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Expression of testicular phosphorylated proteins in types 1 and 2 diabetes mellitus in mice: An experimental study

BACKGROUND: Types 1 and 2 diabetes mellitus (DM) are known to be the cause of sub/infertility. However, the comparisons of potential markers in spermatogenesis and steroidogenesis in DM males have never been elucidated. OBJECTIVE: This study aimed to examine the expressions of tyrosine-phosphorylate...

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Autores principales: Sampannang, Apichakan, Arun, Supatcharee, Burawat, Jaturon, Sukhorum, Wannisa, Iamsaard, Sitthichai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Knowledge E 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6745087/
https://www.ncbi.nlm.nih.gov/pubmed/31583374
http://dx.doi.org/10.18502/ijrm.v17i8.4822
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author Sampannang, Apichakan
Arun, Supatcharee
Burawat, Jaturon
Sukhorum, Wannisa
Iamsaard, Sitthichai
author_facet Sampannang, Apichakan
Arun, Supatcharee
Burawat, Jaturon
Sukhorum, Wannisa
Iamsaard, Sitthichai
author_sort Sampannang, Apichakan
collection PubMed
description BACKGROUND: Types 1 and 2 diabetes mellitus (DM) are known to be the cause of sub/infertility. However, the comparisons of potential markers in spermatogenesis and steroidogenesis in DM males have never been elucidated. OBJECTIVE: This study aimed to examine the expressions of tyrosine-phosphorylated and steroidogenic acute regulatory (StAR) proteins in testis of DM mice. MATERIALS AND METHODS: Fifty-six male C57BL/6 mice were divided into four groups (n░=░14/ each): control of MLD-STZ (multiple low doses of streptozotocin), MLD-STZ, control of HFD-STZ (high-fat diet with STZ), and HFD-STZ. MLD-STZ mice (type 1 DM) were intraperitoneally (i.p.) injected with STZ at 40░mg/kg BW for five days. HFD-STZ mice (type 2 DM) received an HFD for 14 days and i.p.-induced by STZ at 85░mg/kg BW and fed with HFD. At the end of the experiment (days 36 and 72), the expressions of phosphorylated proteins and StAR were examined. RESULTS: Tyrosine phosphorylated proteins were localized in late spermatids, luminal fluid, and Leydig cells. The intensities of phosphorylated 110, 85, 72, 60, and 55░kDas were lower in the 36 day-DM mice. Although such intensities were present in both groups, only 85░kDa in the MLD-STZ mice was higher in HFD mice at 72 days. StAR expressions in both groups were decreased than that of the controls. CONCLUSION: Decreased expressions of StAR and tyrosine-phosphorylated proteins may be directly involved in low testosterone levels and impaired spermatogenesis. These findings support the notion that both DM types play a role in male infertility.
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spelling pubmed-67450872019-10-03 Expression of testicular phosphorylated proteins in types 1 and 2 diabetes mellitus in mice: An experimental study Sampannang, Apichakan Arun, Supatcharee Burawat, Jaturon Sukhorum, Wannisa Iamsaard, Sitthichai Int J Reprod Biomed Original Article BACKGROUND: Types 1 and 2 diabetes mellitus (DM) are known to be the cause of sub/infertility. However, the comparisons of potential markers in spermatogenesis and steroidogenesis in DM males have never been elucidated. OBJECTIVE: This study aimed to examine the expressions of tyrosine-phosphorylated and steroidogenic acute regulatory (StAR) proteins in testis of DM mice. MATERIALS AND METHODS: Fifty-six male C57BL/6 mice were divided into four groups (n░=░14/ each): control of MLD-STZ (multiple low doses of streptozotocin), MLD-STZ, control of HFD-STZ (high-fat diet with STZ), and HFD-STZ. MLD-STZ mice (type 1 DM) were intraperitoneally (i.p.) injected with STZ at 40░mg/kg BW for five days. HFD-STZ mice (type 2 DM) received an HFD for 14 days and i.p.-induced by STZ at 85░mg/kg BW and fed with HFD. At the end of the experiment (days 36 and 72), the expressions of phosphorylated proteins and StAR were examined. RESULTS: Tyrosine phosphorylated proteins were localized in late spermatids, luminal fluid, and Leydig cells. The intensities of phosphorylated 110, 85, 72, 60, and 55░kDas were lower in the 36 day-DM mice. Although such intensities were present in both groups, only 85░kDa in the MLD-STZ mice was higher in HFD mice at 72 days. StAR expressions in both groups were decreased than that of the controls. CONCLUSION: Decreased expressions of StAR and tyrosine-phosphorylated proteins may be directly involved in low testosterone levels and impaired spermatogenesis. These findings support the notion that both DM types play a role in male infertility. Knowledge E 2019-09-03 /pmc/articles/PMC6745087/ /pubmed/31583374 http://dx.doi.org/10.18502/ijrm.v17i8.4822 Text en Copyright © 2019 Apichakan Sampannang et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Original Article
Sampannang, Apichakan
Arun, Supatcharee
Burawat, Jaturon
Sukhorum, Wannisa
Iamsaard, Sitthichai
Expression of testicular phosphorylated proteins in types 1 and 2 diabetes mellitus in mice: An experimental study
title Expression of testicular phosphorylated proteins in types 1 and 2 diabetes mellitus in mice: An experimental study
title_full Expression of testicular phosphorylated proteins in types 1 and 2 diabetes mellitus in mice: An experimental study
title_fullStr Expression of testicular phosphorylated proteins in types 1 and 2 diabetes mellitus in mice: An experimental study
title_full_unstemmed Expression of testicular phosphorylated proteins in types 1 and 2 diabetes mellitus in mice: An experimental study
title_short Expression of testicular phosphorylated proteins in types 1 and 2 diabetes mellitus in mice: An experimental study
title_sort expression of testicular phosphorylated proteins in types 1 and 2 diabetes mellitus in mice: an experimental study
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6745087/
https://www.ncbi.nlm.nih.gov/pubmed/31583374
http://dx.doi.org/10.18502/ijrm.v17i8.4822
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