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
.jpg)
- Institución
- Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturales
- OAI Identificador
- paperaa:paper_0020711X_v20_n9_p1015_WainstokDeCalmanovici
Ver los metadatos del registro completo
| 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/ar2025-10-23T11:18:30Zpaperaa: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:18962025-10-23 11:18:32.688Biblioteca 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 |
| _version_ |
1846784881039769600 |
| score |
12.982451 |