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Impact of uteroplacental insufficiency on postnatal rat male gonad
Prenatal events such as intrauterine growth restriction can affect gonadal development of the offspring and have an impact on reproductive health. To investigate the effects of intrauterine growth restriction induced by uterine artery ligation on the postnatal rat testis. Pregnant rats underwent ute...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Bioscientifica Ltd
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5184772/ https://www.ncbi.nlm.nih.gov/pubmed/27885054 http://dx.doi.org/10.1530/JOE-16-0418 |
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author | Pampanini, Valentina Germani, Daniela Puglianiello, Antonella Stukenborg, Jan-Bernd Reda, Ahmed Savchuk, Iuliia Kjartansdóttir, Kristín Rós Cianfarani, Stefano Söder, Olle |
author_facet | Pampanini, Valentina Germani, Daniela Puglianiello, Antonella Stukenborg, Jan-Bernd Reda, Ahmed Savchuk, Iuliia Kjartansdóttir, Kristín Rós Cianfarani, Stefano Söder, Olle |
author_sort | Pampanini, Valentina |
collection | PubMed |
description | Prenatal events such as intrauterine growth restriction can affect gonadal development of the offspring and have an impact on reproductive health. To investigate the effects of intrauterine growth restriction induced by uterine artery ligation on the postnatal rat testis. Pregnant rats underwent uterine artery ligation at day 19 of gestation. Offspring were killed at 5, 20 and 40 days post-partum (dpp). At killing, one gonad was snap-frozen in liquid nitrogen and processed for RNA and steroid extraction. The other gonad was formalin-fixed for histology. Gene expression was analyzed by TaqMan Low-Density Array. Intratesticular testosterone, estradiol and serum gonadotrophins were measured. Thirty genes were dysregulated in intrauterine growth-restricted rats compared to controls, among which markers of Sertoli cell and Leydig cell function, cell metabolism and growth factors. Testis weights were significantly reduced at 5 and 20 dpp in intrauterine growth-restricted rats and caught-up by 40 dpp. Accordingly, Sertoli cell number was significantly lower in 5 dpp intrauterine growth-restricted rats. At 20 dpp, intratesticular testosterone was significantly increased in intrauterine growth-restricted rats, whereas serum gonadotrophins were unchanged. IUGR altered the gene expression in the rat testes up to peripubertal age and reduced testis size and Sertoli cell number in neonatal age. Multiple mechanisms encompassing genetic changes and steroid production by the testis may be involved in the catch-up growth phase that restored testis size by 40 dpp. Permanent consequences on organ function and gamete integrity cannot be excluded and deserve further investigations. |
format | Online Article Text |
id | pubmed-5184772 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Bioscientifica Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-51847722017-01-04 Impact of uteroplacental insufficiency on postnatal rat male gonad Pampanini, Valentina Germani, Daniela Puglianiello, Antonella Stukenborg, Jan-Bernd Reda, Ahmed Savchuk, Iuliia Kjartansdóttir, Kristín Rós Cianfarani, Stefano Söder, Olle J Endocrinol Research Prenatal events such as intrauterine growth restriction can affect gonadal development of the offspring and have an impact on reproductive health. To investigate the effects of intrauterine growth restriction induced by uterine artery ligation on the postnatal rat testis. Pregnant rats underwent uterine artery ligation at day 19 of gestation. Offspring were killed at 5, 20 and 40 days post-partum (dpp). At killing, one gonad was snap-frozen in liquid nitrogen and processed for RNA and steroid extraction. The other gonad was formalin-fixed for histology. Gene expression was analyzed by TaqMan Low-Density Array. Intratesticular testosterone, estradiol and serum gonadotrophins were measured. Thirty genes were dysregulated in intrauterine growth-restricted rats compared to controls, among which markers of Sertoli cell and Leydig cell function, cell metabolism and growth factors. Testis weights were significantly reduced at 5 and 20 dpp in intrauterine growth-restricted rats and caught-up by 40 dpp. Accordingly, Sertoli cell number was significantly lower in 5 dpp intrauterine growth-restricted rats. At 20 dpp, intratesticular testosterone was significantly increased in intrauterine growth-restricted rats, whereas serum gonadotrophins were unchanged. IUGR altered the gene expression in the rat testes up to peripubertal age and reduced testis size and Sertoli cell number in neonatal age. Multiple mechanisms encompassing genetic changes and steroid production by the testis may be involved in the catch-up growth phase that restored testis size by 40 dpp. Permanent consequences on organ function and gamete integrity cannot be excluded and deserve further investigations. Bioscientifica Ltd 2016-12-13 /pmc/articles/PMC5184772/ /pubmed/27885054 http://dx.doi.org/10.1530/JOE-16-0418 Text en © 2017 The authors http://creativecommons.org/licenses/by/3.0/ This work is licensed under a Creative Commons Attribution 3.0 Unported License (http://creativecommons.org/licenses/by/3.0/) . |
spellingShingle | Research Pampanini, Valentina Germani, Daniela Puglianiello, Antonella Stukenborg, Jan-Bernd Reda, Ahmed Savchuk, Iuliia Kjartansdóttir, Kristín Rós Cianfarani, Stefano Söder, Olle Impact of uteroplacental insufficiency on postnatal rat male gonad |
title | Impact of uteroplacental insufficiency on postnatal rat male gonad |
title_full | Impact of uteroplacental insufficiency on postnatal rat male gonad |
title_fullStr | Impact of uteroplacental insufficiency on postnatal rat male gonad |
title_full_unstemmed | Impact of uteroplacental insufficiency on postnatal rat male gonad |
title_short | Impact of uteroplacental insufficiency on postnatal rat male gonad |
title_sort | impact of uteroplacental insufficiency on postnatal rat male gonad |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5184772/ https://www.ncbi.nlm.nih.gov/pubmed/27885054 http://dx.doi.org/10.1530/JOE-16-0418 |
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