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An Update on the Anxiolytic and Neuroprotective Properties of Etifoxine: from Brain GABA Modulation to a Whole-Body Mode of Acti An update on the anxiolytic and neuroprotective properties of etifoxine: from brain GABA modulation to a whole-body mode of action Philippe Nuss, Florian Ferreri, Michel Bourin To cite this version: Philippe Nuss, Florian Ferreri, Michel Bourin. An update on the anxiolytic and neuroprotective properties of etifoxine: from brain GABA modulation to a whole-body mode of action. Neuropsychi- atric Disease and Treatment, Dove Medical Press, 2019, 15, pp.1781-1795. 10.2147/NDT.S200568. hal-02273267 HAL Id: hal-02273267 https://hal.sorbonne-universite.fr/hal-02273267 Submitted on 28 Aug 2019 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. Neuropsychiatric Disease and Treatment Dovepress open access to scientific and medical research Open Access Full Text Article REVIEW An update on the anxiolytic and neuroprotective properties of etifoxine: from brain GABA modulation to a whole-body mode of action This article was published in the following Dove Press journal: Neuropsychiatric Disease and Treatment Philippe Nuss1,2 Abstract: Treating the signs and symptoms of anxiety is an everyday challenge in clinical Florian Ferreri1 practice. When choosing between treatment options, anxiety needs to be understood in the Michel Bourin3 situational, psychiatric, and biological context in which it arises. Etifoxine, a non- benzodiazepine anxiolytic drug belonging to the benzoxazine class, is an effective treatment 1Department of Adult Psychiatry and Medical Psychology, Sorbonne University, for anxiety in response to a stressful situation. In the present review, we focused on several Saint-Antoine Hospital, Paris, France; aspects of the cerebral and somatic biological mechanisms involved in anxiety and investi- 2 Inserm UMR_S938, Saint-Antoine gated the extent to which etifoxine’s mode of action can explain its anxiolytic activity. Its Research Centre, Sorbonne University, Paris, France; 3Department of two mechanisms of action are the modulation of GABAergic neurotransmission and neuro- Neurobiology of Anxiety and Depression, steroid synthesis. Recent data suggest that the molecule possesses neuroprotective, neuro- Faculty of Medicine, Nantes University, fl fi For personal use only. plastic, and anti-in ammatory properties. Etifoxine was rst shown to be an effective Nantes, France anxiolytic in patients in clinical studies comparing it with clobazam, sulpiride, and placebo. Randomized controlled studies have demonstrated its anxiolytic efficacy in patients with adjustment disorders (ADs) with anxiety, showing it to be superior to buspirone and comparable to lorazepam and phenazepam, with a greater number of markedly improved responders and a better therapeutic index. Etifoxine’s noninferiority to alprazolam has also been demonstrated in a comparative trial. Significantly less rebound anxiety was observed after abrupt cessation of etifoxine compared with lorazepam or alprazolam. Consistent with this finding, etifoxine appears to have a very low dependence potential. Unlike lorazepam, it has no effect on psychomotor performance, vigilance, or free recall. Severe adverse events are in general rare. Skin and subcutaneous disorders are the most frequently reported, but these generally resolve after drug cessation. Taken together, its dual mechanisms of action in anxiety and the positive data yielded by clinical trials support the use of etifoxine for treating the anxiety signs and symptoms of individuals with ADs. Neuropsychiatric Disease and Treatment downloaded from https://www.dovepress.com/ by 134.157.148.106 on 29-Aug-2019 Keywords: etifoxine, adjustment disorders, TSPO, translocator protein 18 kDa, 3α, allopregnanolone, 5α-THP, GABA, benzodiazepines, anxiety, neuroprotection Introduction Anxiety, an emotional experience characterized by a state of arousal and the expectation of danger, has been part of human experience throughout the ages. Over time, numerous conceptions of anxiety and classifications have been pro- posed, particularly in the medical field. Classifications of anxiety regularly redraw Correspondence: Philippe Nuss the boundaries between its different clinical manifestations, and new research Department of Psychiatry and Medical Psychology, Hospital Saint-Antoine, 184 continues to reveal further layers of complexity in its pathophysiological mechan- rue du Faubourg Saint-Antoine, Paris isms. In the present review, we focused on the treatment of anxiety with etifoxine, 75012, France Email [email protected] a non-benzodiazepine (BZD) anxiolytic. Our aim was to provide an overall picture submit your manuscript | www.dovepress.com Neuropsychiatric Disease and Treatment 2019:15 1781–1795 1781 DovePress © 2019 Nuss et al. This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work http://doi.org/10.2147/NDT.S200568 you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). Powered by TCPDF (www.tcpdf.org) 1 / 1 Nuss et al Dovepress of the anxiolytic properties of etifoxine, both within the The traditional concept of the pathophysiology of anxi- traditional conceptual framework of anxiety disorders and ety has focused on structural and functional brain with respect to the new perspectives opened up by recent dysfunction.5 It regards anxiety as the result of an alteration research. of the coordinated activity of brain pathways, modulated by We focused on the treatment of adjustment disorders local and distant synaptic relays via neurotransmitters. (ADs), a category that was recently redefined in the DSM-5 Structurally, a set of limbic structures have been implicated and ICD-11. Previously, the emphasis was on subjective in anxiety. These include the amygdala, which is tightly distress and emotional disturbances in ADs, principally in connected to the prefrontal cortex and appears to be critical terms of anxious or depressive symptomatology, leading to for the regulation of negative emotion. Various neurotrans- the identification of ADs with anxiety (ADWA) and ADs mitters and modulators play an important functional role in with depression. ADWA were described as being more fre- modulating anxiety-related behaviors. These include med- quent than their depressive counterpart, mainly affecting iators associated with the hypothalamic-pituitary-adrenal young and professionally active individuals.1 The manifesta- (HPA) axis,6 monoaminergic and GABAergic neurotrans- tions of anxiety in ADWA were considered to be just as mission systems,7,8 neuropeptides such as cholecystokinin, severe as those of generalized anxiety disorders.2 and lipid neuromodulators.9 Nonetheless, criticisms were voiced regarding the validity In addition to this brain-centered approach to the patho- of the DSM-IV and ICD-10 diagnostic criteria for ADs. physiology of anxiety, there is increasing evidence to sug- Some of these have been addressed in the newly published gest that anxiety states can also be modulated by the effect classifications, where there has been a shift towardconcep- on the brain of somatic physiological processes such as tualizing ADs as trauma- and stressor-related disorders. inflammation, immunity, and oxidative stress, as well as DSM-5 diagnostic criteria for ADs include transient mala- gut microbiota.10 For instance, dysfunctional interactions daptive or pathological reactions to identifiable stressors or involving the HPA axis and gut microbiota11 have been changes in life circumstances, with symptoms emerging described as contributing to the pathophysiology of anxiety. For personal use only. within 3 months of stress or onset. Anxiety, depression, and In humans, stress, a common feature of all anxiety disorders behavioral disturbances are now seen as potentially asso- has been shown to be associated with several pro- ciated qualifiers, rather than as specifiers. Clinical manifesta- inflammatory response phenotypes that may be unrespon- tions are described as being out of all proportion with the sive to the anti-inflammatory actions of glucocorticoids.12 event. In addition to its intrinsic nature, the stressor must be Moreover, several drugs known to reduce the clinical man- seen within the personal and interpersonal context in which it ifestations of anxiety (antidepressants, certain BZD, and has occurred, and cultural norms. The ICD-11 classification non-BZD anxiolytics) have been shown to attenuate the goes one step further, by identifying core clinical manifesta- above-mentioned abnormal physiological processes, point- tions, namely 1) “preoccupation with the stressor or its con- ing to a possible – and previously underestimated – aspect sequences, including excessive
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