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Effects of Lacosamide Treatment on Epileptogenesis,Neuronal Damage and Behavioral Comorbidities in a Rat Model of Temporal Lobe Epilepsy
Authors:Michaela Shishmanova-Doseva  Dimitrinka Atanasova  Yordanka Uzunova  Lyubka Yoanidu  Lyudmil Peychev  Pencho Marinov  Jana Tchekalarova
Affiliation:1.Department of Pharmacology Toxicology and Pharmacotherapy, Medical University-Plovdiv, 4002 Plovdiv, Bulgaria;2.Institute of Neurobiology, Bulgarian Academy of Sciences (BAS), 1113 Sofia, Bulgaria;3.Department of Anatomy, Faculty of Medicine, Trakia University, 6003 Stara Zagora, Bulgaria;4.Department of Bioorganic Chemistry, Medical University-Plovdiv, 4002 Plovdiv, Bulgaria; (Y.U.); (L.Y.);5.Institute of Information and Communication Technologies, BAS, 1113 Sofia, Bulgaria;
Abstract:Clinically, temporal lobe epilepsy (TLE) is the most prevalent type of partial epilepsy and often accompanied by various comorbidities. The present study aimed to evaluate the effects of chronic treatment with the antiepileptic drug (AED) lacosamide (LCM) on spontaneous motor seizures (SMS), behavioral comorbidities, oxidative stress, neuroinflammation, and neuronal damage in a model of TLE. Vehicle/LCM treatment (30 mg/kg, p.o.) was administered 3 h after the pilocarpine-induced status epilepticus (SE) and continued for up to 12 weeks in Wistar rats. Our study showed that LCM attenuated the number of SMS and corrected comorbid to epilepsy impaired motor activity, anxiety, memory, and alleviated depressive-like responses measured in the elevated plus maze, object recognition test, radial arm maze test, and sucrose preference test, respectively. This AED suppressed oxidative stress through increased superoxide dismutase activity and glutathione levels, and alleviated catalase activity and lipid peroxidation in the hippocampus. Lacosamide treatment after SE mitigated the increased levels of IL-1β and TNF-α in the hippocampus and exerted strong neuroprotection both in the dorsal and ventral hippocampus, basolateral amygdala, and partially in the piriform cortex. Our results suggest that the antioxidant, anti-inflammatory, and neuroprotective activity of LCM is an important prerequisite for its anticonvulsant and beneficial effects on SE-induced behavioral comorbidities.
Keywords:lacosamide  pilocarpine  oxidative stress  inflammation  neuronal loss  hippocampus
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