Training-Associated Emotional Arousal Shapes Endocannabinoid Modulation of Spatial Memory Retrieval in Rats

Autor: Valentina De Castro, Viviana Trezza, Benno Roozendaal, Maria Morena, Patrizia Campolongo, Matthew N. Hill, Maura Palmery, J. Megan Gray
Přispěvatelé: Morena, Maria, De Castro, Valentina, Gray, J. Megan, Palmery, Maura, Trezza, Viviana, Roozendaal, Benno, Hill, Matthew N, Campolongo, Patrizia
Rok vydání: 2015
Předmět:
Male
Cannabinoid receptor
Emotions
Stress-related disorders Donders Center for Medical Neuroscience [Radboudumc 13]
cannabinoid receptors
emotional arousal
endocannabinoids
memory for emotional experiences
stress
neuroscience (all)
Hippocampus
Water maze
Developmental psychology
Rats
Sprague-Dawley

chemistry.chemical_compound
Enzyme Inhibitors
JZL184
memory for emotional experience
General Neuroscience
Temperature
Articles
Calcium Channel Blockers
Endocannabinoid system
Benzamides
lipids (amino acids
peptides
and proteins)

Arousal
Psychology
Neuroinformatics
Morpholines
Spatial Learning
Effects of stress on memory
Neurophysiology
Arachidonic Acids
Naphthalenes
Glycerides
Animals
Maze Learning
Cannabinoid Receptor Agonists
Dose-Response Relationship
Drug

Recall
cannabinoid receptor
endocannabinoid
URB597
Benzoxazines
Rats
chemistry
Mental Recall
Carbamates
Corticosterone
Neuroscience
Stress
Psychological

Endocannabinoids
Zdroj: The Journal of Neuroscience, 35, 13962-74
The Journal of Neuroscience, 35, 41, pp. 13962-74
ISSN: 1529-2401
0270-6474
Popis: Contains fulltext : 150747.pdf (Publisher’s version ) (Open Access) Variations in environmental aversiveness influence emotional memory processes in rats. We have previously shown that cannabinoid effects on memory are dependent on the stress level at the time of training as well as on the aversiveness of the environmental context. Here, we investigated whether the hippocampal endocannabinoid system modulates memory retrieval depending on the training-associated arousal level. Male adult Sprague Dawley rats were trained on a water maze spatial task at two different water temperatures (19 degrees C and 25 degrees C) to elicit either higher or lower stress levels, respectively. Rats trained under the higher stress condition had better memory and higher corticosterone concentrations than rats trained at the lower stress condition. The cannabinoid receptor agonist WIN55212-2 (10-30 ng/side), the 2-arachidonoyl glycerol (2-AG) hydrolysis inhibitor JZL184 (0.1-1 mug/side), and the anandamide (AEA) hydrolysis inhibitor URB597 (10-30 ng/side) were administered bilaterally into the hippocampus 60 min before probe-trial retention testing. WIN55212-2 or JZL184, but not URB597, impaired probe-trial performances only of rats trained at the higher stressful condition. Furthermore, rats trained under higher stress levels displayed an increase in hippocampal 2-AG, but not AEA, levels at the time of retention testing and a decreased affinity of the main 2-AG-degrading enzyme for its substrate. The present findings indicate that the endocannabinoid 2-AG in the hippocampus plays a key role in the selective regulation of spatial memory retrieval of stressful experience, shedding light on the neurobiological mechanisms involved in the impact of stress effects on memory processing. SIGNIFICANCE STATEMENT: Endogenous cannabinoids play a central role in the modulation of memory for emotional events. Here we demonstrate that the endocannabinoid 2-arachidonoylglycerol in the hippocampus, a brain region crucially involved in the regulation of memory processes, selectively modulates spatial memory recall of stressful experiences. Thus, our findings provide evidence that the endocannabinoid 2-arachidonoylglycerol is a key player in mediating the impact of stress on memory retrieval. These findings can pave the way to new potential therapeutic intervention for the treatment of neuropsychiatric disorders, such as post-traumatic stress disorder, where a previous exposure to traumatic events could alter the response to traumatic memory recall leading to mental illness.
Databáze: OpenAIRE