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Pharm Res. 2009 Jan;26(1):172-81. doi: 10.1007/s11095-008-9726-9. Epub 2008 Sep 27.

Transport mechanisms of carnosine in SKPT cells: contribution of apical and basolateral membrane transporters.

Author information

1
Department of Pharmaceutical Sciences, University of Michigan, Ann Arbor, Michigan 48109, USA.

Abstract

PURPOSE:

The aim of this study was to investigate the transport properties of carnosine in kidney using SKPT cell cultures as a model of proximal tubular transport, and to isolate the functional activities of renal apical and basolateral transporters in this process.

METHODS:

The membrane transport kinetics of 10 microM [3H]carnosine was studied in SKPT cells as a function of time, pH, potential inhibitors and substrate concentration. A cellular compartment model was constructed in which the influx, efflux and transepithelial clearances of carnosine were determined. Peptide transporter expression was probed by RT-PCR.

RESULTS:

Carnosine uptake was 15-fold greater from the apical than basolateral surface of SKPT cells. However, the apical-to-basolateral transepithelial transport of carnosine was severely rate-limited by its cellular efflux across the basolateral membrane. The high-affinity, proton-dependence, concentration-dependence and inhibitor specificity of carnosine supports the contention that PEPT2 is responsible for its apical uptake. In contrast, the basolateral transporter is saturable, inhibited by PEPT2 substrates but non-concentrative, thereby, suggesting a facilitative carrier.

CONCLUSIONS:

Carnosine is expected to have a substantial cellular accumulation in kidney but minimal tubular reabsorption in blood because of its high influx clearance across apical membranes by PEPT2 and very low efflux clearance across basolateral membranes.

PMID:
18820998
PMCID:
PMC2913304
DOI:
10.1007/s11095-008-9726-9
[Indexed for MEDLINE]
Free PMC Article

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