Protective effects of gabapentin against the seizure susceptibility and comorbid behavioral abnormalities in the early socially isolated mice
Autor: | Arya Haj-Mirzaian, Armin Shirzadian, Mohammad-Reza Zarrindast, Maryam Rahimi-Balaei, Shayan Amiri, Arman Mohsenzadeh, Carl O. Olson, Ali Razmi, Hossein Amini-Khoei, Mojgan Rastegar, Mahmoud Ghazi-Khansari |
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Rok vydání: | 2016 |
Předmět: |
0301 basic medicine
Drug Brain development Gabapentin Cyclohexanecarboxylic Acids media_common.quotation_subject Comorbidity Anxiety Bioinformatics 03 medical and health sciences Epilepsy Mice 0302 clinical medicine Animal model Seizures medicine Animals Social isolation Amines Maze Learning gamma-Aminobutyric Acid media_common Pharmacology Behavior Animal Dose-Response Relationship Drug medicine.disease Aggression Seizure susceptibility 030104 developmental biology Social Isolation Seizure Disorders Anesthesia Housing Anticonvulsants Disease Susceptibility medicine.symptom Psychology 030217 neurology & neurosurgery Locomotion Stress Psychological medicine.drug |
Zdroj: | European journal of pharmacology. 797 |
ISSN: | 1879-0712 |
Popis: | Adolescence is a pivotal period of brain development during lifespan, which is sensitive to stress exposure. Early social isolation stress (SIS) is known to provoke a variety of psychiatric comorbidities as well as seizure risk. Psychiatric comorbidities present challenging dilemmas for treatment and management in people with seizure disorders. In this study, we aimed to investigate whether gabapentin (GBP) as an anti-epileptic drug is able to alleviate the seizure activity as well as comorbid behavioral abnormalities in socially isolated mice. Results showed that early SIS induced proconvulsant effects along with depressive, aggressive and anxiety-like behaviors. Whereas the administration of both acute and chronic GBP at sub-effective doses produced no alterations in the behavioral profile of socially conditioned counterparts the same treatments effectively reversed the seizure susceptibility to pentylenetetrazole and behavioral deficits in isolated mice. Results of the study indicate that 1) Early SIS could be considered as an animal model of psychosocial stress to investigate the psychiatric comorbidities in seizure disorders, 2) Chronic administration of low dose GBP prevented the shaping of behavioral abnormalities in adulthood, 3) Chronic administration of low dose GBP produced no negative behavioral effects in socially conditioned mice suggesting the safety of the drug, 4) Gabapentin at low doses may be considered as an agent for management of epilepsy in individuals with psychiatric comorbidities. |
Databáze: | OpenAIRE |
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