Brief Article
Copyright ©2013 Baishideng Publishing Group Co.
World J Pharmacol. Dec 9, 2013; 2(4): 115-121
Published online Dec 9, 2013. doi: 10.5497/wjp.v2.i4.115
Figure 2
Figure 2 Inhibitory effects of apigenin and kaemperol on the uptake of the specific substrates of organic anion transporters and organic cation transporters. A: Uptake of each radio-labelled substrate was measured in the absence (white bars) and presence of 10 μmol/L apigenin (black bars); B: Uptake of each radio-labelled substrate was measured in the absence (white bars) and presence of 10 μmol/L kaemperol (black bars). The specific substrates used in this experiment were 1 µmol/L [3H]-PAH for OAT1; 500 nmol/L [3H]-ES for OAT2 (pH 5.5); 300 nmol/L [3H]-ES for OAT3 and OAT4; 1 μmol/L [3H]-L-ergothioneine for OCTN1; 5 μmol/L [14C]-L-carnitine for OCTN2. The transporter-mediated uptake of each substrate was calculated by subtracting the uptake of vector control and expressed as a percentage of the uptake to the control (without apigenin or kaemperol). Values were mean ± SE (n = 3) of triplicate repeats in three independent experiments. bP < 0.01, vs absence group. OAT: Organic anion transporter; ES: Estrone-3-sulfate; OCTN: Organic cation transporter.