The effect of agonist and antagonist of Nociceptine/Orphanin FQ receptor on seizure and cognitive dysfunction in experimental model of temporal lobe epilepsy in male rat

N. Jamali-Raeufy, M. Zeinivand, Mina Goudarzi, Sobhan Haghani
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Abstract

Background: Temporal lobe epilepsy is a chronic neurological disorder characterized by spontaneous seizures, learning and memory deficiency, loss of neurons, mossy fiber sprouting and tissue apoptosis. This study was to investigate the effect of NOP receptor agonist (MCOPPB) and antagonist (SB612111) on seizure and cognitive dysfunction and histological studies in experimental model of temporal lobe epilepsy in male rat. Materials and methods: in this study, 50 male rats were divided into six groups, including sham, epileptic, valperoic treated epileptic, NOP receptor agonist and antagonist treated epileptic. Finally, seizure behavior, short-term (Y-maze) and long-term (shuttle box) memory, GFAP value and also histologic finding (Nissel, Tim and Apoptosis staining) were evaluated. Results: Kinic acid induced seizures associated with significant seizure behavior, impairment of learning and memory and tissue damage. Pretreated epileptic rats with NOP receptor agonist decreased seizure attacks, but did not improve memory. Administration of NOP antagonist was not effective on the seizure behavior, but contribute to improve the memory and learning abilities following treatment. Also, administration of NOP agonist and antagonist increased neuron count, reduced increased sprouting of mossy fibers, cell death and the activity of astrocytes in the hippocampus. Conclusion: pre-treatment of epileptic rets with NOP receptor agonist and antagonist reduced seizures attacks and improved short-term spatial memory and tissue damage in rats.
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诺西西汀/孤啡肽FQ受体激动剂和拮抗剂对雄性大鼠颞叶癫痫实验模型癫痫发作和认知功能障碍的影响
背景:颞叶癫痫是一种慢性神经系统疾病,以自发发作、学习记忆障碍、神经元丧失、苔藓纤维萌发和组织凋亡为特征。本研究旨在探讨NOP受体激动剂(MCOPPB)和拮抗剂(SB612111)对雄性大鼠颞叶癫痫实验模型癫痫发作和认知功能障碍的影响及组织学研究。材料与方法:将50只雄性大鼠分为6组,分别为假药组、癫痫组、丙泊仑治疗组、NOP受体激动剂组和拮抗剂治疗组。最后,评估癫痫发作行为、短期(y形迷宫)和长期(穿梭箱)记忆、GFAP值以及组织学发现(Nissel、Tim和凋亡染色)。结果:运动酸诱导的癫痫发作与显著的癫痫发作行为、学习记忆障碍和组织损伤有关。用NOP受体激动剂预处理的癫痫大鼠癫痫发作次数减少,但没有改善记忆。NOP拮抗剂对癫痫发作行为无明显影响,但有助于改善治疗后的记忆和学习能力。此外,给予NOP激动剂和拮抗剂可增加神经元数量,减少苔藓纤维发芽、细胞死亡和海马星形胶质细胞的活性。结论:NOP受体激动剂和拮抗剂预处理癫痫大鼠可减少癫痫发作次数,改善短时空间记忆和组织损伤。
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