I.M.Sechenov Institute of Evolutionary Physiology and Biochemistry RAS, 44 Thorez pr., St.Petersburg, Russia.
Cell Mol Neurobiol. 2018 May;38(4):869-881. doi: 10.1007/s10571-017-0561-6. Epub 2017 Oct 20.
Acid-sensing ion channels (ASICs) are modulated by various classes of ligands, including the recently described hydrophobic monoamines, which inhibit and potentiate ASICs in a subunit-specific manner. In particular, memantine inhibits ASIC1a and potentiates ASIC2a homomers. The aim of the present work was to characterize action mechanism of memantine on recombinant ASIC1a expressed in CHO (Chinese hamster ovary) cells. We have demonstrated that effect of memantine on ASIC1a strongly depends on membrane voltage, conditioning pH value and application protocol. When applied simultaneously with activating acidification at hyperpolarized voltages, memantine caused the strongest inhibition. Surprisingly, application of memantine between ASIC1a activations at zero voltage caused significant potentiation. Analysis of the data suggests that memantine produces two separate effects, voltage-dependent open-channel block and shift of steady-state desensitization curve to more acidic values. Putative binding sites are discussed based on the computer docking of memantine to the acidic pocket and the pore region.
酸敏离子通道(ASICs)受多种配体调控,包括最近描述的疏水性单胺,它们以亚基特异性方式抑制和增强 ASICs。特别是,美金刚抑制 ASIC1a 并增强 ASIC2a 同源二聚体。本工作旨在表征在 CHO(中国仓鼠卵巢)细胞中表达的重组 ASIC1a 上美金刚的作用机制。我们已经证明,美金刚对 ASIC1a 的作用强烈依赖于膜电压、条件 pH 值和应用方案。当与超极化电压下的激活酸化同时应用时,美金刚引起最强的抑制。令人惊讶的是,在零电压下的 ASIC1a 激活之间应用美金刚会引起显著的增强。数据分析表明,美金刚产生两种独立的效应,电压依赖性开放通道阻断和稳态脱敏曲线向更酸性值的偏移。基于美金刚与酸性口袋和孔区的计算机对接,讨论了假定的结合位点。