Mostrar el registro sencillo del ítem

dc.contributor.author
Goldstein Raij, Jorge  
dc.contributor.author
Ibarra, Cristina Adriana  
dc.contributor.author
Silberstein, Claudia Marcela  
dc.date.available
2022-02-17T17:15:19Z  
dc.date.issued
2002-12  
dc.identifier.citation
Goldstein Raij, Jorge; Ibarra, Cristina Adriana; Silberstein, Claudia Marcela; Adenylyl cyclase types I and VI but not II and V are selectively inhibited by nitric oxide; Associação Brasileira de Divulgação Científica; Brazilian Journal of Medical and Biological Research; 35; 2; 12-2002; 145-151  
dc.identifier.issn
0100-879X  
dc.identifier.uri
http://hdl.handle.net/11336/152212  
dc.description.abstract
Adenylyl cyclase (AC) isoforms catalyze the synthesis of 3′,5′-cyclic AMP from ATP. These isoforms are critically involved in the regulation of gene transcription, metabolism, and ion channel activity among others. Nitric oxide (NO) is a gaseous product whose synthesis from L-arginine is catalyzed by the enzyme NO synthase. It has been well established that NO activates the enzyme guanylyl cyclase, but little has been reported on the effects of NO on other important second messengers, such as AC. In the present study, the effects of sodium nitroprusside (SNP), a nitric oxide-releasing compound, on COS-7 cells transfected with plasmids containing AC types I, II, V and VI were evaluated. Total inhibition (∼98.5%) of cAMP production was observed in COS-7 cells transfected with the AC I isoform and previously treated with SNP (10 mM) for 30 min, when stimulated with ionomycin. A high inhibition (∼76%) of cAMP production was also observed in COS-7 cells transfected with the AC VI isoform and previously treated with SNP (10 mM) for 30 min, when stimulated with forskolin. No effect on cAMP production was observed in cells transfected with AC isoforms II and V.  
dc.format
application/pdf  
dc.language.iso
eng  
dc.publisher
Associação Brasileira de Divulgação Científica  
dc.rights
info:eu-repo/semantics/openAccess  
dc.rights.uri
https://creativecommons.org/licenses/by/2.5/ar/  
dc.subject
ADENYLYL CYLASE  
dc.subject
COS-7 CELLS  
dc.subject
CYCLIC AMP  
dc.subject
NITRIC OXIDE  
dc.subject
SIGNAL TRANSDUCTION  
dc.subject
SODIUM NITROPRUSSIDE  
dc.subject.classification
Biofísica  
dc.subject.classification
Ciencias Biológicas  
dc.subject.classification
CIENCIAS NATURALES Y EXACTAS  
dc.title
Adenylyl cyclase types I and VI but not II and V are selectively inhibited by nitric oxide  
dc.type
info:eu-repo/semantics/article  
dc.type
info:ar-repo/semantics/artículo  
dc.type
info:eu-repo/semantics/publishedVersion  
dc.date.updated
2021-12-03T20:49:54Z  
dc.identifier.eissn
1414-431X  
dc.journal.volume
35  
dc.journal.number
2  
dc.journal.pagination
145-151  
dc.journal.pais
Brasil  
dc.journal.ciudad
San Pablo  
dc.description.fil
Fil: Goldstein Raij, Jorge. Universidad de Buenos Aires. Facultad de Medicina. Departamento de Ciencias Fisiológicas. Laboratorio de Fisiopatogenia; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay; Argentina  
dc.description.fil
Fil: Ibarra, Cristina Adriana. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay; Argentina. Universidad de Buenos Aires. Facultad de Medicina. Departamento de Ciencias Fisiológicas. Laboratorio de Fisiopatogenia; Argentina  
dc.description.fil
Fil: Silberstein, Claudia Marcela. Universidad de Buenos Aires; Argentina. Universidad de Buenos Aires. Facultad de Medicina. Departamento de Ciencias Fisiológicas. Laboratorio de Fisiopatogenia; Argentina  
dc.journal.title
Brazilian Journal of Medical and Biological Research  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://www.scielo.br/j/bjmbr/a/DkM6kWr5mgTkc6wrYGycngH/?lang=en  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1590/S0100-879X2002000200002