The role of hypocretin in driving arousal and goal-oriented behaviors

被引:94
作者
Boutrel, Benjamin [1 ]
Cannella, Nazzareno [2 ]
de Lecea, Luis [2 ]
机构
[1] CHUV, Ctr Psychiat Neurosci, Dept Psychiat, CH-1008 Prilly, Switzerland
[2] Stanford Univ, Dept Psychiat & Behav Sci, Palo Alto, CA 94304 USA
关键词
Orexin; Addiction; Hypothalamus; Drug seeking; Neuropeptide; Optogenetic; HYPOTHALAMIC OREXIN NEURONS; MELANIN-CONCENTRATING HORMONE; RECEPTOR ANTAGONIST; INDUCED REINSTATEMENT; OREXIGENIC PEPTIDES; COCAINE-SEEKING; NEUROPEPTIDE-Y; REWARD; SLEEP; ACTIVATION;
D O I
10.1016/j.brainres.2009.11.054
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The hypocretins (Hcrts), also called orexins, are two neuropeptides secreted by a few thousand neurons restricted to the lateral hypothalamus. The Hcrt peptides bind to two receptors located in nuclei associated with diverse cognitive and physiological functions. Experimental evidence has demonstrated that the physiological roles of hypocretins extend far beyond its initial role in food consumption and has emerged as a key system in the fields of sleep disorders and drug addiction. Here, we discuss recent evidence demonstrating a key role of hypocretin in the motivation for reward seeking in general, and drug taking in particular, and we delineate a physiological framework for this peptidergic system in orchestrating the appropriate levels of alertness required for the elaboration and the execution of goal-oriented behaviors. We propose a general role for hypocretins in mediating arousal, especially when an organism must respond to unexpected stressors and environmental challenges, which serve to shape survival behaviors. We also discuss the limit of the current experimental paradigms to address the question of how a system normally involved in the regulation of vigilance states and hyperarousal may promote a pathological state that elicits compulsive craving and relapse to drug seeking. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:103 / 111
页数:9
相关论文
共 95 条
[1]   Physiological arousal: a role for hypothalamic systems [J].
Adamantidis, A. ;
de Lecea, L. .
CELLULAR AND MOLECULAR LIFE SCIENCES, 2008, 65 (10) :1475-1488
[2]   The hypocretins as sensors for metabolism and arousal [J].
Adamantidis, Antoine ;
de Lecea, Luis .
JOURNAL OF PHYSIOLOGY-LONDON, 2009, 587 (01) :33-40
[3]   Neural substrates of awakening probed with optogenetic control of hypocretin neurons [J].
Adamantidis, Antoine R. ;
Zhang, Feng ;
Aravanis, Alexander M. ;
Deisseroth, Karl ;
De Lecea, Luis .
NATURE, 2007, 450 (7168) :420-U9
[4]  
[Anonymous], PSYCHOPHARMACOLOGY B
[5]   Role of lateral hypothalamic orexin neurons in reward processing and addiction [J].
Aston-Jones, Gary ;
Smith, Rachel J. ;
Moorman, David E. ;
Richardson, Kimberlei A. .
NEUROPHARMACOLOGY, 2009, 56 :112-121
[6]   Overlapping distributions of orexin/hypocretin- and dopamine-β-hydroxylase immunoreactive fibers in rat brain regions mediating arousal, motivation, and stress [J].
Baldo, BA ;
Daniel, RA ;
Berridge, CW ;
Kelley, AE .
JOURNAL OF COMPARATIVE NEUROLOGY, 2003, 464 (02) :220-237
[7]   Exclusive postsynaptic action of hypocretin-orexin on sublayer 6b cortical neurons [J].
Bayer, L ;
Serafin, M ;
Eggermann, E ;
Saint-Mleux, B ;
Marchard, D ;
Jones, BE ;
Mühlethaler, M .
JOURNAL OF NEUROSCIENCE, 2004, 24 (30) :6760-6764
[8]   Orexin A in the VTA is critical for the induction of synaptic plasticity and Behavioral Sensitization to cocaine [J].
Borgland, SL ;
Taha, SA ;
Sarti, F ;
Fields, HL ;
Bonci, A .
NEURON, 2006, 49 (04) :589-601
[9]   Orexin A/Hypocretin-1 Selectively Promotes Motivation for Positive Reinforcers [J].
Borgland, Stephanie L. ;
Chang, Shao-Ju ;
Bowers, M. Scott ;
Thompson, Jennifer L. ;
Vittoz, Nicole ;
Floresco, Stan B. ;
Chou, Jonathan ;
Chen, Billy T. ;
Bonci, Antonello .
JOURNAL OF NEUROSCIENCE, 2009, 29 (36) :11215-11225
[10]   Systemic and intrabasalis administration of the orexin-1 receptor antagonist, SB-334867, disrupts attentional performance in rats [J].
Boschen, Karen E. ;
Fadel, Jim R. ;
Burk, Joshua A. .
PSYCHOPHARMACOLOGY, 2009, 206 (02) :205-213