Department of Biophysics, Panjab University, Chandigarh, 160014, India.
Neurotox Res. 2019 Jan;35(1):83-91. doi: 10.1007/s12640-018-9932-0. Epub 2018 Jul 14.
Excessive stimulation of ionotropic glutamate receptor is associated with glutamate-mediated excitotoxicity, thereby causing oxidative imbalance and mitochondrial dysfunction, resulting in the excitotoxic death of neurons. Eminent role of endoplasmic reticulum under glutamate-induced excitotoxicity has been highlighted in numerous literatures which have been observed to trigger endoplasmic reticulum stress (ER stress) as well as regulating oxidative stress. However, combating ER stress in excitotoxic neurons can provide a novel approach to alleviate the mitochondrial dysfunctioning and ROS generation. Therefore, we propose to investigate the cross-communication of α-amino-3-hydroxy-5-methyl-4-isoxzole-propionate (AMPA) excitotoxicity-induced oxidative injury with ER stress by employing ER stress inhibitor-4-phenlybutyric acid (4-PBA). Male SD rats were divided into four groups viz sham group (group 1), AMPA (10 mM)-induced excitotoxic group (group 2), curative group of AMPA-induced excitotoxic animals given 4-PBA at a dose of 100 mg/kg body weight (group 3), and alone 4-PBA treatment group (100 mg/kg body weight) (group 4). Animals were sacrificed after 15 days of treatment, and hippocampi were analyzed for histopathological examination, ROS, inflammatory markers, mitochondrial dysfunction, and ER stress markers. AMPA-induced excitotoxicity exhibited a significant increase in the levels of ROS, upregulated ER stress markers, inflammation markers, and compromised mitochondrial functioning in the hippocampus. However, 4-PBA administration significantly curtailed the AMPA-induced excitotoxic insult. This study suggests that targeting ER stress with a chemical chaperone can provide a better therapeutic intervention for neurological disorders involving excitotoxicity, and thus, it opens a new avenue to screen chemical chaperones for the therapeutic modalities.
离子型谷氨酸受体的过度刺激与谷氨酸介导的兴奋性毒性有关,从而导致氧化失衡和线粒体功能障碍,导致神经元的兴奋性死亡。内质网在谷氨酸诱导的兴奋性毒性中的重要作用在众多文献中得到了强调,这些文献已经观察到内质网应激(ER 应激)的触发以及调节氧化应激。然而,在兴奋性神经元中对抗 ER 应激可以提供一种减轻线粒体功能障碍和 ROS 产生的新方法。因此,我们建议通过使用 ER 应激抑制剂 4-苯丁酸(4-PBA)来研究 α-氨基-3-羟基-5-甲基-4-异恶唑丙酸(AMPA)兴奋性毒性诱导的氧化损伤与 ER 应激的交叉通讯。雄性 SD 大鼠分为四组:假手术组(第 1 组)、AMPA(10 mM)诱导的兴奋性毒性组(第 2 组)、AMPA 诱导的兴奋性毒性动物的治疗组,给予 4-PBA 剂量为 100 mg/kg 体重(第 3 组),以及单独给予 4-PBA 治疗组(100 mg/kg 体重)(第 4 组)。治疗 15 天后处死动物,分析海马组织病理学检查、ROS、炎症标志物、线粒体功能障碍和 ER 应激标志物。AMPA 诱导的兴奋性毒性导致 ROS 水平显著升高,上调 ER 应激标志物、炎症标志物,并损害海马中的线粒体功能。然而,4-PBA 给药显著减轻了 AMPA 诱导的兴奋性毒性损伤。这项研究表明,用化学伴侣靶向 ER 应激可以为涉及兴奋性毒性的神经紊乱提供更好的治疗干预,因此为筛选治疗方式的化学伴侣开辟了新途径。