Department of Pharmacology Toxicology and Pharmacotherapy, Medical University-Plovdiv, 4002 Plovdiv, Bulgaria.
Institute of Neurobiology, Bulgarian Academy of Sciences (BAS), 1113 Sofia, Bulgaria.
Int J Mol Sci. 2021 Apr 28;22(9):4667. doi: 10.3390/ijms22094667.
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.
临床上,颞叶癫痫(TLE)是最常见的部分性癫痫类型,常伴有各种合并症。本研究旨在评估抗癫痫药物(AED)拉科酰胺(LCM)慢性治疗对 TLE 模型中自发性运动性发作(SMS)、行为合并症、氧化应激、神经炎症和神经元损伤的影响。在匹罗卡品诱导的癫痫持续状态(SE)后 3 小时给予载体/LCM 治疗(30mg/kg,po),并在 Wistar 大鼠中持续治疗长达 12 周。我们的研究表明,LCM 减轻了 SMS 的数量,并纠正了与癫痫相关的运动活动受损、焦虑、记忆和抑郁样反应,这些反应分别在高架十字迷宫、物体识别测试、放射臂迷宫测试和蔗糖偏好测试中进行测量。这种 AED 通过增加超氧化物歧化酶活性和谷胱甘肽水平来抑制氧化应激,并减轻海马中的过氧化氢酶活性和脂质过氧化。SE 后 LCM 治疗减轻了海马中 IL-1β和 TNF-α水平的升高,并在背侧和腹侧海马、基底外侧杏仁核以及部分梨状皮质中发挥了强烈的神经保护作用。我们的结果表明,LCM 的抗氧化、抗炎和神经保护活性是其抗惊厥作用和对 SE 诱导的行为合并症有益作用的重要前提。