2-arachidonoylglycerol signaling impairs short-term fear extinction

• DOI: 10.1038/tp.2016.26
• Publication Date: 2016-03-01T15:34:40Z
• Authors: N D Hartley; O Gunduz-Cinar; L Halladay; O Bukalo; A Holmes; S Patel
• Keywords: Cannabinoid Receptor Agonists; Male; 570; Behavior, Animal; 150; Arachidonic Acids; Fear; Extinction, Psychological; Glycerides; Mice, Inbred C57BL; Mice; 03 medical and health sciences; 0302 clinical medicine; Animals; Original Article; Endocannabinoids; Signal Transduction

AbstractImpairments in fear extinction are thought to be central to the psychopathology of posttraumatic stress disorder, and endocannabinoid (eCB) signaling has been strongly implicated in extinction learning. Here we utilized the monoacylglycerol lipase inhibitor JZL184 to selectively augment brain 2-AG levels combined with an auditory cue fear-conditioning paradigm to test the hypothesis that 2-AG-mediated eCB signaling modulates short-term fear extinction learning in mice. We show that systemic JZL184 impairs short-term extinction learning in a CB1 receptor-dependent manner without affecting non-specific freezing behavior or the acquisition of conditioned fear. This effect was also observed in over-conditioned mice environmentally manipulated to re-acquire fear extinction. Cumulatively, the effects of JZL184 appear to be partly due to augmentation of 2-AG signaling in the basolateral nucleus of the amygdala (BLA), as direct microinfusion of JZL184 into the BLA produced similar results. Moreover, we elucidate a short ~3-day temporal window during which 2-AG augmentation impairs extinction behavior, suggesting a preferential role for 2-AG-mediated eCB signaling in the modulation of short-term behavioral sequelae to acute traumatic stress exposure.