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
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/203885

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spelling 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
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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