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Maternal Protein Restriction Modulates Angiogenesis and AQP9 Expression Leading to a Delay in Postnatal Epididymal Development in Rat

The maternal nutritional status is essential to the health and well-being of the fetus. Maternal protein restriction during the perinatal stage causes sperm alterations in the offspring that are associated with epididymal dysfunctions. Vascular endothelial growth factor (VEGF) and its receptor, VEGF...

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Autores principales: de Mello Santos, Talita, Cavariani, Marilia Martins, Pereira, Dhrielly Natália, Schimming, Bruno César, Chuffa, Luiz Gustavo de Almeida, Domeniconi, Raquel Fantin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6770568/
https://www.ncbi.nlm.nih.gov/pubmed/31533210
http://dx.doi.org/10.3390/cells8091094
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author de Mello Santos, Talita
Cavariani, Marilia Martins
Pereira, Dhrielly Natália
Schimming, Bruno César
Chuffa, Luiz Gustavo de Almeida
Domeniconi, Raquel Fantin
author_facet de Mello Santos, Talita
Cavariani, Marilia Martins
Pereira, Dhrielly Natália
Schimming, Bruno César
Chuffa, Luiz Gustavo de Almeida
Domeniconi, Raquel Fantin
author_sort de Mello Santos, Talita
collection PubMed
description The maternal nutritional status is essential to the health and well-being of the fetus. Maternal protein restriction during the perinatal stage causes sperm alterations in the offspring that are associated with epididymal dysfunctions. Vascular endothelial growth factor (VEGF) and its receptor, VEGFr-2, as well as aquaporins (AQPs) are important regulators of angiogenesis and the epididymal microenvironment and are associated with male fertility. We investigated the effects of maternal protein restriction on epididymal angiogenesis and AQP expression in the early stages of postnatal epididymal development. Pregnant rats were divided into two experimental groups that received either a normoprotein (17% protein) or low-protein diet (6% protein) during gestation and lactation. At postnatal day (PND)7 and PND14, male offspring were euthanized, the epididymides were subjected to morphometric and microvascular density analyses and to VEGF-A, VEGF-r2, AQP1 and AQP9 expression analyses. The maternal low-protein diet decreased AQP9 and VEGFr-2 expression, decreased epididymal microvascularity and altered the morphometric features of the epididymal epithelium; no changes in AQP1 expression were observed at the beginning of postnatal epididymal development. Maternal protein restriction alters microvascularization and affects molecules involved in the epidydimal microenvironment, resulting in morphometric alterations related to a delay in the beginning of epididymis postnatal development.
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spelling pubmed-67705682019-10-30 Maternal Protein Restriction Modulates Angiogenesis and AQP9 Expression Leading to a Delay in Postnatal Epididymal Development in Rat de Mello Santos, Talita Cavariani, Marilia Martins Pereira, Dhrielly Natália Schimming, Bruno César Chuffa, Luiz Gustavo de Almeida Domeniconi, Raquel Fantin Cells Article The maternal nutritional status is essential to the health and well-being of the fetus. Maternal protein restriction during the perinatal stage causes sperm alterations in the offspring that are associated with epididymal dysfunctions. Vascular endothelial growth factor (VEGF) and its receptor, VEGFr-2, as well as aquaporins (AQPs) are important regulators of angiogenesis and the epididymal microenvironment and are associated with male fertility. We investigated the effects of maternal protein restriction on epididymal angiogenesis and AQP expression in the early stages of postnatal epididymal development. Pregnant rats were divided into two experimental groups that received either a normoprotein (17% protein) or low-protein diet (6% protein) during gestation and lactation. At postnatal day (PND)7 and PND14, male offspring were euthanized, the epididymides were subjected to morphometric and microvascular density analyses and to VEGF-A, VEGF-r2, AQP1 and AQP9 expression analyses. The maternal low-protein diet decreased AQP9 and VEGFr-2 expression, decreased epididymal microvascularity and altered the morphometric features of the epididymal epithelium; no changes in AQP1 expression were observed at the beginning of postnatal epididymal development. Maternal protein restriction alters microvascularization and affects molecules involved in the epidydimal microenvironment, resulting in morphometric alterations related to a delay in the beginning of epididymis postnatal development. MDPI 2019-09-17 /pmc/articles/PMC6770568/ /pubmed/31533210 http://dx.doi.org/10.3390/cells8091094 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
de Mello Santos, Talita
Cavariani, Marilia Martins
Pereira, Dhrielly Natália
Schimming, Bruno César
Chuffa, Luiz Gustavo de Almeida
Domeniconi, Raquel Fantin
Maternal Protein Restriction Modulates Angiogenesis and AQP9 Expression Leading to a Delay in Postnatal Epididymal Development in Rat
title Maternal Protein Restriction Modulates Angiogenesis and AQP9 Expression Leading to a Delay in Postnatal Epididymal Development in Rat
title_full Maternal Protein Restriction Modulates Angiogenesis and AQP9 Expression Leading to a Delay in Postnatal Epididymal Development in Rat
title_fullStr Maternal Protein Restriction Modulates Angiogenesis and AQP9 Expression Leading to a Delay in Postnatal Epididymal Development in Rat
title_full_unstemmed Maternal Protein Restriction Modulates Angiogenesis and AQP9 Expression Leading to a Delay in Postnatal Epididymal Development in Rat
title_short Maternal Protein Restriction Modulates Angiogenesis and AQP9 Expression Leading to a Delay in Postnatal Epididymal Development in Rat
title_sort maternal protein restriction modulates angiogenesis and aqp9 expression leading to a delay in postnatal epididymal development in rat
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6770568/
https://www.ncbi.nlm.nih.gov/pubmed/31533210
http://dx.doi.org/10.3390/cells8091094
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