In order to determine the effects of the difference in resting metabolism resulting from the intracellular anatomical architecture the active transport and the dissociating movement of radioisotopic Na and Ca ions from the cell portion and from the fibre portion were comparatively investigated in the ganglion-root preparation of which cell portion is morphologically and hence metabolically different from the fibre portion. The ion movement was studied by washout experiments of
22Na and
45Ca from the ganglia and the roots, and the intracellular amount of Na ions was determined in each portion by flamephotometry. Both the spinal ganglia and the root fibres were used as a whole either to soak with test solutions or to label with radioactive ions, and then divided into the ganglion portion and the fibre portion for the purpose of performing washout experiments of radioisotopes from each portion or of determining Na content within each portion. 1. The effluxes of
22Na or
45Ca were not so uniform not only in resting efflux but in responsive efflux between the cell portion and the fibre portion even under the same experimental condition.
22Na effluxes from the ganglion and the root behaved in a manner which was qualitatively different from each other, whereas
45Ca effluxes from both portions did in a manner which was quantitatively similar, the discrepancy, particularly in the former, being dependent on the difference in intracellular morphological architecture and hence in biochemical nature between two portions.2. The depressive effect of K free Ringer on
22Na efflux was more marked in the cell portion than in the fibre portion. Similarly, ouabain was difficult to demonstrate its inhibitory effect on
22Na efflux from the fibre portion but caused a decrease in it in the cell portion. Cyanide showed a reduction of
22Na efflux only in the cellular portion but demonstrated the same effect on
45Ca dissociation similarly in both portions. With regard to
22Na and
45Ca efflux, the difference in resting efflux between the cellular portion and the fibre portion was not significant but the change in responsive efflux was markedly discrepant between two portions. The more active the resting metabolism the more intense is the change in responsive efflux of Na ions.3. The effect of decalcification on internal Na content and its change was similar in both portions, whereas both K free Ringer and ouabain Ringer known to affect selectively membrane or intracellular metabolism via the activity of membrane ATPase demonstrated Na accumulation more markedly in the cellular portion than in the fibre portion. The effect of K free Ringer on
45Ca efflux and that of ouabain on it were in the opposite direction. There is a difference in responsive Na extruding mechanism between the cellular portion and the fibre portion, and the difference reflects the quantitative difference in intracellular resting metabolism between two portions. On the contrary, the movements of
45Ca which were similar in both portions under the same condition represent that the dissociation of Ca
++ is a superficial phenomenon at the plasma membrane of the tissue and is relatively independent of intracellular metabolism.
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