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Atorvastatin pretreatment attenuates kainic acid-induced hippocampal neuronal death via regulation of lipocalin-2-associated neuroinflammation
Article Dans En | WPRIM | ID: wpr-727588
Responsable en Bibliothèque : WPRO
ABSTRACT
Statins mediate vascular protection and reduce the prevalence of cardiovascular diseases. Recent work indicates that statins have anticonvulsive effects in the brain; however, little is known about the precise mechanism for its protective effect in kainic acid (KA)-induced seizures. Here, we investigated the protective effects of atorvastatin pretreatment on KA-induced neuroinflammation and hippocampal cell death. Mice were treated via intragastric administration of atorvastatin for 7 days, injected with KA, and then sacrificed after 24 h. We observed that atorvastatin pretreatment reduced KA-induced seizure activity, hippocampal cell death, and neuroinflammation. Atorvastatin pretreatment also inhibited KA-induced lipocalin-2 expression in the hippocampus and attenuated KA-induced hippocampal cyclooxygenase-2 expression and glial activation. Moreover, AKT phosphorylation in KA-treated hippocampus was inhibited by atorvastatin pretreatment. These findings suggest that atorvastatin pretreatment may protect hippocampal neurons during seizures by controlling lipocalin-2-associated neuroinflammation.
Sujets)

Texte intégral: 1 Indice: WPRIM Sujet Principal: Phosphorylation / Crises épileptiques / Encéphale / Maladies cardiovasculaires / Prévalence / Mort cellulaire / Inhibiteurs de l'hydroxyméthylglutaryl-CoA réductase / Cyclooxygenase 2 / Atorvastatine / Hippocampe Type d'étude: Prevalence_studies Limites du sujet: Animals langue: En Texte intégral: The Korean Journal of Physiology and Pharmacology Année: 2018 Type: Article
Texte intégral: 1 Indice: WPRIM Sujet Principal: Phosphorylation / Crises épileptiques / Encéphale / Maladies cardiovasculaires / Prévalence / Mort cellulaire / Inhibiteurs de l'hydroxyméthylglutaryl-CoA réductase / Cyclooxygenase 2 / Atorvastatine / Hippocampe Type d'étude: Prevalence_studies Limites du sujet: Animals langue: En Texte intégral: The Korean Journal of Physiology and Pharmacology Année: 2018 Type: Article