School of Pharmacy, Jiangxi University of Chinese Medicine, Nanchang, P. R. China.
Pharmacol Res Perspect. 2023 Jun;11(3):e01105. doi: 10.1002/prp2.1105.
Syringin is a natural chemical compound first isolated from the bark of lilac and is known to have neuroprotective effects in middle cerebral artery occlusion (MCAO). Volume regulated anion channel (VRAC) is a cell swelling-activated anion channel, which is implicated in brain ischemia. However, the mechanism underlying the syringin protecting the neuron from damage in MCAO is still unclear. We hypothesized that syringin has an inhibitory effect on the opening of VRAC channels. To access the effect of syringin on VRAC currents and predict how syringin interacts with VRAC proteins, we performed whole-cell patch-clamp experiments using HEK293 cells. Initially, HEK293 cells were perfused with isotonic extracellular solution, followed by hypotonic extracellular solution to stimulate endogenous VRAC currents. Once the VRAC currents reached a steady state, the hypotonic solution containing syringin was perfused to study the effect of syringin on VRAC currents. The potential interaction between syringin and the VRAC protein was investigated using molecular docking as a predictive model. In this study, we found that syringin moderately inhibited VRAC currents in a dose-dependent manner. The potential binding of syringin to LRRC8 protein was predicted through in silico molecular docking, which suggests an affinity of -6.6 kcal/mol and potential binding sites of arginine 103 and leucine 101. Our results herein characterize syringin as an inhibitor of the VRAC channels, which provides valuable insights for the future development of VRAC channel inhibitors.
丁香苷是一种天然化合物,最初从丁香树皮中分离出来,已知具有大脑中动脉闭塞(MCAO)的神经保护作用。容积调节阴离子通道(VRAC)是一种细胞肿胀激活的阴离子通道,与脑缺血有关。然而,丁香苷在 MCAO 中保护神经元免受损伤的机制尚不清楚。我们假设丁香苷对 VRAC 通道的开放具有抑制作用。为了研究丁香苷对 VRAC 电流的影响,并预测丁香苷与 VRAC 蛋白的相互作用方式,我们使用 HEK293 细胞进行了全细胞膜片钳实验。首先,用等渗细胞外液灌流 HEK293 细胞,然后用低渗细胞外液刺激内源性 VRAC 电流。一旦 VRAC 电流达到稳定状态,用含丁香苷的低渗溶液灌流,研究丁香苷对 VRAC 电流的影响。使用分子对接作为预测模型,研究丁香苷与 VRAC 蛋白的潜在相互作用。在这项研究中,我们发现丁香苷以剂量依赖的方式适度抑制 VRAC 电流。通过计算机分子对接预测丁香苷与 LRRC8 蛋白的潜在结合,表明结合亲和力为-6.6 kcal/mol,潜在结合位点为精氨酸 103 和亮氨酸 101。我们的研究结果表明,丁香苷是 VRAC 通道的抑制剂,为未来 VRAC 通道抑制剂的开发提供了有价值的见解。