Identification of differentially expressed genes in pathways of cerebral neurotransmission of anovulatory mice
Autor(a) principal: | |
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Data de Publicação: | 2017 |
Outros Autores: | |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNIFESP |
Texto Completo: | http://dx.doi.org/10.4238/gmr16039622 https://repositorio.unifesp.br/handle/11600/57161 |
Resumo: | Polycystic ovary syndrome is the classic example of loss of functional cyclicity and anomalous feedback. In this case, the excessive extra-glandular production and conversion of androgens to estrogens are the pathophysiological basis of the chronic anovulation. The literature describes an experimental model of the polymicrocystic ovary in obese diabetic mice with insulin resistance. The fact that these animals exhibit obesity, insulin resistance, and infertility demonstrates their skill as an experimental model for polycystic ovary. A recent study using long protocol for up to 40 weeks showed that anovulatory and obese mice transplanted with adipose tissue from animals with normal weight have multiple changes in their phenotype. These changes include reduction of body weight, prevention of obesity, insulin level normalization, and insulin tolerance tests, preventing the elevation of steroids and especially the reversal of fertility restoration with anovulation. Considering that there are close relationships between the ovulation process and the central nervous system, we propose to evaluate the gene expression levels of 84 different genes involved in neurotransmission and insulin pathways in addition to examining the neurolipidosis differential murine brain before and after reversal of anovulation. The present study showed changes in gene expression of molecular markers in brain tissue of animals for brain neurotransmission pathways as well as pathways for insulin. GABAergic genes, muscarinic, serotonin receptors, receptor tyrosine kinase, and genes of interleukin 6 showed overexpression profile. There was also a change in the lipid content in anovulatory brain, obesity, and insulin resistant mice (Ob-/Ob-) compared with controls. The re-introduction of leptin in these animals appears to reverse, at least in part, this profile. |
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Identification of differentially expressed genes in pathways of cerebral neurotransmission of anovulatory miceDifferentially expressed genesNeurotransmitterAnovulationPolycystic ovary syndrome is the classic example of loss of functional cyclicity and anomalous feedback. In this case, the excessive extra-glandular production and conversion of androgens to estrogens are the pathophysiological basis of the chronic anovulation. The literature describes an experimental model of the polymicrocystic ovary in obese diabetic mice with insulin resistance. The fact that these animals exhibit obesity, insulin resistance, and infertility demonstrates their skill as an experimental model for polycystic ovary. A recent study using long protocol for up to 40 weeks showed that anovulatory and obese mice transplanted with adipose tissue from animals with normal weight have multiple changes in their phenotype. These changes include reduction of body weight, prevention of obesity, insulin level normalization, and insulin tolerance tests, preventing the elevation of steroids and especially the reversal of fertility restoration with anovulation. Considering that there are close relationships between the ovulation process and the central nervous system, we propose to evaluate the gene expression levels of 84 different genes involved in neurotransmission and insulin pathways in addition to examining the neurolipidosis differential murine brain before and after reversal of anovulation. The present study showed changes in gene expression of molecular markers in brain tissue of animals for brain neurotransmission pathways as well as pathways for insulin. GABAergic genes, muscarinic, serotonin receptors, receptor tyrosine kinase, and genes of interleukin 6 showed overexpression profile. There was also a change in the lipid content in anovulatory brain, obesity, and insulin resistant mice (Ob-/Ob-) compared with controls. The re-introduction of leptin in these animals appears to reverse, at least in part, this profile.Univ Fed Sao Paulo, Lab Ginecol Mol, Sao Paulo, SP, BrazilUniv Fed Sao Paulo, Lab Ginecol Mol, Sao Paulo, SP, BrazilWeb of ScienceFunpec-Editora2020-08-04T13:39:53Z2020-08-04T13:39:53Z2017info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion-application/pdfhttp://dx.doi.org/10.4238/gmr16039622Genetics And Molecular Research. Ribeirao Preto, v. 16, n. 3, p. -, 2017.10.4238/gmr16039622WOS000417365000007.pdf1676-5680https://repositorio.unifesp.br/handle/11600/57161WOS:000417365000007engGenetics And Molecular ResearchRibeirao Pretoinfo:eu-repo/semantics/openAccessAzevedo, M. A., Jr. [UNIFESP]Silva, I. D. C. G. [UNIFESP]reponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-08-04T14:45:18Zoai:repositorio.unifesp.br/:11600/57161Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-08-04T14:45:18Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false |
dc.title.none.fl_str_mv |
Identification of differentially expressed genes in pathways of cerebral neurotransmission of anovulatory mice |
title |
Identification of differentially expressed genes in pathways of cerebral neurotransmission of anovulatory mice |
spellingShingle |
Identification of differentially expressed genes in pathways of cerebral neurotransmission of anovulatory mice Azevedo, M. A., Jr. [UNIFESP] Differentially expressed genes Neurotransmitter Anovulation |
title_short |
Identification of differentially expressed genes in pathways of cerebral neurotransmission of anovulatory mice |
title_full |
Identification of differentially expressed genes in pathways of cerebral neurotransmission of anovulatory mice |
title_fullStr |
Identification of differentially expressed genes in pathways of cerebral neurotransmission of anovulatory mice |
title_full_unstemmed |
Identification of differentially expressed genes in pathways of cerebral neurotransmission of anovulatory mice |
title_sort |
Identification of differentially expressed genes in pathways of cerebral neurotransmission of anovulatory mice |
author |
Azevedo, M. A., Jr. [UNIFESP] |
author_facet |
Azevedo, M. A., Jr. [UNIFESP] Silva, I. D. C. G. [UNIFESP] |
author_role |
author |
author2 |
Silva, I. D. C. G. [UNIFESP] |
author2_role |
author |
dc.contributor.author.fl_str_mv |
Azevedo, M. A., Jr. [UNIFESP] Silva, I. D. C. G. [UNIFESP] |
dc.subject.por.fl_str_mv |
Differentially expressed genes Neurotransmitter Anovulation |
topic |
Differentially expressed genes Neurotransmitter Anovulation |
description |
Polycystic ovary syndrome is the classic example of loss of functional cyclicity and anomalous feedback. In this case, the excessive extra-glandular production and conversion of androgens to estrogens are the pathophysiological basis of the chronic anovulation. The literature describes an experimental model of the polymicrocystic ovary in obese diabetic mice with insulin resistance. The fact that these animals exhibit obesity, insulin resistance, and infertility demonstrates their skill as an experimental model for polycystic ovary. A recent study using long protocol for up to 40 weeks showed that anovulatory and obese mice transplanted with adipose tissue from animals with normal weight have multiple changes in their phenotype. These changes include reduction of body weight, prevention of obesity, insulin level normalization, and insulin tolerance tests, preventing the elevation of steroids and especially the reversal of fertility restoration with anovulation. Considering that there are close relationships between the ovulation process and the central nervous system, we propose to evaluate the gene expression levels of 84 different genes involved in neurotransmission and insulin pathways in addition to examining the neurolipidosis differential murine brain before and after reversal of anovulation. The present study showed changes in gene expression of molecular markers in brain tissue of animals for brain neurotransmission pathways as well as pathways for insulin. GABAergic genes, muscarinic, serotonin receptors, receptor tyrosine kinase, and genes of interleukin 6 showed overexpression profile. There was also a change in the lipid content in anovulatory brain, obesity, and insulin resistant mice (Ob-/Ob-) compared with controls. The re-introduction of leptin in these animals appears to reverse, at least in part, this profile. |
publishDate |
2017 |
dc.date.none.fl_str_mv |
2017 2020-08-04T13:39:53Z 2020-08-04T13:39:53Z |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.4238/gmr16039622 Genetics And Molecular Research. Ribeirao Preto, v. 16, n. 3, p. -, 2017. 10.4238/gmr16039622 WOS000417365000007.pdf 1676-5680 https://repositorio.unifesp.br/handle/11600/57161 WOS:000417365000007 |
url |
http://dx.doi.org/10.4238/gmr16039622 https://repositorio.unifesp.br/handle/11600/57161 |
identifier_str_mv |
Genetics And Molecular Research. Ribeirao Preto, v. 16, n. 3, p. -, 2017. 10.4238/gmr16039622 WOS000417365000007.pdf 1676-5680 WOS:000417365000007 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Genetics And Molecular Research |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
- application/pdf |
dc.coverage.none.fl_str_mv |
Ribeirao Preto |
dc.publisher.none.fl_str_mv |
Funpec-Editora |
publisher.none.fl_str_mv |
Funpec-Editora |
dc.source.none.fl_str_mv |
reponame:Repositório Institucional da UNIFESP instname:Universidade Federal de São Paulo (UNIFESP) instacron:UNIFESP |
instname_str |
Universidade Federal de São Paulo (UNIFESP) |
instacron_str |
UNIFESP |
institution |
UNIFESP |
reponame_str |
Repositório Institucional da UNIFESP |
collection |
Repositório Institucional da UNIFESP |
repository.name.fl_str_mv |
Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP) |
repository.mail.fl_str_mv |
biblioteca.csp@unifesp.br |
_version_ |
1814268269546176512 |