GABA UPTAKE IN RAT CENTRAL NERVOUS SYSTEM: COMPARISON OF UPTAKE IN SLICES AND HOMOGENATES AND THE EFFECTS OF SOME INHIBITORS

Abstract

Abstract— Fifty‐two substances were tested as inhibitors of the uptake of [3 H]GABA in slices of rat cerebral cortex. Among GABA analogues tested, only the 2‐fluoro, 3‐hydroxy and 2‐amino compounds had affinities for the uptake mechanism comparable to that of GABA. [3 H]GABA uptake was also potently inhibited by p‐chloromercuriphenylsulphonate, N‐ethylmaleimide, chlorpromazine and haloperidol. No inhibitors were found to act in a competitive manner with respect to GABA. [3 H]GABA uptake was also examined in homogenates of cerebral cortex and other regions of CNS. There was a rapid uptake of [3 H]GABA into particles when homogenate samples were incubated with the labelled amino acid; this uptake had similar kinetic properties and inhibitor sensitivity to that observed in slices of intact tissue. Density gradient centrifugation experiments indicated that the particles responsible for the uptake of [3 H]GABA in homogenates were probably synaptosomes. Uptake of [3 H]GABA also occurred in slices and homogenates of rat spinal cord, and evidence was obtained by the simultaneous labelling of homogenates with [14 C]glycine and [3 H]GABA that these two amino acids were taken up by different nerve terminals in this region.