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

Bryan L. Roth, Estela Lopez, Scott Beischel, Richard B Westkaemper, Jon M Evans

Pharmacology & Therapeutics May 1, 2004 DOI: 10.1016/j.pharmthera.2004.03.004 (opens in new tab)

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Characteristics Review Peer reviewed
Keywords Cns drug discovery Neuroscience drug discovery Psychopharmacology Neurotherapeutics Cns therapeutics Brain drug discovery Psychoactive plants Natural products Ethnobotany Phytochemistry Plant-derived compounds Medicinal plants Receptorome screening Molecular target identification Computational pharmacology In silico screening Bioinformatics Drug target discovery Receptor screening Receptor profiling
Citations 98
Key findings Screening psychoactive plant compounds against the receptorome can uncover their molecular targets and provide validated targets for CNS drug discovery.

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.

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