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

  
@article{APS3542,
	author = {Bian-sheng JI and Ling HE and Guo-qing LIU},
	title = {Modulation of P-glycoprotein function by amlodipine derivatives in brain microvessel endothelial cells of rats},
	journal = {Acta Pharmacologica Sinica},
	volume = {26},
	number = {2},
	year = {2016},
	keywords = {},
	abstract = {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/
F12 (1:1) medium. The amount of intracellular rhodamine (Rh123) 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 10
mol/L (P0.05). 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 mol/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 mol/L from the medium.
Conclusion: CJX1 and CJX2
exhibited a potent effect in the inhibition of P-gp function in vitro.},
	issn = {1745-7254},	url = {http://www.chinaphar.com/article/view/3542}
}