Laboratorio de Patología Vascular Cerebral, Instituto Nacional de Neurología y Neurocirugía Manuel Velasco Suárez, Insurgentes Sur #3877, CDMX, 14269, Mexico City, Mexico.
Departamento Neurociencia Cognitiva, Instituto de Fisiología Celular, Universidad Nacional Autónoma de México, Ciudad Universitaria, CDMX, 04510, Mexico City, Mexico.
Mol Neurobiol. 2024 Apr;61(4):2099-2119. doi: 10.1007/s12035-023-03686-0. Epub 2023 Oct 17.
The SUR1-TRPM4-AQP4 complex is overexpressed in the initial phase of edema induced after cerebral ischemia, allowing the massive internalization of Na and water within the brain micro endothelial cells (BMEC) of the blood-brain barrier. The expression of the Abcc8 gene encoding SUR1 depends on transcriptional factors that are responsive to oxidative stress. Because reactive oxygen species (ROS) are generated during cerebral ischemia, we hypothesized that antioxidant compounds might be able to regulate the expression of SUR1. Therefore, the effect of resveratrol (RSV) on SUR1 expression was evaluated in the BMEC cell line HBEC-5i subjected to oxygen and glucose deprivation (OGD) for 2 h followed by different recovery times. Different concentrations of RSV were administered. ROS production was detected with etidine, and protein levels were evaluated by Western blotting and immunofluorescence. Intracellular Na levels and cellular swelling were detected by imaging; cellular metabolic activity and rupture of the cell membrane were detected by MTT and LDH release, respectively; and EMSA assays measured the activity of transcriptional factors. OGD/recovery increased ROS production induced the AKT kinase activity and the activation of SP1 and NFκB. SUR1 protein expression and intracellular Na concentration in the HBEC-5i cells increased after a few hours of OGD. These effects correlated with cellular swelling and necrotic cell death, responses that the administration of RSV prevented. Our results indicate that the ROS/AKT/SP1-NFκB pathway is involved in SUR1 expression during OGD/recovery in BMEC of the blood-brain barrier. Thus, RSV prevented cellular edema formation through modulation of SUR1 expression.
SUR1-TRPM4-AQP4 复合物在脑缺血后水肿的初始阶段过度表达,允许大量的 Na 和水内在化脑微血管内皮细胞 (BMEC) 的血脑屏障。Abcc8 基因的表达编码 SUR1 取决于对氧化应激有反应的转录因子。因为活性氧 (ROS) 在脑缺血期间产生,我们假设抗氧化化合物可能能够调节 SUR1 的表达。因此,评估了白藜芦醇 (RSV) 在氧和葡萄糖剥夺 (OGD) 2 小时后不同恢复时间的 HBEC-5i BMEC 细胞系中对 SUR1 表达的影响。给予不同浓度的 RSV。用乙二醛检测 ROS 的产生,并通过 Western 印迹和免疫荧光评估蛋白质水平。通过成像检测细胞内 Na 水平和细胞肿胀;通过 MTT 和 LDH 释放分别检测细胞代谢活性和细胞膜破裂;EMSA 测定测量转录因子的活性。OGD/恢复增加 ROS 产生诱导 AKT 激酶活性和 SP1 和 NFκB 的激活。HBEC-5i 细胞中 SUR1 蛋白表达和细胞内 Na 浓度在 OGD 数小时后增加。这些效应与细胞肿胀和坏死性细胞死亡相关,RSV 可预防这些反应。我们的结果表明,ROS/AKT/SP1-NFκB 途径参与了 OGD/恢复期间血脑屏障 BMEC 中的 SUR1 表达。因此,RSV 通过调节 SUR1 表达防止细胞水肿形成。