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  Extinction of avoidance behavior by safety learning depends on endocannabinoid signaling in the hippocampus

Micale, V., Stepan, J., Jurik, A., Pamplona, F. A., Marsch, R., Drago, F., Eder, M., & Wotjak, C. T. (2017). Extinction of avoidance behavior by safety learning depends on endocannabinoid signaling in the hippocampus. JOURNAL OF PSYCHIATRIC RESEARCH, 90, 46-59. doi:10.1016/j.jpsychires.2017.02.002.

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アイテムのパーマリンク: https://hdl.handle.net/21.11116/0000-0001-9E7F-0 版のパーマリンク: https://hdl.handle.net/21.11116/0000-0001-9E81-B
資料種別: 学術論文

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 作成者:
Micale, Vincenzo1, 2, 著者           
Stepan, Jens3, 著者           
Jurik, Angela1, 著者           
Pamplona, Fabricio A.1, 著者           
Marsch, Rudolph1, 著者           
Drago, Filippo2, 著者
Eder, Matthias1, 著者           
Wotjak, Carsten T.1, 著者           
所属:
1Dept. Stress Neurobiology and Neurogenetics, Max Planck Institute of Psychiatry, Max Planck Society, ou_2035294              
2external, ou_persistent22              
3Dept. Translational Research in Psychiatry, Max Planck Institute of Psychiatry, Max Planck Society, ou_2035295              

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キーワード: CONTEXTUAL FEAR MEMORY; TRANSPORT INHIBITOR AM404; ACID AMIDE HYDROLASE; RECEPTOR-TYPE 1; CANNABINOID RECEPTOR; ANANDAMIDE TRANSPORT; SYNAPTIC PLASTICITY; CONDITIONED FEAR; CB1 RECEPTOR; GABAERGIC NEURONSPsychiatry; Avoidance behavior; Response extinction; CB1 receptors; Dopamine D1 receptors; AM404;
 要旨: The development of exaggerated avoidance behavior is largely responsible for the decreased quality of life in patients suffering from anxiety disorders. Studies using animal models have contributed to the understanding of the neural mechanisms underlying the acquisition of avoidance responses. However, much less is known about its extinction. Here we provide evidence in mice that learning about the safety of an environment (i.e., safety learning) rather than repeated execution of the avoided response in absence of negative consequences (i.e., response extinction) allowed the animals to overcome their avoidance behavior in a step-down avoidance task. This process was context-dependent and could be blocked by pharmacological (3 mg/kg, s.c.; SR141716) or genetic (lack of cannabinoid CB1 receptors in neurons expressing dopamine D1 receptors) inactivation of CB1 receptors. In turn, the endocannabinoid reuptake inhibitor AM404 (3 mg/kg, i.p.) facilitated safety learning in a CBI-dependent manner and attenuated the relapse of avoidance behavior 28 days after conditioning. Safety learning crucially depended on endocannabinoid signaling at level of the hippocampus, since intrahippocampal SR141716 treatment impaired, whereas AM404 facilitated safety learning. Other than AM404, treatment with diazepam (1 mg/kg, i.p.) impaired safety learning. Drug effects on behavior were directly mirrored by drug effects on evoked activity propagation through the hippocampal trisynaptic circuit in brain slices: As revealed by voltage-sensitive dye imaging, diazepam impaired whereas AM404 facilitated activity propagation to CA1 in a CB1-dependent manner. In line with this, systemic AM404 enhanced safety learning-induced expression of Egr1 at level of CA1. Together, our data render it likely that AM404 promotes safety learning by enhancing information flow through the trisynaptic circuit to CA1. (C) 2017 Elsevier Ltd. All rights reserved.

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言語: eng - English
 日付: 2017
 出版の状態: 出版
 ページ: 14
 出版情報: -
 目次: -
 査読: -
 識別子(DOI, ISBNなど): ISI: 000404198400007
DOI: 10.1016/j.jpsychires.2017.02.002
 学位: -

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出版物 1

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出版物名: JOURNAL OF PSYCHIATRIC RESEARCH
種別: 学術雑誌
 著者・編者:
所属:
出版社, 出版地: PERGAMON-ELSEVIER SCIENCE LTD
ページ: - 巻号: 90 通巻号: - 開始・終了ページ: 46 - 59 識別子(ISBN, ISSN, DOIなど): ISSN: 0022-3956