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PNU-282987对颞叶癫痫模型大鼠认知功能的影响及机制
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| 篇名： | PNU-282987对颞叶癫痫模型大鼠认知功能的影响及机制 |
| TITLE： | Effect and mechanism of PNU-282987 on cognitive function of temporal lobe epilepsy model rats |
| 摘要： | 目的 研究特异性α7烟碱型乙酰胆碱受体（α7nAChR）激动剂PNU-282987对颞叶癫痫（TLE）模型大鼠认知功能的影响及机制。方法将60只大鼠随机分为对照组、模型组、PNU-282987组（3mg/kg）和甲基牛扁亭（MLA）+PNU-282987组（6mg/kgMLA+3mg/kgPNU-282987），每组15只。除对照组之外，其余各组大鼠均制备TLE模型。造模成功后，各组大鼠腹腔注射相应药物或生理盐水，每天1次，连续2周。观察大鼠癫痫发作行为并进行评分，记录发作持续时间；检测大鼠认知功能；观察海马组织CA1区神经元病理学形态；检测海马组织中肿瘤坏死因子α（TNF-α）、白细胞介素6（IL-6）和IL-1β水平；检测海马组织中离子钙接头蛋白1（IBA-1）阳性表达和α7nAChR、核因子κB（NF-κB）p65、磷酸化NF-κBp65（p-NF-κBp65）蛋白表达水平。结果与模型组比较，PNU-282987组大鼠癫痫评分和发作持续时间，海马组织中IBA-1阳性细胞数量和TNF-α、IL-6、IL-1β水平以及NF-κBp65、p-NF-κBp65蛋白表达水平均显著减少/降低（P＜0.05）；逃避潜伏期时间显著缩短（P＜0.05），原平台象限停留时间及穿越平台次数均显著增加（P＜0.05）；海马组织CA1区神经元损伤明显减轻；海马组织中α7nAChR蛋白表达水平显著升高（P＜0.05）。与PNU-282987组比较，MLA+PNU-282987组大鼠上述指标均显著逆转（P＜0.05）。结论PNU-282987可改善TLE模型大鼠的认知功能障碍，其机制可能是通过激活α7nAChR/NF-κB信号通路，抑制小胶质细胞介导的炎症反应，进而减轻海马神经元损伤。 |
| ABSTRACT： | OBJECTIVE To investigate the effect and mechanism of α7 nicotinic acetylcholine receptor （α7nAChR） agonists PNU-282987 on cognitive function in temporal lobe epilepsy （TLE） model rats. METHODS Sixty rats were randomly divided into control group， model group， PNU-282987 group （3 mg/kg） and methyllycaconitine （MLA）+PNU-282987 group （6 mg/kg MLA+3 mg/kg PNU-282987）， with 15 rats in each group. Except for control group， the TLE model was established in the other groups. After the model was successfully established， each group was given relevant medicine or normal saline intraperitoneally， once a day， for two consecutive weeks. The epilepsy attack of rats was observed and scored， and the duration of seizures was recorded； the cognitive function of rats was detected； pathological morphology of neurons in CA1 region was observed； the levels of tumor necrosis factor-α （TNF-α）， interleukin-6 （IL-6） and IL-1β in the hippocampus were detected； the positive expressions of ionized calcium-binding adapter molecule-1 （IBA-1）， α7nAChR， nuclear factor-κB （NF-κB） p65， p-NF-κB p65 in the hippocampus were detected. RESULTS Compared with model group， the score and duration of seizures， the number of IBA-1 positive cells， the levels of TNF- α， IL-6 and IL-1β， the expressions of NF- κB p65 and p-NF- κB p65 protein decreased significantly in the hippocampus （P＜0.05）； the escape latency time was shortened significantly （P＜0.05）， the time spent in the original platform quadrant and times of crossing the platform increased significantly （P＜0.05）； neuronal damage in the CA1 region of the hippocampus was significantly reduced； the expression of α7nAChR protein increased significantly in hippocampus （P＜0.05）. Compared with PNU-282987 group， the above indexes of rats in MLA+PNU-282987 group were reversed significantly （P＜0.05）. CONCLUSIONS PNU-282987 could improve cognitive dysfunction in TLE model rats， and its mechanism may be associated with inhibiting microglia-mediated inflammatory response through α7nAChR/NF- κB signaling pathway， thus reducing hippocampal neuronal damage. |
| 期刊： | 2023年第34卷第19期 |
| 作者： | 李永格；周舒；刘庆春；未小明；张冬；马凤巧 |
| AUTHORS： | LI Yongge，ZHOU Shu，LIU Qingchun，WEI Xiaoming，ZHANG Dong，MA Fengqiao |
| 关键字： | PNU-282987；癫痫；α7nAChR/NF-κB信号通路；小胶质细胞；炎症反应 |
| KEYWORDS： | PNU-282987； epilepsy； α7nAChR/NF-κB signaling pathway； microglia； inflammatory response |
| 阅读数： | 26 次 |
| 本月下载数： | 3 次 |
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