Ndlovu Babongile C, Daniels Willie M U, Mabandla Musa V
Department of Human Physiology, School of Laboratory Medicine and Medical Sciences, College of Health Sciences, University of KwaZulu-Natal, Westville Campus, Durban 4000, South Africa.
Parkinsons Dis. 2014;2014:929854. doi: 10.1155/2014/929854. Epub 2014 Nov 13.
Preconditioning triggers endogenous protection against subsequent exposure to higher concentrations of a neurotoxin. In this study, we investigated whether exposure to oleanolic acid (OA) enhances the protective effects of preconditioning on PC12 cells exposed to 6-hydroxydopamine (6-OHDA). A concentration response curve was constructed using 6-OHDA (50, 150, 300, and 600 μM). The experiment consisted of 6 groups: untreated, OA only, Group 1: cells treated with 6-OHDA (50 μM) for 1 hour, Group 2: cells treated with 6-OHDA (150 μM) for 1 hour, Group 3: cells treated with 6-OHDA (50 μM) for 30 minutes followed 6 hours later by treatment with 6-OHDA (150 μM) for 30 minutes, and Group 4: cells treated as in group 3 but also received OA immediately after the second 6-OHDA treatment. Cell viability and apoptotic ratio were assessed using the MTT and Annexin V staining tests, respectively. In preconditioned cells, we found that cell viability remained high following exposure to 6-OHDA (150 μM). OA treatment enhanced the protective effects of preconditioning. Similarly, with the annexin V apoptosis test, preconditioning protected the cell and this was enhanced by OA. Therefore, preexposure of PC12 cells to low 6-OHDA concentration can protect against subsequent toxic insults of 6-OHDA and OA enhances this protection.
预处理可触发内源性保护机制,以抵御随后暴露于更高浓度神经毒素的情况。在本研究中,我们调查了齐墩果酸(OA)的暴露是否会增强预处理对暴露于6-羟基多巴胺(6-OHDA)的PC12细胞的保护作用。使用6-OHDA(50、150、300和600μM)构建浓度响应曲线。实验分为6组:未处理组、仅OA组、第1组:用6-OHDA(50μM)处理1小时的细胞、第2组:用6-OHDA(150μM)处理1小时的细胞、第3组:用6-OHDA(50μM)处理30分钟,6小时后再用6-OHDA(150μM)处理30分钟;第4组:细胞处理方式同第3组,但在第二次6-OHDA处理后立即给予OA。分别使用MTT和膜联蛋白V染色试验评估细胞活力和凋亡率。在预处理的细胞中,我们发现暴露于6-OHDA(150μM)后细胞活力仍保持较高水平。OA处理增强了预处理的保护作用。同样,通过膜联蛋白V凋亡试验,预处理可保护细胞,且OA可增强这种保护作用。因此,PC12细胞预先暴露于低浓度6-OHDA可抵御随后6-OHDA的毒性损伤,且OA可增强这种保护作用。