Wang Lin, Kong Qingxia, Leng Xinyi, Leung Howan, Li Yang
Department of Neurology, Affiliated Hospital of Jining Medical University, Jining City, China.
Epilepsy Center, Affiliated Hospital of Jining Medical University, Jining City, China.
Epilepsia Open. 2025 Feb;10(1):55-73. doi: 10.1002/epi4.13112. Epub 2024 Dec 27.
Epilepsy is one of the common chronic neurological diseases, affecting more than 70 million people worldwide. The brains of people with epilepsy exhibit a pathological and persistent propensity for recurrent seizures. Epilepsy often coexists with cardiovascular disease, cognitive dysfunction, depression, etc., which seriously affects the patient's quality of life. Although our understanding of epilepsy has advanced, the pathophysiological mechanisms leading to epileptogenesis, drug resistance, and associated comorbidities remain largely unknown. The use of newer antiepileptic drugs has increased, but this has not improved overall outcomes. We need to deeply study the pathogenesis of epilepsy and find drugs that can not only prevent the epileptogenesis and interfere with the process of epileptogenesis but also treat epilepsy comorbidities. Sphingosine-1-phosphate (S1P) is an important lipid molecule. It not only forms the basis of cell membranes but is also an important bioactive mediator. It can not only act as a second messenger in cells to activate downstream signaling pathways but can also exert biological effects by being secreted outside cells and binding to S1P receptors on the cell membrane. Fingolimod (FTY720) is the first S1P receptor modulator developed and approved for the treatment of multiple sclerosis. More and more studies have proven that the S1P signaling pathway is closely related to epilepsy, drug-resistant epilepsy, epilepsy comorbidities, or other epilepsy-causing diseases. However, there is much controversy over the role of certain natural molecules in the pathway and receptor modulators (such as FTY720) in epilepsy. Here, we summarize and analyze the role of the S1P signaling pathway in epilepsy, provide a basis for finding potential therapeutic targets and/or epileptogenic biomarkers, analyze the reasons for these controversies, and put forward our opinions. PLAIN LANGUAGE SUMMARY: This article combines the latest research literature at home and abroad to review the sphingosine 1-phosphate signaling pathway and epileptogenesis, drug-resistant epilepsy, epilepsy comorbidities, other diseases that can cause epilepsy, as well as the sphingosine-1-phosphate signaling pathway regulators and epilepsy, with the expectation of providing a certain theoretical basis for finding potential epilepsy treatment targets and/or epileptogenic biomarkers in the sphingosine-1-phosphate signaling pathway.
癫痫是常见的慢性神经疾病之一,全球有超过7000万人受其影响。癫痫患者的大脑呈现出复发性癫痫发作的病理性和持续性倾向。癫痫常与心血管疾病、认知功能障碍、抑郁症等并存,严重影响患者的生活质量。尽管我们对癫痫的认识有所进步,但导致癫痫发生、耐药性及相关合并症的病理生理机制在很大程度上仍不清楚。新型抗癫痫药物的使用有所增加,但这并未改善总体治疗效果。我们需要深入研究癫痫的发病机制,找到不仅能预防癫痫发生、干扰癫痫发生过程,还能治疗癫痫合并症的药物。鞘氨醇-1-磷酸(S1P)是一种重要的脂质分子。它不仅是细胞膜的组成基础,也是一种重要的生物活性介质。它不仅能作为细胞内的第二信使激活下游信号通路,还能通过分泌到细胞外并与细胞膜上的S1P受体结合发挥生物学效应。芬戈莫德(FTY720)是首个开发并获批用于治疗多发性硬化症的S1P受体调节剂。越来越多的研究证明,S1P信号通路与癫痫、耐药性癫痫、癫痫合并症或其他致痫疾病密切相关。然而,某些天然分子在该通路以及受体调节剂(如FTY720)在癫痫中的作用存在诸多争议。在此,我们总结并分析S1P信号通路在癫痫中的作用,为寻找潜在治疗靶点和/或致痫生物标志物提供依据,分析这些争议的原因,并提出我们的观点。通俗易懂的总结:本文结合国内外最新研究文献,综述了鞘氨醇-1-磷酸信号通路与癫痫发生、耐药性癫痫、癫痫合并症、其他可导致癫痫的疾病,以及鞘氨醇-1-磷酸信号通路调节剂与癫痫的关系,期望为在鞘氨醇-1-磷酸信号通路中寻找潜在的癫痫治疗靶点和/或致痫生物标志物提供一定的理论基础。