Arginine administration decreases cerebral cortex acetylcholinesterase and serum butyrylcholinesterase probably by oxidative stress induction

Detalhes bibliográficos
Autor(a) principal: Wyse, Angela Terezinha de Souza
Data de Publicação: 2004
Outros Autores: Stefanello, Francieli Moro, Chiarani, Fabria, Delwing, Débora, Wannmacher, Clovis Milton Duval, Wajner, Moacir
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UFRGS
Texto Completo: http://hdl.handle.net/10183/218299
Resumo: In the present study we investigated the action of vitamins E and C on the inhibition of acetylcholinesterase and butyrylcholinesterase activities provoked by arginine in cerebral cortex and serum of 60-day-old rats. Animals were pretreated for 1 week with daily intraperitoneal administration of saline (control) or vitamins E (40 mg/kg) and C (100 mg/kg). Twelve hours after the last injection, animals received one injection of arginine (0.8 M/g of body weight) or saline. Results showed that acetylcholinesterase and butyrylcholinesterase activities were decreased in the arginine-treated rats. Furthermore, pretreatment with vitamins E and C prevented these effects. The data indicate that the reduction of acetylcholinesterase and butyrylcholinesterase activities caused by arginine was probably mediated by oxidative stress. Assuming the possibility that these effects might also occur in the human condition, our findings may be relevant to explain, at least in part, the neurological dysfunction associated with hyperargininemia and might support a novel therapeutic strategy to slow the progression of neurodegeneration in this disorder.
id UFRGS-2_50ac5068af2bd6ee3ef3f31e7f1c1939
oai_identifier_str oai:www.lume.ufrgs.br:10183/218299
network_acronym_str UFRGS-2
network_name_str Repositório Institucional da UFRGS
repository_id_str
spelling Wyse, Angela Terezinha de SouzaStefanello, Francieli MoroChiarani, FabriaDelwing, DéboraWannmacher, Clovis Milton DuvalWajner, Moacir2021-03-02T04:15:40Z20040364-3190http://hdl.handle.net/10183/218299000503522In the present study we investigated the action of vitamins E and C on the inhibition of acetylcholinesterase and butyrylcholinesterase activities provoked by arginine in cerebral cortex and serum of 60-day-old rats. Animals were pretreated for 1 week with daily intraperitoneal administration of saline (control) or vitamins E (40 mg/kg) and C (100 mg/kg). Twelve hours after the last injection, animals received one injection of arginine (0.8 M/g of body weight) or saline. Results showed that acetylcholinesterase and butyrylcholinesterase activities were decreased in the arginine-treated rats. Furthermore, pretreatment with vitamins E and C prevented these effects. The data indicate that the reduction of acetylcholinesterase and butyrylcholinesterase activities caused by arginine was probably mediated by oxidative stress. Assuming the possibility that these effects might also occur in the human condition, our findings may be relevant to explain, at least in part, the neurological dysfunction associated with hyperargininemia and might support a novel therapeutic strategy to slow the progression of neurodegeneration in this disorder.application/pdfengNeurochemical research. New York, NY. Vol. 29, no. 2 (2004), p. 385-389HiperargininemiaAcetilcolinesteraseButirilcolinesteraseArgininaVitamina EÁcido ascórbicoHyperargininemiaAcetylcholinesteraseButyrylcholinesteraseArginineVitamin EVitamin CArginine administration decreases cerebral cortex acetylcholinesterase and serum butyrylcholinesterase probably by oxidative stress inductionEstrangeiroinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFRGSinstname:Universidade Federal do Rio Grande do Sul (UFRGS)instacron:UFRGSTEXT000503522.pdf.txt000503522.pdf.txtExtracted Texttext/plain0http://www.lume.ufrgs.br/bitstream/10183/218299/2/000503522.pdf.txtd41d8cd98f00b204e9800998ecf8427eMD52ORIGINAL000503522.pdfTexto completo (inglês)application/pdf1528730http://www.lume.ufrgs.br/bitstream/10183/218299/1/000503522.pdf132db6cdd22e424f07ba48a25ee16f8dMD5110183/2182992021-04-12 08:31:21.50767oai:www.lume.ufrgs.br:10183/218299Repositório de PublicaçõesPUBhttps://lume.ufrgs.br/oai/requestopendoar:2021-04-12T11:31:21Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS)false
dc.title.pt_BR.fl_str_mv Arginine administration decreases cerebral cortex acetylcholinesterase and serum butyrylcholinesterase probably by oxidative stress induction
title Arginine administration decreases cerebral cortex acetylcholinesterase and serum butyrylcholinesterase probably by oxidative stress induction
spellingShingle Arginine administration decreases cerebral cortex acetylcholinesterase and serum butyrylcholinesterase probably by oxidative stress induction
Wyse, Angela Terezinha de Souza
Hiperargininemia
Acetilcolinesterase
Butirilcolinesterase
Arginina
Vitamina E
Ácido ascórbico
Hyperargininemia
Acetylcholinesterase
Butyrylcholinesterase
Arginine
Vitamin E
Vitamin C
title_short Arginine administration decreases cerebral cortex acetylcholinesterase and serum butyrylcholinesterase probably by oxidative stress induction
title_full Arginine administration decreases cerebral cortex acetylcholinesterase and serum butyrylcholinesterase probably by oxidative stress induction
title_fullStr Arginine administration decreases cerebral cortex acetylcholinesterase and serum butyrylcholinesterase probably by oxidative stress induction
title_full_unstemmed Arginine administration decreases cerebral cortex acetylcholinesterase and serum butyrylcholinesterase probably by oxidative stress induction
title_sort Arginine administration decreases cerebral cortex acetylcholinesterase and serum butyrylcholinesterase probably by oxidative stress induction
author Wyse, Angela Terezinha de Souza
author_facet Wyse, Angela Terezinha de Souza
Stefanello, Francieli Moro
Chiarani, Fabria
Delwing, Débora
Wannmacher, Clovis Milton Duval
Wajner, Moacir
author_role author
author2 Stefanello, Francieli Moro
Chiarani, Fabria
Delwing, Débora
Wannmacher, Clovis Milton Duval
Wajner, Moacir
author2_role author
author
author
author
author
dc.contributor.author.fl_str_mv Wyse, Angela Terezinha de Souza
Stefanello, Francieli Moro
Chiarani, Fabria
Delwing, Débora
Wannmacher, Clovis Milton Duval
Wajner, Moacir
dc.subject.por.fl_str_mv Hiperargininemia
Acetilcolinesterase
Butirilcolinesterase
Arginina
Vitamina E
Ácido ascórbico
topic Hiperargininemia
Acetilcolinesterase
Butirilcolinesterase
Arginina
Vitamina E
Ácido ascórbico
Hyperargininemia
Acetylcholinesterase
Butyrylcholinesterase
Arginine
Vitamin E
Vitamin C
dc.subject.eng.fl_str_mv Hyperargininemia
Acetylcholinesterase
Butyrylcholinesterase
Arginine
Vitamin E
Vitamin C
description In the present study we investigated the action of vitamins E and C on the inhibition of acetylcholinesterase and butyrylcholinesterase activities provoked by arginine in cerebral cortex and serum of 60-day-old rats. Animals were pretreated for 1 week with daily intraperitoneal administration of saline (control) or vitamins E (40 mg/kg) and C (100 mg/kg). Twelve hours after the last injection, animals received one injection of arginine (0.8 M/g of body weight) or saline. Results showed that acetylcholinesterase and butyrylcholinesterase activities were decreased in the arginine-treated rats. Furthermore, pretreatment with vitamins E and C prevented these effects. The data indicate that the reduction of acetylcholinesterase and butyrylcholinesterase activities caused by arginine was probably mediated by oxidative stress. Assuming the possibility that these effects might also occur in the human condition, our findings may be relevant to explain, at least in part, the neurological dysfunction associated with hyperargininemia and might support a novel therapeutic strategy to slow the progression of neurodegeneration in this disorder.
publishDate 2004
dc.date.issued.fl_str_mv 2004
dc.date.accessioned.fl_str_mv 2021-03-02T04:15:40Z
dc.type.driver.fl_str_mv Estrangeiro
info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/10183/218299
dc.identifier.issn.pt_BR.fl_str_mv 0364-3190
dc.identifier.nrb.pt_BR.fl_str_mv 000503522
identifier_str_mv 0364-3190
000503522
url http://hdl.handle.net/10183/218299
dc.language.iso.fl_str_mv eng
language eng
dc.relation.ispartof.pt_BR.fl_str_mv Neurochemical research. New York, NY. Vol. 29, no. 2 (2004), p. 385-389
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.source.none.fl_str_mv reponame:Repositório Institucional da UFRGS
instname:Universidade Federal do Rio Grande do Sul (UFRGS)
instacron:UFRGS
instname_str Universidade Federal do Rio Grande do Sul (UFRGS)
instacron_str UFRGS
institution UFRGS
reponame_str Repositório Institucional da UFRGS
collection Repositório Institucional da UFRGS
bitstream.url.fl_str_mv http://www.lume.ufrgs.br/bitstream/10183/218299/2/000503522.pdf.txt
http://www.lume.ufrgs.br/bitstream/10183/218299/1/000503522.pdf
bitstream.checksum.fl_str_mv d41d8cd98f00b204e9800998ecf8427e
132db6cdd22e424f07ba48a25ee16f8d
bitstream.checksumAlgorithm.fl_str_mv MD5
MD5
repository.name.fl_str_mv Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS)
repository.mail.fl_str_mv
_version_ 1801225008924590080