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In utero protein restriction causes growth delay and alters sperm parameters in adult male rats

BACKGROUND: Recent studies have supported the concept of "fetal programming" which suggests that during the intrauterine development the fetus may be programmed to develop diseases in adulthood. The possible effects of in utero protein restriction on sexual development of rat male offsprin...

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Autores principales: Toledo, Fabíola C, Perobelli, Juliana E, Pedrosa, Flávia PC, Anselmo-Franci, Janete A, Kempinas, Wilma DG
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3141647/
https://www.ncbi.nlm.nih.gov/pubmed/21702915
http://dx.doi.org/10.1186/1477-7827-9-94
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author Toledo, Fabíola C
Perobelli, Juliana E
Pedrosa, Flávia PC
Anselmo-Franci, Janete A
Kempinas, Wilma DG
author_facet Toledo, Fabíola C
Perobelli, Juliana E
Pedrosa, Flávia PC
Anselmo-Franci, Janete A
Kempinas, Wilma DG
author_sort Toledo, Fabíola C
collection PubMed
description BACKGROUND: Recent studies have supported the concept of "fetal programming" which suggests that during the intrauterine development the fetus may be programmed to develop diseases in adulthood. The possible effects of in utero protein restriction on sexual development of rat male offspring were evaluated in the present study. METHODS: Pregnant Wistar rats were divided into two experimental groups: one group treated with standard chow (SC, n = 8, 17% protein) and the other group treated with hypoproteic chow (HC, n = 10, 6% protein) throughout gestation. After gestation the two experimental groups received standard chow. To evaluate the possible late reproductive effects of in utero protein restriction, the male offspring of both groups were assessed at different phases of sexual development: prepubertal (30 days old); peripubertal (60 days old); adult (90 days old). Student's t-test and Mann-Whitney test were utilized. Differences were considered significant when p < 0.05. RESULTS: We found that in utero protein restriction reduced the body weight of male pups on the first postnatal day and during the different sexual development phases (prepubertal, peripubertal and adult). During adulthood, Sertoli cell number, sperm motility and sperm counts in the testis and epididymal cauda were also reduced in HC. Furthermore, the numbers of sperm presenting morphological abnormalities and cytoplasmic drop retention were higher in HC. CONCLUSIONS: In conclusion, in utero protein restriction, under these experimental conditions, causes growth delay and alters male reproductive-system programming in rats, suggesting impairment of sperm quality in adulthood.
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spelling pubmed-31416472011-07-23 In utero protein restriction causes growth delay and alters sperm parameters in adult male rats Toledo, Fabíola C Perobelli, Juliana E Pedrosa, Flávia PC Anselmo-Franci, Janete A Kempinas, Wilma DG Reprod Biol Endocrinol Research BACKGROUND: Recent studies have supported the concept of "fetal programming" which suggests that during the intrauterine development the fetus may be programmed to develop diseases in adulthood. The possible effects of in utero protein restriction on sexual development of rat male offspring were evaluated in the present study. METHODS: Pregnant Wistar rats were divided into two experimental groups: one group treated with standard chow (SC, n = 8, 17% protein) and the other group treated with hypoproteic chow (HC, n = 10, 6% protein) throughout gestation. After gestation the two experimental groups received standard chow. To evaluate the possible late reproductive effects of in utero protein restriction, the male offspring of both groups were assessed at different phases of sexual development: prepubertal (30 days old); peripubertal (60 days old); adult (90 days old). Student's t-test and Mann-Whitney test were utilized. Differences were considered significant when p < 0.05. RESULTS: We found that in utero protein restriction reduced the body weight of male pups on the first postnatal day and during the different sexual development phases (prepubertal, peripubertal and adult). During adulthood, Sertoli cell number, sperm motility and sperm counts in the testis and epididymal cauda were also reduced in HC. Furthermore, the numbers of sperm presenting morphological abnormalities and cytoplasmic drop retention were higher in HC. CONCLUSIONS: In conclusion, in utero protein restriction, under these experimental conditions, causes growth delay and alters male reproductive-system programming in rats, suggesting impairment of sperm quality in adulthood. BioMed Central 2011-06-24 /pmc/articles/PMC3141647/ /pubmed/21702915 http://dx.doi.org/10.1186/1477-7827-9-94 Text en Copyright ©2011 Toledo et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Toledo, Fabíola C
Perobelli, Juliana E
Pedrosa, Flávia PC
Anselmo-Franci, Janete A
Kempinas, Wilma DG
In utero protein restriction causes growth delay and alters sperm parameters in adult male rats
title In utero protein restriction causes growth delay and alters sperm parameters in adult male rats
title_full In utero protein restriction causes growth delay and alters sperm parameters in adult male rats
title_fullStr In utero protein restriction causes growth delay and alters sperm parameters in adult male rats
title_full_unstemmed In utero protein restriction causes growth delay and alters sperm parameters in adult male rats
title_short In utero protein restriction causes growth delay and alters sperm parameters in adult male rats
title_sort in utero protein restriction causes growth delay and alters sperm parameters in adult male rats
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3141647/
https://www.ncbi.nlm.nih.gov/pubmed/21702915
http://dx.doi.org/10.1186/1477-7827-9-94
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