Obese neuronal PPARγ KO mice are leptin sensitive but show impaired glucose tolerance and fertility

Autores
Fernandez, Marina Olga; Sharma, Shweta; Kim, Sun; Rickert, Emily; Hsueh, Katherine; Hwang, Vicky; Olefsky, Jerrold M.; Webster, Nicholas J.G.
Año de publicación
2017
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
PPARγ is expressed in the hypothalamus in areas involved in energy homeostasis and glucose metabolism. In this study, we created a deletion of PPARγ (BKO) in mature neurons in female mice to investigate its involvement in metabolism and reproduction. We observed that there was no difference in age at puberty onset between female BKOs and littermate controls, but the BKOs gave smaller litters when mated and fewer oocytes when ovulated. The female BKO mice had regular cycles but showed an increase in the number of cycles with prolonged estrus. The mice also had increased LH levels during the LH surge and histological examination showed hemorrhagic corpora lutea. The mice were challenged with a 60% high fat diet. Metabolically the female BKO mice showed normal body weight, glucose and insulin tolerance, and leptin levels but were protected from obesity-induced leptin resistance. The neuronal knockout also prevented the reduction in estrous cycles due to the HFD. Examination of ovarian histology showed a decrease in the number of primary and secondary follicles in both genotypes due to the HFD, but the BKO ovaries showed an increase in the number of hemorrhagic follicles. In summary, our results show that neuronal PPARγ is required for optimal female fertility, but is also involved in the adverse effects of diet-induced obesity by creating leptin resistance potentially through induction of the repressor Socs3.
Fil: Fernandez, Marina Olga. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Biología y Medicina Experimental. Fundación de Instituto de Biología y Medicina Experimental. Instituto de Biología y Medicina Experimental; Argentina. University of California at San Diego; Estados Unidos
Fil: Sharma, Shweta. University of California at San Diego; Estados Unidos
Fil: Kim, Sun. University of California at San Diego; Estados Unidos
Fil: Rickert, Emily. University of California at San Diego; Estados Unidos
Fil: Hsueh, Katherine. University of California at San Diego; Estados Unidos
Fil: Hwang, Vicky. University of California at San Diego; Estados Unidos
Fil: Olefsky, Jerrold M.. University of California at San Diego; Estados Unidos
Fil: Webster, Nicholas J.G.. University of California at San Diego; Estados Unidos. VA San Diego Healthcare System,; Estados Unidos
Materia
Leptin
Obesity
Pparg
Reproduction
Ovary Pathology
Nivel de accesibilidad
acceso abierto
Condiciones de uso
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
Repositorio
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/24315

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repository_id_str 3498
network_name_str CONICET Digital (CONICET)
spelling Obese neuronal PPARγ KO mice are leptin sensitive but show impaired glucose tolerance and fertilityFernandez, Marina OlgaSharma, ShwetaKim, SunRickert, EmilyHsueh, KatherineHwang, VickyOlefsky, Jerrold M.Webster, Nicholas J.G.LeptinObesityPpargReproductionOvary Pathologyhttps://purl.org/becyt/ford/3.1https://purl.org/becyt/ford/3https://purl.org/becyt/ford/1.6https://purl.org/becyt/ford/1PPARγ is expressed in the hypothalamus in areas involved in energy homeostasis and glucose metabolism. In this study, we created a deletion of PPARγ (BKO) in mature neurons in female mice to investigate its involvement in metabolism and reproduction. We observed that there was no difference in age at puberty onset between female BKOs and littermate controls, but the BKOs gave smaller litters when mated and fewer oocytes when ovulated. The female BKO mice had regular cycles but showed an increase in the number of cycles with prolonged estrus. The mice also had increased LH levels during the LH surge and histological examination showed hemorrhagic corpora lutea. The mice were challenged with a 60% high fat diet. Metabolically the female BKO mice showed normal body weight, glucose and insulin tolerance, and leptin levels but were protected from obesity-induced leptin resistance. The neuronal knockout also prevented the reduction in estrous cycles due to the HFD. Examination of ovarian histology showed a decrease in the number of primary and secondary follicles in both genotypes due to the HFD, but the BKO ovaries showed an increase in the number of hemorrhagic follicles. In summary, our results show that neuronal PPARγ is required for optimal female fertility, but is also involved in the adverse effects of diet-induced obesity by creating leptin resistance potentially through induction of the repressor Socs3.Fil: Fernandez, Marina Olga. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Biología y Medicina Experimental. Fundación de Instituto de Biología y Medicina Experimental. Instituto de Biología y Medicina Experimental; Argentina. University of California at San Diego; Estados UnidosFil: Sharma, Shweta. University of California at San Diego; Estados UnidosFil: Kim, Sun. University of California at San Diego; Estados UnidosFil: Rickert, Emily. University of California at San Diego; Estados UnidosFil: Hsueh, Katherine. University of California at San Diego; Estados UnidosFil: Hwang, Vicky. University of California at San Diego; Estados UnidosFil: Olefsky, Jerrold M.. University of California at San Diego; Estados UnidosFil: Webster, Nicholas J.G.. University of California at San Diego; Estados Unidos. VA San Diego Healthcare System,; Estados UnidosEndocrine Society2017-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/24315Fernandez, Marina Olga; Sharma, Shweta; Kim, Sun; Rickert, Emily; Hsueh, Katherine; et al.; Obese neuronal PPARγ KO mice are leptin sensitive but show impaired glucose tolerance and fertility; Endocrine Society; Endocrinology; 158; 1; 1-1-2017; 121-1330013-72271945-7170CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://academic.oup.com/endo/article-abstract/158/1/121/2751121/Obese-Neuronal-PPAR-Knockout-Mice-Are-Leptin?redirectedFrom=fulltextinfo:eu-repo/semantics/altIdentifier/doi/10.1210/en.2016-1818info:eu-repo/semantics/altIdentifier/pmid/27841948info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-03T09:50:59Zoai:ri.conicet.gov.ar:11336/24315instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-09-03 09:50:59.406CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Obese neuronal PPARγ KO mice are leptin sensitive but show impaired glucose tolerance and fertility
title Obese neuronal PPARγ KO mice are leptin sensitive but show impaired glucose tolerance and fertility
spellingShingle Obese neuronal PPARγ KO mice are leptin sensitive but show impaired glucose tolerance and fertility
Fernandez, Marina Olga
Leptin
Obesity
Pparg
Reproduction
Ovary Pathology
title_short Obese neuronal PPARγ KO mice are leptin sensitive but show impaired glucose tolerance and fertility
title_full Obese neuronal PPARγ KO mice are leptin sensitive but show impaired glucose tolerance and fertility
title_fullStr Obese neuronal PPARγ KO mice are leptin sensitive but show impaired glucose tolerance and fertility
title_full_unstemmed Obese neuronal PPARγ KO mice are leptin sensitive but show impaired glucose tolerance and fertility
title_sort Obese neuronal PPARγ KO mice are leptin sensitive but show impaired glucose tolerance and fertility
dc.creator.none.fl_str_mv Fernandez, Marina Olga
Sharma, Shweta
Kim, Sun
Rickert, Emily
Hsueh, Katherine
Hwang, Vicky
Olefsky, Jerrold M.
Webster, Nicholas J.G.
author Fernandez, Marina Olga
author_facet Fernandez, Marina Olga
Sharma, Shweta
Kim, Sun
Rickert, Emily
Hsueh, Katherine
Hwang, Vicky
Olefsky, Jerrold M.
Webster, Nicholas J.G.
author_role author
author2 Sharma, Shweta
Kim, Sun
Rickert, Emily
Hsueh, Katherine
Hwang, Vicky
Olefsky, Jerrold M.
Webster, Nicholas J.G.
author2_role author
author
author
author
author
author
author
dc.subject.none.fl_str_mv Leptin
Obesity
Pparg
Reproduction
Ovary Pathology
topic Leptin
Obesity
Pparg
Reproduction
Ovary Pathology
purl_subject.fl_str_mv https://purl.org/becyt/ford/3.1
https://purl.org/becyt/ford/3
https://purl.org/becyt/ford/1.6
https://purl.org/becyt/ford/1
dc.description.none.fl_txt_mv PPARγ is expressed in the hypothalamus in areas involved in energy homeostasis and glucose metabolism. In this study, we created a deletion of PPARγ (BKO) in mature neurons in female mice to investigate its involvement in metabolism and reproduction. We observed that there was no difference in age at puberty onset between female BKOs and littermate controls, but the BKOs gave smaller litters when mated and fewer oocytes when ovulated. The female BKO mice had regular cycles but showed an increase in the number of cycles with prolonged estrus. The mice also had increased LH levels during the LH surge and histological examination showed hemorrhagic corpora lutea. The mice were challenged with a 60% high fat diet. Metabolically the female BKO mice showed normal body weight, glucose and insulin tolerance, and leptin levels but were protected from obesity-induced leptin resistance. The neuronal knockout also prevented the reduction in estrous cycles due to the HFD. Examination of ovarian histology showed a decrease in the number of primary and secondary follicles in both genotypes due to the HFD, but the BKO ovaries showed an increase in the number of hemorrhagic follicles. In summary, our results show that neuronal PPARγ is required for optimal female fertility, but is also involved in the adverse effects of diet-induced obesity by creating leptin resistance potentially through induction of the repressor Socs3.
Fil: Fernandez, Marina Olga. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Biología y Medicina Experimental. Fundación de Instituto de Biología y Medicina Experimental. Instituto de Biología y Medicina Experimental; Argentina. University of California at San Diego; Estados Unidos
Fil: Sharma, Shweta. University of California at San Diego; Estados Unidos
Fil: Kim, Sun. University of California at San Diego; Estados Unidos
Fil: Rickert, Emily. University of California at San Diego; Estados Unidos
Fil: Hsueh, Katherine. University of California at San Diego; Estados Unidos
Fil: Hwang, Vicky. University of California at San Diego; Estados Unidos
Fil: Olefsky, Jerrold M.. University of California at San Diego; Estados Unidos
Fil: Webster, Nicholas J.G.. University of California at San Diego; Estados Unidos. VA San Diego Healthcare System,; Estados Unidos
description PPARγ is expressed in the hypothalamus in areas involved in energy homeostasis and glucose metabolism. In this study, we created a deletion of PPARγ (BKO) in mature neurons in female mice to investigate its involvement in metabolism and reproduction. We observed that there was no difference in age at puberty onset between female BKOs and littermate controls, but the BKOs gave smaller litters when mated and fewer oocytes when ovulated. The female BKO mice had regular cycles but showed an increase in the number of cycles with prolonged estrus. The mice also had increased LH levels during the LH surge and histological examination showed hemorrhagic corpora lutea. The mice were challenged with a 60% high fat diet. Metabolically the female BKO mice showed normal body weight, glucose and insulin tolerance, and leptin levels but were protected from obesity-induced leptin resistance. The neuronal knockout also prevented the reduction in estrous cycles due to the HFD. Examination of ovarian histology showed a decrease in the number of primary and secondary follicles in both genotypes due to the HFD, but the BKO ovaries showed an increase in the number of hemorrhagic follicles. In summary, our results show that neuronal PPARγ is required for optimal female fertility, but is also involved in the adverse effects of diet-induced obesity by creating leptin resistance potentially through induction of the repressor Socs3.
publishDate 2017
dc.date.none.fl_str_mv 2017-01-01
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
http://purl.org/coar/resource_type/c_6501
info:ar-repo/semantics/articulo
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv http://hdl.handle.net/11336/24315
Fernandez, Marina Olga; Sharma, Shweta; Kim, Sun; Rickert, Emily; Hsueh, Katherine; et al.; Obese neuronal PPARγ KO mice are leptin sensitive but show impaired glucose tolerance and fertility; Endocrine Society; Endocrinology; 158; 1; 1-1-2017; 121-133
0013-7227
1945-7170
CONICET Digital
CONICET
url http://hdl.handle.net/11336/24315
identifier_str_mv Fernandez, Marina Olga; Sharma, Shweta; Kim, Sun; Rickert, Emily; Hsueh, Katherine; et al.; Obese neuronal PPARγ KO mice are leptin sensitive but show impaired glucose tolerance and fertility; Endocrine Society; Endocrinology; 158; 1; 1-1-2017; 121-133
0013-7227
1945-7170
CONICET Digital
CONICET
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/url/https://academic.oup.com/endo/article-abstract/158/1/121/2751121/Obese-Neuronal-PPAR-Knockout-Mice-Are-Leptin?redirectedFrom=fulltext
info:eu-repo/semantics/altIdentifier/doi/10.1210/en.2016-1818
info:eu-repo/semantics/altIdentifier/pmid/27841948
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
eu_rights_str_mv openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.format.none.fl_str_mv application/pdf
application/pdf
dc.publisher.none.fl_str_mv Endocrine Society
publisher.none.fl_str_mv Endocrine Society
dc.source.none.fl_str_mv reponame:CONICET Digital (CONICET)
instname:Consejo Nacional de Investigaciones Científicas y Técnicas
reponame_str CONICET Digital (CONICET)
collection CONICET Digital (CONICET)
instname_str Consejo Nacional de Investigaciones Científicas y Técnicas
repository.name.fl_str_mv CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas
repository.mail.fl_str_mv dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar
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