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Salvinorin A: the "magic mint" hallucinogen finds a molecular target in the kappa opioid receptor.

Douglas J Sheffler, Bryan L. Roth

TIPS - Trends in Pharmacological Sciences March 1, 2003 DOI: 10.1016/S0165-6147(03)00027-0 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Review Peer reviewed
Topics Salvia divinorum
Citations 151
Key findings Salvinorin A is a selective, non-nitrogenous agonist of the kappa opioid receptor, which may serve as a molecular target for treating disorders involving altered perception.

Abstract

Salvinorin A, a neoclerodane diterpene, is the most potent naturally occurring hallucinogen known and rivals the synthetic hallucinogen lysergic acid diethylamide in potency. Recently, the molecular target of salvinorin A was identified as the kappa opioid receptor (KOR). Salvinorin A represents the only known non-nitrogenous KOR selective agonist. Based on the selectivity of salvinorin A for the KOR, this receptor represents a potential molecular target for the development of drugs to treat disorders characterized by alterations in perception, including schizophrenia, Alzheimer's disease and bipolar disorder.

In the evidence

This study is part of the evidence base for a synthesis in the library. Here is how each one recorded it.

  • Argues salvinorin A is a selective non-nitrogenous kappa opioid agonist and that the kappa receptor is a potential target for treating disorders of perception such as schizophrenia and bipolar disorder.

    Synthesized

Comparable studies

Other narrative reviews on salvia divinorum, most cited first.

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