Saul R. Korey Department of Neurology, Laboratory of Developmental Epilepsy, Albert Einstein College of Medicine, Bronx New York, USA.
Department of Neuroscience, Monash University, Melbourne, Australia.
J Neurotrauma. 2024 Jan;41(1-2):222-243. doi: 10.1089/neu.2022.0219. Epub 2023 May 2.
Sodium selenate (SS) activates protein phosphatase 2 (PP2A) and reduces phosphorylated tau (pTAU) and late post-traumatic seizures after lateral fluid percussion injury (LFPI). In EpiBioS4Rx Project 2, a multi-center international study for post-traumatic targets, biomarkers, and treatments, we tested the target relevance and modification by SS of pTAU forms and PP2A and in the LFPI model, at two sites: Einstein and Melbourne. In Experiment 1, adult male rats were assigned to LFPI and sham (both sites) and naïve controls (Einstein). Motor function was monitored by neuroscores. Brains were studied with immunohistochemistry (IHC), Western blots (WBs), or PP2A activity assay, from 2 days to 8 weeks post-operatively. In Experiment 2, LFPI rats received SS for 7 days (SS0.33: 0.33 mg/kg/day; SS1: 1 mg/kg/day, subcutaneously) or vehicle (Veh) post-LFPI and pTAU, PR55 expression, or PP2A activity were studied at 2 days and 1 week (on treatment), or 2 weeks (1 week off treatment). Plasma selenium and SS levels were measured. In Experiment 1 IHC, LFPI rats had higher cortical pTAU-Ser/Thr-immunoreactivity (AT8-ir) and pTAU-Ser-ir at 2 days, and pTAU-Thr-ir (AT180-ir) at 2 days, 2 weeks, and 8 weeks, ipsilaterally to LFPI, than controls. LFPI-2d rats also had higher AT8/total-TAU5-ir in cortical extracts ipsilateral to the lesion (WB). PP2A (PR55-ir) showed time- and region-dependent changes in IHC, but not in WB. PP2A activity was lower in LFPI-1wk than in sham rats. In Experiment 2, SS did not affect neuroscores or cellular AT8-ir, AT180-ir, or PR55-ir in IHC. In WB, total cortical AT8/total-TAU-ir was lower in SS0.33 and SS1 LFPI rats than in Veh rats (2 days, 1 week); total cortical PR55-ir (WB) and PP2A activity were higher in SS1 than Veh rats (2 days). SS dose dependently increased plasma selenium and SS levels. Concordant across-sites data confirm time and pTAU form-specific cortical increases ipsilateral to LFPI. The discordant SS effects may either suggest SS-induced reduction in the numbers of cells with increased pTAU-ir, need for longer treatment, or the involvement of other mechanisms of action.
硒酸钠 (SS) 可激活蛋白磷酸酶 2A (PP2A),降低磷酸化 tau (pTAU),并减少侧方液压冲击伤 (LFPI) 后的晚期创伤后癫痫发作。在 EpiBioS4Rx 项目 2 中,这是一项针对创伤后靶点、生物标志物和治疗方法的多中心国际研究,我们在两个地点 (爱因斯坦和墨尔本) 测试了 SS 对 pTAU 形式和 PP2A 的靶标相关性和修饰作用,以及 LFPI 模型中的作用。在实验 1 中,成年雄性大鼠被分配到 LFPI 和假手术 (均为两个地点) 和对照 (爱因斯坦)。通过神经评分监测运动功能。术后 2 天至 8 周,通过免疫组织化学 (IHC)、Western blot (WB) 或 PP2A 活性测定研究大脑。在实验 2 中,LFPI 大鼠在 LFPI 后接受 SS 治疗 7 天 (SS0.33:0.33mg/kg/天;SS1:1mg/kg/天,皮下注射) 或载体 (Veh),并在治疗 2 天和 1 周或治疗 1 周后 (2 周) 研究 pTAU、PR55 表达或 PP2A 活性。测量血浆硒和 SS 水平。在实验 1 的 IHC 中,与对照相比,LFPI 大鼠在 2 天出现更高的皮质 pTAU-Ser/Thr-免疫反应性 (AT8-ir) 和 pTAU-Ser-ir,在 2 天、2 周和 8 周出现更高的 pTAU-Thr-ir (AT180-ir),同侧到 LFPI。LFPI-2d 大鼠皮质提取物中 AT8/总-TAU5-ir 也更高 (WB)。PP2A(PR55-ir)在 IHC 中表现出时间和区域依赖性变化,但在 WB 中没有。与假手术大鼠相比,LFPI-1wk 大鼠的 PP2A 活性较低。在实验 2 中,SS 对 IHC 中的神经评分或细胞 AT8-ir、AT180-ir 或 PR55-ir 没有影响。在 WB 中,与 Veh 大鼠相比,SS0.33 和 SS1 LFPI 大鼠的总皮质 AT8/总-TAU-ir 较低 (2 天、1 周);与 Veh 大鼠相比,总皮质 PR55-ir (WB)和 PP2A 活性较高 (2 天)。SS 呈剂量依赖性增加血浆硒和 SS 水平。跨地点的一致数据证实了 LFPI 同侧皮质 pTAU 形式的时间特异性增加。SS 的不一致作用可能表明 SS 诱导的增加 pTAU-ir 的细胞数量减少、需要更长的治疗时间或涉及其他作用机制。