Nikolaev Maxim V, Fedorova Irina M, Chistyakova Oxana V, Postnikova Tatiana Yu, Kim Kira Kh, Dron Mikhail Yu, Zaitsev Aleksey V, Tikhonov Denis B
Sechenov Institute of Evolutionary Physiology and Biochemistry, Russian Academy of Sciences, 194223 Saint Petersburg, Russia.
Int J Mol Sci. 2025 May 30;26(11):5299. doi: 10.3390/ijms26115299.
The search for novel compounds with anticonvulsant properties remains a key focus in neuropharmacology. Recently, the diazepine-benzimidazole derivative, DAB-19, has emerged as a promising candidate due to its demonstrated anxiolytic and analgesic effects. In this study, we investigate the mechanisms underlying DAB-19's activity, focusing on its impact on glutamatergic transmission, a key target in the pathophysiology of various central nervous system disorders. Intriguingly, while DAB-19 suppressed evoked glutamatergic transmission in rat brain slices, it simultaneously enhanced spontaneous neurotransmission. Further experiments on glutamatergic neuromuscular synapses in fly larvae revealed two distinct mechanisms: calcium-dependent potentiation of glutamate release and inhibition of spike propagation via blockade of voltage-gated sodium channels. The latter effect was directly confirmed in rat brain neurons. Given its action on sodium channels, we tested DAB-19 in the pentylenetetrazole model, where it delayed seizure onset but did not prevent seizures. These findings position DAB-19 as a multifaceted compound with significant therapeutic potential.
寻找具有抗惊厥特性的新型化合物仍然是神经药理学的一个关键重点。最近,二氮杂卓 - 苯并咪唑衍生物DAB - 19因其已证实的抗焦虑和镇痛作用而成为一个有前景的候选物。在本研究中,我们研究了DAB - 19活性的潜在机制,重点关注其对谷氨酸能传递的影响,谷氨酸能传递是各种中枢神经系统疾病病理生理学中的一个关键靶点。有趣的是,虽然DAB - 19抑制了大鼠脑片中诱发的谷氨酸能传递,但它同时增强了自发神经传递。对果蝇幼虫谷氨酸能神经肌肉突触的进一步实验揭示了两种不同的机制:钙依赖性增强谷氨酸释放以及通过阻断电压门控钠通道抑制动作电位传播。后一种效应在大鼠脑神经元中得到了直接证实。鉴于其对钠通道的作用,我们在戊四氮模型中测试了DAB - 19,它延迟了癫痫发作的起始,但并未预防癫痫发作。这些发现表明DAB - 19是一种具有显著治疗潜力的多面化合物。