Glutamate-induced obesity leads to decreased sperm reserves and acceleration of transit time in the epididymis of adult male rats
Autor(a) principal: | |
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Data de Publicação: | 2012 |
Outros Autores: | , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://dx.doi.org/10.1186/1477-7827-10-105 http://hdl.handle.net/11449/12276 |
Resumo: | Background: Given the established fact that obesity interferes with male reproductive functions, the present study aimed to evaluate sperm production in the testis and storage in the epididymis in a glutamate-induced model of obesity.Methods: Male rats were treated neonatally with monosodium glutamate (MSG) at doses of 4 mg/kg subcutaneously, or with saline solution (control group), on postnatal days 2, 4, 6, 8 and 10. on day 120, obesity was confirmed by the Lee index in all MSG-treated rats. After this, all animals from the two experimental groups were anesthetized and killed to evaluate body and reproductive organ weights, sperm parameters, plasma hormone levels (FSH, LH and testosterone), testicular and epididymal histo-morphometry and histopathology.Results: Significant reductions in absolute and relative weights of testis, epididymis, prostate and seminal vesicle were noted in MSG-treated animals. In these same animals plasma testosterone and follicle-stimulating hormone (FSH) concentrations were decreased, as well as sperm counts in the testis and epididymis and seminiferous epithelium height and tubular diameter. The sperm transit time was accelerated in obese rats. However, the number of Sertoli cells per seminiferous tubule and stereological findings on the epididymis were not markedly changed by obesity.Conclusions: Neonatal MSG-administered model of obesity lowers sperm production and leads to a reduction in sperm storage in the epididymis of adult male rats. The acceleration of sperm transit time can have implications for the sperm quality of these rats. |
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Glutamate-induced obesity leads to decreased sperm reserves and acceleration of transit time in the epididymis of adult male ratsObesityMonosodium glutamateEpididymisTestosteroneSpermRatBackground: Given the established fact that obesity interferes with male reproductive functions, the present study aimed to evaluate sperm production in the testis and storage in the epididymis in a glutamate-induced model of obesity.Methods: Male rats were treated neonatally with monosodium glutamate (MSG) at doses of 4 mg/kg subcutaneously, or with saline solution (control group), on postnatal days 2, 4, 6, 8 and 10. on day 120, obesity was confirmed by the Lee index in all MSG-treated rats. After this, all animals from the two experimental groups were anesthetized and killed to evaluate body and reproductive organ weights, sperm parameters, plasma hormone levels (FSH, LH and testosterone), testicular and epididymal histo-morphometry and histopathology.Results: Significant reductions in absolute and relative weights of testis, epididymis, prostate and seminal vesicle were noted in MSG-treated animals. In these same animals plasma testosterone and follicle-stimulating hormone (FSH) concentrations were decreased, as well as sperm counts in the testis and epididymis and seminiferous epithelium height and tubular diameter. The sperm transit time was accelerated in obese rats. However, the number of Sertoli cells per seminiferous tubule and stereological findings on the epididymis were not markedly changed by obesity.Conclusions: Neonatal MSG-administered model of obesity lowers sperm production and leads to a reduction in sperm storage in the epididymis of adult male rats. The acceleration of sperm transit time can have implications for the sperm quality of these rats.Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Univiversidade Estadual de Londrina (UEL), UEL, Ctr Biol Sci, Londrina, PR, BrazilUNESP UnivEstadualPaulista, Inst Biosci, Dept Morphol, Botucatu, SP, BrazilUniv Fed Mato Grosso, UFMT, Inst Biol & Hlth Sci, Barra do Garca, MT, BrazilUniv São Paulo, Ribeirao Preto Med Sch, Dept Physiol, Ribeirao Preto, SP, BrazilUNESP UnivEstadualPaulista, Lab Expt Res Gynecol & Obstet, Dept Gynecol & Obstet, Botucatu Med Sch, Botucatu, SP, BrazilUNESP UnivEstadualPaulista, Inst Biosci, Dept Morphol, Botucatu, SP, BrazilUNESP UnivEstadualPaulista, Lab Expt Res Gynecol & Obstet, Dept Gynecol & Obstet, Botucatu Med Sch, Botucatu, SP, BrazilBiomed Central Ltd.Universidade Estadual de Londrina (UEL)Universidade Estadual Paulista (Unesp)Univ Fed Mato GrossoUniversidade de São Paulo (USP)Fernandes, Glaura S. A.Arena, Arielle C. [UNESP]Campos, Kleber E.Volpato, Gustavo T.Anselmo-Franci, Janete A.Damasceno, Débora Cristina [UNESP]Kempinas, Wilma G. [UNESP]2014-05-20T13:35:40Z2014-05-20T13:35:40Z2012-12-05info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article6application/pdfhttp://dx.doi.org/10.1186/1477-7827-10-105Reproductive Biology and Endocrinology. London: Biomed Central Ltd., v. 10, p. 6, 2012.1477-7827http://hdl.handle.net/11449/1227610.1186/1477-7827-10-105WOS:000314708600002WOS000314708600002.pdfWeb of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengReproductive Biology and Endocrinology2.8521,203info:eu-repo/semantics/openAccess2024-08-16T14:06:31Zoai:repositorio.unesp.br:11449/12276Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-16T14:06:31Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Glutamate-induced obesity leads to decreased sperm reserves and acceleration of transit time in the epididymis of adult male rats |
title |
Glutamate-induced obesity leads to decreased sperm reserves and acceleration of transit time in the epididymis of adult male rats |
spellingShingle |
Glutamate-induced obesity leads to decreased sperm reserves and acceleration of transit time in the epididymis of adult male rats Fernandes, Glaura S. A. Obesity Monosodium glutamate Epididymis Testosterone Sperm Rat |
title_short |
Glutamate-induced obesity leads to decreased sperm reserves and acceleration of transit time in the epididymis of adult male rats |
title_full |
Glutamate-induced obesity leads to decreased sperm reserves and acceleration of transit time in the epididymis of adult male rats |
title_fullStr |
Glutamate-induced obesity leads to decreased sperm reserves and acceleration of transit time in the epididymis of adult male rats |
title_full_unstemmed |
Glutamate-induced obesity leads to decreased sperm reserves and acceleration of transit time in the epididymis of adult male rats |
title_sort |
Glutamate-induced obesity leads to decreased sperm reserves and acceleration of transit time in the epididymis of adult male rats |
author |
Fernandes, Glaura S. A. |
author_facet |
Fernandes, Glaura S. A. Arena, Arielle C. [UNESP] Campos, Kleber E. Volpato, Gustavo T. Anselmo-Franci, Janete A. Damasceno, Débora Cristina [UNESP] Kempinas, Wilma G. [UNESP] |
author_role |
author |
author2 |
Arena, Arielle C. [UNESP] Campos, Kleber E. Volpato, Gustavo T. Anselmo-Franci, Janete A. Damasceno, Débora Cristina [UNESP] Kempinas, Wilma G. [UNESP] |
author2_role |
author author author author author author |
dc.contributor.none.fl_str_mv |
Universidade Estadual de Londrina (UEL) Universidade Estadual Paulista (Unesp) Univ Fed Mato Grosso Universidade de São Paulo (USP) |
dc.contributor.author.fl_str_mv |
Fernandes, Glaura S. A. Arena, Arielle C. [UNESP] Campos, Kleber E. Volpato, Gustavo T. Anselmo-Franci, Janete A. Damasceno, Débora Cristina [UNESP] Kempinas, Wilma G. [UNESP] |
dc.subject.por.fl_str_mv |
Obesity Monosodium glutamate Epididymis Testosterone Sperm Rat |
topic |
Obesity Monosodium glutamate Epididymis Testosterone Sperm Rat |
description |
Background: Given the established fact that obesity interferes with male reproductive functions, the present study aimed to evaluate sperm production in the testis and storage in the epididymis in a glutamate-induced model of obesity.Methods: Male rats were treated neonatally with monosodium glutamate (MSG) at doses of 4 mg/kg subcutaneously, or with saline solution (control group), on postnatal days 2, 4, 6, 8 and 10. on day 120, obesity was confirmed by the Lee index in all MSG-treated rats. After this, all animals from the two experimental groups were anesthetized and killed to evaluate body and reproductive organ weights, sperm parameters, plasma hormone levels (FSH, LH and testosterone), testicular and epididymal histo-morphometry and histopathology.Results: Significant reductions in absolute and relative weights of testis, epididymis, prostate and seminal vesicle were noted in MSG-treated animals. In these same animals plasma testosterone and follicle-stimulating hormone (FSH) concentrations were decreased, as well as sperm counts in the testis and epididymis and seminiferous epithelium height and tubular diameter. The sperm transit time was accelerated in obese rats. However, the number of Sertoli cells per seminiferous tubule and stereological findings on the epididymis were not markedly changed by obesity.Conclusions: Neonatal MSG-administered model of obesity lowers sperm production and leads to a reduction in sperm storage in the epididymis of adult male rats. The acceleration of sperm transit time can have implications for the sperm quality of these rats. |
publishDate |
2012 |
dc.date.none.fl_str_mv |
2012-12-05 2014-05-20T13:35:40Z 2014-05-20T13:35:40Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.1186/1477-7827-10-105 Reproductive Biology and Endocrinology. London: Biomed Central Ltd., v. 10, p. 6, 2012. 1477-7827 http://hdl.handle.net/11449/12276 10.1186/1477-7827-10-105 WOS:000314708600002 WOS000314708600002.pdf |
url |
http://dx.doi.org/10.1186/1477-7827-10-105 http://hdl.handle.net/11449/12276 |
identifier_str_mv |
Reproductive Biology and Endocrinology. London: Biomed Central Ltd., v. 10, p. 6, 2012. 1477-7827 10.1186/1477-7827-10-105 WOS:000314708600002 WOS000314708600002.pdf |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Reproductive Biology and Endocrinology 2.852 1,203 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
6 application/pdf |
dc.publisher.none.fl_str_mv |
Biomed Central Ltd. |
publisher.none.fl_str_mv |
Biomed Central Ltd. |
dc.source.none.fl_str_mv |
Web of Science reponame:Repositório Institucional da UNESP instname:Universidade Estadual Paulista (UNESP) instacron:UNESP |
instname_str |
Universidade Estadual Paulista (UNESP) |
instacron_str |
UNESP |
institution |
UNESP |
reponame_str |
Repositório Institucional da UNESP |
collection |
Repositório Institucional da UNESP |
repository.name.fl_str_mv |
Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP) |
repository.mail.fl_str_mv |
|
_version_ |
1808128114614599680 |