Abstract

Cannabinoid agonists generally have a disruptive effect on memory, learning, and operant behavior that is considered to be hippocampus-dependent. Nevertheless, under certain conditions, cannabinoid receptor activation may facilitate neuronal learning processes. For example, CB1 receptors are essential for the extinction of conditioned fear associations, indicating an important role for this receptor in neuronal emotional learning and memory. This review examines the diverse effects of cannabinoids on hippocampal memory and plasticity. It shows how the effects of cannabinoid receptor activation may vary depending on the route of administration, the nature of the task (aversive or not), and whether it involves emotional memory formation (e.g., conditioned fear and extinction learning) or non-emotional memory formation (e.g., spatial learning). It also examines the memory stage under investigation (acquisition, consolidation, retrieval, extinction), and the brain areas involved. Differences between the effects of exogenous and endogenous agonists are also discussed. The apparently biphasic effects of cannabinoids on anxiety is noted as this implies that the effects of cannabinoid receptor agonists on hippocampal learning and memory may be attributable to a general modulation of anxiety or stress levels and not to memory per se. The review concludes that cannabinoids have diverse effects on hippocampal memory and plasticity that cannot be categorized simply into an impairing or an enhancing effect. A better understanding of the involvement of cannabinoids in memory processes will help determine whether the benefits of the clinical use of cannabinoids outweigh the risks of possible memory impairments.

Highlights

  • Considerable evidence suggests that cannabinoids impair hippocampal-dependent learning and memory processes, such as spatial learning and context-related memory tasks (Sullivan, 2000; Riedel and Davies, 2005)

  • We have recently examined cannabinoid modulation of long-term potentiation (LTP) symptoms, such as reexperiencing trauma in PTSD (Rothbaum and long-term depression (LTD) in a different experimental model: acute anesthetized rats. and Davis, 2003; Milad et al, 2006; Quirk et al, 2006; Rauch et al, Using this experimental condition, we found that i.p. administra- 2006)

  • We found that WIN 55,212-2 administered into the CA1 facilitates the extinction of inhibitory avoidance, with no effect on extinction kinetics when microinjected into the BLA (Ganon-Elazar and Akirav, 2009; Abush and Akirav, 2010)

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Summary

Irit Akirav*

Edited by: Patrizia Campolongo, Università degli Studi di Roma La Sapienza, Italy. Reviewed by: Antonella Gasbarri, University of L’Aquila, Italy Cathy Fernandes, King’s College London, UK. This review examines the diverse effects of cannabinoids on hippocampal memory and plasticity. It shows how the effects of cannabinoid receptor activation may vary depending on the route of administration, the nature of the task (aversive or not), and whether it involves emotional memory formation (e.g., conditioned fear and extinction learning) or non-emotional memory formation (e.g., spatial learning). It examines the memory stage under investigation (acquisition, consolidation, retrieval, extinction), and the brain areas involved.

Introduction
Cannabinoids effects on hippocampal memory
Findings
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Full Text
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