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纸质出版日期:2015
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孟祥乐, 郭艳丽, 苏成福, 等. 连翘脂苷A抑制Caco-2细胞膜上P-糖蛋白的外排功能及作用机制探讨[J]. 中国实验方剂学杂志, 2015,21(17):5-8.
MENG Xiang-le, GUO Yan-li, SU Cheng-fu, et al. Discussion of Inhibitory of Forsythoside A on Efflux Function and Mechanism of P-glycoprotein in Caco-2 Cell Membrane[J]. Chinese journal of experimental traditional medical formulae, 2015, 21(17): 5-8.
孟祥乐, 郭艳丽, 苏成福, 等. 连翘脂苷A抑制Caco-2细胞膜上P-糖蛋白的外排功能及作用机制探讨[J]. 中国实验方剂学杂志, 2015,21(17):5-8. DOI: 10.13422/j.cnki.syfjx.2015170005.
MENG Xiang-le, GUO Yan-li, SU Cheng-fu, et al. Discussion of Inhibitory of Forsythoside A on Efflux Function and Mechanism of P-glycoprotein in Caco-2 Cell Membrane[J]. Chinese journal of experimental traditional medical formulae, 2015, 21(17): 5-8. DOI: 10.13422/j.cnki.syfjx.2015170005.
目的: 探讨连翘脂苷A对人克隆结肠癌细胞(Caco-2)细胞膜上P-糖蛋白(P-gp)的外排功能及作用机制。 方法: 采用刃天青法检测不同质量浓度连翘脂苷A对Caco-2的细胞毒性作用。以P-gp底物罗丹明123(Rh-123)为荧光探针
采用流式细胞术评价不同质量浓度连翘脂苷A对Rh-123细胞蓄积的影响
考察不同质量浓度连翘脂苷A对P-gp三磷酸腺苷 (ATP)酶活性的影响。 结果: 连翘脂苷A在1~80 mg·L-1时
与阴性组比较
差异无统计学意义
细胞存活率>90%
对Caco-2 细胞形态无影响。连翘脂苷A的荧光强度较空白组显著增加
其中80 mg·L-1连翘脂苷A荧光强度(223.43±5.6)%增加最多。连翘脂苷A不同质量浓度均有抑制P-gp ATP酶耗能的作用。 结论: 连翘脂苷A可通过抑制P-gp ATP酶产生抑制P-gp外排的作用。
Objective: To discuss effect of forsythoside A (FTA) on efflux function and mechanism of P-glycoprotein(P-gp) in Caco-2 cell membrane. Method: Caco-2 cell viability was measured by resazurin assay in the presence of FTA at different concentrations.Effects of FTA and verapamil (inhibitor of P-gp) on cellular drug accumulation in caco-2 cells were investigated
rhodamine 123 (R-123) measured by flowcytometer
was selected as fluorescent probe.Caco-2 cell membrane were exposed to FTA with different concentrations and then ATPase activity of P-gp was assayed. Result: Viability of cells treated by FTA (1-80 mg·L-1) was above 90%
difference was not statistically significant by compared with the negative group
which suggested that Caco-2 cells could maintain their viability under these experiment conditions.Fluorescence intensity of FTA significantly increased by comparing with the blank group
Rh-123 accumulation reached maximum levels of (223.43±5.6)% when the concentration of FTA was 80 mg·L-1.FTA treatments decreased P-gp ATPase activity in Caco-2 cell membranes expressing P-gp. Conclusion: FTA can modulate drug efflux by inhibiting P-gp activity in Caco-2 cell membrane.
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