Pattarachotanant Nattaporn, Tencomnao Tewin
Department of Clinical Chemistry, Faculty of Allied Health Sciences, Chulalongkorn University, Bangkok 10330, Thailand.
Age-Related Inflammation and Degeneration Research Unit, Chulalongkorn University, Bangkok 10330, Thailand.
Pharmaceuticals (Basel). 2020 Sep 30;13(10):283. doi: 10.3390/ph13100283.
(CH) is a beneficial plant utilized in traditional folk medicine to relieve various health ailments. The antisenescent mechanisms of CH extracts were investigated using human neuroblastoma cells (SH-SY5Y). Phytochemical contents and antioxidant activities of CH extracts were analyzed using a gas chromatograph-mass spectrometer (GC-MS), 2,2-diphenyl-1-picryl-hydrazyl-hydrate (DPPH) assay and 2,2'-azino-bis (3-ethylbenzthiazoline-6-sulphonic acid) (ABTS) assay. Effects of CH extracts on high glucose-induced cytotoxicity, reactive oxygen species (ROS) generation, cell cycle arrest and cell cycle-associated proteins were assessed using a 3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide tetrazolium (MTT) assay, non-fluorescent 2', 7'-dichloro-dihydrofluorescein diacetate (HDCFDA) assay, flow cytometer and Western blot. The extracts protected neuronal senescence by inhibiting ROS generation. CH extracts induced cell cycle progression by releasing senescent cells from the G1 phase arrest. As the Western blot confirmed, the mechanism involved in cell cycle progression was associated with the downregulation of cyclin D1, phospho-cell division cycle 2 (pcdc2) and phospho-Retinoblastoma (pRb) proteins. Furthermore, the Western blot showed that extracts increased Surtuin 1 (SIRT1) expression by increasing the phosphorylation of Glyceraldehyde 3-phosphate dehydrogenase (GAPDH). Collectively, CH extracts could protect high glucose-induced human neuronal senescence by inducing cell cycle progression and up-regulation of SIRT1, thus leading to the improvement of the neuronal cell functions.
长春花是一种在传统民间医学中用于缓解各种健康问题的有益植物。使用人神经母细胞瘤细胞(SH-SY5Y)研究了长春花提取物的抗衰老机制。使用气相色谱-质谱联用仪(GC-MS)、2,2-二苯基-1-苦基肼基水合物(DPPH)测定法和2,2'-联氮-双-(3-乙基苯并噻唑啉-6-磺酸)(ABTS)测定法分析了长春花提取物的植物化学成分和抗氧化活性。使用3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐(MTT)测定法、非荧光2',7'-二氯二氢荧光素二乙酸酯(HDCFDA)测定法、流式细胞仪和蛋白质免疫印迹法评估了长春花提取物对高糖诱导的细胞毒性、活性氧(ROS)生成、细胞周期阻滞和细胞周期相关蛋白的影响。提取物通过抑制ROS生成来保护神经元衰老。长春花提取物通过使衰老细胞从G1期阻滞中释放出来诱导细胞周期进程。正如蛋白质免疫印迹所证实的,细胞周期进程所涉及的机制与细胞周期蛋白D1、磷酸化细胞分裂周期2(pcdc2)和磷酸化视网膜母细胞瘤(pRb)蛋白的下调有关。此外,蛋白质免疫印迹显示提取物通过增加甘油醛-3-磷酸脱氢酶(GAPDH)的磷酸化来增加沉默调节蛋白1(SIRT1)的表达。总的来说,长春花提取物可以通过诱导细胞周期进程和上调SIRT1来保护高糖诱导的人神经元衰老,从而改善神经元细胞功能。