Orexin-mediated motivated arousal and reward seeking

被引:4
作者
Bjorness, Theresa E. [1 ,2 ]
Greene, Robert W. [2 ,3 ,4 ]
机构
[1] VA North Texas Hlth Care Syst, Res Serv, Dallas, TX 75126 USA
[2] Univ Texas Southwestern Med Ctr, Dept Psychiat, Dallas, TX 75390 USA
[3] Univ Texas Southwestern Med Ctr, Peter ODonnell Jr Brain Inst, Dept Neurosci, Dallas, TX 75390 USA
[4] Univ Tsukuba, Int Inst Integrat Sleep Med, Tsukuba 3058577, Japan
关键词
Hypocretin; Reward; Motivation; Sleep deprivation; Outline; narcolepsy; CONDITIONED PLACE PREFERENCE; VENTRAL TEGMENTAL AREA; RECEPTOR ANTAGONIST SB-334867; CUE-INDUCED REINSTATEMENT; MELANIN-CONCENTRATING HORMONE; STRESS-INDUCED REINSTATEMENT; BINGE-LIKE CONSUMPTION; RAT NUCLEUS-ACCUMBENS; PALATABLE FOOD-INTAKE; HYPOCRETIN-OREXIN;
D O I
10.1016/j.peptides.2024.171280
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The neuromodulator orexin has been identified as a key factor for motivated arousal including recent evidence that sleep deprivation-induced enhancement of reward behavior is modulated by orexin. While orexin is not necessary for either reward or arousal behavior, orexin neurons' broad projections, ability to sense the internal state of the animal, and high plasticity of signaling in response to natural rewards and drugs of abuse may underlie heightened drug seeking, particularly in a subset of highly motivated reward seekers. As such, orexin receptor antagonists have gained deserved attention for putative use in addiction treatments. Ongoing and future clinical trials are expected to identify individuals most likely to benefit from orexin receptor antagonist treatment to promote abstinence, such as those with concurrent sleep disorders or high craving, while attention to methodological considerations will aid interpretation of the numerous preclinical studies investigating disparate aspects of the role of orexin in reward and arousal.
引用
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页数:23
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