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Bryan A Killinger

Department of Psychology, Western Michigan University, Kalamazoo, MI 49008-5439, USA.

2 papers in the library · 98 citations · publishing 2009-2010

Papers

Comparison of the discriminative stimulus effects of salvinorin A and its derivatives to U69,593 and U50,488 in rats.

Psychopharmacology April 1, 2009 Lisa E Baker, John J Panos, Bryan A Killinger et al. 57 citations

Salvinorin A, the active compound in the hallucinogenic plant Salvia divinorum, produces its effects through kappa opioid receptors. In experiments with male Sprague-Dawley rats trained to discriminate between two different kappa opioid agonists (U69,593 or U50,488), salvinorin A and two synthetic derivatives of salvinorin B fully substituted for the training drugs, indicating they produce similar internal sensations. Additional rats trained to discriminate salvinorin A also recognized the other kappa agonists. These results confirm that salvinorin A's discriminative stimulus effects are mediated by kappa receptors, supporting the potential use of salvinorin A analogs as therapeutic agents for conditions like drug dependence and mood disorders.

Salvinorin A fails to substitute for the discriminative stimulus effects of LSD or ketamine in Sprague-Dawley rats.

Pharmacology, biochemistry, and behavior September 1, 2010 Bryan A Killinger, Mary M Peet, Lisa E Baker 41 citations

Salvinorin A, the active compound in Salvia divinorum, is an atypical hallucinogen that selectively binds to kappa opioid receptors and is structurally distinct from other opioids. In a drug discrimination study, 16 male rats trained to recognize either LSD or ketamine did not generalize to salvinorin A, meaning the rats did not treat it as similar to those hallucinogens. This supports evidence that salvinorin A is pharmacologically distinct from traditional hallucinogens like LSD and ketamine, offering a unique tool for studying the neurochemical mechanisms of hallucination.