Department of Anatomy, College of Veterinary Medicine, Research Institute of Life Science, Gyeongsang National University, Jinju, South Korea.
PLoS One. 2024 Mar 1;19(3):e0299042. doi: 10.1371/journal.pone.0299042. eCollection 2024.
Epigallocatechin gallate (EGCG) is a polyphenolic component of green tea that has anti-oxidative and anti-inflammatory effects in neurons. Ischemic stroke is a major neurological disease that causes irreversible brain disorders. It increases the intracellular calcium concentration and induces apoptosis. The regulation of intracellular calcium concentration is important to maintain the function of the nervous system. Hippocalcin is a neuronal calcium sensor protein that controls intracellular calcium concentration. We investigated whether EGCG treatment regulates the expression of hippocalcin in stroke animal model and glutamate-induced neuronal damage. We performed middle cerebral artery occlusion (MCAO) to induce cerebral ischemia. EGCG (50 mg/kg) or phosphate buffered saline was injected into the abdominal cavity just before MCAO surgery. The neurobehavioral tests were performed 24 h after MCAO surgery and cerebral cortex tissue was collected. MCAO damage induced severe neurobehavioral disorders, increased infarct volume, and decreased the expression of hippocalcin in the cerebral cortex. However, EGCG treatment improved these deficits and alleviated the decrease in hippocalcin expression in cerebral cortex. In addition, EGCG dose-dependently alleviated neuronal cell death and intracellular calcium overload in glutamate-exposed neurons. Glutamate exposure reduced hippocalcin expression, decreased Bcl-2 expression, and increased Bax expression. However, EGCG treatment mitigated these changes caused by glutamate toxicity. EGCG also attenuated the increase in caspase-3 and cleaved caspase-3 expressions caused by glutamate exposure. The effect of EGCG was more pronounced in non-transfected cells than in hippocalcin siRNA-transfected cells. These findings demonstrate that EGCG protects neurons against glutamate toxicity through the regulation of Bcl-2 family proteins and caspase-3. It is known that hippocalcin exerts anti-apoptotic effect through the modulation of apoptotic pathway. Thus, we can suggest evidence that EGCG has a neuroprotective effect by regulating hippocalcin expression in ischemic brain damage and glutamate-exposed cells.
没食子儿茶素没食子酸酯(EGCG)是绿茶中的一种多酚成分,具有抗氧化和抗炎作用神经元。缺血性中风是一种主要的神经系统疾病,可导致不可逆的脑功能障碍。它会增加细胞内钙离子浓度并诱导细胞凋亡。调节细胞内钙离子浓度对于维持神经系统的功能非常重要。钙调蛋白是一种神经元钙传感器蛋白,可控制细胞内钙离子浓度。我们研究了 EGCG 治疗是否调节了中风动物模型和谷氨酸诱导的神经元损伤中 hippocalcin 的表达。我们进行了大脑中动脉闭塞(MCAO)以诱导脑缺血。在 MCAO 手术前,将 EGCG(50mg/kg)或磷酸盐缓冲盐水注入腹腔。在 MCAO 手术后 24 小时进行神经行为测试,并收集大脑皮质组织。MCAO 损伤导致严重的神经行为障碍,梗塞体积增加,大脑皮质 hippocalcin 表达减少。然而,EGCG 治疗改善了这些缺陷,并减轻了大脑皮质 hippocalcin 表达的减少。此外,EGCG 剂量依赖性地减轻了谷氨酸暴露神经元中的细胞死亡和细胞内钙超载。谷氨酸暴露降低了 hippocalcin 的表达,降低了 Bcl-2 的表达,增加了 Bax 的表达。然而,EGCG 治疗减轻了谷氨酸毒性引起的这些变化。EGCG 还减轻了谷氨酸暴露引起的 caspase-3 和 cleaved caspase-3 表达的增加。与未转染细胞相比,EGCG 在 hippocalcin siRNA 转染细胞中的作用更为明显。这些发现表明,EGCG 通过调节 Bcl-2 家族蛋白和 caspase-3 来保护神经元免受谷氨酸毒性。已知 hippocalcin 通过调节凋亡途径发挥抗凋亡作用。因此,我们可以提出证据表明,EGCG 通过调节缺血性脑损伤和谷氨酸暴露细胞中的 hippocalcin 表达来发挥神经保护作用。