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Article

Effect of five novel 5‑substituted tetrandrine derivatives on P‑glycoprotein‑mediated inhibition and transport in Caco‑2 cells

  • Authors:
    • Zhonglian Cao
    • Dan Li
    • Li Liu
    • Ping Yang
  • View Affiliations / Copyright

    Affiliations: Instrumental Analysis Centre, School of Pharmacy, Fudan University, Shanghai 201203, P.R. China, Department of Pharmacology, Center for Pharmacological Evaluation and Research of SIPI, Shanghai Institute of Pharmaceutical Industry, Shanghai 200437, P.R. China
  • Pages: 6808-6814
    |
    Published online on: September 24, 2018
       https://doi.org/10.3892/ol.2018.9492
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Abstract

Tetrandrine (Tet) is a potent inhibitor that reverses P‑glycoprotein‑mediated multidrug resistance (MDR). A number of novel 5‑substituted tetrandrine derivatives were synthesized by the authors. The present study aimed at identifying potential P‑gp inhibitor candidates, and intracellular uptake and efflux experiments and Caco‑2 cell‑based Transwell transport studies were performed. It was demonstrated that all five test compounds were able to inhibit efflux and increase intracellular uptake of the P‑gp substrate, rhodamine‑123 (Rho‑123); the test compounds were P‑gp inhibitors. The transepithelial transport experiment indicated that the secretory (basolateral‑to‑apical) of Rho‑123 decreased, the absorption (apical‑to‑basolateral) increased and the transport efflux ratio (ER) reduced in the presence of the five compounds. Among the compounds, fluobenzene‑Tet (TF) exhibited similar inhibitory effect as Tet. Although the other four test compounds exhibited weaker inhibitory effects than Tet and TF, the compounds exhibited stronger inhibitory effects compared with the reference compound verapamil. The study demonstrated that the five novel 5‑substituted tetrandrine derivatives are able to act as inhibitors of P‑gp to overcome P‑gp‑mediated drug resistance.
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Copy and paste a formatted citation
Spandidos Publications style
Cao Z, Li D, Liu L and Yang P: Effect of five novel 5‑substituted tetrandrine derivatives on P‑glycoprotein‑mediated inhibition and transport in Caco‑2 cells. Oncol Lett 16: 6808-6814, 2018.
APA
Cao, Z., Li, D., Liu, L., & Yang, P. (2018). Effect of five novel 5‑substituted tetrandrine derivatives on P‑glycoprotein‑mediated inhibition and transport in Caco‑2 cells. Oncology Letters, 16, 6808-6814. https://doi.org/10.3892/ol.2018.9492
MLA
Cao, Z., Li, D., Liu, L., Yang, P."Effect of five novel 5‑substituted tetrandrine derivatives on P‑glycoprotein‑mediated inhibition and transport in Caco‑2 cells". Oncology Letters 16.5 (2018): 6808-6814.
Chicago
Cao, Z., Li, D., Liu, L., Yang, P."Effect of five novel 5‑substituted tetrandrine derivatives on P‑glycoprotein‑mediated inhibition and transport in Caco‑2 cells". Oncology Letters 16, no. 5 (2018): 6808-6814. https://doi.org/10.3892/ol.2018.9492
Copy and paste a formatted citation
x
Spandidos Publications style
Cao Z, Li D, Liu L and Yang P: Effect of five novel 5‑substituted tetrandrine derivatives on P‑glycoprotein‑mediated inhibition and transport in Caco‑2 cells. Oncol Lett 16: 6808-6814, 2018.
APA
Cao, Z., Li, D., Liu, L., & Yang, P. (2018). Effect of five novel 5‑substituted tetrandrine derivatives on P‑glycoprotein‑mediated inhibition and transport in Caco‑2 cells. Oncology Letters, 16, 6808-6814. https://doi.org/10.3892/ol.2018.9492
MLA
Cao, Z., Li, D., Liu, L., Yang, P."Effect of five novel 5‑substituted tetrandrine derivatives on P‑glycoprotein‑mediated inhibition and transport in Caco‑2 cells". Oncology Letters 16.5 (2018): 6808-6814.
Chicago
Cao, Z., Li, D., Liu, L., Yang, P."Effect of five novel 5‑substituted tetrandrine derivatives on P‑glycoprotein‑mediated inhibition and transport in Caco‑2 cells". Oncology Letters 16, no. 5 (2018): 6808-6814. https://doi.org/10.3892/ol.2018.9492
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