Intracellular accumulation of radiolabeled organic cations agmatine, TEA, and choline was significantly increased in bcrp1-transfected MDCKII cells, as compared to wild-type cells, consistent with the observed increase in OCT2 expression. Prazosin uptake, a representative positive control for bcrp1-mediated efflux, was significantly decreased in bcrp1 cells as compared to wild-type counterparts. Results are expressed as mean ± S.D (n = 3). (*p < 0.01 comparing with wild-type group)