山东大学学报 (医学版) ›› 2023, Vol. 61 ›› Issue (7): 34-39.doi: 10.6040/j.issn.1671-7554.0.2023.0272
• 基础医学 • 上一篇
刘凤祺*,高峰*,薛彩彩,乔秀梅,王金红
LIU Fengqi*, GAO Feng*, XUE Caicai, QIAO Xiumei, WANG Jinhong
摘要: 目的 探讨不同条件下高浓度葡萄糖(高糖)对大鼠肾上腺嗜铬细胞瘤细胞系PC12细胞的损伤作用,分析建立高糖损伤细胞模型的影响因素,并用确定的细胞模型观察梓醇的保护作用。 方法 PC12细胞种植密度为1×103、1×104、1×105个/mL,高糖加入时间点分别为细胞种植后24 h和48 h,葡萄糖终浓度为30、40、50和75 mmol/L,据此分为HG30、HG40、HG50、HG75组,另外对照组细胞加入等容积生理盐水。分别作用24、48、72 h,MTT法检测细胞存活率。用确定条件建立的细胞损伤模型观察梓醇的保护作用,细胞分为对照组、模型组、梓醇低剂量组(1×10-5mol/L)和梓醇高剂量组(1×10-4mol/L),ELISA法和荧光探针检测细胞活性氧(ROS)含量,ELISA测定乳酸脱氢酶(LDH)的释放量。 结果 不同葡萄糖作用条件下,与对照组比较,HG30组细胞存活率不变或降低(P>0.05或P<0.05),HG40、HG50和HG75组细胞存活率降低(P<0.05或P<0.01)。与对照组比较,模型组的细胞ROS含量增加(P<0.01),LDH释放量升高(P<0.01);与模型组比较,梓醇低剂量组和梓醇高剂量组细胞存活率升高(P<0.01),细胞ROS含量和LDH释放量降低(P<0.01)。 结论 高糖诱导的PC12细胞损伤受细胞种植密度、葡萄糖浓度和作用时间等因素影响;以1×104个/mL密度种植细胞、种植后24 h加入终浓度50 mmol/L葡萄糖作用时长24 h,可成功建立PC12细胞高糖损伤模型,梓醇对该细胞模型有保护作用。
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