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
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/30373

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network_name_str CONICET Digital (CONICET)
spelling 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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