Katzman Martin A, Katzman Matthew P
Stress, Trauma, Anxiety, Rehabilitation and Treatment (START) Clinic for the Mood and Anxiety Disorders, Toronto, ON M4W 2N4, Canada.
Department of Psychology, Adler Graduate Professional School, Toronto, ON M4W 3P4, Canada.
Brain Sci. 2022 Jan 24;12(2):150. doi: 10.3390/brainsci12020150.
Orexin peptides comprise two neuropeptides, orexin A and orexin B, that bind two G-protein coupled receptors (GPCRs), orexin receptor 1 (OXR1) and orexin receptor 2 (OXR2). Although cell bodies that produce orexin peptides are localized in a small area comprising the lateral hypothalamus and adjacent regions, orexin-containing fibres project throughout the neuraxis. Although orexins were initially described as peptides that regulate feeding behaviour, research has shown that orexins are involved in diverse functions that range from the modulation of autonomic functions to higher cognitive functions, including reward-seeking, behaviour, attention, cognition, and mood. Furthermore, disruption in orexin signalling has been shown in mood disorders that are associated with low hedonic tone or anhedonia, including depression, anxiety, attention deficit hyperactivity disorder, and addiction. Notably, projections of orexin neurons overlap circuits involved in the modulation of hedonic tone. Evidence shows that orexins may potentiate hedonic behaviours by increasing the feeling of pleasure or reward to various signalling, whereas dysregulation of orexin signalling may underlie low hedonic tone or anhedonia. Further, orexin appears to play a key role in regulating behaviours in motivationally charged situations, such as food-seeking during hunger, or drug-seeking during withdrawal. Therefore, it would be expected that dysregulation of orexin expression or signalling is associated with changes in hedonic tone. Further studies investigating this association are warranted.
食欲素肽由两种神经肽组成,即食欲素A和食欲素B,它们与两种G蛋白偶联受体(GPCRs),即食欲素受体1(OXR1)和食欲素受体2(OXR2)结合。尽管产生食欲素肽的细胞体位于包括下丘脑外侧和相邻区域的一个小区域内,但含食欲素的纤维投射到整个神经轴。尽管食欲素最初被描述为调节进食行为的肽,但研究表明,食欲素参与了从自主功能调节到更高认知功能的多种功能,包括寻求奖励、行为、注意力、认知和情绪。此外,在与低享乐基调或快感缺乏相关的情绪障碍中,包括抑郁症、焦虑症、注意力缺陷多动障碍和成瘾,都显示出食欲素信号传导的破坏。值得注意的是,食欲素神经元的投射与参与享乐基调调节的神经回路重叠。证据表明,食欲素可能通过增加对各种信号的愉悦或奖励感来增强享乐行为,而食欲素信号传导的失调可能是低享乐基调或快感缺乏的基础。此外,食欲素似乎在调节充满动机的情境中的行为中起关键作用,例如饥饿时觅食或戒断时觅药。因此,可以预期食欲素表达或信号传导的失调与享乐基调的变化有关。有必要进行进一步的研究来调查这种关联。