Animal models of narcolepsy and the hypocretin/orexin system: Past, present, and future
Autor: | Thomas S. Kilduff, Ryan K Tisdale, Akihiro Yamanaka |
---|---|
Jazyk: | angličtina |
Rok vydání: | 2020 |
Předmět: |
Cataplexy
Neurotransmitter systems Basic Science of Sleep and Circadian Rhythms Pathognomonic symptom 03 medical and health sciences 0302 clinical medicine Dogs Physiology (medical) mental disorders medicine Animals 030304 developmental biology Narcolepsy 0303 health sciences Sleep disorder Orexins business.industry Intracellular Signaling Peptides and Proteins medicine.disease Sleep in non-human animals Orexin Disease Models Animal nervous system Models Animal Neurology (clinical) medicine.symptom business Neuroscience 030217 neurology & neurosurgery psychological phenomena and processes Hypocretin orexin |
Zdroj: | Sleep |
Popis: | Animal models have advanced not only our understanding of the etiology and phenotype of the sleep disorder narcolepsy but have also informed sleep/wake regulation more generally. The identification of an inheritable narcolepsy phenotype in dogs in the 1970s allowed the establishment of a breeding colony at Stanford University, resulting in studies that provided the first insights into the genetics and neurotransmitter systems that underlie cataplexy and rapid-eye movement sleep atonia. Although the discovery of the hypocretin/orexin neuropeptides in 1998 initially seemed unrelated to sleep/wake control, the description of the phenotype of the prepro-orexin knockout (KO) mouse as strongly resembling cataplexy, the pathognomonic symptom of narcolepsy, along with identification of a mutation in hypocretin receptor-2 gene as the source of canine narcolepsy, unequivocally established the relationship between this system and narcolepsy. The subsequent discovery of hypocretin neuron degeneration in human narcolepsy demystified a disorder whose etiology had been unknown since its initial description 120 years earlier. These breakthroughs prompted the development of numerous other animal models that have allowed manipulation of the hypocretin/orexin system, thereby advancing our understanding of sleep/wake circuitry. While animal models have greatly informed understanding of this fascinating disorder and the role of the hypocretin/orexin system in sleep/wake control, the question of why these neurons degenerate in human narcolepsy is only beginning to be understood. The development of new immune-mediated narcolepsy models are likely to further inform the etiology of this sleep disorder and animal models will undoubtedly play a critical role in the development of novel narcolepsy therapeutics. |
Databáze: | OpenAIRE |
Externí odkaz: |