PT - JOURNAL ARTICLE AU - Qi Wang AU - Marilyn E. Morris TI - The Role of Monocarboxylate Transporter 2 and 4 in the Transport of γ-Hydroxybutyric Acid in Mammalian Cells AID - 10.1124/dmd.107.014852 DP - 2007 Aug 01 TA - Drug Metabolism and Disposition PG - 1393--1399 VI - 35 IP - 8 4099 - http://dmd.aspetjournals.org/content/35/8/1393.short 4100 - http://dmd.aspetjournals.org/content/35/8/1393.full SO - Drug Metab Dispos2007 Aug 01; 35 AB - Monocarboxylate transporter 1 (MCT1) is an important determinant of the renal transport of the drug of abuse, γ-hydroxybutyric acid (GHB). The objective of this study was to investigate the role of MCT2 and MCT4, present in tissues including intestine, kidney, skeletal muscle, and brain, in the membrane transport of GHB and the MCT substrate l-lactate. mRNA and protein of MCT2 and MCT4 were expressed in MDA-MB231 cells, as detected by reverse transcription-polymerase chain reaction and Western blot analysis; MCT1 and MCT3 were not detected. The uptake of GHB or l-lactate by MDA-MB231 cells was pH-dependent but not sodium-dependent. The concentration-dependent uptake of GHB was best fitted to a single-transporter model with a diffusional clearance component (Km of 17.6 ± 1.5 mM, Vmax of 50.6 ± 9.0 nmol · mg–1 min–1 and diffusional clearance of 0.20 ± 0.07 μl · mg–1 min–1). On the other hand, the concentration-dependent uptake of l-lactate was best fitted to a two-transporter model (Km of 21 ± 2.5 and 3.0 ± 1.5 mM, and Vmax of 268 ± 72 and 62.9 ± 42.2 nmol · mg–1min–1, respectively). The uptake of GHB and l-lactate was inhibited by MCT inhibitors α-cyano-4-hydroxycinnamate (CHC), phloretin, and p-chloromercuribenzoic acid; CHC inhibited GHB and l-lactate uptake with IC50 values of 1.71 ± 0.39 and 0.71 ± 0.11 mM, respectively. Small interfering RNA treatment to silence MCT2 or MCT4 significantly decreased their protein expression and the uptake of l-lactate and GHB; however, the decrease in GHB uptake with MCT2 inhibition was smaller than that for MCT4. This investigation demonstrated that GHB is a substrate for both MCT2 and MCT4; these transporters may be important in the nonlinear disposition of GHB, as well as influencing its tissue distribution. The American Society for Pharmacology and Experimental Therapeutics