Laboratory of Molecular Neurodegeneration, Peter the Great St. Petersburg Polytechnic University, St. Petersburg, 195251, Russia.
Laboratory of Structural Bioinformatics, Institute of Biomedicine and Pharmacy, Russian-Armenian University, Yerevan, 0051, Armenia.
Sci Rep. 2024 Oct 9;14(1):23512. doi: 10.1038/s41598-024-73849-z.
Alzheimer disease (AD) is characterized by progressive loss of memory. Synaptic loss is now the best correlate of cognitive dysfunction in patients with Alzheimer's disease. Thus, restoration or limitation of synapse loss is a promising strategy for pharmacotherapy of AD. N-N substituted piperazines are widely used chemical compounds for drug interventions to treat different illnesses including CNS diseases such as drug abuse, mental and anxiety disorders. Piperazine derivatives are small molecules that are usually well tolerated and cross blood brain barrier (BBB). Thus, disubstituted piperazines are good tools for searching and developing novel disease-modifying drugs. Previously, we have determined the piperazine derivative, 51164, as an activator of TRPC6 in dendritic spines. We have demonstrated synaptoprotective properties of 51164 in AD mouse models. However, 51164 was not able to cross BBB. Within the current study, we identified a novel piperazine derivative, cmp2, that is structurally similar to 51164 but is able to cross BBB. Cmp2 binds central part of monomeric TRPC6 in similar way as hypeforin does. Cmp2 selectively activates TRPC6 but not structurally related TRPC3 and TRPC7. Novel piperazine derivative exhibits synaptoprotective properties in culture and slices and penetrates the BBB. In vivo study indicated cmp2 (10 mg/kg I.P.) reversed deficits in synaptic plasticity in the 5xFAD mice. Thus, we suggest that cmp2 is a novel lead compound for drug development. The mechanism of cmp2 action is based on selective TRPC6 stimulation and it is expected to treat synaptic deficiency in hippocampal neurons.
阿尔茨海默病(AD)的特征是记忆逐渐丧失。突触丢失现在是阿尔茨海默病患者认知功能障碍的最佳相关因素。因此,恢复或限制突触丢失是 AD 药物治疗的一种有前途的策略。N-N 取代的哌嗪是广泛用于药物干预的化学化合物,可用于治疗包括中枢神经系统疾病在内的各种疾病,如药物滥用、精神和焦虑障碍。哌嗪衍生物是小分子,通常耐受性良好且可穿透血脑屏障(BBB)。因此,取代的哌嗪是寻找和开发新型疾病修饰药物的良好工具。此前,我们已经确定哌嗪衍生物 51164 是树突棘中 TRPC6 的激活剂。我们已经证明了 51164 在 AD 小鼠模型中的突触保护特性。然而,51164 无法穿透 BBB。在当前的研究中,我们确定了一种新型哌嗪衍生物 cmp2,它在结构上与 51164 相似,但能够穿透 BBB。Cmp2 以类似于海呋林的方式结合单体 TRPC6 的中心部分。Cmp2 选择性激活 TRPC6,但不激活结构相关的 TRPC3 和 TRPC7。新型哌嗪衍生物在培养物和切片中表现出突触保护特性,并穿透 BBB。体内研究表明,cmp2(10mg/kg I.P.)逆转了 5xFAD 小鼠突触可塑性的缺陷。因此,我们认为 cmp2 是一种新型的药物开发先导化合物。cmp2 的作用机制基于选择性 TRPC6 刺激,预计可治疗海马神经元中的突触缺乏。