Department of Biochemistry and Biotechnology, Faculty of Science, Annamalai University, Annamalai Nagar, Tamil Nadu, 608002, India.
Department of Pharmacology, JSS College of Pharmacy, JSS University, SS Nagar, Mysore, Karnataka, 570015, India.
Neurotox Res. 2019 Feb;35(2):318-330. doi: 10.1007/s12640-018-9956-5. Epub 2018 Sep 21.
The neuroprotective role of tannoid principles of Emblica officinalis (EoT), an Indian and Chinese traditional medicinal plant against memory loss in aluminum chloride-induced in vivo model of Alzheimer's disease through attenuating AChE activity, oxidative stress, amyloid and tau toxicity, and apoptosis, was recently reported in our lab. However, to further elucidate the mechanism of neuroprotective effect of EoT, the current study was designed to evaluate endoplasmic reticulum stress-suppressing and anti-inflammatory role of EoT in PC 12 and SH-SY 5Y cells. These cells were divided into four groups: control (aluminum maltolate (Al(mal)), EoT + Al(mal), and EoT alone based on 3-(4, 5-dimethyl 2-yl)-2, and 5-diphenyltetrazolium bromide (MTT) assay. EoT significantly reduced Al(mal)-induced cell death and attenuated ROS, mitochondrial membrane dysfunction, and apoptosis (protein expressions of Bax; Bcl-2; cleaved caspases 3, 6, 9, 12; and cytochrome c) by regulating endoplasmic reticulum stress (PKR-like ER kinase (PERK), α subunit of eukaryotic initiation factor 2 (EIF2-α), C/EBP-homologous protein (CHOP), and high-mobility group box 1 protein (HMGB1)). Moreover, inflammatory response (NF-κB, IL-1β, IL-6, and TNF-α) and Aβ toxicity (Aβ) triggered by Al(mal) was significantly normalized by EoT. Our results suggested that EoT could be a possible/promising and novel therapeutic lead against Al-induced neurotoxicity. However, further extensive research is needed to prove its efficacy in clinical studies.
最近,我们实验室报道了印度和中国传统药用植物余甘子的鞣质成分(EoT)通过抑制乙酰胆碱酯酶(AChE)活性、氧化应激、淀粉样蛋白和 tau 毒性以及细胞凋亡,对氯化铝诱导的体内阿尔茨海默病模型的记忆丧失具有神经保护作用。然而,为了进一步阐明 EoT 的神经保护作用机制,本研究旨在评估 EoT 对 PC12 和 SH-SY5Y 细胞的内质网应激抑制和抗炎作用。这些细胞分为四组:对照组(铝麦芽醇(Al(mal))、EoT+Al(mal)和 EoT 单独组),基于 3-(4,5-二甲基-2-噻唑基)-2,5-二苯基四氮唑溴盐(MTT)测定法。EoT 显著降低了 Al(mal)诱导的细胞死亡,并通过调节内质网应激(PKR 样内质网激酶(PERK)、真核起始因子 2(EIF2-α)的α亚基、C/EBP 同源蛋白(CHOP)和高迁移率族蛋白 B1 蛋白(HMGB1))来减轻 ROS、线粒体膜功能障碍和细胞凋亡(Bax;Bcl-2;裂解的半胱天冬酶 3、6、9、12;和细胞色素 c)。此外,EoT 还显著调节了由 Al(mal)引发的炎症反应(NF-κB、IL-1β、IL-6 和 TNF-α)和 Aβ 毒性(Aβ)。我们的结果表明,EoT 可能是一种针对铝诱导神经毒性的潜在和新型治疗药物。然而,还需要进一步的广泛研究来证明其在临床研究中的疗效。