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. 2024 Feb 26;9:17. doi: 10.1186/s41181-024-00244-4

Fig. 2.

Fig. 2

Cellular uptake and release of [211At]At-NpGT, [125I]I-NpGT and [18F]F-NpGT from C6 cells. a Time-course study of uptake. b Time-course study of extracellular release. The Y-axis shows the percentage release of each agent. c Inhibition of each agent’s uptake with amino acids and a LAT1-selective inhibitor (1 mM). The Y-axis shows the percentage of the control. The inhibitors were as follows Tyr = L-tyrosine; BCH = 2-aminobicyclo-(2,2,1)-heptane-2-carboxylic acid; MeAIB = α-methyl-aminoisobutyric acid; AMT = α-methyl-L-tyrosine