Suppr超能文献

发作性睡病中组胺能结节乳头体神经元的增加。

Increase of histaminergic tuberomammillary neurons in narcolepsy.

机构信息

Department of Neurology, Beth Israel Deaconess Medical Center, Boston, MA; Department of Neurology, University Hospital of Zurich, Zurich, Switzerland.

出版信息

Ann Neurol. 2013 Dec;74(6):794-804. doi: 10.1002/ana.24019.

Abstract

OBJECTIVE

Narcolepsy is caused by loss of the hypothalamic neurons producing the orexin/hypocretin neuropeptides. One key target of the orexin system is the histaminergic neurons of the tuberomammillary nucleus (TMN), an essential wake-promoting system. As cerebrospinal fluid histamine levels may be low in patients with narcolepsy, we examined histaminergic neurons in patients with narcolepsy and in 2 mouse models of narcolepsy.

METHODS

We counted the number of hypothalamic neurons producing orexin, melanin-concentrating hormone, and histamine in 7 narcolepsy patients and 12 control subjects using stereological techniques. We identified histaminergic neurons using immunostaining for histidine decarboxylase. We also examined these systems in 6 wild-type mice, 6 orexin/ataxin-3 transgenic mice, and 5 orexin ligand knockout mice.

RESULTS

Compared to controls, narcolepsy patients had 94% more histaminergic TMN neurons (233,572 ± 49,476 vs 120,455 ± 10,665, p < 0.001). This increase was higher in 5 narcolepsy patients with >90% orexin neuron loss than in 2 patients with ≤75% orexin neuron loss (252,279 ± 46,264 vs 186,804 ± 1,256, p = 0.03). Similarly, the number of histaminergic TMN neurons was increased 53% in orexin ligand knockout mice compared to wild-type mice, whereas orexin/ataxin-3 transgenic mice showed an intermediate 28% increase.

INTERPRETATION

This surprising increase in histaminergic neurons in narcolepsy may be a compensatory response to loss of excitatory drive from the orexin neurons and may contribute to some of the symptoms of narcolepsy such as preserved consciousness during cataplexy and fragmented nighttime sleep. In addition, this finding may have therapeutic implications, as medications that enhance histamine signaling are now under development.

摘要

目的

发作性睡病是由产生食欲素/下丘脑分泌素神经肽的下丘脑神经元丧失引起的。食欲素系统的一个关键靶点是结节乳头核(TMN)中的组胺能神经元,TMN 是促进觉醒的重要系统。由于发作性睡病患者脑脊液中的组胺水平可能较低,我们检查了发作性睡病患者和 2 种发作性睡病小鼠模型中的组胺能神经元。

方法

我们使用立体学技术对 7 名发作性睡病患者和 12 名对照者的下丘脑产生食欲素、黑色素浓缩激素和组胺的神经元数量进行计数。我们使用组氨酸脱羧酶免疫染色来鉴定组胺能神经元。我们还在 6 只野生型小鼠、6 只食欲素/ataxin-3 转基因小鼠和 5 只食欲素配体敲除小鼠中检查了这些系统。

结果

与对照组相比,发作性睡病患者的 TMN 组胺能神经元增加了 94%(233572 ± 49476 比 120455 ± 10665,p < 0.001)。在 5 名食欲素神经元丢失>90%的发作性睡病患者中,这种增加高于 2 名食欲素神经元丢失≤75%的患者(252279 ± 46264 比 186804 ± 1256,p = 0.03)。同样,与野生型小鼠相比,食欲素配体敲除小鼠的 TMN 组胺能神经元数量增加了 53%,而食欲素/ataxin-3 转基因小鼠则增加了 28%。

结论

发作性睡病中组胺能神经元的这种惊人增加可能是对来自食欲素神经元的兴奋性驱动丧失的代偿性反应,可能导致发作性睡病的一些症状,如猝倒期间意识保留和夜间睡眠片段化。此外,这一发现可能具有治疗意义,因为目前正在开发增强组胺信号的药物。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验