The GPER1 agonist G1 reduces brain injury and improves the qEEG and behavioral outcome of experimental ischemic stroke

Stroke is one of the principal cerebrovascular diseases in human populations and contributes to a majority of the functional impairments in the elderly. Recent discoveries have led to the inclusion of electroencephalography (EEG) in the complementary prognostic evaluation of patients. The present st...

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Detalles Bibliográficos
Autores: Ferreira, Luan Oliveira, Souza, Rafael Dias de, Teixeira, Leonan Lima, Pinto, Laine Celestino, Rodrigues, João Cleiton Martins, Martins Filho, Arnaldo Jorge, Costa, Edmar Tavares da, Hamoy, Moisés, Lopes, Dielly Catrina Favacho
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2023
País:Brasil
Institución:Instituto Evandro Chagas (IEC)
Repositorio:Repositório Digital do Instituto Evandro Chagas (Patuá)
Idioma:inglés
OAI Identifier:oai:patua.iec.gov.br:iec/6895
Acceso en línea:https://patua.iec.gov.br/handle/iec/6895
Access Level:acceso embargado
Palabra clave:Sistema Nervoso Central
Acidente Vascular Cerebral / tratamento farmacológico
Isquemia Encefálica
Eletroencefalografia / métodos
Neurofarmacologia / métodos
Descripción
Sumario:Stroke is one of the principal cerebrovascular diseases in human populations and contributes to a majority of the functional impairments in the elderly. Recent discoveries have led to the inclusion of electroencephalography (EEG) in the complementary prognostic evaluation of patients. The present study describes the EEG, behavioral, and histological changes that occur following cerebral ischemia associated with treatment by G1, a potent and selective G protein-coupled estrogen receptor 1 (GPER1) agonist in a rat model. Treatment with G1 attenuated the neurological deficits induced by ischemic stroke from the second day onward, and reduced areas of infarction. Treatment with G1 also improved the total brainwave power, as well as the theta and alpha wave activity, specifically, and restored the delta band power to levels similar to those observed in the controls. Treatment with G1 also attenuated the peaks of harmful activity observed in the EEG indices. These improvements in brainwave activity indicate that GPER1 plays a fundamental role in the mediation of cerebral injury and in the behavioral outcome of ischemic brain injuries, which points to treatment with G1 as a potential pharmacological strategy for the therapy of stroke.