We have demonstrated that the crude synaptosome P2 fraction prepared from t
he rat brain is able to accumulate [H-3]D-serine in a saturable, temperatur
e-dependent and partially sodium- and potassium-dependent manner with an af
finity of a hundred micromolar range. The inhibition profile of D-serine ac
cumulation by various amino acids is different from those of uptake systems
reported for glycine and other amino acids. The present data suggest that
the endogenous D-serine may be taken up mainly through a carrier-mediated t
ransport system to regulate its extracellular concentration in the mammalia
n brain. (C) 2001 Wiley-Liss, Inc.