Journal of Biological Chemistry · 1989 · 161 citations · 20 references
MedicineBiochemistryPharmacologyIntracellular TransportMolecular PharmacologyNeuropharmacologyIon PermeationMembrane TransportSerotonergic PharmacologyTransport Across Biological MembranesTransport In CellsTransporter PharmacologyBrush Border Membrane TransportConcentration-dependent UptakePh DependencePlacental Transport MechanismsPlacental TransportersPlacental Uptake TransportersSerotonin Transporter FunctionVesicular Monoamine Transporters
Serotonin is actively transported into brush-border membrane vesicles isolated from normal human term placentas and an inward-directed NaCl gradient provides the driving force for this process. Uptake is negligible if Na+ is replaced by Li+, K+, Rb+, Cs+ or choline. The presence of Cl- seems necessary for the maximal activity of this Na+-dependent uptake system. Intravesicular K+ (20-40 mM) stimulates serotonin uptake, the stimulation being considerably greater at pH 7.5 than at pH 6.5. But, in the absence of K+, uptake at pH 6.5 was twice the uptake at pH 7.5. Unlabeled serotonin and dopamine inhibit the uptake of radiolabeled serotonin and the IC50 values are 70 nM and 20 microM, respectively. Histamine and 5-hydroxytryptophan do not significantly interact with the system (IC50 greater than 1 mM). Kinetic analysis reveals that serotonin uptake in these vesicles occurs via a single, saturable, high affinity system (Kt = 51 +/- 2 nM; Vmax = 6.4 +/- 0.1 pmol/mg of protein/15 s). The transporter is highly sensitive to inhibition by imipramine (IC50 = 32 nM) and desipramine (IC50 = 160 nM) but relatively insensitive to reserpine and hydralazine.
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Stephen M. Stahl, Herbert Y. Meltzer · Journal of Pharmacology and Experimental Therapeutics · 1978 · 161 citations
Medicine, Neuroscience, Pharmacology +11