Acute physiologic and chronic histologic changes in rats and mice exposed to the unique hallucinogen salvinorin A.
Mark Mowry, Michael Mosher, Wayne Briner
Journal of psychoactive drugs January 1, 2003 DOI: 10.1080/02791072.2003.10400021 via PubMed
Summary
AI-generated from the abstractSalvinorin A, a hallucinogen used as a legal alternative to controlled substances, has low physical toxicity even at doses far exceeding typical human exposure. In anesthetized rats given 1600 mcg/kg, no effects were observed on cardiac conduction, temperature, or galvanic skin response, though a nonsignificant rise in pulse pressure occurred. Mice chronically exposed to doses up to 6400 mcg/kg for two weeks showed no significant histologic changes in brain, heart, kidney, bone marrow, blood, or spleen. These findings indicate minimal acute and chronic organ damage, but further research on blood pressure and psychological effects is warranted.
Study at a glance
| Characteristics | Animal study Peer reviewed |
|---|---|
| Population | Rats and mice |
| Intervention | Salvinorin A |
| Dose | 1600 mcg/kg (rats); 400, 800, 1600, 3200, or 6400 mcg/kg (mice) |
| Duration | 100 minutes (rats); two weeks (mice) |
| Keywords | Physical impact Acute exposure Chronic organ changes Tissue damage Toxicity |
| Citations | 54 |
| Key finding | Salvinorin A showed no significant histologic changes or acute physiological effects at high doses, suggesting low physical toxicity. |
Abstract
Salvinorin A is a unique hallucinogen that is seeing increased use in humans. It is not currently a controlled substance and is used as a legal alternative to controlled substances. Usually smoked or buccally absorbed by chewing, doses of approximately 200 mcg can produce profound hallucinogenic effects of short duration. The mechanism of action of salvinorin A is at the kappa-opioid receptor. Little data is available on the medical effects of this substance so animal studies were undertaken to explore the acute toxic effects of this substance in rats and the chronic effects in mice. Rats were anesthetized and administered salvinorin A at 1600 mcg/kg or vehicle. Recordings were made of galvanic skin response, EKG, temperature, and pulse pressure for 100 minutes. Mice were chronically exposed to vehicle or 400, 800, 1600, 3200, or 6400 mcg/kg of salvinorin A for two weeks. After exposure the animals were sacrificed and brain, heart, kidney, bone marrow, blood and spleen were removed, fixed, sectioned, stained and examined by light microscopy. No effects were seen on cardiac conduction, temperature, or galvanic skin response. A nonsignificant rise was seen in pulse pressure. Histologic studies of spleen, blood, brain, liver, kidney, and bone marrow did not find any significant histologic changes at any of the doses examined. These data suggests that the toxicity of salvinorin A is relatively low, even at doses many times greater than what humans are exposed to. However, further studies should be done on blood pressure effects. The psychological impact of this potent hallucinogen should also be investigated.