After chronic preganglionic denervation of the superior cervical ganglion of the cat, methonium compounds no longer block but potentiate the effects of injected acetylcholine and, in some 50 % of experiments, themselves cause stimulation of the ganglion cells, as judged by contraction of the nictitating membrane, Furthermore, in normal ganglia, perfused with modified Locke's solution containing a reduced concentration of potassium, the same changes in response to the methonium compounds occur, although even in such conditions these drugs still block preganglionic stimulation (Perry & Reinert, 1954).It was suggested that the methonium compounds could only block transmission when the extracellular potassium ion concentration was normal; and their success in blocking preganglionic stimulation during perfusion with potassium-free Locke's solution was attributed to a local release of potassium from the activated preganglionic nerve endings. That potassium ions appeared to play an important role in these reactions was further indicated by our findings that L-glutamate, which has been shown by and Davies & Krebs (1952) to promote the inwards transfer of potassium ions into many cells against the ionic gradient, when added to the fluid perfusing a denervated ganglion, reversed the effects of denervation (Perry & Reinert, 1954). In this paper we describe further experiments which we have carried out in order to study in more detail the role of potassium ions in these reactions.Krebs and his co-workers found that, of the amino-acids which they studied, only L-glutamate and L-aspartate had a 'potassium carrier-function'. We have, therefore, investigated the action of a number of amino-acids other than L-glutamate, including D-glutamate, L-and D-aspartate, L-and D-alanine, ,B-alanine, L-arginine and L-lysine, in both normal and chronically denervated ganglia.