Nash Family Department of Neuroscience, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Nash Family Department of Neuroscience, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Trends Pharmacol Sci. 2021 Mar;42(3):203-215. doi: 10.1016/j.tips.2020.12.002. Epub 2021 Jan 16.
G protein-gated inwardly rectifying potassium (GIRK) channels are essential regulators of cell excitability in the brain. While they are implicated in a variety of neurological diseases in both human and animal model studies, their therapeutic potential has been largely untapped. Here, we review recent advances in the development of small molecule compounds that specifically modulate GIRK channels and compare them with first-generation compounds that exhibit off-target activity. We describe the method of discovery of these small molecule modulators, their chemical features, and their effects in vivo. These studies provide a promising outlook on the future development of subunit-specific GIRK modulators to regulate neuronal excitability in a brain region-specific manner.
G 蛋白门控内向整流钾 (GIRK) 通道是大脑细胞兴奋性的重要调节因子。虽然它们在人类和动物模型研究的各种神经疾病中都有牵连,但它们的治疗潜力在很大程度上尚未被开发。在这里,我们回顾了近年来开发专门调节 GIRK 通道的小分子化合物的最新进展,并将其与表现出非靶向活性的第一代化合物进行了比较。我们描述了这些小分子调节剂的发现方法、它们的化学特征以及它们在体内的作用。这些研究为未来以亚基特异性方式调节神经元兴奋性的 GIRK 调节剂的开发提供了有希望的前景。