Neuroscience Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Phytomedicine. 2013 Jul 15;20(10):939-46. doi: 10.1016/j.phymed.2013.03.013. Epub 2013 Apr 29.
There is an increasing amount of experimental evidence that oxidative stress has a central role in the neuropathology of neurodegenerative diseases. It has been suggested that the loss of cell function results from the increased oxidative damage to proteins and DNA. Herein, we investigated the effect of a natural neuroprotective flavonoid, calycopterin, on H₂O₂-induced disruption of phase II detoxifying enzyme system and cAMP response element binding protein (CREB) phosphorylation.
PC12 cells were treated with 25, 50 and 100 μM of calycopterin for 3h, followed by adding H₂O₂ (150 μM) for 24 h. The extent of apoptosis was assessed by comet assay. The level of phosphorylated CREB, nuclear factor erythroid 2-related factor 2 (Nrf2), glutamylcysteine synthetase (γ-GCS) and heme oxygenase 1 (HO-1) were measured by western blot method. The concentration of glutathione (GSH) was determined in whole cell lysate using dithionitrobenzoic acid method. Superoxide dismutase (SOD) activity was measured by colorimetric assay.
Morphological analysis of protection induced by calycopterin, determined by comet assay, showed that calycopterin reduced DNA in tail. We found that H₂O₂ decreased mitochondrial membrane potential (MMP), while, calycopterin prevented this decrease in MMP in presence of H₂O₂. In H₂O₂-treated cells, calycopterin also suppressed cytochrome C release to cytosol that is necessary for maintaining mitochondrial homeostasis in survived cells. Moreover, calycopterin, in presence of H₂O₂ inhibited the decrease caused by oxidative stress in stress-sensing transcription factors, CREB and Nrf2, which play an important role in antioxidant capacity of the cell. There was also an increase in γ-GCS and HO-1 levels in calycopterin pretreated cells. In the presence of H₂O₂, calycopterin inhibited decrease in GSH level and SOD activity.
We provided documentation of neuroprotective effect of a natural flavone, calycopterin, against H₂O₂-induced oxidative stress in differentiated PC12 cells by modulating the level of CREB phosphorylation and Nrf2 pathway.
越来越多的实验证据表明,氧化应激在神经退行性疾病的神经病理学中起核心作用。有人认为,细胞功能的丧失是由于蛋白质和 DNA 的氧化损伤增加所致。在此,我们研究了天然神经保护黄酮类化合物白杨素对 H₂O₂诱导的 II 相解毒酶系统和 cAMP 反应元件结合蛋白(CREB)磷酸化破坏的影响。
用 25、50 和 100 μM 白杨素处理 PC12 细胞 3 小时,然后加入 H₂O₂(150 μM)24 小时。通过彗星试验评估细胞凋亡程度。通过 Western blot 法测定磷酸化 CREB、核因子红细胞 2 相关因子 2(Nrf2)、谷氨酰半胱氨酸合成酶(γ-GCS)和血红素加氧酶 1(HO-1)的水平。用二硫代硝基苯甲酸法测定全细胞裂解物中的谷胱甘肽(GSH)浓度。通过比色法测定超氧化物歧化酶(SOD)活性。
通过彗星试验确定的白杨素诱导的形态保护分析表明,白杨素减少了尾部的 DNA。我们发现 H₂O₂降低了线粒体膜电位(MMP),而白杨素在存在 H₂O₂的情况下阻止了 MMP 的这种降低。在 H₂O₂处理的细胞中,白杨素还抑制了细胞色素 C 向细胞质的释放,这对于维持线粒体在存活细胞中的稳态是必需的。此外,白杨素在存在 H₂O₂的情况下抑制了应激感应转录因子 CREB 和 Nrf2 的降低,这些转录因子在细胞的抗氧化能力中起着重要作用。在白杨素预处理的细胞中,γ-GCS 和 HO-1 水平也增加。在 H₂O₂存在的情况下,白杨素抑制了 GSH 水平和 SOD 活性的降低。
我们通过调节 CREB 磷酸化和 Nrf2 途径的水平,为天然类黄酮白杨素对分化 PC12 细胞中 H₂O₂诱导的氧化应激的神经保护作用提供了证据。