Effects of Cabergoline and Levetiracetam on the Histological and Stereological Structure of the Cerebral Cortex, Hippocampus and Cerebellum of Rats With Pentylenetetrazol-Induced Seizure

Mohammad Hossein Hajati Pishvari, Y. Panahi, Gholamreza Hamidian
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Abstract

Background: Epilepcy is a chronic neurological disease, and due to its complex mechanism, the current therapeutic drugs for it are not effective enough. It may have a non-neurological origin such as astrocytes and microglia. Objective This study aims to investigate the effect of cabergoline and levetiracetam (alone or combined) on the histological and stereological structure of the cerebral cortex, hippocampus, and cerebellum in rats with pentylenetetrazol (PTZ)-induced seizure. Methods: In this experimental study, samples were 30 female rats in five groups of control, seizure (PTZ-induced kindling), seizure+levetiracetam, seizure+cabergoline, seizure+levetiracetam+cabergoline. Levetiracetam and cabergoline were used at 50 and 0.05 mg/kg doses, respectively, and half of these doses were used in the seizure+levetiracetam+cabergoline group. After anesthesia, animals’ brain tissue was removed and after preparing tissue slices, the number of neurons and neuroglia was examined using stereology technique. Results: In the cerebral cortex and in the molecular and granular layers of the cerebellum, the numbers of neurons and neuroglia in the treatment groups were not significantly different from those in the control group, but a significant decrease was observed in the CA1, CA2, and CA3 regions of the hippocampus in the seizure group compared to the control group. In dentate gyrus, the number of neurons in all treatment groups and the number of neuroglia in the seizure group showed a significant decrease compared to the control group. In the Purkinje layer of the cerebellum, there was no significant change in the number of neurons compared to that in the control group. Conclusion: The hippocampus is more involved in the occurrence of seizure activity than other parts of the brain. Neurons and neuroglia play an essential role in seizures, but more studies are needed for determining the relationship between the number of these cells and the use of cabergoline because their number decreases in different parts of the hippocampus following chronic seizures, where the relationship is different between dendrite gyrus and CA regions.
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卡麦角林和左乙曲西坦对戊四唑致癫痫大鼠大脑皮质、海马和小脑组织和体视结构的影响
背景:癫痫是一种慢性神经系统疾病,由于其发病机制复杂,目前的治疗药物疗效不足。它可能有非神经起源,如星形胶质细胞和小胶质细胞。目的探讨卡麦角林和左乙莱西坦(单独或联合)对戊四唑(PTZ)致癫痫大鼠大脑皮层、海马和小脑的组织学和体视学结构的影响。方法:本实验选取30只雌性大鼠,分为5组:对照组、癫痫发作(pz诱导点燃)、癫痫发作+左乙拉西坦、癫痫发作+卡麦角林、癫痫发作+左乙拉西坦+卡麦角林。左乙拉西坦和卡麦角林的剂量分别为50和0.05 mg/kg,其中癫痫+左乙拉西坦+卡麦角林组占一半剂量。麻醉后,取动物脑组织,制备组织切片,用体视技术检测神经元和神经胶质细胞的数量。结果:在大脑皮层、小脑分子层和颗粒层,各治疗组的神经元和神经胶质细胞数量与对照组相比无显著差异,但癫痫发作组海马CA1、CA2、CA3区与对照组相比明显减少。在齿状回,与对照组相比,各治疗组的神经元数量和癫痫发作组的神经胶质细胞数量均显著减少。在小脑浦肯野层,与对照组相比,神经元数量无明显变化。结论:海马比其他脑区更能参与癫痫发作的发生。神经元和神经胶质细胞在癫痫发作中起着至关重要的作用,但由于慢性癫痫发作后海马不同部位的神经元和神经胶质细胞数量减少,其中树突回和CA区域之间的关系不同,因此需要更多的研究来确定这些细胞数量与卡麦角林使用之间的关系。
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