Modulation of P-glycoprotein function by amlodipine derivatives in brain microvessel endothelial cells of rats

• 来源期刊: 中国药理学报（英文版）
• 关键词: amlodipine derivatives CJX1 CJX2 verapamil P-glycoprotein blood brain barrier vascularendothelium
• 年，卷（期）: 2005,（2）
• 页码范围: 166-170
• 页数: 5页
• 语种: 英文

摘要

Aim: To investigate whether the amlodipine derivatives, CJX1 and CJX2, have a modulative effect on P-glycoprotein (P-gp) function in rat brain microvessel endothelial cells (RBMEC). Methods: Isolated RBMEC were cultured in DMEM/ F1 2 (1:1) medium. The amount of intracellular rhodamine (Rh 123) was determined, using a fluorescence spectrophotometer, to evaluate the function of P-gp. Results:The accumulation of Rh123 in RBMEC was potentiated in a concentrationdependent manner after incubation with CJX1 and CJX2 at 1, 2.5, 5, and 10μmol/L (P＜0.01), but no accumulation of Rh123 was observed in human umbilical vein endothelial cells after incubation with CJX1 and CJX2 10 μmol/L (P＞0.05). Accumulation of intracellular Rh123 was increased and efflux of intracellular Rh123 was decreased in a time-dependent manner from 0-100 min after CJX1 and CXJ2 at 10 μmol/L treatment. The inhibitory effect of CJX1 and CJX2 on P-gp function was reversible and remained even at 120 min after removal of CJX1 and CJX2 at 2.5 μmol/L from the medium. Conclusion: CJX1 and CJX2 exhibited a potent effect in the inhibition of P-gp function in vitro.