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

被引:58
|
作者
Morena, Maria [1 ,2 ,3 ,4 ]
De Castro, Valentina [1 ]
Gray, J. Megan [2 ,3 ,4 ]
Palmery, Maura [1 ]
Trezza, Viviana [5 ]
Roozendaal, Benno [6 ,7 ]
Hill, Matthew N. [2 ,3 ,4 ]
Campolongo, Patrizia [1 ]
机构
[1] Univ Roma La Sapienza, Dept Physiol & Pharmacol, I-00185 Rome, Italy
[2] Univ Calgary, Hotchkiss Brain Inst, Calgary, AB T2N 4N1, Canada
[3] Univ Calgary, Dept Cell Biol & Anat, Calgary, AB T2N 4N1, Canada
[4] Univ Calgary, Dept Psychiat, Calgary, AB T2N 4N1, Canada
[5] Univ Roma Tre, Sect Biomed Sci & Technol, Dept Sci, I-00146 Rome, Italy
[6] Radboud Univ Nijmegen, Dept Cognit Neurosci, Med Ctr, NL-6525 EZ Nijmegen, Netherlands
[7] Radboud Univ Nijmegen, Donders Inst Brain Cognit & Behav, NL-6525 EZ Nijmegen, Netherlands
来源
JOURNAL OF NEUROSCIENCE | 2015年 / 35卷 / 41期
基金
加拿大健康研究院;
关键词
cannabinoid receptors; emotional arousal; endocannabinoids; memory for emotional experiences; stress; MONOACYLGLYCEROL LIPASE INHIBITION; REPEATED HOMOTYPIC STRESS; LONG-TERM POTENTIATION; CANNABINOID RECEPTOR; CB1; RECEPTOR; DORSAL HIPPOCAMPUS; CONTEXTUAL RETRIEVAL; INDUCED IMPAIRMENT; RESTRAINT STRESS; AMYGDALA;
D O I
10.1523/JNEUROSCI.1983-15.2015
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
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 mu g/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.
引用
收藏
页码:13962 / 13974
页数:13
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