“…It has been suggested that the pharmacological mode of action of the phenothiazine type drugs is related to their presence in or at biological membranes (Guth & Spirtes, 1964;Bhise et al, 1983). In particular, the reduction in membrane permeability to dopamine has been cited as the origin of their antipsychotic function (Bhise et al, 1983; Creese et al, 1976). The specific interactions responsible may be quite complex and involve disordering of the lipid (Pang et al, 1980), disruption of ion channels (Lee, 1976), interaction with membrane protein (LaBella, 1981), or modification of the membrane surface (Bhise et al, 1983;Zografi & Munshi, 1970;Seeman & Bialy, 1963).…”