PEPT2-mediated uptake of neuropeptides in rat choroid plexus

NS Teuscher, RF Keep, DE Smith - Pharmaceutical research, 2001 - Springer
NS Teuscher, RF Keep, DE Smith
Pharmaceutical research, 2001Springer
Purpose. The peptide transporter PEPT2 was recently shown to be functionally active in rat
choroid plexus, suggesting that it may play a role in neuropeptide homeostasis in the
cerebrospinal fluid. This study, therefore, examined the role of PEPT2 in mediating
neuropeptide uptake into choroid plexus. Methods. Whole-tissue rat choroid plexus uptake
studies were performed on GlySar in the absence and presence of neuropeptides and on
carnosine. Results. The neuropeptides NAAG, CysGly, GlyGln, kyotorphin, and carnosine …
Abstract
Purpose. The peptide transporter PEPT2 was recently shown to be functionally active in rat choroid plexus, suggesting that it may play a role in neuropeptide homeostasis in the cerebrospinal fluid. This study, therefore, examined the role of PEPT2 in mediating neuropeptide uptake into choroid plexus.
Methods. Whole-tissue rat choroid plexus uptake studies were performed on GlySar in the absence and presence of neuropeptides and on carnosine.
Results. The neuropeptides NAAG, CysGly, GlyGln, kyotorphin, and carnosine inhibited the uptake of radiolabeled GlySar at 1.0 mM concentrations. In contrast, TRH, [D-Arg2]-kyotorphin, glutathione, and homocarnosine did not inhibit GlySar uptake. Kyotorphin, an analgesic, was a competitive inhibitor of GlySar with a Ki of 8.0 μM. The direct uptake of carnosine was also shown to be mediated by PEPT2 in isolated choroid plexus (Km = 39.3 μM; Vmax = 73.9 pmol/mg/min). Radiolabeled carnosine uptake was inhibited by 1.0 mM concentrations of GlySar or carnosine but not homocarnosine, L-histidine, or β-alanine.
Conclusions. These findings indicate that PEPT2 mediates the uptake of a diverse group of neuropeptides in choroid plexus, and suggests a role for PEPT2 in the regulation of neuropeptides, peptide fragments, and peptidomimetics in cerebrospinal fluid.
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