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
- Institución
- Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturales
- OAI Identificador
- paperaa:paper_0020711X_v21_n4_p377_WainstokdeCalmanovici
Ver los metadatos del registro completo
id |
BDUBAFCEN_86c9136c68ce8cadfe3ec3be43df65e0 |
---|---|
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 |
_version_ |
1844618735021719552 |
score |
13.070432 |