The editors instructed me to be "fiercely selective" in the material that I was to include in this chapter. In one respect that is an easily followed in struction for a general physiologist who studies cell membranes and attempts to use pharmacology as a tool to help decipher the electrogenic phenomena of excitable cells. Electrophysiology is fortunate in having a theory which links electrogenesis with the permeability of the cell membrane to ions (25, 100). The dazzlingly quantitative application of this theory to account for the spike of the squid axon (101) is meeting with the stubborn complexities of living membranes (13,14,95,144,188,189). Nevertheless, some rela tively simple modifications of the ionic theory permit the latter to account, although only qualitatively at present, for the bulk of a large variety of electrophysiological and pharmacological phenomena (84,85,89,90).The situation appears to be quite different in pharmacology. The periodi cal literature seems to be styled after the biblical "begat" chapters and much of it is about equally innocent of theory. Even in the restricted field of neuro pharmacology the data are almost entirely based on various reactions of whole animals or of their individual organ systems. When theory is attempted it seems to regard as irrelevant the morphology and functional properties of individual neurons and effectors, and of their organization into the complex organ system of the neuraxis and its peripheral appendages.In another respect, however, this instruction must be disobeyed. The present reviewer arrived at his interest in neuropharmacology from an at tempt to use a relatively simple conceptual framework, gained from the study of peripheral junctions (78 to 80), to account for the actions of drugs on cells, including those of the central nervous system (77, 81). The studies on electrocortical phenomenon with Purpura and other colleagues (82, 148, 151, 152, 154 to 156) in which pharmacological tools were used extensively 1 The survey of the literature pertaining to this teview was concluded in July 1963.