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作 者:王春苗[1] 侯华新[1] 黎丹戎[2] 陈云龙[1] 莫春燕[1] 李竟[1] 莫媛媛[1]
机构地区:[1]广西医科大学药学院,广西南宁530021 [2]广西医科大学医学科学实验中心,广西南宁530021
出 处:《中国激光》2014年第5期92-96,共5页Chinese Journal of Lasers
基 金:国家自然科学基金(81060270);广西医学科学实验中心开放基金(KFJJ2011-25)
摘 要:利用激光扫描共聚焦显微镜动态研究大黄素β-环糊精包合物在鼻咽癌CNE-1细胞的跨膜转运及分布。结果显示,大黄素β-环糊精包合物以颗粒的形式主要分布于胞浆中,在其浓度为5~40mg·L-1时细胞对其摄取量随浓度的增加呈非线性增加;NaN3、甘露醇可抑制CNE-1细胞对大黄素β-环糊精包合物的摄入量,环孢菌素A(CsA)在药物浓度低(小于5mg·L-1)时可显著增加细胞对大黄素β-环糊精包合物的摄入量,而在药物浓度大时,反而抑制细胞的摄取量。相对大黄素而言,大黄素β-环糊精包合物在细胞内持续时间较长。大黄素β环糊精包合物在鼻咽癌CNE-1细胞的跨膜转运主要遵循能量依赖的内吞模式且受P-gp蛋白的调控,这一特性可为药物剂型研究提供参考。The transmembrane transport and distribution characteristics of emodin-^-CD inclusion complex in the nasopharyngeal carcinoma CNE-1 cells are observed using laser scanning confocal microscope. The results show that both emodin and emodin-β3-CD inclusion complex are mainly distributed in the cytoplasm in granules. In the concentration range of 5-4.0 mg~ L -1, the intake of emodin-β-CD inclusion complex nonlinearly increases with the increase of concentrations. Compared with the control group, emodin-β-CD inclusion complex uptake in cells is significantly lower than that of treatment with NaNs and mannitol, After treatment with P-glycoprotein inhibitors cyclosporin A (CsA), intake of emodin-β-CD inclusion complex at low concentrations (smaller than 5 mg L 1) significantly increases, but at high concentrations, intake of emodin-β-CD inclusion complex significantly decreases. Emodin-β-CD inclusion complex has long time of maintaining high concentration in cell relative to emodin. The mechanism of emodin-β-CD inclusion complex uptake in cells may involve energy-dependent endocytosis and P-glycoproteins participates in the conveying process of emodin-β-CD inclusion complex in CNE-1 cells. It provides a reference to improving emodin formulations.
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