A Quantitative Structure-Activity Relationship for the Modulation Effects of Flavonoids on P-Glycoprotein-Mediated Transport

作者：Sheu Ming Thau; Liou Yi Bo; Kao Yu Han; Lin Ying Ku; Ho Hsiu O^*

来源：Chemical & Pharmaceutical Bulletin, 2010, 58(9): 1187-1194.

DOI：10.1248/cpb.58.1187

• flavonoid
• P-glycoprotein
• quantitative structure-activity relationship
• multidrug resistance
• fexofenadine

P-Glycoprotein accounts for multidrug resistance in chemotherapy patients and contributes to reduced oral bioavailability and distribution of drugs in the brain. The aim of this study was to establish the qualitative and quantitative structure activity relationships (QSAR) of flavonoid modulation effects on P-glycoprotein (P-gp)'s function. Using human colorectal adenocarcinoma (HCT15) cells as an in vitro model and fexofenadine as a P-gp substrate, the modulation effects on P-gp at three concentration levels of 22 representative compounds from four flavonoid families were evaluated. Results showed that the modulation (enhanced or inhibitory) effects could be divided into three ranges designated as enhanced (<100%) as compared to the control, low inhibitory (100-217%) and high inhibitory (>217%) as compared to verapamil. An optimal QSAR was constructed for Y1 (adjusted R-2=0.4798), Y2 (adjusted R-2=0.6809), and Y3 (adjusted R-2=0.5902), respectively. This was further confirmed by a highly correlated plot of the predicted percent inhibition against observed values from a respective QSAR equation.

• 出版日期2010-9