Role of brain cytochrome P450 mono‑oxygenases in bilirubin oxidation‑specific induction and activity
- Autores
- Gambaro, Sabrina Eliana; Robert, María Celeste; Tiribelli, Claudio; Gazzin, Silvia
- Año de publicación
- 2014
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- In the Crigler–Najjar type I syndrome, the genetic absence of efficient hepatic glucuronidation of unconjugated bilirubin (UCB) by the uridine 5′-diphospho-glucuronosyltransferase1A1 (UGT1A1) enzyme produces the rise of UCB level in blood. Its entry to central nervous system could generate toxicity and neurological damage, and even death. In the past years, a compensatory mechanism to liver glucuronidation has been indicated in the hepatic cytochromes P450 enzymes (Cyps) which are able to oxidize bilirubin. Cyps are expressed also in the central nervous system, the target of bilirubin toxicity, thus making them theoretically important to confer a protective activity toward bilirubin accumulation and neurotoxicity. We therefore investigated the functional induction (mRNA, EROD/MROD) and the ability to oxidize bilirubin of Cyp1A1, 1A2, and 2A3 in primary astrocytes cultures obtained from two rat brain region (cortex: Cx and cerebellum: Cll). We observed that Cyp1A1 was the Cyp isoform more easily induced by beta-naphtoflavone (βNF) in both Cx and Cll astrocytes, but oxidized bilirubin only after uncoupling by 3, 4,3′,4′-tetrachlorobiphenyl (TCB). On the contrary, Cyp1A2 was the most active Cyp in bilirubin clearance without uncoupling, but its induction was confined only in Cx cells. Brain Cyp2A3 was not inducible. In conclusion, the exposure of astrocytes to βNF plus TCB significantly enhanced Cyp1A1 mediating bilirubin clearance, improving cell viability in both regions. These results may be a relevant groundwork for the manipulation of brain Cyps as a therapeutic approach in reducing bilirubin-induced neurological damage
Fil: Gambaro, Sabrina Eliana. Italian Liver Foundation; Italia. Fundación Favaloro; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Fil: Robert, María Celeste. Italian Liver Foundation; Italia. Universidad Nacional de Rosario. Secretaria de Ciencia y Tecnica. Centro Binacional de Investigación en Criobiologia Clinica y Aplicada; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Fil: Tiribelli, Claudio. Italian Liver Foundation; Italia. Università degli Studi di Trieste; Italia
Fil: Gazzin, Silvia. Italian Liver Foundation; Italia - Materia
-
Cytochrome P450 Enzymes (Cyp)
Bilirubin Oxidation
Kernicterus
Astrocytes
Βnf
Erod/Mrod - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
- Repositorio
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/30373
Ver los metadatos del registro completo
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Role of brain cytochrome P450 mono‑oxygenases in bilirubin oxidation‑specific induction and activityGambaro, Sabrina ElianaRobert, María CelesteTiribelli, ClaudioGazzin, SilviaCytochrome P450 Enzymes (Cyp)Bilirubin OxidationKernicterusAstrocytesΒnfErod/Mrodhttps://purl.org/becyt/ford/1.6https://purl.org/becyt/ford/1In the Crigler–Najjar type I syndrome, the genetic absence of efficient hepatic glucuronidation of unconjugated bilirubin (UCB) by the uridine 5′-diphospho-glucuronosyltransferase1A1 (UGT1A1) enzyme produces the rise of UCB level in blood. Its entry to central nervous system could generate toxicity and neurological damage, and even death. In the past years, a compensatory mechanism to liver glucuronidation has been indicated in the hepatic cytochromes P450 enzymes (Cyps) which are able to oxidize bilirubin. Cyps are expressed also in the central nervous system, the target of bilirubin toxicity, thus making them theoretically important to confer a protective activity toward bilirubin accumulation and neurotoxicity. We therefore investigated the functional induction (mRNA, EROD/MROD) and the ability to oxidize bilirubin of Cyp1A1, 1A2, and 2A3 in primary astrocytes cultures obtained from two rat brain region (cortex: Cx and cerebellum: Cll). We observed that Cyp1A1 was the Cyp isoform more easily induced by beta-naphtoflavone (βNF) in both Cx and Cll astrocytes, but oxidized bilirubin only after uncoupling by 3, 4,3′,4′-tetrachlorobiphenyl (TCB). On the contrary, Cyp1A2 was the most active Cyp in bilirubin clearance without uncoupling, but its induction was confined only in Cx cells. Brain Cyp2A3 was not inducible. In conclusion, the exposure of astrocytes to βNF plus TCB significantly enhanced Cyp1A1 mediating bilirubin clearance, improving cell viability in both regions. These results may be a relevant groundwork for the manipulation of brain Cyps as a therapeutic approach in reducing bilirubin-induced neurological damageFil: Gambaro, Sabrina Eliana. Italian Liver Foundation; Italia. Fundación Favaloro; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaFil: Robert, María Celeste. Italian Liver Foundation; Italia. Universidad Nacional de Rosario. Secretaria de Ciencia y Tecnica. Centro Binacional de Investigación en Criobiologia Clinica y Aplicada; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaFil: Tiribelli, Claudio. Italian Liver Foundation; Italia. Università degli Studi di Trieste; ItaliaFil: Gazzin, Silvia. Italian Liver Foundation; ItaliaSpringer2014-11info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfapplication/pdfapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/30373Gambaro, Sabrina Eliana; Robert, María Celeste; Tiribelli, Claudio; Gazzin, Silvia; Role of brain cytochrome P450 mono‑oxygenases in bilirubin oxidation‑specific induction and activity; Springer; Archives of Toxicology; 90; 2; 11-2014; 279-2900340-5761CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://link.springer.com/article/10.1007%2Fs00204-014-1394-4info:eu-repo/semantics/altIdentifier/doi/10.1007/s00204-014-1394-4info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-03T10:01:57Zoai:ri.conicet.gov.ar:11336/30373instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-09-03 10:01:57.755CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
dc.title.none.fl_str_mv |
Role of brain cytochrome P450 mono‑oxygenases in bilirubin oxidation‑specific induction and activity |
title |
Role of brain cytochrome P450 mono‑oxygenases in bilirubin oxidation‑specific induction and activity |
spellingShingle |
Role of brain cytochrome P450 mono‑oxygenases in bilirubin oxidation‑specific induction and activity Gambaro, Sabrina Eliana Cytochrome P450 Enzymes (Cyp) Bilirubin Oxidation Kernicterus Astrocytes Βnf Erod/Mrod |
title_short |
Role of brain cytochrome P450 mono‑oxygenases in bilirubin oxidation‑specific induction and activity |
title_full |
Role of brain cytochrome P450 mono‑oxygenases in bilirubin oxidation‑specific induction and activity |
title_fullStr |
Role of brain cytochrome P450 mono‑oxygenases in bilirubin oxidation‑specific induction and activity |
title_full_unstemmed |
Role of brain cytochrome P450 mono‑oxygenases in bilirubin oxidation‑specific induction and activity |
title_sort |
Role of brain cytochrome P450 mono‑oxygenases in bilirubin oxidation‑specific induction and activity |
dc.creator.none.fl_str_mv |
Gambaro, Sabrina Eliana Robert, María Celeste Tiribelli, Claudio Gazzin, Silvia |
author |
Gambaro, Sabrina Eliana |
author_facet |
Gambaro, Sabrina Eliana Robert, María Celeste Tiribelli, Claudio Gazzin, Silvia |
author_role |
author |
author2 |
Robert, María Celeste Tiribelli, Claudio Gazzin, Silvia |
author2_role |
author author author |
dc.subject.none.fl_str_mv |
Cytochrome P450 Enzymes (Cyp) Bilirubin Oxidation Kernicterus Astrocytes Βnf Erod/Mrod |
topic |
Cytochrome P450 Enzymes (Cyp) Bilirubin Oxidation Kernicterus Astrocytes Βnf Erod/Mrod |
purl_subject.fl_str_mv |
https://purl.org/becyt/ford/1.6 https://purl.org/becyt/ford/1 |
dc.description.none.fl_txt_mv |
In the Crigler–Najjar type I syndrome, the genetic absence of efficient hepatic glucuronidation of unconjugated bilirubin (UCB) by the uridine 5′-diphospho-glucuronosyltransferase1A1 (UGT1A1) enzyme produces the rise of UCB level in blood. Its entry to central nervous system could generate toxicity and neurological damage, and even death. In the past years, a compensatory mechanism to liver glucuronidation has been indicated in the hepatic cytochromes P450 enzymes (Cyps) which are able to oxidize bilirubin. Cyps are expressed also in the central nervous system, the target of bilirubin toxicity, thus making them theoretically important to confer a protective activity toward bilirubin accumulation and neurotoxicity. We therefore investigated the functional induction (mRNA, EROD/MROD) and the ability to oxidize bilirubin of Cyp1A1, 1A2, and 2A3 in primary astrocytes cultures obtained from two rat brain region (cortex: Cx and cerebellum: Cll). We observed that Cyp1A1 was the Cyp isoform more easily induced by beta-naphtoflavone (βNF) in both Cx and Cll astrocytes, but oxidized bilirubin only after uncoupling by 3, 4,3′,4′-tetrachlorobiphenyl (TCB). On the contrary, Cyp1A2 was the most active Cyp in bilirubin clearance without uncoupling, but its induction was confined only in Cx cells. Brain Cyp2A3 was not inducible. In conclusion, the exposure of astrocytes to βNF plus TCB significantly enhanced Cyp1A1 mediating bilirubin clearance, improving cell viability in both regions. These results may be a relevant groundwork for the manipulation of brain Cyps as a therapeutic approach in reducing bilirubin-induced neurological damage Fil: Gambaro, Sabrina Eliana. Italian Liver Foundation; Italia. Fundación Favaloro; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina Fil: Robert, María Celeste. Italian Liver Foundation; Italia. Universidad Nacional de Rosario. Secretaria de Ciencia y Tecnica. Centro Binacional de Investigación en Criobiologia Clinica y Aplicada; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina Fil: Tiribelli, Claudio. Italian Liver Foundation; Italia. Università degli Studi di Trieste; Italia Fil: Gazzin, Silvia. Italian Liver Foundation; Italia |
description |
In the Crigler–Najjar type I syndrome, the genetic absence of efficient hepatic glucuronidation of unconjugated bilirubin (UCB) by the uridine 5′-diphospho-glucuronosyltransferase1A1 (UGT1A1) enzyme produces the rise of UCB level in blood. Its entry to central nervous system could generate toxicity and neurological damage, and even death. In the past years, a compensatory mechanism to liver glucuronidation has been indicated in the hepatic cytochromes P450 enzymes (Cyps) which are able to oxidize bilirubin. Cyps are expressed also in the central nervous system, the target of bilirubin toxicity, thus making them theoretically important to confer a protective activity toward bilirubin accumulation and neurotoxicity. We therefore investigated the functional induction (mRNA, EROD/MROD) and the ability to oxidize bilirubin of Cyp1A1, 1A2, and 2A3 in primary astrocytes cultures obtained from two rat brain region (cortex: Cx and cerebellum: Cll). We observed that Cyp1A1 was the Cyp isoform more easily induced by beta-naphtoflavone (βNF) in both Cx and Cll astrocytes, but oxidized bilirubin only after uncoupling by 3, 4,3′,4′-tetrachlorobiphenyl (TCB). On the contrary, Cyp1A2 was the most active Cyp in bilirubin clearance without uncoupling, but its induction was confined only in Cx cells. Brain Cyp2A3 was not inducible. In conclusion, the exposure of astrocytes to βNF plus TCB significantly enhanced Cyp1A1 mediating bilirubin clearance, improving cell viability in both regions. These results may be a relevant groundwork for the manipulation of brain Cyps as a therapeutic approach in reducing bilirubin-induced neurological damage |
publishDate |
2014 |
dc.date.none.fl_str_mv |
2014-11 |
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/11336/30373 Gambaro, Sabrina Eliana; Robert, María Celeste; Tiribelli, Claudio; Gazzin, Silvia; Role of brain cytochrome P450 mono‑oxygenases in bilirubin oxidation‑specific induction and activity; Springer; Archives of Toxicology; 90; 2; 11-2014; 279-290 0340-5761 CONICET Digital CONICET |
url |
http://hdl.handle.net/11336/30373 |
identifier_str_mv |
Gambaro, Sabrina Eliana; Robert, María Celeste; Tiribelli, Claudio; Gazzin, Silvia; Role of brain cytochrome P450 mono‑oxygenases in bilirubin oxidation‑specific induction and activity; Springer; Archives of Toxicology; 90; 2; 11-2014; 279-290 0340-5761 CONICET Digital CONICET |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/url/https://link.springer.com/article/10.1007%2Fs00204-014-1394-4 info:eu-repo/semantics/altIdentifier/doi/10.1007/s00204-014-1394-4 |
dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
eu_rights_str_mv |
openAccess |
rights_invalid_str_mv |
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
dc.format.none.fl_str_mv |
application/pdf application/pdf application/pdf application/pdf application/pdf |
dc.publisher.none.fl_str_mv |
Springer |
publisher.none.fl_str_mv |
Springer |
dc.source.none.fl_str_mv |
reponame:CONICET Digital (CONICET) instname:Consejo Nacional de Investigaciones Científicas y Técnicas |
reponame_str |
CONICET Digital (CONICET) |
collection |
CONICET Digital (CONICET) |
instname_str |
Consejo Nacional de Investigaciones Científicas y Técnicas |
repository.name.fl_str_mv |
CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas |
repository.mail.fl_str_mv |
dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar |
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1842269726873485312 |
score |
13.13397 |