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      Cannabidiol regulation of emotion and emotional memory processing: relevance for treating anxiety‐related and substance abuse disorders

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          Abstract

          Learning to associate cues or contexts with potential threats or rewards is adaptive and enhances survival. Both aversive and appetitive memories are therefore powerful drivers of behaviour, but the inappropriate expression of conditioned responding to fear‐ and drug‐related stimuli can develop into anxiety‐related and substance abuse disorders respectively. These disorders are associated with abnormally persistent emotional memories and inadequate treatment, often leading to symptom relapse. Studies show that cannabidiol, the main non‐psychotomimetic phytocannabinoid found in Cannabis sativa, reduces anxiety via 5‐HT 1A and (indirect) cannabinoid receptor activation in paradigms assessing innate responses to threat. There is also accumulating evidence from animal studies investigating the effects of cannabidiol on fear memory processing indicating that it reduces learned fear in paradigms that are translationally relevant to phobias and post‐traumatic stress disorder. Cannabidiol does so by reducing fear expression acutely and by disrupting fear memory reconsolidation and enhancing fear extinction, both of which can result in a lasting reduction of learned fear. Recent studies have also begun to elucidate the effects of cannabidiol on drug memory expression using paradigms with translational relevance to addiction. The findings suggest that cannabidiol reduces the expression of drug memories acutely and by disrupting their reconsolidation. Here, we review the literature demonstrating the anxiolytic effects of cannabidiol before focusing on studies investigating its effects on various fear and drug memory processes. Understanding how cannabidiol regulates emotion and emotional memory processing may eventually lead to its use as a treatment for anxiety‐related and substance abuse disorders.

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          This article is part of a themed section on Pharmacology of Cognition: a Panacea for Neuropsychiatric Disease? To view the other articles in this section visit http://onlinelibrary.wiley.com/doi/10.1111/bph.v174.19/issuetoc

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          Isolation, Structure, and Partial Synthesis of an Active Constituent of Hashish

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            A two-dimensional neuropsychology of defense: fear/anxiety and defensive distance.

            We present in this paper a picture of the neural systems controlling defense that updates and simplifies Gray's "Neuropsychology of Anxiety". It is based on two behavioural dimensions: 'defensive distance' as defined by the Blanchards and 'defensive direction'. Defensive direction is a categorical dimension with avoidance of threat corresponding to fear and approach to threat corresponding to anxiety. These two psychological dimensions are mapped to underlying neural dimensions. Defensive distance is mapped to neural level, with the shortest defensive distances involving the lowest neural level (periaqueductal grey) and the largest defensive distances the highest neural level (prefrontal cortex). Defensive direction is mapped to separate parallel streams that run across these levels. A significant departure from prior models is the proposal that both fear and anxiety are represented at all levels. The theory is presented in a simplified form that does not incorporate the interactions that must occur between non-adjacent levels of the system. It also requires expansion to include the dimension of escapability of threat. Our current development and these proposed future extensions do not change the core concepts originally proposed by Gray and, we argue, demonstrate their enduring value.
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              Non-psychotropic plant cannabinoids: new therapeutic opportunities from an ancient herb.

              Delta(9)-tetrahydrocannabinol binds cannabinoid (CB(1) and CB(2)) receptors, which are activated by endogenous compounds (endocannabinoids) and are involved in a wide range of physiopathological processes (e.g. modulation of neurotransmitter release, regulation of pain perception, and of cardiovascular, gastrointestinal and liver functions). The well-known psychotropic effects of Delta(9)-tetrahydrocannabinol, which are mediated by activation of brain CB(1) receptors, have greatly limited its clinical use. However, the plant Cannabis contains many cannabinoids with weak or no psychoactivity that, therapeutically, might be more promising than Delta(9)-tetrahydrocannabinol. Here, we provide an overview of the recent pharmacological advances, novel mechanisms of action, and potential therapeutic applications of such non-psychotropic plant-derived cannabinoids. Special emphasis is given to cannabidiol, the possible applications of which have recently emerged in inflammation, diabetes, cancer, affective and neurodegenerative diseases, and to Delta(9)-tetrahydrocannabivarin, a novel CB(1) antagonist which exerts potentially useful actions in the treatment of epilepsy and obesity.
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                Author and article information

                Contributors
                carl.stevenson@nottingham.ac.uk
                Journal
                Br J Pharmacol
                Br. J. Pharmacol
                10.1111/(ISSN)1476-5381
                BPH
                British Journal of Pharmacology
                John Wiley and Sons Inc. (Hoboken )
                0007-1188
                1476-5381
                09 March 2017
                October 2017
                : 174
                : 19 , Themed Section: Pharmacology of Cognition: a Panacea for Neuropsychiatric Disease? Guest Editors: Sarah J Bailey, Joanna C Neill and Paula M Moran ( doiID: 10.1111/bph.v174.19 )
                : 3242-3256
                Affiliations
                [ 1 ] School of Psychology University of Birmingham Birmingham UK
                [ 2 ] Department of Pharmacology Federal University of Santa Catarina Florianopolis SC Brazil
                [ 3 ] Department of Pharmacology University of São Paulo Ribeirão Preto SP Brazil
                [ 4 ] School of Biosciences University of Nottingham, Sutton Bonington Campus Loughborough UK
                Author notes
                [*] [* ] Correspondence

                Carl Stevenson, School of Biosciences, University of Nottingham, Sutton Bonington Campus, Loughborough LE12 5RD, UK. E‐mail: carl.stevenson@ 123456nottingham.ac.uk

                Author information
                http://orcid.org/0000-0001-8143-8415
                Article
                PMC5595771 PMC5595771 5595771 BPH13724 2016-BJP-1000-RCT-G.R1
                10.1111/bph.13724
                5595771
                28268256
                098cb5c0-a9db-4d7f-8d8d-55eb88c06d54
                © 2017 The British Pharmacological Society
                History
                : 07 November 2016
                : 31 December 2016
                : 18 January 2017
                Page count
                Figures: 1, Tables: 3, Pages: 15, Words: 5367
                Funding
                Funded by: Fundação de Amparo à Pesquisa do Estado de São Paulo
                Award ID: 2012/50896‐8
                Funded by: Conselho Nacional de Desenvolvimento Científico e Tecnológico
                Award ID: 307895/2013‐0
                Categories
                Review Article
                Themed Section: Review Articles
                Custom metadata
                2.0
                bph13724
                October 2017
                Converter:WILEY_ML3GV2_TO_NLMPMC version:5.1.9 mode:remove_FC converted:12.09.2017

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