Chronic, intermittent treatment with a cannabinoid receptor agonist impairs recognition memory and brain network functional connectivity. Issue 1 (27th September 2018)

• Record Type: Journal Article
• Authors: Mouro, Francisco M.; Ribeiro, Joaquim A.; Sebastião, Ana M.; Dawson, Neil
• Is Part Of: Journal of neurochemistry. Volume 147:Issue 1(2018)
• Page Start: 71
• Page End: 83
• Publication Date: 2018-09-27
• Subjects: cannabinoids -- chronic -- functional connectivity -- recognition memory; Neurochemistry -- Periodicals; 616.8042
• DOI: 10.1111/jnc.14549
• Languages: English
• ISSNs: 0022-3042

Abstract

Abstract: Elucidating how cannabinoids affect brain function is instrumental for the development of therapeutic tools aiming to mitigate 'on target' side effects of cannabinoid‐based therapies. A single treatment with the cannabinoid receptor agonist, WIN 55, 212‐2, disrupts recognition memory in mice. Here, we evaluate how prolonged, intermittent (30 days) exposure to WIN 55, 212‐2 (1 mg/kg) alters recognition memory and impacts on brain metabolism and functional connectivity. We show that chronic, intermittent treatment with WIN 55, 212‐2 disrupts recognition memory (Novel Object Recognition Test) without affecting locomotion and anxiety‐like behaviour (Open Field and Elevated Plus Maze). Through 14 C‐2‐deoxyglucose functional brain imaging we show that chronic, intermittent WIN 55, 212‐2 exposure induces hypometabolism in the hippocampal dorsal subiculum and in the mediodorsal nucleus of the thalamus, two brain regions directly involved in recognition memory. In addition, WIN 55, 212‐2 exposure induces hypometabolism in the habenula with a contrasting hypermetabolism in the globus pallidus. Through the application of the Partial Least Squares Regression (PLSR) algorithm to the brain imaging data, we observed that prolonged WIN 55, 212‐2 administration alters functional connectivity in brain networks that underlie recognition memory, including that between the hippocampus and prefrontal cortex, the thalamus and prefrontal cortex, and between the hippocampus and the perirhinal cortex. In addition, our results support disturbed lateral habenula and serotonin system functional connectivity following WIN 55, 212‐2 exposure. Overall, this study provides new insight into the functional mechanisms underlying the impact of chronic cannabinoid exposure on memory and highlights the serotonin system as a particularly vulnerable target. Abstract : We show that chronic intermittent treatment with cannabinoid agonist WIN 55, 212‐2 leads to disruption in recognition memory. Autoradiographic image analysis revealed that chronic WIN 55, 212‐2 administration altered brain metabolism in several brain regions. Finally, we show that this treatment modified functional brain connectivity directly in recognition memory circuits. These data give new insight into the mechanisms by which chronic cannabinoid exposure impacts on behaviour and cognition, and highlight the value of considering cannabinoid actions at the systems‐level perspective.