Université Côte d'Azur, CNRS, IPMC, France; LabEx Ion Channel Science and Therapeutics, IPMC, France.
Université Côte d'Azur, CNRS, IPMC, France; LabEx Ion Channel Science and Therapeutics, IPMC, France.
Neuropharmacology. 2017 Oct;125:429-440. doi: 10.1016/j.neuropharm.2017.08.004. Epub 2017 Aug 9.
Acid-Sensing Ion Channels (ASICs) are cation channels activated by extracellular acidification that emerge as potential pharmacological targets in pain and other neurological disorders. Here, we compare the pharmacological modulation of ASIC1a and ASIC3 channels by amiloride and 2-guanidine-4-methylquinazoline (GMQ), two compounds commonly used for their in vitro and in vivo investigation. We analyzed the effect of amiloride on the pH-dependent activation and inactivation, the relative influence of the extracellular domain and the transmembrane/cytosolic domains on the effect of amiloride and GMQ using chimeras between ASIC1a and ASIC3, and how these compounds potentiate the physiologically relevant ASIC3 sustained window current. We showed that amiloride and GMQ shift the pH-dependent activation and inactivation in the same directions, which depend on the channel, and that their effects rely on the nature of the extracellular domain but can be indirectly modulated in their amplitude by the transmembrane/cytosolic domains. The extracellular domain explains the pharmacological potentiating effect of amiloride and GMQ on the window current in ASIC3, and why these compounds failed to generate a window current in ASIC1a. Amiloride and GMQ have similar and purely additive effects suggesting that they act through a common unique binding site different from acidic pockets. Finally, a simple cycle analysis using GMQ that targets the nonproton ligand-sensor, and two peptide inhibitors of ASIC1a targeting the acidic pockets (PcTx1 and mambalgin-1), shows overlap between the mechanisms by which GMQ and PcTx1 modify inactivation and suggests shared mechanisms of regulation of the pH-dependent inactivation of ASIC1a between these two regions.
酸敏离子通道(ASICs)是一种由细胞外酸化激活的阳离子通道,在疼痛和其他神经疾病中成为潜在的药物靶点。在这里,我们比较了阿米洛利和 2-胍基-4-甲基喹唑啉(GMQ)对 ASIC1a 和 ASIC3 通道的药理学调节,这两种化合物常用于体外和体内研究。我们分析了阿米洛利对 pH 依赖性激活和失活的影响,以及细胞外结构域和跨膜/细胞质结构域对阿米洛利和 GMQ 作用的相对影响,使用 ASIC1a 和 ASIC3 之间的嵌合体,并研究了这些化合物如何增强生理相关的 ASIC3 持续窗口电流。我们表明,阿米洛利和 GMQ 以依赖于通道的相同方向改变 pH 依赖性激活和失活,其作用依赖于细胞外结构域的性质,但可以通过跨膜/细胞质结构域间接调节其幅度。细胞外结构域解释了阿米洛利和 GMQ 对 ASIC3 窗口电流的药理学增强作用,以及为什么这些化合物在 ASIC1a 中不能产生窗口电流。阿米洛利和 GMQ 具有相似的纯加和作用,表明它们通过不同于酸性口袋的共同独特结合位点起作用。最后,使用靶向非质子配体传感器的 GMQ 和靶向 ASIC1a 酸性口袋的两种 ASIC1a 肽抑制剂(PcTx1 和 mambalgin-1)的简单循环分析表明,GMQ 和 PcTx1 修饰失活的机制存在重叠,并提示 GMQ 和 PcTx1 之间存在共享的调节机制 ASIC1a 的 pH 依赖性失活。