Influence of the strain of rats on the induction of hexachlorobenzene induced porphyria

Autores
Wainstok de Calmanovici, R.; Billi de Catabbi, S.C.; Aldonatti, C.A.; San Martin de Viale, L.C.
Año de publicación
1989
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
1. 1. The present work undertakes a comparative study on the hexachlorobenzene (HCB) porphyria induction in female rats of Wistar and CHBBTHOM strains. The purpose was to characterize the CHBBTHOM strain with respect to the haem metabolic pathway, its regulatory mechanisms and its response to foreign drugs. 2. 2. After 7 weeks of treatment it was observed that the hepatic porphyrins increased 140 times, ALA-synthase 4 times and PCL was 73% inhibited in the Wistar strain. 3. 3. On the other hand the animals of CHBBTHOM strain showed lesser alteration on these parameters; hepatic porphyrins increased only 3-fold, ALA-synthase 1.7-fold and PCL was only 22% inhibited. 4. 4. Total iron liver content was nearly equal in both strains of rats. 5. 5. The results obtained would indicate that the lower susceptibility of the CHBBTHOM strain to acquire porphyria does not seem to be due to either: (1) congenital alterations of any parameters of the haem metabolic pathway, since the behaviour of normal animals from both strains was similar; or (2) a lower hepatic iron content in such animals. 6. 6. These findings would suggest that the differential response to HCB to this strain would be looked for in another metabolic pathway, such as that involved in the metabolization process of the toxic. © 1989.
Fil:Wainstok de Calmanovici, R. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.
Fil:Billi de Catabbi, S.C. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.
Fil:San Martin de Viale, L.C. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.
Fuente
Int. J. Biochem. 1989;21(4):377-381
Materia
5 aminolevulinate synthase
aminolevulinic acid
heme
hexachlorobenzene
porphobilinogen
porphyrin
uroporphyrinogen decarboxylase
xenobiotic agent
animal cell
animal experiment
animal model
female
hepatic porphyria
iron liver level
nonhuman
oral drug administration
rat
regulatory mechanism
strain difference
urinary excretion
5-Aminolevulinate Synthetase
Animal
Carboxy-Lyases
Chlorobenzenes
Comparative Study
Female
Hexachlorobenzene
Iron
Liver
Liver Diseases
Porphyria
Porphyrins
Rats
Rats, Inbred Strains
Species Specificity
Support, Non-U.S. Gov't
Nivel de accesibilidad
acceso abierto
Condiciones de uso
http://creativecommons.org/licenses/by/2.5/ar
Repositorio
Biblioteca Digital (UBA-FCEN)
Institución
Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturales
OAI Identificador
paperaa:paper_0020711X_v21_n4_p377_WainstokdeCalmanovici

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oai_identifier_str paperaa:paper_0020711X_v21_n4_p377_WainstokdeCalmanovici
network_acronym_str BDUBAFCEN
repository_id_str 1896
network_name_str Biblioteca Digital (UBA-FCEN)
spelling Influence of the strain of rats on the induction of hexachlorobenzene induced porphyriaWainstok de Calmanovici, R.Billi de Catabbi, S.C.Aldonatti, C.A.San Martin de Viale, L.C.5 aminolevulinate synthaseaminolevulinic acidhemehexachlorobenzeneporphobilinogenporphyrinuroporphyrinogen decarboxylasexenobiotic agentanimal cellanimal experimentanimal modelfemalehepatic porphyriairon liver levelnonhumanoral drug administrationratregulatory mechanismstrain differenceurinary excretion5-Aminolevulinate SynthetaseAnimalCarboxy-LyasesChlorobenzenesComparative StudyFemaleHexachlorobenzeneIronLiverLiver DiseasesPorphyriaPorphyrinsRatsRats, Inbred StrainsSpecies SpecificitySupport, Non-U.S. Gov't1. 1. The present work undertakes a comparative study on the hexachlorobenzene (HCB) porphyria induction in female rats of Wistar and CHBBTHOM strains. The purpose was to characterize the CHBBTHOM strain with respect to the haem metabolic pathway, its regulatory mechanisms and its response to foreign drugs. 2. 2. After 7 weeks of treatment it was observed that the hepatic porphyrins increased 140 times, ALA-synthase 4 times and PCL was 73% inhibited in the Wistar strain. 3. 3. On the other hand the animals of CHBBTHOM strain showed lesser alteration on these parameters; hepatic porphyrins increased only 3-fold, ALA-synthase 1.7-fold and PCL was only 22% inhibited. 4. 4. Total iron liver content was nearly equal in both strains of rats. 5. 5. The results obtained would indicate that the lower susceptibility of the CHBBTHOM strain to acquire porphyria does not seem to be due to either: (1) congenital alterations of any parameters of the haem metabolic pathway, since the behaviour of normal animals from both strains was similar; or (2) a lower hepatic iron content in such animals. 6. 6. These findings would suggest that the differential response to HCB to this strain would be looked for in another metabolic pathway, such as that involved in the metabolization process of the toxic. © 1989.Fil:Wainstok de Calmanovici, R. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.Fil:Billi de Catabbi, S.C. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.Fil:San Martin de Viale, L.C. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.1989info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfhttp://hdl.handle.net/20.500.12110/paper_0020711X_v21_n4_p377_WainstokdeCalmanoviciInt. J. Biochem. 1989;21(4):377-381reponame:Biblioteca Digital (UBA-FCEN)instname:Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturalesinstacron:UBA-FCENenginfo:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by/2.5/ar2025-09-29T13:42:54Zpaperaa:paper_0020711X_v21_n4_p377_WainstokdeCalmanoviciInstitucionalhttps://digital.bl.fcen.uba.ar/Universidad públicaNo correspondehttps://digital.bl.fcen.uba.ar/cgi-bin/oaiserver.cgiana@bl.fcen.uba.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:18962025-09-29 13:42:56.005Biblioteca Digital (UBA-FCEN) - Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturalesfalse
dc.title.none.fl_str_mv Influence of the strain of rats on the induction of hexachlorobenzene induced porphyria
title Influence of the strain of rats on the induction of hexachlorobenzene induced porphyria
spellingShingle Influence of the strain of rats on the induction of hexachlorobenzene induced porphyria
Wainstok de Calmanovici, R.
5 aminolevulinate synthase
aminolevulinic acid
heme
hexachlorobenzene
porphobilinogen
porphyrin
uroporphyrinogen decarboxylase
xenobiotic agent
animal cell
animal experiment
animal model
female
hepatic porphyria
iron liver level
nonhuman
oral drug administration
rat
regulatory mechanism
strain difference
urinary excretion
5-Aminolevulinate Synthetase
Animal
Carboxy-Lyases
Chlorobenzenes
Comparative Study
Female
Hexachlorobenzene
Iron
Liver
Liver Diseases
Porphyria
Porphyrins
Rats
Rats, Inbred Strains
Species Specificity
Support, Non-U.S. Gov't
title_short Influence of the strain of rats on the induction of hexachlorobenzene induced porphyria
title_full Influence of the strain of rats on the induction of hexachlorobenzene induced porphyria
title_fullStr Influence of the strain of rats on the induction of hexachlorobenzene induced porphyria
title_full_unstemmed Influence of the strain of rats on the induction of hexachlorobenzene induced porphyria
title_sort Influence of the strain of rats on the induction of hexachlorobenzene induced porphyria
dc.creator.none.fl_str_mv Wainstok de Calmanovici, R.
Billi de Catabbi, S.C.
Aldonatti, C.A.
San Martin de Viale, L.C.
author Wainstok de Calmanovici, R.
author_facet Wainstok de Calmanovici, R.
Billi de Catabbi, S.C.
Aldonatti, C.A.
San Martin de Viale, L.C.
author_role author
author2 Billi de Catabbi, S.C.
Aldonatti, C.A.
San Martin de Viale, L.C.
author2_role author
author
author
dc.subject.none.fl_str_mv 5 aminolevulinate synthase
aminolevulinic acid
heme
hexachlorobenzene
porphobilinogen
porphyrin
uroporphyrinogen decarboxylase
xenobiotic agent
animal cell
animal experiment
animal model
female
hepatic porphyria
iron liver level
nonhuman
oral drug administration
rat
regulatory mechanism
strain difference
urinary excretion
5-Aminolevulinate Synthetase
Animal
Carboxy-Lyases
Chlorobenzenes
Comparative Study
Female
Hexachlorobenzene
Iron
Liver
Liver Diseases
Porphyria
Porphyrins
Rats
Rats, Inbred Strains
Species Specificity
Support, Non-U.S. Gov't
topic 5 aminolevulinate synthase
aminolevulinic acid
heme
hexachlorobenzene
porphobilinogen
porphyrin
uroporphyrinogen decarboxylase
xenobiotic agent
animal cell
animal experiment
animal model
female
hepatic porphyria
iron liver level
nonhuman
oral drug administration
rat
regulatory mechanism
strain difference
urinary excretion
5-Aminolevulinate Synthetase
Animal
Carboxy-Lyases
Chlorobenzenes
Comparative Study
Female
Hexachlorobenzene
Iron
Liver
Liver Diseases
Porphyria
Porphyrins
Rats
Rats, Inbred Strains
Species Specificity
Support, Non-U.S. Gov't
dc.description.none.fl_txt_mv 1. 1. The present work undertakes a comparative study on the hexachlorobenzene (HCB) porphyria induction in female rats of Wistar and CHBBTHOM strains. The purpose was to characterize the CHBBTHOM strain with respect to the haem metabolic pathway, its regulatory mechanisms and its response to foreign drugs. 2. 2. After 7 weeks of treatment it was observed that the hepatic porphyrins increased 140 times, ALA-synthase 4 times and PCL was 73% inhibited in the Wistar strain. 3. 3. On the other hand the animals of CHBBTHOM strain showed lesser alteration on these parameters; hepatic porphyrins increased only 3-fold, ALA-synthase 1.7-fold and PCL was only 22% inhibited. 4. 4. Total iron liver content was nearly equal in both strains of rats. 5. 5. The results obtained would indicate that the lower susceptibility of the CHBBTHOM strain to acquire porphyria does not seem to be due to either: (1) congenital alterations of any parameters of the haem metabolic pathway, since the behaviour of normal animals from both strains was similar; or (2) a lower hepatic iron content in such animals. 6. 6. These findings would suggest that the differential response to HCB to this strain would be looked for in another metabolic pathway, such as that involved in the metabolization process of the toxic. © 1989.
Fil:Wainstok de Calmanovici, R. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.
Fil:Billi de Catabbi, S.C. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.
Fil:San Martin de Viale, L.C. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.
description 1. 1. The present work undertakes a comparative study on the hexachlorobenzene (HCB) porphyria induction in female rats of Wistar and CHBBTHOM strains. The purpose was to characterize the CHBBTHOM strain with respect to the haem metabolic pathway, its regulatory mechanisms and its response to foreign drugs. 2. 2. After 7 weeks of treatment it was observed that the hepatic porphyrins increased 140 times, ALA-synthase 4 times and PCL was 73% inhibited in the Wistar strain. 3. 3. On the other hand the animals of CHBBTHOM strain showed lesser alteration on these parameters; hepatic porphyrins increased only 3-fold, ALA-synthase 1.7-fold and PCL was only 22% inhibited. 4. 4. Total iron liver content was nearly equal in both strains of rats. 5. 5. The results obtained would indicate that the lower susceptibility of the CHBBTHOM strain to acquire porphyria does not seem to be due to either: (1) congenital alterations of any parameters of the haem metabolic pathway, since the behaviour of normal animals from both strains was similar; or (2) a lower hepatic iron content in such animals. 6. 6. These findings would suggest that the differential response to HCB to this strain would be looked for in another metabolic pathway, such as that involved in the metabolization process of the toxic. © 1989.
publishDate 1989
dc.date.none.fl_str_mv 1989
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/20.500.12110/paper_0020711X_v21_n4_p377_WainstokdeCalmanovici
url http://hdl.handle.net/20.500.12110/paper_0020711X_v21_n4_p377_WainstokdeCalmanovici
dc.language.none.fl_str_mv eng
language eng
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
http://creativecommons.org/licenses/by/2.5/ar
eu_rights_str_mv openAccess
rights_invalid_str_mv http://creativecommons.org/licenses/by/2.5/ar
dc.format.none.fl_str_mv application/pdf
dc.source.none.fl_str_mv Int. J. Biochem. 1989;21(4):377-381
reponame:Biblioteca Digital (UBA-FCEN)
instname:Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturales
instacron:UBA-FCEN
reponame_str Biblioteca Digital (UBA-FCEN)
collection Biblioteca Digital (UBA-FCEN)
instname_str Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturales
instacron_str UBA-FCEN
institution UBA-FCEN
repository.name.fl_str_mv Biblioteca Digital (UBA-FCEN) - Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturales
repository.mail.fl_str_mv ana@bl.fcen.uba.ar
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score 13.070432