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一种用于诱导小鼠慢性间歇性低氧的新型可调节自动化系统。

A novel adjustable automated system for inducing chronic intermittent hypoxia in mice.

作者信息

Polšek Dora, Bago Marcel, Živaljić Marija, Rosenzweig Ivana, Lacza Zsombor, Gajović Srećko

机构信息

Croatian Institute for Brain Research, University of Zagreb School of Medicine, Zagreb, Croatia.

Institute of Clinical Experimental Research, Semmelweis University, Budapest, Hungary.

出版信息

PLoS One. 2017 Mar 31;12(3):e0174896. doi: 10.1371/journal.pone.0174896. eCollection 2017.

Abstract

BACKGROUND

Sleep apnea is a chronic, widely underdiagnosed condition characterized by disruption of sleep architecture and intermittent hypoxia due to short cessations of breathing. It is a major independent risk factor for myocardial infarction, congestive heart failure and stroke as well as one of the rare modifiable risk factors for Alzheimer's Dementia. Reliable animal disease models are needed to understand the link between sleep apnea and the various clinically linked disorders.

NEW METHOD

An automated system for inducing hypoxia was developed, in which the major improvement was the possibility to efficiently adjust the length and intensity of hypoxia in two different periods. The chamber used a small volume of gas allowing for fast exchanges of different oxygen levels. The mice were kept in their cages adapted with the system on the cage lid. As a proof of principle, they were exposed to a three week period of intermittent hypoxia for 8 hours a day, with 90 s intervals of 5, 7% and 21% oxygen to validate the model. Treated (n = 8) and control mice (no hypoxia, n = 7) were handled in the same manner and their hippocampal brain regions compared by histology.

RESULTS

The chamber provided a fast, reliable and precise intermittent hypoxia, without inducing noticeable side effects to the animals. The validation experiment showed that apoptotic neurons in the hippocampus were more numerous in the mice exposed to intermittent hypoxia than in the control group, in all tested hippocampal regions (cornu ammonis 1 (CA1) P <0.001; cornu ammonis 3 (CA3) P <0.001; and dentate gyrus (DG) P = 0.023). In both, control and hypoxic conditions, there was a significantly higher number of apoptotic neurons in the DG compared to the CA1 and CA3 subfields (P <0.001).

CONCLUSION

The new design of a hypoxic chamber provides a fast, adjustable and reliable model of obstructive sleep apnea, which was validated by apoptosis of hippocampal neurons.

摘要

背景

睡眠呼吸暂停是一种慢性疾病,普遍存在诊断不足的情况,其特征是睡眠结构紊乱以及因呼吸短暂停止导致间歇性缺氧。它是心肌梗死、充血性心力衰竭和中风的主要独立危险因素,也是阿尔茨海默病中少数可改变的危险因素之一。需要可靠的动物疾病模型来理解睡眠呼吸暂停与各种临床相关疾病之间的联系。

新方法

开发了一种用于诱导缺氧的自动化系统,其主要改进之处在于能够在两个不同阶段有效调节缺氧的时长和强度。该实验箱使用少量气体,可实现不同氧气水平的快速交换。小鼠饲养在其笼子中,笼子盖子上适配了该系统。作为原理验证,它们每天暴露于间歇性缺氧环境8小时,为期三周,期间以90秒的间隔交替给予5%、7%和21%的氧气,以验证该模型。对经过处理的小鼠(n = 8)和对照小鼠(未缺氧,n = 7)采用相同方式处理,并通过组织学比较它们的海马脑区。

结果

该实验箱提供了快速、可靠且精确的间歇性缺氧,且未对动物产生明显副作用。验证实验表明,在所有测试的海马区域(海马1区(CA1)P <0.001;海马3区(CA3)P <0.001;齿状回(DG)P = 0.023),暴露于间歇性缺氧的小鼠海马中凋亡神经元比对照组更多。在对照和缺氧条件下,与CA1和CA3亚区相比,DG中的凋亡神经元数量均显著更高(P <0.001)。

结论

缺氧实验箱的新设计提供了一种快速、可调节且可靠的阻塞性睡眠呼吸暂停模型,该模型通过海马神经元凋亡得到了验证。

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