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下丘脑泌素系统在斑马鱼中的作用及机制()

The Role and Mechanisms of the Hypocretin System in Zebrafish ().

作者信息

Dyachuk Vyacheslav

机构信息

A.V. Zhirmunsky National Scientific Center of Marine Biology, Far Eastern Branch, Russian Academy of Sciences, 690041 Vladivostok, Russia.

出版信息

Int J Mol Sci. 2024 Dec 30;26(1):256. doi: 10.3390/ijms26010256.

Abstract

Sleep is the most important physiological function of all animals studied to date. Sleep disorders include narcolepsy, which is characterized by excessive daytime sleepiness, disruption of night sleep, and muscle weakness-cataplexy. Narcolepsy is known to be caused by the degeneration of orexin-synthesizing neurons (hypocretin (HCRT) neurons or orexin neurons) in the hypothalamus. In mammals, HCRT neurons primarily regulate the sleep/wake cycle, nutrition, reward seeking, and addiction development. The hypocretin system of the brain is involved in a number of neurological disorders. The distinctive pathologies associated with the disruption of HCRT neurons are narcolepsy and cataplexy, which are caused by the loss of hypocretin neurons that produce HCRT. In Danio, the hypocretin system is also involved in the regulation of sleep and wakefulness. It is represented by a single gene that encodes the peptides HCRT1 and HCRT2, as well as one HCRT receptor (HCRTR), which is structurally closest to the mammalian HCRTR2. The overexpression of the gene in larvae causes wakefulness, whereas the physical destruction of HCRT cells or a pharmacological blockade of the type 2 hypocretin receptor leads to fragmentation of sleep in fish larvae, which is also observed in patients with narcolepsy. These data confirm the evolutionary conservatism of the hypocretin system. Thus, is an ideal model for studying the functions of HCRT neural networks and their functions.

摘要

睡眠是迄今为止所研究的所有动物最重要的生理功能。睡眠障碍包括发作性睡病,其特征为日间过度嗜睡、夜间睡眠中断以及肌肉无力——猝倒。已知发作性睡病是由下丘脑中促食欲素合成神经元(下丘脑泌素(HCRT)神经元或促食欲素神经元)的退化所引起。在哺乳动物中,HCRT神经元主要调节睡眠/觉醒周期、营养、寻求奖励以及成瘾发展。大脑的下丘脑泌素系统涉及多种神经疾病。与HCRT神经元破坏相关的独特病理表现为发作性睡病和猝倒,这是由产生HCRT的下丘脑泌素神经元丧失所致。在斑马鱼中,下丘脑泌素系统也参与睡眠和觉醒的调节。它由一个单一基因所代表,该基因编码肽HCRT1和HCRT2,以及一个HCRT受体(HCRTR),其在结构上与哺乳动物的HCRTR2最为接近。该基因在斑马鱼幼体中的过表达会导致清醒,而HCRT细胞的物理破坏或2型下丘脑泌素受体的药理学阻断会导致斑马鱼幼体睡眠碎片化,这在发作性睡病患者中也有观察到。这些数据证实了下丘脑泌素系统的进化保守性。因此,斑马鱼是研究HCRT神经网络功能及其作用的理想模型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db98/11719587/044cf7c4eac0/ijms-26-00256-g001.jpg

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