The accumulation of carnitine was measured in cerebral cortex neurons isola
ted from adult rat brain. This process was found to be lowered by 40% after
preincubation with ouabain and with SH-group reagents (N-ethylmaleimide an
d mersalyl). The initial velocity of carnitine transport was found to be in
hibited by LF-aminobutyrate (GABA) in a competitive way (K-i = 20.9 +/- 2.4
mM). However, of various inhibitors of GABA transporters, only nipecotic a
cid and very high concentrations of 1-[2-([(diphenylmethylene) amino] oxy)e
thyl] -1,2,5,6-tetrahydro-3 -pyridine-carboxylic acid hydrochloride (NO-711
) acid decreased carnitine accumulation while betaine, taurine and p-alanin
e had no effect. The GABA transporters expressed in Xenopus laevis oocytes
did not transport carnitine. Moreover, carnitine was not observed to dimini
sh the accumulation of GABA in cerebral cortex neurons, which further exclu
ded a possible involvement of the GABA transporter GAT1 in the process of c
arnitine accumulation, despite the expression of this protein in the cells
under study. The absence of carnitine transporter OCTN2 in rat cerebral cor
tex neurons (K. A. Nalecz, D. Dymna, J. E. Mroczkowska, A. Broer, S. Broer
M. J. Nalecz and R. Cecchelli, unpublished results), together with the inse
nsitivity of carnitine accumulation towards betaines, implies that a novel
transporting protein is present in these cells.