Effect of some antineoplasics on metabolic heme pathway

Autores
Wainstok De Calmanovici, R.; San Martin De Viale, L.C.
Año de publicación
1988
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
1. 1. The porphyrinogenic ability of several antineoplasics used in the therapy of the different cancers was evaluated. The action of cyclophosphamide, busulfan and 5-fluorouracil on the amount and nature of the accumulated hepatic porphyrins and on the activity of δ-aminolaevulinate synthase(ALA-S). were estimated at different doses and times of drug treatment in 17-day-old chick embryos. 2. 2. It was observed that cyclophosphamide produces a significant increase in the accumulation of hepatic porphyrins at different doses as well as in the activity of the ALA-S, at all the incubation times. Cyclophosphamide alters the pattern of porphyrins accumulated in the liver, where a coproporphyrin: protoporphyrin ratio higher than in the controls can be observed. 3. 3. Busulfan increased the hepatic porphyrins accumulated in the liver but to a lesser degree than cyclophosphamide. 4. 4. 5-Fluorouracil did not modify the hepatic porphyrin content when it was administered at doses up to 40 mg/embryo. 5. 5. When the embryos were injected with busulfan or 5-fluorouracil no significant differences were observed in the activity of ALA-S up to 11 hr of incubation. 6. 6. These results indicate that cyclophosphamide has a remarkable porphyrinogenic capacity in chick embryo while busulfan. notwithstancling the fact that it alters the haem pathway, it does so to a degree that does not impair the regulation of ALA-S activity. Fluorouracil seems to be non porphyrinogenic in this system, up to 40 mg/embryo. © 1988.
Fil:Wainstok De Calmanovici, R. 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. 1988;20(9):1015-1020
Materia
5 aminolevulinate synthase
antineoplastic agent
busulfan
cyclophosphamide
fluorouracil
heme
porphyrin
5 aminolevulinate synthase
busulfan
cyclophosphamide
fluorouracil
porphyrin
animal
article
chick embryo
drug effect
liver
metabolism
chicken
nonhuman
porphyrin synthesis
5-Aminolevulinate Synthetase
Animal
Antineoplastic Agents
Busulfan
Chick Embryo
Cyclophosphamide
Fluorouracil
Heme
Liver
Porphyrins
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_v20_n9_p1015_WainstokDeCalmanovici

id BDUBAFCEN_5428e99461be6d0926948ac663f93fee
oai_identifier_str paperaa:paper_0020711X_v20_n9_p1015_WainstokDeCalmanovici
network_acronym_str BDUBAFCEN
repository_id_str 1896
network_name_str Biblioteca Digital (UBA-FCEN)
spelling Effect of some antineoplasics on metabolic heme pathwayWainstok De Calmanovici, R.San Martin De Viale, L.C.5 aminolevulinate synthaseantineoplastic agentbusulfancyclophosphamidefluorouracilhemeporphyrin5 aminolevulinate synthasebusulfancyclophosphamidefluorouracilporphyrinanimalarticlechick embryodrug effectlivermetabolismchickennonhumanporphyrin synthesis5-Aminolevulinate SynthetaseAnimalAntineoplastic AgentsBusulfanChick EmbryoCyclophosphamideFluorouracilHemeLiverPorphyrinsSupport, Non-U.S. Gov't1. 1. The porphyrinogenic ability of several antineoplasics used in the therapy of the different cancers was evaluated. The action of cyclophosphamide, busulfan and 5-fluorouracil on the amount and nature of the accumulated hepatic porphyrins and on the activity of δ-aminolaevulinate synthase(ALA-S). were estimated at different doses and times of drug treatment in 17-day-old chick embryos. 2. 2. It was observed that cyclophosphamide produces a significant increase in the accumulation of hepatic porphyrins at different doses as well as in the activity of the ALA-S, at all the incubation times. Cyclophosphamide alters the pattern of porphyrins accumulated in the liver, where a coproporphyrin: protoporphyrin ratio higher than in the controls can be observed. 3. 3. Busulfan increased the hepatic porphyrins accumulated in the liver but to a lesser degree than cyclophosphamide. 4. 4. 5-Fluorouracil did not modify the hepatic porphyrin content when it was administered at doses up to 40 mg/embryo. 5. 5. When the embryos were injected with busulfan or 5-fluorouracil no significant differences were observed in the activity of ALA-S up to 11 hr of incubation. 6. 6. These results indicate that cyclophosphamide has a remarkable porphyrinogenic capacity in chick embryo while busulfan. notwithstancling the fact that it alters the haem pathway, it does so to a degree that does not impair the regulation of ALA-S activity. Fluorouracil seems to be non porphyrinogenic in this system, up to 40 mg/embryo. © 1988.Fil:Wainstok De Calmanovici, R. 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.1988info: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_v20_n9_p1015_WainstokDeCalmanoviciInt. J. Biochem. 1988;20(9):1015-1020reponame: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/ar2025-09-29T13:43:05Zpaperaa:paper_0020711X_v20_n9_p1015_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 13:43:06.988Biblioteca Digital (UBA-FCEN) - Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturalesfalse
dc.title.none.fl_str_mv Effect of some antineoplasics on metabolic heme pathway
title Effect of some antineoplasics on metabolic heme pathway
spellingShingle Effect of some antineoplasics on metabolic heme pathway
Wainstok De Calmanovici, R.
5 aminolevulinate synthase
antineoplastic agent
busulfan
cyclophosphamide
fluorouracil
heme
porphyrin
5 aminolevulinate synthase
busulfan
cyclophosphamide
fluorouracil
porphyrin
animal
article
chick embryo
drug effect
liver
metabolism
chicken
nonhuman
porphyrin synthesis
5-Aminolevulinate Synthetase
Animal
Antineoplastic Agents
Busulfan
Chick Embryo
Cyclophosphamide
Fluorouracil
Heme
Liver
Porphyrins
Support, Non-U.S. Gov't
title_short Effect of some antineoplasics on metabolic heme pathway
title_full Effect of some antineoplasics on metabolic heme pathway
title_fullStr Effect of some antineoplasics on metabolic heme pathway
title_full_unstemmed Effect of some antineoplasics on metabolic heme pathway
title_sort Effect of some antineoplasics on metabolic heme pathway
dc.creator.none.fl_str_mv Wainstok De Calmanovici, R.
San Martin De Viale, L.C.
author Wainstok De Calmanovici, R.
author_facet Wainstok De Calmanovici, R.
San Martin De Viale, L.C.
author_role author
author2 San Martin De Viale, L.C.
author2_role author
dc.subject.none.fl_str_mv 5 aminolevulinate synthase
antineoplastic agent
busulfan
cyclophosphamide
fluorouracil
heme
porphyrin
5 aminolevulinate synthase
busulfan
cyclophosphamide
fluorouracil
porphyrin
animal
article
chick embryo
drug effect
liver
metabolism
chicken
nonhuman
porphyrin synthesis
5-Aminolevulinate Synthetase
Animal
Antineoplastic Agents
Busulfan
Chick Embryo
Cyclophosphamide
Fluorouracil
Heme
Liver
Porphyrins
Support, Non-U.S. Gov't
topic 5 aminolevulinate synthase
antineoplastic agent
busulfan
cyclophosphamide
fluorouracil
heme
porphyrin
5 aminolevulinate synthase
busulfan
cyclophosphamide
fluorouracil
porphyrin
animal
article
chick embryo
drug effect
liver
metabolism
chicken
nonhuman
porphyrin synthesis
5-Aminolevulinate Synthetase
Animal
Antineoplastic Agents
Busulfan
Chick Embryo
Cyclophosphamide
Fluorouracil
Heme
Liver
Porphyrins
Support, Non-U.S. Gov't
dc.description.none.fl_txt_mv 1. 1. The porphyrinogenic ability of several antineoplasics used in the therapy of the different cancers was evaluated. The action of cyclophosphamide, busulfan and 5-fluorouracil on the amount and nature of the accumulated hepatic porphyrins and on the activity of δ-aminolaevulinate synthase(ALA-S). were estimated at different doses and times of drug treatment in 17-day-old chick embryos. 2. 2. It was observed that cyclophosphamide produces a significant increase in the accumulation of hepatic porphyrins at different doses as well as in the activity of the ALA-S, at all the incubation times. Cyclophosphamide alters the pattern of porphyrins accumulated in the liver, where a coproporphyrin: protoporphyrin ratio higher than in the controls can be observed. 3. 3. Busulfan increased the hepatic porphyrins accumulated in the liver but to a lesser degree than cyclophosphamide. 4. 4. 5-Fluorouracil did not modify the hepatic porphyrin content when it was administered at doses up to 40 mg/embryo. 5. 5. When the embryos were injected with busulfan or 5-fluorouracil no significant differences were observed in the activity of ALA-S up to 11 hr of incubation. 6. 6. These results indicate that cyclophosphamide has a remarkable porphyrinogenic capacity in chick embryo while busulfan. notwithstancling the fact that it alters the haem pathway, it does so to a degree that does not impair the regulation of ALA-S activity. Fluorouracil seems to be non porphyrinogenic in this system, up to 40 mg/embryo. © 1988.
Fil:Wainstok De Calmanovici, R. 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 porphyrinogenic ability of several antineoplasics used in the therapy of the different cancers was evaluated. The action of cyclophosphamide, busulfan and 5-fluorouracil on the amount and nature of the accumulated hepatic porphyrins and on the activity of δ-aminolaevulinate synthase(ALA-S). were estimated at different doses and times of drug treatment in 17-day-old chick embryos. 2. 2. It was observed that cyclophosphamide produces a significant increase in the accumulation of hepatic porphyrins at different doses as well as in the activity of the ALA-S, at all the incubation times. Cyclophosphamide alters the pattern of porphyrins accumulated in the liver, where a coproporphyrin: protoporphyrin ratio higher than in the controls can be observed. 3. 3. Busulfan increased the hepatic porphyrins accumulated in the liver but to a lesser degree than cyclophosphamide. 4. 4. 5-Fluorouracil did not modify the hepatic porphyrin content when it was administered at doses up to 40 mg/embryo. 5. 5. When the embryos were injected with busulfan or 5-fluorouracil no significant differences were observed in the activity of ALA-S up to 11 hr of incubation. 6. 6. These results indicate that cyclophosphamide has a remarkable porphyrinogenic capacity in chick embryo while busulfan. notwithstancling the fact that it alters the haem pathway, it does so to a degree that does not impair the regulation of ALA-S activity. Fluorouracil seems to be non porphyrinogenic in this system, up to 40 mg/embryo. © 1988.
publishDate 1988
dc.date.none.fl_str_mv 1988
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_v20_n9_p1015_WainstokDeCalmanovici
url http://hdl.handle.net/20.500.12110/paper_0020711X_v20_n9_p1015_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. 1988;20(9):1015-1020
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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