Salvinorin A: a potent naturally occurring nonnitrogenous kappa opioid selective agonist.
Bryan L. Roth, Karen Baner, Richard B Westkaemper, Daniel J Siebert, Kenner C Rice, Seanna Steinberg, Paul Ernsberger, Richard B Rothman
Proceedings of the National Academy of Sciences September 3, 2002 DOI: 10.1073/pnas.182234399 (opens in new tab)
Study at a glance
AI-extracted from the abstract| Characteristics | Experimental study Peer reviewed |
|---|---|
| Intervention | Salvinorin A |
| Topics | Salvia divinorum |
| Keywords | Natural compound Plant compound Kappa opioid receptor Kor Receptor activation Human perception Brain function Perceptual disorders Drug discovery Therapeutics New treatments Pharmacology |
| Citations | 782 |
| Key findings | Salvinorin A is a potent and selective kappa opioid receptor agonist with no activity at the 5-HT(2A) serotonin receptor, indicating that kappa opioid receptors modulate human perception. |
Abstract
Salvia divinorum, whose main active ingredient is the neoclerodane diterpene Salvinorin A, is a hallucinogenic plant in the mint family that has been used in traditional spiritual practices for its psychoactive properties by the Mazatecs of Oaxaca, Mexico. More recently, S. divinorum extracts and Salvinorin A have become more widely used in the U.S. as legal hallucinogens. We discovered that Salvinorin A potently and selectively inhibited (3)H-bremazocine binding to cloned kappa opioid receptors. Salvinorin A had no significant activity against a battery of 50 receptors, transporters, and ion channels and showed a distinctive profile compared with the prototypic hallucinogen lysergic acid diethylamide. Functional studies demonstrated that Salvinorin A is a potent kappa opioid agonist at cloned kappa opioid receptors expressed in human embryonic kidney-293 cells and at native kappa opioid receptors expressed in guinea pig brain. Importantly, Salvinorin A had no actions at the 5-HT(2A) serotonin receptor, the principal molecular target responsible for the actions of classical hallucinogens. Salvinorin A thus represents, to our knowledge, the first naturally occurring nonnitrogenous opioid-receptor subtype-selective agonist. Because Salvinorin A is a psychotomimetic selective for kappa opioid receptors, kappa opioid-selective antagonists may represent novel psychotherapeutic compounds for diseases manifested by perceptual distortions (e.g., schizophrenia, dementia, and bipolar disorders). Additionally, these results suggest that kappa opioid receptors play a prominent role in the modulation of human perception.
In the evidence
This study is part of the evidence base for a synthesis in the library. Here is how each one recorded it.
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Salvinorin A potently and selectively activated kappa opioid receptors with no activity at 5-HT2A or 50 other targets, indicating kappa opioid receptors modulate human perception.
Synthesized
Comparable studies
Other experimental studies on salvia divinorum, most cited first.
| Study | Year | Design | Participants |
|---|---|---|---|
| Salvinorin A, an active component of the hallucinogenic sage salvia divinorum is a highly efficacious kappa-opioid receptor agonist: structural and functional considerations. Cloned human kappa-opioid receptors expressed in human embryonic kidney-293 cells and... | 2004 | Experimental study | |
| Synthesis and κ-opioid receptor activity of furan-substituted salvinorin A analogues. Animal model | 2014 | Experimental study | |
| Identification of the molecular mechanisms by which the diterpenoid salvinorin A binds to kappa-opioid receptors. | 2005 | Experimental study | |
| Dopamine D2High receptors stimulated by phencyclidines, lysergic acid diethylamide, salvinorin A, and modafinil. Rat brain striatum homogenates | 2009 | Laboratory experiment | |
| Structure-based design, synthesis, and biochemical and pharmacological characterization of novel salvinorin A analogues as active state probes of the kappa-opioid receptor. | 2009 | Experimental study |
Citations in the library
Cited by 271
- Crystal structure of an LSD-bound human serotonin receptor Cell January 26, 2017
- Here today, gone tomorrow…and back again? A review of herbal marijuana alternatives (K2, Spice), synthetic cathinones (bath salts), kratom, Salvia divinorum, methoxetamine, and piperazines. Journal of Medical Toxicology March 1, 2012
- Psychedelics and the Human Receptorome PLoS One 2010
- The Serotonin System and Spiritual Experiences American Journal of Psychiatry November 1, 2003
- Opioid receptors and legal highs:Salvia divinorumand Kratom Clinical Toxicology 2008
and 266 more in the library
Cites 8
- Evidence for 5-HT2 involvement in the mechanism of action of hallucinogenic agents. Life Sciences December 17, 1984
- Divinorin A, a psychotropic terpenoid, and divinorin B from the hallucinogenic Mexican mint, Salvia divinorum The Journal of Organic Chemistry November 1, 1984
- Salvia divinorum and the unique diterpene hallucinogen, Salvinorin (divinorin) A. Journal of Psychoactive Drugs 1994
- Salvinorin C, a new neoclerodane diterpene from a bioactive fraction of the hallucinogenic Mexican mint Salvia divinorum. Organic Letters November 29, 2001
- Salvia divinorum: an hallucinogenic mint which might become a new recreational drug in Switzerland. Forensic Science International August 14, 2000
and 3 more in the library