The cannabinoid receptor agonist WIN 55,212-2 facilitates the extinction of contextual fear memory and spatial memory in rats
Abstract
Rationale Previous studies demonstrated that pharmacological blockade of CB1 cannabinoid receptors decreases the extinction of conditioned fear and spatial memory in rodents. However, the effects of CB1 cannabinoid receptor activation in this response remain unclear.Objectives To evaluate the effects of the cannabinoid agonist WIN 55,212-2 (WIN) and the cannabinoid antagonist SR 147778 (SR) on the extinction of contextual fear memory in rats 24 h or 30 days after fear conditioning.Methods For fear conditioning, rats were placed in the conditioning chamber for 3 min and received a 1-s electric foot shock (1.5 mA). Retrieval testing consisted of a 3-min exposure to the conditioning chamber and extinction training consisted of successive 9-min exposures at 24-h intervals. Rats were also evaluated in the open field and water maze reversal task.Results The administration of SR (1.0 mg/kg, i.p.) and WIN (0.25 mg/kg, i.p.) before extinction training disrupted and facilitated, respectively, the extinction of 24 h contextual fear memory. These effects were not related to any disturbance in memory retrieval, unconditioned freezing expression, or locomotor activity. WIN (0.25 mg/kg, i.p.) also facilitated the extinction of 30-day-old contextual fear memory, while the prior administration of SR (0.2 mg/kg, i.p.) antagonized this response. The facilitative effect of WIN on memory extinction does not seem to be specific for contextual fear memory because it was also observed in the water maze reversal task.Conclusions These results suggest cannabinoid receptor agonists as potential drugs to treat anxiety disorders related to the retrieval of aversive memories.
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Activating CB1R via systemic or intra-hippocampal or intra-mPFC administration of WIN55212-2, AM404, or AEA facilitates rodent fear extinction, in most cases without affecting conditioned fear.
“Activating CB1R via systemic or intra-hippocampal or -mPFC administration of either the CB1R agonist, WIN55212-2, the ECB reuptake blocker, AM404, or AEA itself has been shown to facilitate rodent fear extinction, in most cases without affecting conditioned fear [89,95–98] (but see [90]).”
From Amygdala FAAH and anandamide: mediating protection and recovery from stress (2013) · cites this paper as [89]
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References 30 · Cited by 211
- Authors
- Pamplona, F. A., Prediger, R. D. S., Pandolfo, P., & Takahashi, R. N.
- Affiliations
- Universidade Federal de Santa Catarina (BR)
- Corresponding author
- Takahashi, Reinaldo N.
- Venue
- Psychopharmacology
- Published
- 2006-09-01
- Volume
- 188
- Issue
- 4
- Pages
- 641-649
- ISSN
- 0033-3158 (ISSN-L)
- 1432-2072
- OpenAlex
- W2073513282
- Cited by
- 211
- References
- 30
- Citations by year
- 2026: 6 · 2025: 8 · 2024: 5 · 2023: 6 · 2022: 7 · 2021: 9 · 2020: 4 · 2019: 7 · 2018: 8 · 2017: 12 · 2016: 9 · 2015: 15 · 2014: 20 · 2013: 17 · 2012: 10
- FWCI
- 8.52
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Psychopharmacology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Sanofi
- Conselho Nacional de Desenvolvimento Científico e Tecnológico
- Topics
- Health Sciences › Medicine › Pharmacology › Cannabis and Cannabinoid Research
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory Processes and Influences
- Keywords
- WIN 55,212-2, CB1 receptor, cannabinoid receptor agonists, fear extinction, contextual fear memory, spatial memory, anxiety disorders, fear conditioning
- MeSH terms
- Animals, Conditioning, Psychological, Extinction, Psychological, Fear, Male, Memory, Morpholines, Naphthalenes, Piperidines, Pyrazoles, Rats, Wistar, Maze Learning, Receptor, Cannabinoid, CB1, Freezing Reaction, Cataleptic, Benzoxazines, Rats
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