Intervenção farmacológica sobre o sistema serotoninérgico durante o desenvolvimento testicular pré-natal e neonatal de ratos Wistar utilizando cloridrato de fluoxetina

Detalhes bibliográficos
Autor(a) principal: MONTEIRO FILHO, Waldo Oliveira
Data de Publicação: 2009
Tipo de documento: Dissertação
Idioma: por
Título da fonte: Biblioteca Digital de Teses e Dissertações da UFRPE
Texto Completo: http://www.tede2.ufrpe.br:8080/tede2/handle/tede2/5884
Resumo: Currently, selective serotonin reuptake inhibitors (SSRIs) are the most frequently prescribed antidepressants for the treatment of depression and major side effects in adults related to sexual dysfunction. Depressive disorders are common both during the prenatal period and early months after birth and fluoxetine is widely used to treat depression in this period. Until the present moment, no further study on the pharmacological intervention in the serotonin system during the critical period for testicular development in neonatal rats and the effects on the spermatogenic process in sexually mature rats was performed. We carried out 3 experiments using fluoxetine hydrochloride. In the first experiment observed the effect of direct administration of fluoxetine during postnatal testicular development in rats, but with assessment at 150 days of age. In this paper, we observed reduction in testicular weight gross and net volume of tubules and seminiferous epithelium. The tubular diameter was reduced in animals treated with 20 mg/Kg which caused an increase in total length of seminiferous tubules in this group. There were no histological changes in the population of Sertoli cells, daily sperm production and efficiency of the spermatogenic process. The second experiment studied the effects of transplacental transfer of fluoxetine and breast milk on the testicular development of prepubertal rats. In this experiment, were observed changes in the body weight development, in the testicular volumetric parameters and total length of seminiferous tubules, mainly in higher doses of fluoxetine. There was a trend of reduction of Sertoli cells population and delay in the appearance tubular lumen in animals exposed to higher dose. Inthe third experiment was used the same protocol of the second experiment, but the testis were performed in rats sexually mature. According to the results was observed that fetal and neonatal contact with fluoxetine during the critical period of Sertoli cells proliferation influenced the somatic development of animals and induced changes in testicular parameters, such as the weight of the epididymis and seminal gland, volumes of the seminiferous epithelium, the total Leydig cells volume, total length of seminiferous tubules and a trend of reduction in sperm production per testis. Although fluoxetine has interfered with the Leydig cells volumetry, were not observed changes in plasma levels of testosterone and spermatogenesis. Most of the changes were related to the group treated with the highest dosage of the antidepressant, 20 mg/kg, implying that this dosage fluoxetine may actually cause changes in somatic development and reproductive function.
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spelling SILVA JUNIOR, Valdemiro Amaro daEVÊNCIO NETO, JoaquimMENDONÇA, Fábio de SouzaMAIA, Frederico Celso Lirahttp://lattes.cnpq.br/8920849880729899MONTEIRO FILHO, Waldo Oliveira2016-11-08T12:52:57Z2009-07-31MONTEIRO FILHO, Waldo Oliveira. Intervenção farmacológica sobre o sistema serotoninérgico durante o desenvolvimento testicular pré-natal e neonatal de ratos Wistar utilizando cloridrato de fluoxetina. 2009. 113 f. Dissertação (Programa de Pós-Graduação em Ciência Veterinária) - Universidade Federal Rural de Pernambuco, Recife.http://www.tede2.ufrpe.br:8080/tede2/handle/tede2/5884Currently, selective serotonin reuptake inhibitors (SSRIs) are the most frequently prescribed antidepressants for the treatment of depression and major side effects in adults related to sexual dysfunction. Depressive disorders are common both during the prenatal period and early months after birth and fluoxetine is widely used to treat depression in this period. Until the present moment, no further study on the pharmacological intervention in the serotonin system during the critical period for testicular development in neonatal rats and the effects on the spermatogenic process in sexually mature rats was performed. We carried out 3 experiments using fluoxetine hydrochloride. In the first experiment observed the effect of direct administration of fluoxetine during postnatal testicular development in rats, but with assessment at 150 days of age. In this paper, we observed reduction in testicular weight gross and net volume of tubules and seminiferous epithelium. The tubular diameter was reduced in animals treated with 20 mg/Kg which caused an increase in total length of seminiferous tubules in this group. There were no histological changes in the population of Sertoli cells, daily sperm production and efficiency of the spermatogenic process. The second experiment studied the effects of transplacental transfer of fluoxetine and breast milk on the testicular development of prepubertal rats. In this experiment, were observed changes in the body weight development, in the testicular volumetric parameters and total length of seminiferous tubules, mainly in higher doses of fluoxetine. There was a trend of reduction of Sertoli cells population and delay in the appearance tubular lumen in animals exposed to higher dose. Inthe third experiment was used the same protocol of the second experiment, but the testis were performed in rats sexually mature. According to the results was observed that fetal and neonatal contact with fluoxetine during the critical period of Sertoli cells proliferation influenced the somatic development of animals and induced changes in testicular parameters, such as the weight of the epididymis and seminal gland, volumes of the seminiferous epithelium, the total Leydig cells volume, total length of seminiferous tubules and a trend of reduction in sperm production per testis. Although fluoxetine has interfered with the Leydig cells volumetry, were not observed changes in plasma levels of testosterone and spermatogenesis. Most of the changes were related to the group treated with the highest dosage of the antidepressant, 20 mg/kg, implying that this dosage fluoxetine may actually cause changes in somatic development and reproductive function.Atualmente, os inibidores da recaptação seletiva da serotonina (ISRS) são os antidepressivos mais freqüentemente prescritos para o tratamento da depressão, sendo o principal efeito colateral em adultos relacionado às disfunções sexuais. Distúrbios depressivos são comuns tanto durante o período pré-natal quanto nos meses iniciais após o nascimento e a fluoxetina é largamente utilizado no tratamento da depressão neste período. Até o presente momento, nenhum estudo mais pormenorizado sobre a intervenção farmacológica do sistema serotoninérgico durante o período crítico do desenvolvimento testicular em ratos neonatos e os seus reflexos no processo espermatogênico em ratos maturos sexualmente foi realizado. Neste trabalho foram realizados 3 experimentos utilizando cloridrato de fluoxetina. No primeiro experimento foi observado o efeito da administração direta da fluoxetina durante o período pós-natal do desenvolvimento testicular de ratos Wistar porém, com avaliação aos 150 dias de idade. Neste trabalho se observou redução o peso testicular bruto e líquido, volume de túbulos e epitélio seminíferos. O diâmetro tubular foi reduzido nos animais tratados com 20mg/Kg o que gerou aumento no comprimento total de túbulos seminíferos neste grupo. Não foram observadas alterações morfométricas na população de células de Sertoli, produção espermática diária e eficiência do processo espermatogênico. No segundo experimento foram estudados os efeitos da transferência de fluoxetina transplacentária e pelo leite materno sobre o desenvolvimento testicular de ratos Wistar pré-buberes. Neste experimento se observou alterações no desenvolvimento ponderal de peso corporal, em parâmetros volumétricos testiculares e comprimento total de túbulos seminíferos em dosagensmais elevadas de fluoxetina. Notou-se tendência de redução da população total de células de Sertoli por testículo e atraso no aparecimento do lume tubular nos animais expostos a maior dose. No terceiro experimento se utilizou o mesmo protocolo do segundo experimento, porém as análises foram realizadas em animais maturos sexualmente. De acordo com os resultados observados o contato fetal e neonatal com fluoxetina, no período crítico de proliferação das células de Sertoli influenciou no desenvolvimento somático dos animais e ocasionou alterações em parâmetros testiculares, tais como o peso de epidídimo e glândula seminal, volumetria do epitélio seminífero, volumetria total das células de Leydig, comprimento total dos túbulos seminíferos e uma tendência de redução na produção espermática por testículo. Ainda que a fluoxetina tenha interferido na volumetria das células de Leydig, não se constatou alteração nos níveis plasmáticos de testosterona e da espermatogênese. A maior parte das alterações está relacionada ao grupo tratado com a maior dosagem do antidepressivo, 20mg/Kg, inferindo que nessa dosagem a fluoxetina pode, de fato, causar alterações no desenvolvimento somático e do aparelho reprodutivo.Submitted by (edna.saturno@ufrpe.br) on 2016-11-08T12:52:57Z No. of bitstreams: 1 Waldo Oliveira Monteiro Filho.pdf: 1607300 bytes, checksum: aa0749d6dd1cc7f00a1f19730ca34d59 (MD5)Made available in DSpace on 2016-11-08T12:52:57Z (GMT). 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dc.title.por.fl_str_mv Intervenção farmacológica sobre o sistema serotoninérgico durante o desenvolvimento testicular pré-natal e neonatal de ratos Wistar utilizando cloridrato de fluoxetina
title Intervenção farmacológica sobre o sistema serotoninérgico durante o desenvolvimento testicular pré-natal e neonatal de ratos Wistar utilizando cloridrato de fluoxetina
spellingShingle Intervenção farmacológica sobre o sistema serotoninérgico durante o desenvolvimento testicular pré-natal e neonatal de ratos Wistar utilizando cloridrato de fluoxetina
MONTEIRO FILHO, Waldo Oliveira
Rato
Testículo
Célula de Sertoli
Serotonina
Fluoxetina
Rat
Sertoli cell
Fluoxetine
CIENCIAS AGRARIAS::MEDICINA VETERINARIA
title_short Intervenção farmacológica sobre o sistema serotoninérgico durante o desenvolvimento testicular pré-natal e neonatal de ratos Wistar utilizando cloridrato de fluoxetina
title_full Intervenção farmacológica sobre o sistema serotoninérgico durante o desenvolvimento testicular pré-natal e neonatal de ratos Wistar utilizando cloridrato de fluoxetina
title_fullStr Intervenção farmacológica sobre o sistema serotoninérgico durante o desenvolvimento testicular pré-natal e neonatal de ratos Wistar utilizando cloridrato de fluoxetina
title_full_unstemmed Intervenção farmacológica sobre o sistema serotoninérgico durante o desenvolvimento testicular pré-natal e neonatal de ratos Wistar utilizando cloridrato de fluoxetina
title_sort Intervenção farmacológica sobre o sistema serotoninérgico durante o desenvolvimento testicular pré-natal e neonatal de ratos Wistar utilizando cloridrato de fluoxetina
author MONTEIRO FILHO, Waldo Oliveira
author_facet MONTEIRO FILHO, Waldo Oliveira
author_role author
dc.contributor.advisor1.fl_str_mv SILVA JUNIOR, Valdemiro Amaro da
dc.contributor.referee1.fl_str_mv EVÊNCIO NETO, Joaquim
dc.contributor.referee2.fl_str_mv MENDONÇA, Fábio de Souza
dc.contributor.referee3.fl_str_mv MAIA, Frederico Celso Lira
dc.contributor.authorLattes.fl_str_mv http://lattes.cnpq.br/8920849880729899
dc.contributor.author.fl_str_mv MONTEIRO FILHO, Waldo Oliveira
contributor_str_mv SILVA JUNIOR, Valdemiro Amaro da
EVÊNCIO NETO, Joaquim
MENDONÇA, Fábio de Souza
MAIA, Frederico Celso Lira
dc.subject.por.fl_str_mv Rato
Testículo
Célula de Sertoli
Serotonina
Fluoxetina
topic Rato
Testículo
Célula de Sertoli
Serotonina
Fluoxetina
Rat
Sertoli cell
Fluoxetine
CIENCIAS AGRARIAS::MEDICINA VETERINARIA
dc.subject.eng.fl_str_mv Rat
Sertoli cell
Fluoxetine
dc.subject.cnpq.fl_str_mv CIENCIAS AGRARIAS::MEDICINA VETERINARIA
description Currently, selective serotonin reuptake inhibitors (SSRIs) are the most frequently prescribed antidepressants for the treatment of depression and major side effects in adults related to sexual dysfunction. Depressive disorders are common both during the prenatal period and early months after birth and fluoxetine is widely used to treat depression in this period. Until the present moment, no further study on the pharmacological intervention in the serotonin system during the critical period for testicular development in neonatal rats and the effects on the spermatogenic process in sexually mature rats was performed. We carried out 3 experiments using fluoxetine hydrochloride. In the first experiment observed the effect of direct administration of fluoxetine during postnatal testicular development in rats, but with assessment at 150 days of age. In this paper, we observed reduction in testicular weight gross and net volume of tubules and seminiferous epithelium. The tubular diameter was reduced in animals treated with 20 mg/Kg which caused an increase in total length of seminiferous tubules in this group. There were no histological changes in the population of Sertoli cells, daily sperm production and efficiency of the spermatogenic process. The second experiment studied the effects of transplacental transfer of fluoxetine and breast milk on the testicular development of prepubertal rats. In this experiment, were observed changes in the body weight development, in the testicular volumetric parameters and total length of seminiferous tubules, mainly in higher doses of fluoxetine. There was a trend of reduction of Sertoli cells population and delay in the appearance tubular lumen in animals exposed to higher dose. Inthe third experiment was used the same protocol of the second experiment, but the testis were performed in rats sexually mature. According to the results was observed that fetal and neonatal contact with fluoxetine during the critical period of Sertoli cells proliferation influenced the somatic development of animals and induced changes in testicular parameters, such as the weight of the epididymis and seminal gland, volumes of the seminiferous epithelium, the total Leydig cells volume, total length of seminiferous tubules and a trend of reduction in sperm production per testis. Although fluoxetine has interfered with the Leydig cells volumetry, were not observed changes in plasma levels of testosterone and spermatogenesis. Most of the changes were related to the group treated with the highest dosage of the antidepressant, 20 mg/kg, implying that this dosage fluoxetine may actually cause changes in somatic development and reproductive function.
publishDate 2009
dc.date.issued.fl_str_mv 2009-07-31
dc.date.accessioned.fl_str_mv 2016-11-08T12:52:57Z
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dc.identifier.citation.fl_str_mv MONTEIRO FILHO, Waldo Oliveira. Intervenção farmacológica sobre o sistema serotoninérgico durante o desenvolvimento testicular pré-natal e neonatal de ratos Wistar utilizando cloridrato de fluoxetina. 2009. 113 f. Dissertação (Programa de Pós-Graduação em Ciência Veterinária) - Universidade Federal Rural de Pernambuco, Recife.
dc.identifier.uri.fl_str_mv http://www.tede2.ufrpe.br:8080/tede2/handle/tede2/5884
identifier_str_mv MONTEIRO FILHO, Waldo Oliveira. Intervenção farmacológica sobre o sistema serotoninérgico durante o desenvolvimento testicular pré-natal e neonatal de ratos Wistar utilizando cloridrato de fluoxetina. 2009. 113 f. Dissertação (Programa de Pós-Graduação em Ciência Veterinária) - Universidade Federal Rural de Pernambuco, Recife.
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