Learning and memory impairment induced by salvinorin A, the principal ingredient of Salvia divinorum, in wistar rats.
Daniela Braida, Andrea Donzelli, Roberta Martucci, Valeria Capurro, Mariaelvina Sala
International journal of toxicology December 1, 2011 DOI: 10.1177/1091581811418538 via PubMed
Summary
AI-generated from the abstractSalvinorin A, the main psychoactive compound in Salvia divinorum, impairs spatial long-term memory, episodic memory, and aversive memory in rats, but does not affect short-term memory. These memory deficits are blocked by a selective κ-opioid receptor antagonist, indicating the effects are mediated through that receptor. Additionally, salvinorin A disrupts latent inhibition, a measure of attention, suggesting broader cognitive impairment. The findings demonstrate that salvinorin A has deleterious effects on learning and memory via a κ-opioid receptor mechanism.
Study at a glance
| Characteristics | Experimental study Peer reviewed |
|---|---|
| Population | Wistar rats |
| Interventions | Salvinorin A nor-binaltorphimine |
| Dose | 80-640 μg/kg subcutaneous; 160-640 μg/kg for episodic and aversive memory; 160 μg/kg for latent inhibition; nor-binaltorphimine 0.5-1 mg/kg intraperitoneal |
| Topics | Salvia divinorum |
| Keywords | Memory impairment Kappa opioid receptor Neuropharmacology |
| Citations | 29 |
| Key finding | Salvinorin A impairs spatial long-term memory, episodic memory, and aversive memory in rats through a κ-opioid receptor mechanism, without affecting short-term memory. |
Abstract
The effects of salvinorin A (Salvia divinorum principal ingredient), a potent κ-opioid natural hallucinogen, on learning and memory were investigated. Wistar rats were tested in the 8-arm radial maze, for object recognition and passive avoidance tasks for spatial, episodic, and aversive memory. Attention was assessed using a latent inhibition task. Salvinorin A (80-640 μg/kg subcutaneous [sc]) did not affect short-term memory, but it impaired spatial long-term memory. Episodic and aversive memories were impaired by salvinorin A (160-640 μg/kg). Memory impairment was blocked by the selective κ-opioid receptor antagonist, nor-binaltorphimine ([nor-B]; 0.5-1 mg/kg, intraperitoneal [ip]). Salvinorin A (160 μg/kg) disrupted latent inhibition, after LiCl treatment, such as reduced sucrose intake, suggesting an attention would result in an impairment of cognitive behavior. These findings demonstrate for the first time that salvinorin A has deleterious effects on learning and memory, through a κ-opioid receptor mechanism.