TY - JOUR
T1 - Modeling sleep and neuropsychiatric disorders in zebrafish
AU - Levitas-Djerbi, Talia
AU - Appelbaum, Lior
N1 - Publisher Copyright: © 2017 Elsevier Ltd
PY - 2017/6/1
Y1 - 2017/6/1
N2 - What are the molecular and cellular mechanisms that link neurological disorders and sleep disturbances? The transparent zebrafish model could bridge this gap in knowledge due to its unique genetic and imaging toolbox, and amenability to high-throughput screening. Sleep is well-characterized in zebrafish and key regulators of the sleep/wake cycle are conserved, including melatonin and hypocretin/orexin (Hcrt), whereas novel sleep regulating proteins are continually being identified, such as Kcnh4a, Neuromedin U, and QRFP. Sleep deficiencies have been observed in various zebrafish models for genetic neuropsychiatric disorders, ranging from psychomotor retardation and autism to anxiety disorders. Understanding the link between neuropsychiatric disorders and sleep phenotypes in zebrafish may ultimately provide a platform for identifying therapeutic targets for clinical trials in humans.
AB - What are the molecular and cellular mechanisms that link neurological disorders and sleep disturbances? The transparent zebrafish model could bridge this gap in knowledge due to its unique genetic and imaging toolbox, and amenability to high-throughput screening. Sleep is well-characterized in zebrafish and key regulators of the sleep/wake cycle are conserved, including melatonin and hypocretin/orexin (Hcrt), whereas novel sleep regulating proteins are continually being identified, such as Kcnh4a, Neuromedin U, and QRFP. Sleep deficiencies have been observed in various zebrafish models for genetic neuropsychiatric disorders, ranging from psychomotor retardation and autism to anxiety disorders. Understanding the link between neuropsychiatric disorders and sleep phenotypes in zebrafish may ultimately provide a platform for identifying therapeutic targets for clinical trials in humans.
UR - http://www.scopus.com/inward/record.url?scp=85017558361&partnerID=8YFLogxK
U2 - https://doi.org/10.1016/j.conb.2017.02.017
DO - https://doi.org/10.1016/j.conb.2017.02.017
M3 - مقالة مرجعية
C2 - 28414966
SN - 0959-4388
VL - 44
SP - 89
EP - 93
JO - Current Opinion in Neurobiology
JF - Current Opinion in Neurobiology
ER -