Nishino Seiji
Center for Narcolepsy, Stanford University, School of Medicine, Psychiatry and Behavioral Sciences, Palo Alto, California 94304, USA.
Biol Psychiatry. 2003 Jul 15;54(2):87-95. doi: 10.1016/s0006-3223(03)00349-4.
Using positional cloning in a canine model of narcolepsy and mouse gene knockouts, genes involved in the pathogenesis of narcolepsy in animals have been identified. Hypocretin/orexin ligand and hypocretin/orexin receptor genes are key to the pathogenesis of narcolepsy in animals. Mutations in hypocretin-related genes are rare in humans, but hypocretin-ligand deficiency is found in many cases. Hypocretins/orexins are novel hypothalamic neuropeptides involved in various hypothalamic mechanisms, such as energy homeostasis and neuroendocrine function. Hypocretin-deficient human narcolepsy appears to be a more complex condition than a simple sleep disorder, and it may serve as an important disease model for studying hypothalamic function in health and disease.
利用发作性睡病犬模型中的定位克隆技术和小鼠基因敲除技术,已鉴定出与动物发作性睡病发病机制相关的基因。下丘脑分泌素/食欲素配体基因和下丘脑分泌素/食欲素受体基因是动物发作性睡病发病机制的关键。下丘脑分泌素相关基因的突变在人类中很少见,但在许多病例中发现了下丘脑分泌素配体缺乏的情况。下丘脑分泌素/食欲素是参与各种下丘脑机制的新型下丘脑神经肽,如能量稳态和神经内分泌功能。下丘脑分泌素缺乏的人类发作性睡病似乎是一种比单纯睡眠障碍更复杂的病症,它可能作为研究健康和疾病状态下下丘脑功能的重要疾病模型。