SIRT1 in astrocytes regulates glucose metabolism and reproductive function
- Autores
- Choi, Irene; Rickert, Emily; Fernandez, Marina Olga; Webster, Nicholas J.G.
- Año de publicación
- 2019
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- Sirtuin 1 (Sirt1) is an NAD-dependent class III deacetylase that functions as a cellular energy sensor. In addition to its well-characterized effects in peripheral tissues, evidence suggests that SIRT1 in neurons plays a role in the central regulation of energy balance and reproduction, but no studies have addressed the contribution of astrocytes. We show here that overexpression of SIRT1 in astrocytes causes markedly increased food intake, body weight gain, and glucose intolerance, but expression of a deacetylase-deficient SIRT1 mutant decreases food intake and body weight and improves glucose tolerance, particularly in female mice. Paradoxically, the effect of these SIRT1 mutants on insulin tolerance was reversed, with overexpression showing greater insulin sensitivity. The mice overexpressing SIRT1 were more active, generated more heat, and had elevated oxygen consumption, possibly in compensation for the increased food intake. The female overexpressing mice were also more sensitive to diet-induced obesity. Reproductively, the mice expressing the deacetylase-deficient SIRT1 mutant had impaired estrous cycles, decreased LH surges, and fewer corpora lutea, indicating decreased ovulation. The GnRH neurons were responsive to kisspeptin stimulation, but hypothalamic expression of Kiss1 was reduced in the mutant mice. Our results showed that SIRT1 signaling in astrocytes can contribute to metabolic and reproductive regulation independent of SIRT1 effects in neurons.
Fil: Choi, Irene. VA San Diego Healthcare System; Estados Unidos
Fil: Rickert, Emily. University of California at San Diego; Estados Unidos
Fil: Fernandez, Marina Olga. University of California at San Diego; Estados Unidos. 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
Fil: Webster, Nicholas J.G.. VA San Diego Healthcare System; Estados Unidos. University of California at San Diego; Estados Unidos - Materia
-
ASTROCYTE KNOCK-OUT
ENERGY BALANCE
REPRODUCTION
SIRTUIN 1 - 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:11336/106233
Ver los metadatos del registro completo
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SIRT1 in astrocytes regulates glucose metabolism and reproductive functionChoi, IreneRickert, EmilyFernandez, Marina OlgaWebster, Nicholas J.G.ASTROCYTE KNOCK-OUTENERGY BALANCEREPRODUCTIONSIRTUIN 1https://purl.org/becyt/ford/3.1https://purl.org/becyt/ford/3Sirtuin 1 (Sirt1) is an NAD-dependent class III deacetylase that functions as a cellular energy sensor. In addition to its well-characterized effects in peripheral tissues, evidence suggests that SIRT1 in neurons plays a role in the central regulation of energy balance and reproduction, but no studies have addressed the contribution of astrocytes. We show here that overexpression of SIRT1 in astrocytes causes markedly increased food intake, body weight gain, and glucose intolerance, but expression of a deacetylase-deficient SIRT1 mutant decreases food intake and body weight and improves glucose tolerance, particularly in female mice. Paradoxically, the effect of these SIRT1 mutants on insulin tolerance was reversed, with overexpression showing greater insulin sensitivity. The mice overexpressing SIRT1 were more active, generated more heat, and had elevated oxygen consumption, possibly in compensation for the increased food intake. The female overexpressing mice were also more sensitive to diet-induced obesity. Reproductively, the mice expressing the deacetylase-deficient SIRT1 mutant had impaired estrous cycles, decreased LH surges, and fewer corpora lutea, indicating decreased ovulation. The GnRH neurons were responsive to kisspeptin stimulation, but hypothalamic expression of Kiss1 was reduced in the mutant mice. Our results showed that SIRT1 signaling in astrocytes can contribute to metabolic and reproductive regulation independent of SIRT1 effects in neurons.Fil: Choi, Irene. VA San Diego Healthcare System; Estados UnidosFil: Rickert, Emily. University of California at San Diego; Estados UnidosFil: Fernandez, Marina Olga. University of California at San Diego; Estados Unidos. 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; ArgentinaFil: Webster, Nicholas J.G.. VA San Diego Healthcare System; Estados Unidos. University of California at San Diego; Estados UnidosEndocrine Society2019-06info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/106233Choi, Irene; Rickert, Emily; Fernandez, Marina Olga; Webster, Nicholas J.G.; SIRT1 in astrocytes regulates glucose metabolism and reproductive function; Endocrine Society; Endocrinology; 160; 6; 6-2019; 1547-15600013-7227CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://academic.oup.com/endo/article/160/6/1547/5479348info:eu-repo/semantics/altIdentifier/doi/10.1210/en.2019-00223info:eu-repo/semantics/altIdentifier/url/https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6542483/info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-10T13:06:44Zoai:ri.conicet.gov.ar:11336/106233instacron: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:34982025-09-10 13:06:44.462CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
dc.title.none.fl_str_mv |
SIRT1 in astrocytes regulates glucose metabolism and reproductive function |
title |
SIRT1 in astrocytes regulates glucose metabolism and reproductive function |
spellingShingle |
SIRT1 in astrocytes regulates glucose metabolism and reproductive function Choi, Irene ASTROCYTE KNOCK-OUT ENERGY BALANCE REPRODUCTION SIRTUIN 1 |
title_short |
SIRT1 in astrocytes regulates glucose metabolism and reproductive function |
title_full |
SIRT1 in astrocytes regulates glucose metabolism and reproductive function |
title_fullStr |
SIRT1 in astrocytes regulates glucose metabolism and reproductive function |
title_full_unstemmed |
SIRT1 in astrocytes regulates glucose metabolism and reproductive function |
title_sort |
SIRT1 in astrocytes regulates glucose metabolism and reproductive function |
dc.creator.none.fl_str_mv |
Choi, Irene Rickert, Emily Fernandez, Marina Olga Webster, Nicholas J.G. |
author |
Choi, Irene |
author_facet |
Choi, Irene Rickert, Emily Fernandez, Marina Olga Webster, Nicholas J.G. |
author_role |
author |
author2 |
Rickert, Emily Fernandez, Marina Olga Webster, Nicholas J.G. |
author2_role |
author author author |
dc.subject.none.fl_str_mv |
ASTROCYTE KNOCK-OUT ENERGY BALANCE REPRODUCTION SIRTUIN 1 |
topic |
ASTROCYTE KNOCK-OUT ENERGY BALANCE REPRODUCTION SIRTUIN 1 |
purl_subject.fl_str_mv |
https://purl.org/becyt/ford/3.1 https://purl.org/becyt/ford/3 |
dc.description.none.fl_txt_mv |
Sirtuin 1 (Sirt1) is an NAD-dependent class III deacetylase that functions as a cellular energy sensor. In addition to its well-characterized effects in peripheral tissues, evidence suggests that SIRT1 in neurons plays a role in the central regulation of energy balance and reproduction, but no studies have addressed the contribution of astrocytes. We show here that overexpression of SIRT1 in astrocytes causes markedly increased food intake, body weight gain, and glucose intolerance, but expression of a deacetylase-deficient SIRT1 mutant decreases food intake and body weight and improves glucose tolerance, particularly in female mice. Paradoxically, the effect of these SIRT1 mutants on insulin tolerance was reversed, with overexpression showing greater insulin sensitivity. The mice overexpressing SIRT1 were more active, generated more heat, and had elevated oxygen consumption, possibly in compensation for the increased food intake. The female overexpressing mice were also more sensitive to diet-induced obesity. Reproductively, the mice expressing the deacetylase-deficient SIRT1 mutant had impaired estrous cycles, decreased LH surges, and fewer corpora lutea, indicating decreased ovulation. The GnRH neurons were responsive to kisspeptin stimulation, but hypothalamic expression of Kiss1 was reduced in the mutant mice. Our results showed that SIRT1 signaling in astrocytes can contribute to metabolic and reproductive regulation independent of SIRT1 effects in neurons. Fil: Choi, Irene. VA San Diego Healthcare System; Estados Unidos Fil: Rickert, Emily. University of California at San Diego; Estados Unidos Fil: Fernandez, Marina Olga. University of California at San Diego; Estados Unidos. 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 Fil: Webster, Nicholas J.G.. VA San Diego Healthcare System; Estados Unidos. University of California at San Diego; Estados Unidos |
description |
Sirtuin 1 (Sirt1) is an NAD-dependent class III deacetylase that functions as a cellular energy sensor. In addition to its well-characterized effects in peripheral tissues, evidence suggests that SIRT1 in neurons plays a role in the central regulation of energy balance and reproduction, but no studies have addressed the contribution of astrocytes. We show here that overexpression of SIRT1 in astrocytes causes markedly increased food intake, body weight gain, and glucose intolerance, but expression of a deacetylase-deficient SIRT1 mutant decreases food intake and body weight and improves glucose tolerance, particularly in female mice. Paradoxically, the effect of these SIRT1 mutants on insulin tolerance was reversed, with overexpression showing greater insulin sensitivity. The mice overexpressing SIRT1 were more active, generated more heat, and had elevated oxygen consumption, possibly in compensation for the increased food intake. The female overexpressing mice were also more sensitive to diet-induced obesity. Reproductively, the mice expressing the deacetylase-deficient SIRT1 mutant had impaired estrous cycles, decreased LH surges, and fewer corpora lutea, indicating decreased ovulation. The GnRH neurons were responsive to kisspeptin stimulation, but hypothalamic expression of Kiss1 was reduced in the mutant mice. Our results showed that SIRT1 signaling in astrocytes can contribute to metabolic and reproductive regulation independent of SIRT1 effects in neurons. |
publishDate |
2019 |
dc.date.none.fl_str_mv |
2019-06 |
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/11336/106233 Choi, Irene; Rickert, Emily; Fernandez, Marina Olga; Webster, Nicholas J.G.; SIRT1 in astrocytes regulates glucose metabolism and reproductive function; Endocrine Society; Endocrinology; 160; 6; 6-2019; 1547-1560 0013-7227 CONICET Digital CONICET |
url |
http://hdl.handle.net/11336/106233 |
identifier_str_mv |
Choi, Irene; Rickert, Emily; Fernandez, Marina Olga; Webster, Nicholas J.G.; SIRT1 in astrocytes regulates glucose metabolism and reproductive function; Endocrine Society; Endocrinology; 160; 6; 6-2019; 1547-1560 0013-7227 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/160/6/1547/5479348 info:eu-repo/semantics/altIdentifier/doi/10.1210/en.2019-00223 info:eu-repo/semantics/altIdentifier/url/https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6542483/ |
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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1842980286202118144 |
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12.993085 |