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Atorvastatin pretreatment attenuates kainic acid-induced hippocampal neuronal death via regulation of lipocalin-2-associated neuroinflammation
The Korean Journal of Physiology and Pharmacology ; : 301-309, 2018.
Article in English | WPRIM | ID: wpr-727588
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.
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Full text: Available Index: WPRIM (Western Pacific) Main subject: Phosphorylation / Seizures / Brain / Cardiovascular Diseases / Prevalence / Cell Death / Hydroxymethylglutaryl-CoA Reductase Inhibitors / Cyclooxygenase 2 / Atorvastatin / Hippocampus Type of study: Prevalence study Limits: Animals Language: English Journal: The Korean Journal of Physiology and Pharmacology Year: 2018 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Phosphorylation / Seizures / Brain / Cardiovascular Diseases / Prevalence / Cell Death / Hydroxymethylglutaryl-CoA Reductase Inhibitors / Cyclooxygenase 2 / Atorvastatin / Hippocampus Type of study: Prevalence study Limits: Animals Language: English Journal: The Korean Journal of Physiology and Pharmacology Year: 2018 Type: Article