苯妥英-左乙乙坦辅助治疗诱导的雄性Wistar大鼠神经毒性和胆碱能神经传递失调,伴有神经认知障碍

Pub Date : 2021-01-01 DOI:10.1080/20905068.2021.1948157
O. Osuntokun, Mary Olabisi Aderoju, Ifeoluwa Esther Adebisi, T. Abayomi, Olorunfemi Samuel Tokunbo, G. Olayiwola
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引用次数: 1

摘要

摘要简介研究了长期给药苯妥英(PHT)、左乙西坦(LEV)和PHT + LEV辅助治疗对雄性大鼠认知功能的影响。方法雄性Wistar大鼠28只(150 ~ 180 g),随机分为4组(N = 7), I-IV组每日腹腔注射生理盐水(0.2 ml)、治疗剂量PHT (50 mg/kg)、LEV (50 mg/kg)或亚治疗剂量PHT (25 mg/kg)与LEV (25 mg/kg)联合用药,连续28 d。随后对大鼠进行行为学评价、乙酰胆碱酯酶活性评价、脂质过氧化活性评价和脑形态学评价。数据分析采用描述性和推断性统计。结果以图或表的平均值±SEM表示,p < 0.05为显著性水平。结果PHT和PHT + LEV辅助治疗后,工作和空间记忆、探索活动和运动协调指标显著(p = 0.0099)受损,额叶和海马重量减少。PHT和PHT + LEV辅助治疗后,大鼠额叶和海马乙酰胆碱酯酶活性显著升高(p = 0.0437)。与对照组相比,PHT、LEV和PHT + LEV组丙二醛浓度显著升高(p = 0.0473)。在前额皮质、海马体和小脑组织中,特别是在PHT + LEV治疗的大鼠,存在染色质溶解、透明化和神经空泡化的组织结构紊乱。结论PHT及PHT + LEV辅助治疗后认知功能损害可能与胆碱能传递的解除和神经毒性有关。
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Phenytoin–levetiracetam adjunctive treatment-induced neurotoxicity and deregulation of cholinergic neurotransmission with evidence of neurocognitive impairment in male Wistar rats
ABSTRACT Introduction The effects of chronic administration of phenytoin (PHT), levetiracetam (LEV), and PHT + LEV adjunctive treatments were examined on the cognitive functions of male rats. Methods Twenty-eight male Wistar rats (150–180 g) were randomized into 4 groups (N = 7). Groups I–IV received daily intraperitoneal administration of normal saline (0.2 ml), therapeutic doses of PHT (50 mg/kg), LEV (50 mg/kg) or sub-therapeutic dose of PHT (25 mg/kg) and LEV (25 mg/kg) combination, respectively, for 28 days. Thereafter, the animals were subjected to behavioral assessment and evaluation of the activities of acetylcholinesterase, lipid peroxidation, and lastly the morphological evaluation of the brain. Data were analyzed using descriptive and inferential statistics. The results were presented as mean ± SEM in graphs or tables, while the level of significance was taken at p < 0.05. Results Working & spatial memory, exploratory activities, and motor-coordination indices were significantly (p = 0.0099) impaired with a reduction in the frontal lobe and hippocampal weight following PHT and PHT + LEV adjunctive treatments. The frontal lobe and hippocampal activities of acetylcholinesterase increased significantly (p = 0.0437) following PHT and PHT + LEV adjunctive treatment. The concentrations of malondialdehyde increased significantly (p = 0.0473) in PHT, LEV, and PHT + LEV compared with the control. There was disorganization in the histoarchitectural profile with chromatolysis, hyalinization, and neural vacuolation in the pre-frontal cortex, hippocampus, and cerebellar tissue, especially in the PHT + LEV treated rats. Conclusion Impairment of cognitive functions following PHT and PHT + LEV adjunctive treatments may be attributable to the deregulation of cholinergic transmission and neurotoxicity.
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