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. 2002 Oct 30;137(6):910–918. doi: 10.1038/sj.bjp.0704926

Figure 3.

Figure 3

Inhibition by compound DMPBI of specific MPP+ uptake into 293 cells expressing EMTr or EMTh in (a) standard buffer or (b) high potassium buffer. In K+ buffer, all Na+ ions were replaced by K+ to depolarize and clamp membrane potential. For both conditions, cells were preincubated without inhibitor in the respective uptake buffers for 24 min. For EMTr, control uptake in K+ buffer was 44% of uptake in Na+ buffer, and non-specific uptake amounted to 5% of total uptake in Na+ buffer and 7% in K+ buffer. For further details see legend to Figure 2.