swim-out spermatozoa were analyzed for count, motility, morphology and viability. The sperm chromatin quality and DNA integrity, was evaluated with Aniline Blue (AB), Toluidine blue (TB), Acridine orange (AO) and Chromomycin A3 (CMA3) staining. Results: In sperm analysis, the diabetic mice had poor parameters in comparison with control animals (p=0.000). Regarding sperm chromatin quality, the results of TB and AO tests showed statically significant differences between two groups, but in AB and CMA3 staining, we didn’t see any differences between them. Conclusion: The results showed that STZ-induced diabetes mellitus may influence the male fertility potential via affecting sperm parameters and DNA integrity in mice. However, according to our data, the diabetes doesn’t have any detrimental effects on histone-protamines replacement during the testicular phase of sperm chromatin packaging. |
format | Online Article Text |
id | pubmed-3941382 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Research and Clinical Center for Infertility |
record_format | MEDLINE/PubMed |
spelling | pubmed-39413822014-03-17 Effects of experimentally-induced diabetes on sperm parameters and chromatin quality in mice Mangoli, Esmat Talebi, Ali Reza Anvari, Morteza Pourentezari, Majid Iran J Reprod Med Background: Diabetes mellitus (DM), primary or idiopathic is a chronic disorder of the carbohydrate, lipid and protein metabolism. DM may impact male reproductive function at several levels. It is shown that DM has detrimental effects on sperm parameters in human and experimental animals. Objective: The aim of this study was to observe the effects of diabetes on sperm parameters (viability, count, morphology and motility) and evaluation of sperm chromatin quality in mice. Materials and Methods: Totally twenty adult male Syrian mice were divided randomly into 2 groups (n=10). The animals of group A were considered as controls while group B mice were diabetic that received a single dose (200 mg/kg) streptozotocin (STZ) intra peritoneally. After 35 days, the cauda epididymis of each diabetic mouse was dissected and placed in culture medium for 30 min. The swim-out spermatozoa were analyzed for count, motility, morphology and viability. The sperm chromatin quality and DNA integrity, was evaluated with Aniline Blue (AB), Toluidine blue (TB), Acridine orange (AO) and Chromomycin A3 (CMA3) staining. Results: In sperm analysis, the diabetic mice had poor parameters in comparison with control animals (p=0.000). Regarding sperm chromatin quality, the results of TB and AO tests showed statically significant differences between two groups, but in AB and CMA3 staining, we didn’t see any differences between them. Conclusion: The results showed that STZ-induced diabetes mellitus may influence the male fertility potential via affecting sperm parameters and DNA integrity in mice. However, according to our data, the diabetes doesn’t have any detrimental effects on histone-protamines replacement during the testicular phase of sperm chromatin packaging. Research and Clinical Center for Infertility 2013-01 /pmc/articles/PMC3941382/ /pubmed/24639693 Text en This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Mangoli, Esmat Talebi, Ali Reza Anvari, Morteza Pourentezari, Majid Effects of experimentally-induced diabetes on sperm parameters and chromatin quality in mice |
title | Effects of experimentally-induced diabetes on sperm parameters and chromatin quality in mice |
title_full | Effects of experimentally-induced diabetes on sperm parameters and chromatin quality in mice |
title_fullStr | Effects of experimentally-induced diabetes on sperm parameters and chromatin quality in mice |
title_full_unstemmed | Effects of experimentally-induced diabetes on sperm parameters and chromatin quality in mice |
title_short | Effects of experimentally-induced diabetes on sperm parameters and chromatin quality in mice |
title_sort | effects of experimentally-induced diabetes on sperm parameters and chromatin quality in mice |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3941382/ https://www.ncbi.nlm.nih.gov/pubmed/24639693 |
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