Skip to content

Kappa-opioid receptor-mediated effects of the plant-derived hallucinogen, salvinorin A, on inverted screen performance in the mouse.

William E Fantegrossi, Kelly M Kugle, Leander J. Valdés, Masato Koreeda, James H Woods

Behavioural Pharmacology December 1, 2005 DOI: 10.1097/00008877-200512000-00005 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Preclinical experimental study Peer reviewed
Population Mice
Interventions Salvinorin A remifentanil U69 593 nor-binaltorphamine
Topics Salvia divinorum
Keywords Natural compound Mexican mint extract Mint compound Kappa-opioid receptors Kappa receptors Receptor activation Pharmacology Mechanism of action Drug action Receptor interaction Pharmacodynamics Drug discovery Therapeutic potential New therapeutics Compound development Drug development
Citations 80
Key findings Salvinorin A disrupts motor coordination in mice via kappa-opioid receptor activation, but its binding may differ from that of traditional kappa-agonists like U69,593.

Abstract

Salvinorin A is a pharmacologically active diterpene that occurs naturally in the Mexican mint Ska Maria Pastora (Salvia divinorum) and represents the first naturally occurring kappa-opioid receptor agonist. The chemical structure of salvinorin A is novel among the opioids, and thus defines a new structural class of kappa-opioid-receptor selective drugs. Few studies have examined the effects of salvinorin A in vivo, and fewer still have attempted to assess the agonist actions of this compound at mu-opioid, delta-opioid, and kappa-opioid receptors using selective antagonists. In the mouse, salvinorin A disrupted climbing behavior on an inverted screen task, indicating a rapid, but short-lived induction of sedation/motor incoordination. Similar effects were observed with the mu-agonist remifentanil and the synthetic kappa-agonist U69,593. When behaviorally equivalent doses of all three opioids were challenged with antagonists at doses selective for mu-opioid, delta-opioid, or kappa-opioid receptors, results suggested that the motoric effects of remifentanil were mediated by mu-receptors, whereas those of salvinorin A and U69,593 were mediated via kappa-receptors. Despite similar potencies and degrees of effectiveness, salvinorin A and U69,593 differed with regard to their susceptibility to antagonism by the kappa-antagonist nor-binaltorphamine. This later finding, coupled with the novel chemical structure of the compound, is consistent with recent findings that the diterpene salvinorin A may bind to the kappa-receptor in a manner that is qualitatively different from that of more traditional kappa-agonists such as the benzeneacetamide U69,593. Such pharmacological differences among these kappa-opioids raise the possibility that the development of other diterpene-based opioids may yield important therapeutic compounds.

Comparable studies

Other preclinical and animal studies on salvia divinorum, most cited first.

Citations in the library

Cited by 42

and 37 more in the library

Cites 13

and 8 more in the library

Explore topics