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
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/24315
Ver los metadatos del registro completo
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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 |
_version_ |
1842269065147580416 |
score |
13.13397 |