Mindscape Collective is now The Consciousness Library. Same library, new name. You may need to sign in again. About the change
Skip to content

Salvia divinorum increases alcohol intake and tonic immobility whilst decreasing food intake in Wistar rats.

Priscila Vázquez-león, Ulises Arenas-Martínez, Dafne Córdova-maqueda, Tomás Fregoso-Aguilar, Eduardo Ramírez-san Juan, Abraham Miranda-Páez

Acta neurobiologiae experimentalis January 1, 2021 DOI: 10.21307/ane-2021-005 (opens in new tab) via PubMed

Summary

AI-generated from the abstract

Salvia divinorum extract (SDE) and its active compound salvinorin-A (Sal-A) increased voluntary alcohol intake in male Wistar rats. SDE boosted alcohol consumption especially in rats with a history of forced alcohol intake from a young age, while Sal-A increased alcohol intake regardless of prior alcohol exposure. Both SDE and Sal-A also prolonged tonic immobility, a sign of anxiety-like behavior, and reduced food intake. These findings suggest that activation of the kappa-opioid system by Sal-A or SDE can stimulate alcohol consumption and produce anorexigenic and anxiety-like effects in rats.

Study at a glance

Characteristics Randomized controlled trial Peer reviewed
Sample size 48
Population Adult male Wistar rats
Intervention salvinorin-A (Sal-A)
Dose ~1 mg/kg of Sal-A
Duration Two weeks of alcohol and food intake assessment with one week of daily intraperitoneal injections in the middle
Citations 3
Key finding Salvia divinorum extract and salvinorin-A increased voluntary alcohol intake and prolonged tonic immobility while decreasing food intake in rats.

Abstract

The kappa-opioid system (KOP) is the key in drug abuse. Of all the compounds isolated from Salvia divinorum (S. divinorum), salvinorin-A (Sal-A) is predominant. Further, Sal-A is the only compound within S. divinorum which is reported to have psychoactive properties as a powerful kappa-opioid receptor (KOPr) agonist. Based on the key role of the KOP system in the consumption of drugs, S. divinorum extract (SDE) and Sal-A may modify the alcohol intake in Wistar rats. Assessing voluntary alcohol intake as a drug consummatory behavior, food intake as natural reward behavior and tonic immobility as indicative of anxiety-like behavior, the present study sought to identify the role of both SDE and Sal-A in the Wistar rat model. Forty-eight adult male rats were randomly divided into six groups: control, alcohol naive and vehicle, alcohol-naive and SDE, alcohol-naive and Sal-A, alcohol-consumption and vehicle, alcohol-consumption and SDE, and alcohol-consumption and Sal-A. Alcohol and food intake were assessed for two weeks. In the middle of these two weeks, vehicle, SDE (containing ~1 mg/kg of Sal-A) or Sal-A was injected intraperitoneally once a day for a week. Tonic immobility testing was performed once. The administration of SDE produced a significant increase in voluntary alcohol intake especially in rats with a history of forced alcohol consumption from a juvenile age, Sal-A elicited an increase in alcohol intake in animals with or without previous alcohol exposure, SDE and Sal-A prolonged the tonic immobility duration and decreased food intake. In conclusion, S. divinorum or Sal-A stimulated alcohol consumption in rats with a history of alcohol intake and independent of previous exposure respectively, also SDE or Sal-A elicited an anorexigenic effect, and increased tonic immobility as indicative of anxious-like behavior. The kappa-opioid system (KOP) is the key in drug abuse. Of all the compounds isolated from Salvia divinorum (S. divinorum), salvinorin-A (Sal-A) is predominant. Further, Sal-A is the only compound within S. divinorum which is reported to have psychoactive properties as a powerful kappa-opioid receptor (KOPr) agonist. Based on the key role of the KOP system in the consumption of drugs, S. divinorum extract (SDE) and Sal-A may modify the alcohol intake in Wistar rats. Assessing voluntary alcohol intake as a drug consummatory behavior, food intake as natural reward behavior and tonic immobility as indicative of anxiety-like behavior, the present study sought to identify the role of both SDE and Sal-A in the Wistar rat model. Forty-eight adult male rats were randomly divided into six groups: control, alcohol naive and vehicle, alcohol-naive and SDE, alcohol-naive and Sal-A, alcohol-consumption and vehicle, alcohol-consumption and SDE, and alcohol-consumption and Sal-A. Alcohol and food intake were assessed for two weeks. In the middle of these two weeks, vehicle, SDE (containing ~1 mg/kg of Sal-A) or Sal-A was injected intraperitoneally once a day for a week. Tonic immobility testing was performed once. The administration of SDE produced a significant increase in voluntary alcohol intake especially in rats with a history of forced alcohol consumption from a juvenile age, Sal-A elicited an increase in alcohol intake in animals with or without previous alcohol exposure, SDE and Sal-A prolonged the tonic immobility duration and decreased food intake. In conclusion, S. divinorum or Sal-A stimulated alcohol consumption in rats with a history of alcohol intake and independent of previous exposure respectively, also SDE or Sal-A elicited an anorexigenic effect, and increased tonic immobility as indicative of anxious-like behavior.

Comments

No comments yet.

Log in to comment