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Provedor de dados:  Anais da ABC (AABC)
País:  Brazil
Título:  Acute administration of fenproporex increased acetylcholinesterase activity in brain of young rats
Autores:  TEODORAK,BRENA P.
FERREIRA,GABRIELA K.
SCAINI,GISELLI
WESSLER,LETÍCIA B.
HEYLMANN,ALEXANDRA S.
DEROZA,PEDRO
VALVASSORI,SAMIRA S.
ZUGNO,ALEXANDRA I.
QUEVEDO,JOÃO
STRECK,EMILIO L.
Data:  2015-08-01
Ano:  2015
Palavras-chave:  Acetylcholinesterase
Amphetamine
Dopamine
Fenproporex
Resumo:  Fenproporex is the second most commonly amphetamine-based anorectic consumed worldwide; this drug is rapidly converted into amphetamine, in vivo, and acts by increasing dopamine levels in the synaptic cleft. Considering that fenproporex effects on the central nervous system are still poorly known and that acetylcholinesterase is a regulatory enzyme which is involved in cholinergic synapses and may indirectly modulate the release of dopamine, the present study investigated the effects of acute administration of fenproporex on acetylcholinesterase activity in brain of young rats. Young male Wistar rats received a single injection of fenproporex (6.25, 12.5 or 25mg/kg i.p.) or vehicle (2% Tween 80). Two hours after the injection, the rats were killed by decapitation and the brain was removed for evaluation of acetylcholinesterase activity. Results showed that fenproporex administration increased acetylcholinesterase activity in the hippocampus and posterior cortex, whereas in the prefrontal cortex, striatum and cerebellum the enzyme activity was not altered. In conclusion, in the present study we demonstrated that acute administration of fenproporex exerts an effect in the cholinergic system causing an increase in the activity of acetylcholinesterase in a dose-dependent manner in the hippocampus and posterior cortex. Thus, we suggest that the imbalance in cholinergic homeostasis could be considered as an important pathophysiological mechanism underlying the brain damage observed in patients who use amphetamines such as fenproporex.
Tipo:  Info:eu-repo/semantics/article
Idioma:  Inglês
Identificador:  http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0001-37652015000301389
Editor:  Academia Brasileira de Ciências
Relação:  10.1590/0001-3765201520140638
Formato:  text/html
Fonte:  Anais da Academia Brasileira de Ciências v.87 n.2 suppl.0 2015
Direitos:  info:eu-repo/semantics/openAccess
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