UPTAKE AND RELEASE OF EXOGENOUS [ACETYLCHOLINE-1-C-14 BY BRAIN CORTEX SLICES FROM THE RAT

Abstract— Radioactive acetylcholine ([14C]ACh) that is taken up by rat cerebral cortex slices, incubated aerobically in a physiological saline‐glucose paraoxon‐[14C]ACh medium, apparently by a passive diffusion process at concentrations > 1 mm consists essentially of two forms, a readily exchangeable and releaseable or mobile form, and a bound or retained form, poorly (or not) exchangeable. The quantity of retained ACh consists of a considerable fraction of that taken up amounting to 54% with external 0.1 mm‐[14C]ACh and about constant, 27%, for the range 5‐50mm‐[14C]ACh. All its ACh is released on homogenization with 0.1 n‐perchloric acid or on tissue disintegration in distilled water. The cerebral uptake of ACh differs basically from that of urea as there is no retention of the latter following its uptake. Cerebral cortex slices are superior to those of cerebellar cortex, subcortical white matter, kidney cortex, liver and spleen in taking up and retaining [14C]ACh. Deprivation in the incubation media of glucose or Na+ or Ca2+. or the presence of dinitrophenol, whilst causing little change in ACh uptake, induces considerable changes in swelling and ACh retention; the greater the amount of swelling the smaller is that of retention. It seems that the latter is segregated in compartments characterized by a low permeability to exogenous ACh. About half of it is independent of changes in incubation conditions whilst the other half enters the compartment by an Na+, Ca2+ and energy‐dependent process. At least part of the retention is neuronal as it is diminished by protovera‐trine, the diminution being blocked by tetrodotoxin. Mobile ACh (i.e. total uptake minus retained ACh) is largely unaffected by protoveratrine, ouabain, etc. It seems that the retained ACh is directly proportional to the amount of mobile ACh minus the amount that enters with swelling. If the latter is largely glial in location, then the retained ACh is simply proportional to the mobile neuronal ACh. Suggestions are made as to the location of the retained ACh in the brain cells and to the processes involved in its segregation there. Release of retained ACh occurs on change of the Na+ gradient. Atropine and d‐tubocurarine also diminish the amount of retained ACh but the percentage diminution falls with increase of the concentration of exogenous ACh. Copyright © 1979, Wiley Blackwell. All rights reserved