Orexin/hypocretin system modulates amygdala-dependent threat learning through the locus coeruleus

被引:138
|
作者
Sears, Robert M. [1 ]
Fink, Ann E. [1 ]
Wigestrand, Mattis B. [1 ,2 ]
Farb, Claudia R. [1 ]
de Lecea, Luis [3 ,4 ,5 ]
LeDoux, Joseph E. [1 ,6 ]
机构
[1] NYU, Ctr Neurosci, New York, NY 10003 USA
[2] Univ Oslo, Dept Mol Biosci, N-0371 Oslo, Norway
[3] Stanford Univ, Neurosci Program, Stanford, CA 94305 USA
[4] Stanford Univ, Dept Psychiat, Stanford, CA 94305 USA
[5] Stanford Univ, Dept Behav Sci, Stanford, CA 94305 USA
[6] Nathan S Kline Inst Psychiat Res, Emot Brain Inst, Orangeburg, NY 10962 USA
基金
美国国家卫生研究院;
关键词
norepinephrine; fear conditioning; channelrhodopsin-2; POSTTRAUMATIC-STRESS-DISORDER; OREXIN; 2; RECEPTORS; GLUTAMATERGIC TRANSMISSION; MEMORY CONSOLIDATION; EMOTIONAL BEHAVIOR; REWARD-SEEKING; NEURONS; HYPOCRETIN; ACTIVATION; BRAIN;
D O I
10.1073/pnas.1320325110
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Survival in a dangerous environment requires learning about stimuli that predict harm. Although recent work has focused on the amygdala as the locus of aversive memory formation, the hypothalamus has long been implicated in emotional regulation, and the hypothalamic neuropeptide orexin (hypocretin) is involved in anxiety states and arousal. Nevertheless, little is known about the role of orexin in aversive memory formation. Using a combination of behavioral pharmacology, slice physiology, and optogenetic techniques, we show that orexin acts upstream of the amygdala via the noradrenergic locus coeruleus to enable threat (fear) learning, specifically during the aversive event. Our results are consistent with clinical studies linking orexin levels to aversive learning and anxiety in humans and dysregulation of the orexin system may contribute to the etiology of fear and anxiety disorders.
引用
收藏
页码:20260 / 20265
页数:6
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