Li Zhen, Ge Biying, Li Haoqi, Huang Chunyao, Ji Yunhan, Schachner Melitta, Yin Shengming, Li Sheng, Zhao Jie
National-Local Joint Engineering Research Center for Drug Research and Development (R&D) of Neurodegenerative Diseases, Dalian Medical University, Dalian 116044, China.
Functional Laboratory, College of Basic Medical Sciences, Dalian Medical University, Dalian 116044, China.
Biomolecules. 2025 Jul 17;15(7):1032. doi: 10.3390/biom15071032.
Temporal lobe epilepsy (TLE) is a common drug-resistant form of epilepsy, often accompanied by cognitive and emotional disturbances, highlighting the urgent need for novel therapies. Scorpion Venom Heat-Resistant Synthetic Peptide (SVHRSP), isolated and synthetically derived from scorpion venom, has shown anti-epileptic and neuroprotective potential. This study evaluated the anti-epileptic effects of SVHRSP in a kainic acid (KA)-induced TLE rat model. Our results demonstrated that SVHRSP (0.81 mg/kg/day) reduced the frequency and severity of spontaneous seizures. Behavioral tests showed improved cognitive performance in the novel object recognition, object location, and T-maze tasks, as well as reduced anxiety-like behavior in the open-field test. Moreover, SVHRSP mitigated hippocampal neuronal loss and glial activation. Transcriptomic analysis indicated that SVHRSP upregulates genes involved in adhesion molecule-triggered and axon guidance pathways. Western blotting and immunofluorescence further confirmed that SVHRSP restored dendritic (MAP2), axonal (NFL), and synaptic (PSD95) marker expression, elevated the functionally important L1CAM fragment (L1-70), and increased myelin basic protein-induced serine protease activity responsible for L1-70 generation. Blockade of L1CAM expression diminished the neuroprotective effects of SVHRSP, suggesting a critical role for L1CAM-mediated synapse functions. This study is the first to reveal the therapeutic potential of SVHRSP in TLE via L1CAM-associated mechanisms.
颞叶癫痫(TLE)是一种常见的耐药性癫痫形式,常伴有认知和情绪障碍,凸显了对新型疗法的迫切需求。蝎毒耐热合成肽(SVHRSP)是从蝎毒中分离并合成得到的,已显示出抗癫痫和神经保护潜力。本研究评估了SVHRSP在 kainic 酸(KA)诱导的 TLE 大鼠模型中的抗癫痫作用。我们的结果表明,SVHRSP(0.81 mg/kg/天)降低了自发癫痫发作的频率和严重程度。行为测试显示,在新物体识别、物体定位和 T 迷宫任务中认知表现得到改善,在旷场试验中焦虑样行为减少。此外,SVHRSP 减轻了海马神经元损失和神经胶质细胞激活。转录组分析表明,SVHRSP 上调了参与黏附分子触发和轴突导向途径的基因。蛋白质免疫印迹和免疫荧光进一步证实,SVHRSP 恢复了树突(MAP2)、轴突(NFL)和突触(PSD95)标志物的表达,提高了功能重要的 L1CAM 片段(L1-70),并增加了髓鞘碱性蛋白诱导的负责 L1-70 产生的丝氨酸蛋白酶活性。阻断 L1CAM 的表达减弱了 SVHRSP 的神经保护作用,表明 L1CAM 介导的突触功能起关键作用。本研究首次揭示了 SVHRSP 通过与 L1CAM 相关的机制在 TLE 中的治疗潜力。