中南大学学报(医学版)
中南大學學報(醫學版)
중남대학학보(의학판)
JOURNAL OF CENTRAL SOUTH UNIVERSITY (MEDICAL SCIENCES)
2014年
7期
703-707
,共5页
黄亮%唐正严%李东杰%王桂林%黄珂%周杰%黎勇林%高本敏%陈俊杰
黃亮%唐正嚴%李東傑%王桂林%黃珂%週傑%黎勇林%高本敏%陳俊傑
황량%당정엄%리동걸%왕계림%황가%주걸%려용림%고본민%진준걸
氯胺酮%膀胱炎%SV-HUC-1%膀胱上皮细胞%凋亡
氯胺酮%膀胱炎%SV-HUC-1%膀胱上皮細胞%凋亡
록알동%방광염%SV-HUC-1%방광상피세포%조망
目的:研究氯胺酮对人膀胱SV-HUC-1细胞凋亡的影响,初步探讨氯胺酮相关性膀胱功能损伤的发病机制。方法:培养人膀胱SV-HUC-1永生化上皮细胞系,用不同质量浓度的氯胺酮作用于SV-HUC-1细胞,作用不同时间后用Annexin V-FITC/PI双染法流式细胞术检测细胞凋亡率,用Western印迹法检测Bax,Bcl-2, pro-caspase-3,cleaved caspase-3蛋白表达的含量。结果:与对照组相比,加入氯胺酮后SV-HUC-1细胞凋亡率增加, Bax表达增高,Bcl-2表达减弱,Bax与Bcl-2比值增高,pro-caspase-3表达减少,cleaved caspase-3表达增高(P<0.05),且与氯胺酮质量浓度和作用时间相关(P<0.05)。结论:氯胺酮能够明显促进人膀胱SV-HUC-1细胞的凋亡,并呈浓度依赖性和时间依赖性。
目的:研究氯胺酮對人膀胱SV-HUC-1細胞凋亡的影響,初步探討氯胺酮相關性膀胱功能損傷的髮病機製。方法:培養人膀胱SV-HUC-1永生化上皮細胞繫,用不同質量濃度的氯胺酮作用于SV-HUC-1細胞,作用不同時間後用Annexin V-FITC/PI雙染法流式細胞術檢測細胞凋亡率,用Western印跡法檢測Bax,Bcl-2, pro-caspase-3,cleaved caspase-3蛋白錶達的含量。結果:與對照組相比,加入氯胺酮後SV-HUC-1細胞凋亡率增加, Bax錶達增高,Bcl-2錶達減弱,Bax與Bcl-2比值增高,pro-caspase-3錶達減少,cleaved caspase-3錶達增高(P<0.05),且與氯胺酮質量濃度和作用時間相關(P<0.05)。結論:氯胺酮能夠明顯促進人膀胱SV-HUC-1細胞的凋亡,併呈濃度依賴性和時間依賴性。
목적:연구록알동대인방광SV-HUC-1세포조망적영향,초보탐토록알동상관성방광공능손상적발병궤제。방법:배양인방광SV-HUC-1영생화상피세포계,용불동질량농도적록알동작용우SV-HUC-1세포,작용불동시간후용Annexin V-FITC/PI쌍염법류식세포술검측세포조망솔,용Western인적법검측Bax,Bcl-2, pro-caspase-3,cleaved caspase-3단백표체적함량。결과:여대조조상비,가입록알동후SV-HUC-1세포조망솔증가, Bax표체증고,Bcl-2표체감약,Bax여Bcl-2비치증고,pro-caspase-3표체감소,cleaved caspase-3표체증고(P<0.05),차여록알동질량농도화작용시간상관(P<0.05)。결론:록알동능구명현촉진인방광SV-HUC-1세포적조망,병정농도의뢰성화시간의뢰성。
Objective:To determine the effect of ketamine on the apoptosis of human uroepithelial cells (SV-HUC-1) and the pathogenesis of ketamine-associated cystitis. Methods:SV-HUC-1 cells were cultured under various concentrations of ketamine and different time. Flow cytometry was used to analyze the rate of cell apoptosis. hTe protein levels of Bax, Bcl-2, pro-caspase-3, and cleaved caspase-3 were detected by Western blot. Results:Compared with the control group, the apoptotic rate of ketamine cultured SV-HUC-1 cells increased. hTe expression of Bax increased, Bcl-2 expression decreased, and Bax/Bcl-2 in the ketamine cultured SV-HUC-1 cells was signiifcantly higher. hTe protein level of pro-caspase-3 was signiifcantly lower, and that of cleaved caspase-3 was signiifcantly higher than that in the control group (P<0.05), positively correlated with the dose of ketamine and time of culture (P<0.05). Conclusion:Ketamine can induce the apoptosis of SV-HUC-1 cells in a dose and time dependent manner.