The Lateral Habenula Directs Coping Styles Under Conditions of Stress via Recruitment of the Endocannabinoid System

被引:43
作者
Berger, Anthony L. [1 ]
Henricks, Angela M. [1 ]
Lugo, Janelle M. [2 ]
Wright, Hayden R. [2 ]
Warrick, Collin R. [2 ]
Sticht, Martin A. [3 ,4 ]
Morena, Maria [3 ,4 ]
Bonilla, Itziar [5 ,6 ]
Laredo, Sarah A. [7 ]
Craft, Rebecca M. [1 ]
Parsons, Loren H. [7 ]
Grandes, Pedro R. [5 ,6 ,8 ]
Hillard, Cecilia J. [9 ,10 ]
Hill, Matthew N. [3 ,4 ]
McLaughlin, Ryan J. [1 ,2 ]
机构
[1] Washington State Univ, Dept Psychol, Pullman, WA 99164 USA
[2] Washington State Univ, Dept Integrat Physiol & Neurosci, Pullman, WA 99164 USA
[3] Univ Calgary, Hotchkiss Brain Inst, Dept Cell Biol & Anat, Calgary, AB, Canada
[4] Univ Calgary, Hotchkiss Brain Inst, Dept Psychiat, Calgary, AB, Canada
[5] Univ Basque Country, Euskal Herriko Unibertsitatea, Univ Basque Country, Dept Neurosci, Leioa, Spain
[6] Univ Basque Country, Euskal Herriko Unibertsitatea, Achucarro Basque Ctr Neurosci, Sci Pk, Leioa, Spain
[7] Scripps Res Inst, Dept Neurosci, La Jolla, CA 92037 USA
[8] Univ Victoria, Div Med Sci, Victoria, BC, Canada
[9] Med Coll Wisconsin, Dept Pharmacol & Toxicol, Milwaukee, WI 53226 USA
[10] Med Coll Wisconsin, Neurosci Res Ctr, Milwaukee, WI 53226 USA
基金
美国国家卫生研究院; 加拿大健康研究院;
关键词
Anxiety; CB1; receptor; Endocannabinoid; Lateral habenula; Rat; Stress coping; CANNABINOID CB1 RECEPTOR; VENTRAL TEGMENTAL AREA; MEDIAL PREFRONTAL CORTEX; DEEP BRAIN-STIMULATION; PITUITARY-ADRENAL AXIS; DORSAL RAPHE NUCLEUS; ANTIDEPRESSANT-LIKE; SYNAPTIC POTENTIATION; PRELIMBIC CORTEX; MEMORY FORMATION;
D O I
10.1016/j.biopsych.2018.04.018
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
BACKGROUND: The ability to effectively cope with stress is a critical determinant of disease susceptibility. The lateral habenula (LHb) and the endocannabinoid (ECB) system have independently been shown to be involved in the selection of stress coping strategies, yet the role of ECB signaling in the LHb remains unknown. METHODS: Using a battery of complementary techniques in rats, we examined the localization of type-1 cannabinoid receptors (CB(1)Rs) and assessed the behavioral and neuroendocrine effects of intra-LHb CB1R manipulations. We further tested the extent to which the ECB system in the LHb is impacted following chronic unpredictable stress or social defeat stress, and whether manipulation of LHb CB(1)Rs can bias coping strategies in rats with a history of chronic stress. RESULTS: Electron microscopy studies revealed CB1R expression on presynaptic axon terminals, postsynaptic membranes, mitochondria, and glial processes in the rat LHb. In vivo microdialysis experiments indicated that acute stress increased the amount of 2-arachidonoylglycerol in the LHb, while intra-LHb CB1R blockade increased basal corticosterone, augmented proactive coping strategies, and reduced anxiety-like behavior. Basal LHb 2-arachidonoylglycerol content was similarly elevated in rats that were subjected to chronic unpredictable stress or social defeat stress and positively correlated with adrenal weight. Finally, intra-LHb CB1R blockade increased proactive behaviors in response to a novel conspecific, increasing approach behaviors irrespective of stress history and decreasing the latency to be attacked during an agonistic encounter. CONCLUSIONS: Alterations in LHb ECB signaling may be relevant for development of stress-related pathologies in which LHb dysfunction and stress-coping impairments are hallmark symptoms.
引用
收藏
页码:611 / 623
页数:13
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