Screening the receptorome to discover the molecular targets for plant-derived psychoactive compounds: a novel approach for CNS drug discovery.

Psychoactive plants alter perception, emotion, and cognition, and understanding their molecular mechanisms may reveal the biological basis of consciousness and provide validated targets for central nervous system drug discovery. This review describes an unbiased, discovery-based approach that screens the main active ingredients of psychoactive plants against the 'receptorome'—the portion of the proteome encoding receptors. It overviews the receptorome, describes public-domain in silico resources, and details new tools for mining data from the National Institute of Mental Health Psychoactive Drug Screening Program's K(i) Database. Three case studies on Hypericum perforatum, Salvia divinorum, and Ephedra sinica illustrate the approach, and recommendations for future studies are offered.

Study at a glance

Abstract

Because psychoactive plants exert profound effects on human perception, emotion, and cognition, discovering the molecular mechanisms responsible for psychoactive plant actions will likely yield insights into the molecular underpinnings of human consciousness. Additionally, it is likely that elucidation of the molecular targets responsible for psychoactive drug actions will yield validated targets for CNS drug discovery. This review article focuses on an unbiased, discovery-based approach aimed at uncovering the molecular targets responsible for psychoactive drug actions wherein the main active ingredients of psychoactive plants are screened at the "receptorome" (that portion of the proteome encoding receptors). An overview of the receptorome is given and various in silico, public-domain resources are described. Newly developed tools for the in silico mining of data derived from the National Institute of Mental Health Psychoactive Drug Screening Program's (NIMH-PDSP) K(i) Database (K(i) DB) are described in detail. Additionally, three case studies aimed at discovering the molecular targets responsible for Hypericum perforatum, Salvia divinorum, and Ephedra sinica actions are presented. Finally, recommendations are made for future studies.