Alternation between dietary protein depletion and normal feeding cause liver damage in mouse

Autores
Caballero, Veronica Jorgelina; Mendieta, Julieta Renee; Giudici, Ana Marcela; Crupkin, Andrea Carina; Barbeito, Claudio Gustavo; Ronchi, Virginia Paola; Chisari, Andrea; Conde, Ruben Danilo
Año de publicación
2010
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
The effect of frequent protein malnutrition on liver function has not been intensively examined. Thus, the effects of alternating 5 days of a protein and amino acid-free diet followed by 5 days of a complete diet repeated three times (3 PFD-CD) on female mouse liver were examined. The expression of carbonic anhydrase III (CAIII), fatty acid synthase (FAS), glyceraldehyde 3-phosphate dehydrogenase (GAPDH) and glutathione S-transferase P1 (GSTP1) in liver were assessed by proteomics, reverse transcriptase-polymerase chain reaction and Northern blotting. The activities of liver GSTs, glutathione reductase (GR) and catalase (CAT), as well as serum glutamic-oxaloacetic transaminase (SGOT) and glutamic-pyruvic transaminase (SGPT) were also tested. Additionally, oxidative damage was examined by measuring of protein carbonylation and lipid peroxidation. Liver histology was examined by light and electron microscopy. Compared with control mice, 3 PFD-CD increased the content of FAS protein (+90%) and FAS mRNA (+30%), while the levels of CAIII and CAIII mRNAs were decreased (-48% and -64%, respectively). In addition, 3 PFD-CD did not significantly change the content of GSTP1 but produced an increase in its mRNA level (+20%), while it decreased the activities of both CAT (-66%) and GSTs (-26%). After 3 PFD-CD, liver protein carbonylation and lipid peroxidation were increased by +55% and +95%, respectively. In serum, 3 PFD-CD increased the activities of both SGOT (+30%) and SGPT (+61%). In addition, 3 PFD-CD showed a histological pattern characteristic of hepatic damage. All together, these data suggest that frequent dietary amino acid deprivation causes hepatic metabolic and ultrastructural changes in a fashion similar to precancerous or cancerous conditions.
Facultad de Ciencias Veterinarias
Materia
Veterinaria
Ciencias Exactas
Mouse liver
Cycles of protein depletion
Liver damage
Oxidative stress
Nivel de accesibilidad
acceso abierto
Condiciones de uso
http://creativecommons.org/licenses/by/4.0/
Repositorio
SEDICI (UNLP)
Institución
Universidad Nacional de La Plata
OAI Identificador
oai:sedici.unlp.edu.ar:10915/142085

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network_acronym_str SEDICI
repository_id_str 1329
network_name_str SEDICI (UNLP)
spelling Alternation between dietary protein depletion and normal feeding cause liver damage in mouseCaballero, Veronica JorgelinaMendieta, Julieta ReneeGiudici, Ana MarcelaCrupkin, Andrea CarinaBarbeito, Claudio GustavoRonchi, Virginia PaolaChisari, AndreaConde, Ruben DaniloVeterinariaCiencias ExactasMouse liverCycles of protein depletionLiver damageOxidative stressThe effect of frequent protein malnutrition on liver function has not been intensively examined. Thus, the effects of alternating 5 days of a protein and amino acid-free diet followed by 5 days of a complete diet repeated three times (3 PFD-CD) on female mouse liver were examined. The expression of carbonic anhydrase III (CAIII), fatty acid synthase (FAS), glyceraldehyde 3-phosphate dehydrogenase (GAPDH) and glutathione S-transferase P1 (GSTP1) in liver were assessed by proteomics, reverse transcriptase-polymerase chain reaction and Northern blotting. The activities of liver GSTs, glutathione reductase (GR) and catalase (CAT), as well as serum glutamic-oxaloacetic transaminase (SGOT) and glutamic-pyruvic transaminase (SGPT) were also tested. Additionally, oxidative damage was examined by measuring of protein carbonylation and lipid peroxidation. Liver histology was examined by light and electron microscopy. Compared with control mice, 3 PFD-CD increased the content of FAS protein (+90%) and FAS mRNA (+30%), while the levels of CAIII and CAIII mRNAs were decreased (-48% and -64%, respectively). In addition, 3 PFD-CD did not significantly change the content of GSTP1 but produced an increase in its mRNA level (+20%), while it decreased the activities of both CAT (-66%) and GSTs (-26%). After 3 PFD-CD, liver protein carbonylation and lipid peroxidation were increased by +55% and +95%, respectively. In serum, 3 PFD-CD increased the activities of both SGOT (+30%) and SGPT (+61%). In addition, 3 PFD-CD showed a histological pattern characteristic of hepatic damage. All together, these data suggest that frequent dietary amino acid deprivation causes hepatic metabolic and ultrastructural changes in a fashion similar to precancerous or cancerous conditions.Facultad de Ciencias Veterinarias2010-09-29info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionArticulohttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdf43-52http://sedici.unlp.edu.ar/handle/10915/142085enginfo:eu-repo/semantics/altIdentifier/issn/1877-8755info:eu-repo/semantics/altIdentifier/issn/1138-7548info:eu-repo/semantics/altIdentifier/doi/10.1007/s13105-010-0047-1info:eu-repo/semantics/altIdentifier/pmid/20878513info:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by/4.0/Creative Commons Attribution 4.0 International (CC BY 4.0)reponame:SEDICI (UNLP)instname:Universidad Nacional de La Platainstacron:UNLP2025-09-03T11:04:18Zoai:sedici.unlp.edu.ar:10915/142085Institucionalhttp://sedici.unlp.edu.ar/Universidad públicaNo correspondehttp://sedici.unlp.edu.ar/oai/snrdalira@sedici.unlp.edu.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:13292025-09-03 11:04:18.469SEDICI (UNLP) - Universidad Nacional de La Platafalse
dc.title.none.fl_str_mv Alternation between dietary protein depletion and normal feeding cause liver damage in mouse
title Alternation between dietary protein depletion and normal feeding cause liver damage in mouse
spellingShingle Alternation between dietary protein depletion and normal feeding cause liver damage in mouse
Caballero, Veronica Jorgelina
Veterinaria
Ciencias Exactas
Mouse liver
Cycles of protein depletion
Liver damage
Oxidative stress
title_short Alternation between dietary protein depletion and normal feeding cause liver damage in mouse
title_full Alternation between dietary protein depletion and normal feeding cause liver damage in mouse
title_fullStr Alternation between dietary protein depletion and normal feeding cause liver damage in mouse
title_full_unstemmed Alternation between dietary protein depletion and normal feeding cause liver damage in mouse
title_sort Alternation between dietary protein depletion and normal feeding cause liver damage in mouse
dc.creator.none.fl_str_mv Caballero, Veronica Jorgelina
Mendieta, Julieta Renee
Giudici, Ana Marcela
Crupkin, Andrea Carina
Barbeito, Claudio Gustavo
Ronchi, Virginia Paola
Chisari, Andrea
Conde, Ruben Danilo
author Caballero, Veronica Jorgelina
author_facet Caballero, Veronica Jorgelina
Mendieta, Julieta Renee
Giudici, Ana Marcela
Crupkin, Andrea Carina
Barbeito, Claudio Gustavo
Ronchi, Virginia Paola
Chisari, Andrea
Conde, Ruben Danilo
author_role author
author2 Mendieta, Julieta Renee
Giudici, Ana Marcela
Crupkin, Andrea Carina
Barbeito, Claudio Gustavo
Ronchi, Virginia Paola
Chisari, Andrea
Conde, Ruben Danilo
author2_role author
author
author
author
author
author
author
dc.subject.none.fl_str_mv Veterinaria
Ciencias Exactas
Mouse liver
Cycles of protein depletion
Liver damage
Oxidative stress
topic Veterinaria
Ciencias Exactas
Mouse liver
Cycles of protein depletion
Liver damage
Oxidative stress
dc.description.none.fl_txt_mv The effect of frequent protein malnutrition on liver function has not been intensively examined. Thus, the effects of alternating 5 days of a protein and amino acid-free diet followed by 5 days of a complete diet repeated three times (3 PFD-CD) on female mouse liver were examined. The expression of carbonic anhydrase III (CAIII), fatty acid synthase (FAS), glyceraldehyde 3-phosphate dehydrogenase (GAPDH) and glutathione S-transferase P1 (GSTP1) in liver were assessed by proteomics, reverse transcriptase-polymerase chain reaction and Northern blotting. The activities of liver GSTs, glutathione reductase (GR) and catalase (CAT), as well as serum glutamic-oxaloacetic transaminase (SGOT) and glutamic-pyruvic transaminase (SGPT) were also tested. Additionally, oxidative damage was examined by measuring of protein carbonylation and lipid peroxidation. Liver histology was examined by light and electron microscopy. Compared with control mice, 3 PFD-CD increased the content of FAS protein (+90%) and FAS mRNA (+30%), while the levels of CAIII and CAIII mRNAs were decreased (-48% and -64%, respectively). In addition, 3 PFD-CD did not significantly change the content of GSTP1 but produced an increase in its mRNA level (+20%), while it decreased the activities of both CAT (-66%) and GSTs (-26%). After 3 PFD-CD, liver protein carbonylation and lipid peroxidation were increased by +55% and +95%, respectively. In serum, 3 PFD-CD increased the activities of both SGOT (+30%) and SGPT (+61%). In addition, 3 PFD-CD showed a histological pattern characteristic of hepatic damage. All together, these data suggest that frequent dietary amino acid deprivation causes hepatic metabolic and ultrastructural changes in a fashion similar to precancerous or cancerous conditions.
Facultad de Ciencias Veterinarias
description The effect of frequent protein malnutrition on liver function has not been intensively examined. Thus, the effects of alternating 5 days of a protein and amino acid-free diet followed by 5 days of a complete diet repeated three times (3 PFD-CD) on female mouse liver were examined. The expression of carbonic anhydrase III (CAIII), fatty acid synthase (FAS), glyceraldehyde 3-phosphate dehydrogenase (GAPDH) and glutathione S-transferase P1 (GSTP1) in liver were assessed by proteomics, reverse transcriptase-polymerase chain reaction and Northern blotting. The activities of liver GSTs, glutathione reductase (GR) and catalase (CAT), as well as serum glutamic-oxaloacetic transaminase (SGOT) and glutamic-pyruvic transaminase (SGPT) were also tested. Additionally, oxidative damage was examined by measuring of protein carbonylation and lipid peroxidation. Liver histology was examined by light and electron microscopy. Compared with control mice, 3 PFD-CD increased the content of FAS protein (+90%) and FAS mRNA (+30%), while the levels of CAIII and CAIII mRNAs were decreased (-48% and -64%, respectively). In addition, 3 PFD-CD did not significantly change the content of GSTP1 but produced an increase in its mRNA level (+20%), while it decreased the activities of both CAT (-66%) and GSTs (-26%). After 3 PFD-CD, liver protein carbonylation and lipid peroxidation were increased by +55% and +95%, respectively. In serum, 3 PFD-CD increased the activities of both SGOT (+30%) and SGPT (+61%). In addition, 3 PFD-CD showed a histological pattern characteristic of hepatic damage. All together, these data suggest that frequent dietary amino acid deprivation causes hepatic metabolic and ultrastructural changes in a fashion similar to precancerous or cancerous conditions.
publishDate 2010
dc.date.none.fl_str_mv 2010-09-29
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Articulo
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status_str publishedVersion
dc.identifier.none.fl_str_mv http://sedici.unlp.edu.ar/handle/10915/142085
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dc.language.none.fl_str_mv eng
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info:eu-repo/semantics/altIdentifier/issn/1138-7548
info:eu-repo/semantics/altIdentifier/doi/10.1007/s13105-010-0047-1
info:eu-repo/semantics/altIdentifier/pmid/20878513
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
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Creative Commons Attribution 4.0 International (CC BY 4.0)
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rights_invalid_str_mv http://creativecommons.org/licenses/by/4.0/
Creative Commons Attribution 4.0 International (CC BY 4.0)
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repository.name.fl_str_mv SEDICI (UNLP) - Universidad Nacional de La Plata
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