España R A, Baldo B A, Kelley A E, Berridge C W
Department of Psychology, University of Wisconsin, Madison 53706-1611, USA.
Neuroscience. 2001;106(4):699-715. doi: 10.1016/s0306-4522(01)00319-0.
The hypocretins (orexins) are a newly identified peptide family comprised of two peptides, hypocretin-1 and hypocretin-2. Recent observations suggest an involvement of these peptides in the regulation of behavioral state. For example, these peptides are found in a variety of brain regions associated with the regulation of forebrain neuronal and behavioral activity states. Furthermore, when infused into the lateral ventricles in awake animals, hypocretin-1 elicits increased duration of waking beyond that observed in vehicle-treated animals. Previous studies have been limited to an examination of the sleep-wake effects of hypocretin-1 in awake animals. Currently, the sleep-wake effects of hypocretin-2 and the extent to which hypocretins can initiate waking in the sleeping animal remain unclear. To better characterize the wake-promoting actions of the hypocretins, the current studies examined the sleep-wake effects of varying doses (0.007, 0.07 and 0.7 nmol) of hypocretin-1 and hypocretin-2 when administered into sleeping rats (e.g. remote-controlled infusions). Infusions of hypocretin-1 and hypocretin-2 into the lateral ventricles elicited a short latency (0.7 nmol hypocretin-1; 93+/-30 s from the start of the 120-s infusion) increase in electroencephalographic, electromyographic, and behavioral indices of waking. These infusions also produced substantial decreases in slow-wave and rapid-eye movement sleep. Hypocretin-1 was more potent than hypocretin-2 in these actions. Interestingly, hypocretin-1 infused into the fourth ventricle elicited less robust waking which occurred with a longer latency than infusions into the lateral ventricles. These latter observations suggest a forebrain site of action participates in hypocretin-1-induced waking. Within the forebrain, a variety of basal forebrain structures, including the medial preoptic area, the medial septal area and the substantia innominata, receive a moderate hypocretin innervation. Therefore, additional studies examined the sleep-wake effects of bilateral hypocretin-1 infusions into these basal forebrain structures. Robust increases in waking were observed following infusions into, but not outside, the medial septal area, the medial preoptic area and the substantia innominata. These results indicate a potentially prominent role of hypocretins in sleep-wake regulation via actions within certain basal forebrain structures and are consistent with studies indicating a prominent role of hypocretins in sleep/arousal disorders.
下丘脑泌素(食欲素)是一个新发现的肽家族,由两种肽组成,即下丘脑泌素 -1 和下丘脑泌素 -2。最近的观察结果表明,这些肽参与行为状态的调节。例如,这些肽存在于与前脑神经元和行为活动状态调节相关的多种脑区。此外,当将下丘脑泌素 -1 注入清醒动物的侧脑室时,其引起的清醒持续时间比给予赋形剂处理的动物更长。以往的研究仅限于考察下丘脑泌素 -1 对清醒动物睡眠 - 觉醒的影响。目前,下丘脑泌素 -2 对睡眠 - 觉醒的影响以及下丘脑泌素能在睡眠动物中引发觉醒的程度仍不清楚。为了更好地表征下丘脑泌素促进觉醒的作用,当前研究考察了将不同剂量(0.007、0.07 和 0.7 nmol)的下丘脑泌素 -1 和下丘脑泌素 -2 注入睡眠大鼠(如遥控输注)时的睡眠 - 觉醒效应。将下丘脑泌素 -1 和下丘脑泌素 -2 注入侧脑室会引发脑电图、肌电图和行为觉醒指标的短潜伏期增加(0.7 nmol 下丘脑泌素 -1;从 120 秒输注开始起 93±30 秒)。这些输注还使慢波睡眠和快速眼动睡眠大幅减少。在这些作用中,下丘脑泌素 -1 比下丘脑泌素 -2 更有效。有趣的是,将下丘脑泌素 -1 注入第四脑室引发的觉醒较弱,且潜伏期比注入侧脑室更长。这些后来的观察结果表明,前脑作用部位参与下丘脑泌素 -1 诱导的觉醒。在前脑内,多种基底前脑结构,包括视前内侧区、内侧隔区和无名质,接受适度的下丘脑泌素神经支配。因此,进一步的研究考察了将双侧下丘脑泌素 -1 注入这些基底前脑结构时的睡眠 - 觉醒效应。在注入内侧隔区、视前内侧区和无名质内而非其外后,观察到觉醒显著增加。这些结果表明,下丘脑泌素通过在某些基底前脑结构内发挥作用,在睡眠 - 觉醒调节中可能具有重要作用,并且与表明下丘脑泌素在睡眠 / 觉醒障碍中起重要作用的研究一致。