Liver sex dimorphism and zonation shaped by growth hormone
- Autores
- Becu, Damasia
- Año de publicación
- 2022
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- In clinical medicine, the consideration of sex-specific differences in diagnosis and treatment of many diseases is gaining acceptance. In this context, sex differences in liver function and gene expression are important, although not highlighted in medical practice. In humans, significant sex differences in the bioavailability and clearance of drugs and other xenobiotics, as well as sex-biased proneness to different liver disorders, have been described. Sexually dimorphic gene expression of the liver depends mainly on growth hormone (GH) secretory patterns, and to a lesser extent on sex steroids. The brain is paramount in organizing GH pulses through synchronization of growth hormone–releasing hormone and somatostatin release and feedback responses (1), thus shaping liver sex dimorphism in accordance with the need for sex-specific steroid metabolism, and metabolic or even behavioral performance. High intermittent GH pulses are found in males, while females have a more constant secretory pattern in rodents; this pattern is found also in humans, although to a minor extent. This differential pulsatility is a key factor for the establishment and maintenance of sexual dimorphism in the transcription of liver genes (2-4). More than 1000 liver genes are sexually dimorphic, and of these approximately 90% are GH dependent (2). Sex differences in gene expression range from less than 2-fold to >1000-fold in the mouse, and this should alert to the need of considering sex as a variable when instrumenting different liver therapies, or administering drugs metabolized in a sex-specific manner.
Fil: Becu, Damasia. Academia Nacional de Ciencias de Buenos Aires; Argentina. 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 - Materia
-
GROWTH HORMONE
LIVER
SEX DIMORPHISM
SNRNASEQ
ZONATION - 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:11336/203885
Ver los metadatos del registro completo
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Liver sex dimorphism and zonation shaped by growth hormoneBecu, DamasiaGROWTH HORMONELIVERSEX DIMORPHISMSNRNASEQZONATIONhttps://purl.org/becyt/ford/3.1https://purl.org/becyt/ford/3In clinical medicine, the consideration of sex-specific differences in diagnosis and treatment of many diseases is gaining acceptance. In this context, sex differences in liver function and gene expression are important, although not highlighted in medical practice. In humans, significant sex differences in the bioavailability and clearance of drugs and other xenobiotics, as well as sex-biased proneness to different liver disorders, have been described. Sexually dimorphic gene expression of the liver depends mainly on growth hormone (GH) secretory patterns, and to a lesser extent on sex steroids. The brain is paramount in organizing GH pulses through synchronization of growth hormone–releasing hormone and somatostatin release and feedback responses (1), thus shaping liver sex dimorphism in accordance with the need for sex-specific steroid metabolism, and metabolic or even behavioral performance. High intermittent GH pulses are found in males, while females have a more constant secretory pattern in rodents; this pattern is found also in humans, although to a minor extent. This differential pulsatility is a key factor for the establishment and maintenance of sexual dimorphism in the transcription of liver genes (2-4). More than 1000 liver genes are sexually dimorphic, and of these approximately 90% are GH dependent (2). Sex differences in gene expression range from less than 2-fold to >1000-fold in the mouse, and this should alert to the need of considering sex as a variable when instrumenting different liver therapies, or administering drugs metabolized in a sex-specific manner.Fil: Becu, Damasia. Academia Nacional de Ciencias de Buenos Aires; Argentina. 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; ArgentinaEndocrine Society2022info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/203885Becu, Damasia; Liver sex dimorphism and zonation shaped by growth hormone; Endocrine Society; Endocrinology; 163; 8; 2022; 1-20013-7227CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/doi/10.1210/endocr/bqac087info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-03T09:46:22Zoai:ri.conicet.gov.ar:11336/203885instacron: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 09:46:22.921CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
dc.title.none.fl_str_mv |
Liver sex dimorphism and zonation shaped by growth hormone |
title |
Liver sex dimorphism and zonation shaped by growth hormone |
spellingShingle |
Liver sex dimorphism and zonation shaped by growth hormone Becu, Damasia GROWTH HORMONE LIVER SEX DIMORPHISM SNRNASEQ ZONATION |
title_short |
Liver sex dimorphism and zonation shaped by growth hormone |
title_full |
Liver sex dimorphism and zonation shaped by growth hormone |
title_fullStr |
Liver sex dimorphism and zonation shaped by growth hormone |
title_full_unstemmed |
Liver sex dimorphism and zonation shaped by growth hormone |
title_sort |
Liver sex dimorphism and zonation shaped by growth hormone |
dc.creator.none.fl_str_mv |
Becu, Damasia |
author |
Becu, Damasia |
author_facet |
Becu, Damasia |
author_role |
author |
dc.subject.none.fl_str_mv |
GROWTH HORMONE LIVER SEX DIMORPHISM SNRNASEQ ZONATION |
topic |
GROWTH HORMONE LIVER SEX DIMORPHISM SNRNASEQ ZONATION |
purl_subject.fl_str_mv |
https://purl.org/becyt/ford/3.1 https://purl.org/becyt/ford/3 |
dc.description.none.fl_txt_mv |
In clinical medicine, the consideration of sex-specific differences in diagnosis and treatment of many diseases is gaining acceptance. In this context, sex differences in liver function and gene expression are important, although not highlighted in medical practice. In humans, significant sex differences in the bioavailability and clearance of drugs and other xenobiotics, as well as sex-biased proneness to different liver disorders, have been described. Sexually dimorphic gene expression of the liver depends mainly on growth hormone (GH) secretory patterns, and to a lesser extent on sex steroids. The brain is paramount in organizing GH pulses through synchronization of growth hormone–releasing hormone and somatostatin release and feedback responses (1), thus shaping liver sex dimorphism in accordance with the need for sex-specific steroid metabolism, and metabolic or even behavioral performance. High intermittent GH pulses are found in males, while females have a more constant secretory pattern in rodents; this pattern is found also in humans, although to a minor extent. This differential pulsatility is a key factor for the establishment and maintenance of sexual dimorphism in the transcription of liver genes (2-4). More than 1000 liver genes are sexually dimorphic, and of these approximately 90% are GH dependent (2). Sex differences in gene expression range from less than 2-fold to >1000-fold in the mouse, and this should alert to the need of considering sex as a variable when instrumenting different liver therapies, or administering drugs metabolized in a sex-specific manner. Fil: Becu, Damasia. Academia Nacional de Ciencias de Buenos Aires; Argentina. 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 |
description |
In clinical medicine, the consideration of sex-specific differences in diagnosis and treatment of many diseases is gaining acceptance. In this context, sex differences in liver function and gene expression are important, although not highlighted in medical practice. In humans, significant sex differences in the bioavailability and clearance of drugs and other xenobiotics, as well as sex-biased proneness to different liver disorders, have been described. Sexually dimorphic gene expression of the liver depends mainly on growth hormone (GH) secretory patterns, and to a lesser extent on sex steroids. The brain is paramount in organizing GH pulses through synchronization of growth hormone–releasing hormone and somatostatin release and feedback responses (1), thus shaping liver sex dimorphism in accordance with the need for sex-specific steroid metabolism, and metabolic or even behavioral performance. High intermittent GH pulses are found in males, while females have a more constant secretory pattern in rodents; this pattern is found also in humans, although to a minor extent. This differential pulsatility is a key factor for the establishment and maintenance of sexual dimorphism in the transcription of liver genes (2-4). More than 1000 liver genes are sexually dimorphic, and of these approximately 90% are GH dependent (2). Sex differences in gene expression range from less than 2-fold to >1000-fold in the mouse, and this should alert to the need of considering sex as a variable when instrumenting different liver therapies, or administering drugs metabolized in a sex-specific manner. |
publishDate |
2022 |
dc.date.none.fl_str_mv |
2022 |
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/11336/203885 Becu, Damasia; Liver sex dimorphism and zonation shaped by growth hormone; Endocrine Society; Endocrinology; 163; 8; 2022; 1-2 0013-7227 CONICET Digital CONICET |
url |
http://hdl.handle.net/11336/203885 |
identifier_str_mv |
Becu, Damasia; Liver sex dimorphism and zonation shaped by growth hormone; Endocrine Society; Endocrinology; 163; 8; 2022; 1-2 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/doi/10.1210/endocr/bqac087 |
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 |
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CONICET Digital (CONICET) |
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CONICET Digital (CONICET) |
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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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1842268790498263040 |
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13.13397 |