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作 者:孙学军[1] 邵彦[2] 张红星[1] 周芳[1] 赵曦[1] 马虹[1]
机构地区:[1]110001沈阳市,中国医科大学附属第一医院麻醉学教研室 [2]大连医科大学附属第二医院
出 处:《中华麻醉学杂志》2013年第9期1076-1078,共3页Chinese Journal of Anesthesiology
摘 要:目的 评价骨髓间充质干细胞(BMSC)对利多卡因致大鼠脊髓背根神经节细胞(DRGC)凋亡的影响.方法 对数生长期大鼠DRGC以2×104个/cm2的密度接种于培养板中,共27孔,采用随机数字表法,将其分为3组(n=9):对照组(C组)、利多卡因组(L组)和BMSC处理组(B组).C组常规培养;L组和B组分别用终浓度50 mmol/L利多卡因孵育2h,随后L组正常培养,B组取大鼠BM-SC接种于Transwell小室内,密度2× 104个/cm2,建立共培养体系.孵育48 h时,收集DRGC,采用流式细胞术检测凋亡率.结果 与C组比较,L组和B组凋亡率增加(P<0.05);与L组比较,B组凋亡率降低(P<0.05).结论 BMSC可减少利多卡因导致的大鼠DRGC凋亡,提示其可能减轻局麻药的外周神经毒性.Objective To evaluate the effect of bone mesenchymal stem cells (BMSCs) on lidocaine-induced apoptosis in dorsal root ganglion cells (DRGCs) of rats in vitro.Methods DRGCs in the logarithmic phase were incubated in culture plates at the density of 2 × 104 cells/cm2 (27 wells in total).DRGCs were randomly divided into 3 groups (n =9 each) using a random number table:control group (group C),lidocaine treatment group (group L) and BMSC treatment group (group B).The DRGCs in group C were incubated routinely without lidocaine,while the DRGCs were incubated for 2 h with lidocaine with the final concentration of 50 mmol/L in L and B groups.The DRGCs were then incubated normally in group L.The DRGCs were then co-cultured with the BMSCs which were incubated in Transwell chambers with the density of 2 × 104 cells/cm2 in group B.DRGCs were collected at 48 h of incubation for detection of apoptosis by flow cytometry.Apoptosis rate was calculated.Results Compared with group C,the apoptosis rate was significantly increased in L and B groups (P 〈 0.05).The apoptosis rate was significantly lower in group B than in group L (P 〈 0.05).Conclusion BMSCs can reduce lidocaine-induced apoptosis in DRGCs of rats in vitro,indicating that BMSCs may reduce local anesthetics-produced toxicity to the peripheral nerve. Keywords:Mesenchymal stem cells ; Ganglia, spinal; Apoptosis; Lidocaine ; Postoperative complications
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