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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 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.

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