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Kcna1 基因敲除小鼠(一种癫痫伴发的猝死模型)的呼吸功能障碍随年龄增长而进展。

Respiratory dysfunction progresses with age in Kcna1-null mice, a model of sudden unexpected death in epilepsy.

机构信息

Department of Pharmacology, Creighton University School of Medicine, Omaha, NE, USA.

Department of Pharmacology and Experimental Neuroscience, University of Nebraska Medical Center, Omaha, NE, USA.

出版信息

Epilepsia. 2018 Feb;59(2):345-357. doi: 10.1111/epi.13971. Epub 2018 Jan 12.

Abstract

OBJECTIVE

Increased breathing rate, apnea, and respiratory failure are associated with sudden unexpected death in epilepsy (SUDEP). We recently demonstrated the progressive nature of epilepsy and mortality in Kcna1 mice, a model of temporal lobe epilepsy and SUDEP. Here we tested the hypothesis that respiratory dysfunction progresses with age in Kcna1 mice, thereby increasing risk of respiratory failure and sudden death (SD).

METHODS

Respiratory parameters were determined in conscious mice at baseline and following increasing doses of methacholine (MCh) using noninvasive airway mechanics (NAM) systems. Kcna1 , Kcna1 , and Kcna1 littermates were assessed during 3 age ranges when up to ~30%, ~55%, and ~90% of Kcna1 mice have succumbed to SUDEP: postnatal day (P) 32-36, P40-46, and P48-56, respectively. Saturated arterial O (SaO ) was determined with pulse oximetry. Lung and brain tissues were isolated and Kcna1 gene and protein expression were evaluated by reverse transcriptase quantitative polymerase chain reaction (RT-qPCR) and Western blot techniques. Airway smooth muscle responsiveness was assessed in isolated trachea exposed to MCh.

RESULTS

Kcna1 mice experienced an increase in basal respiratory drive, chronic oxygen desaturation, frequent apnea-hypopnea (A-H), an atypical breathing sequence of A-H-tachypnea-A-H, increased tidal volume, and hyperventilation induced by MCh. The MCh-provoked hyperventilation was dramatically attenuated with age. Of interest, only Kcna1 mice developed seizures following exposure to MCh. Seizures were provoked by lower concentrations of MCh as Kcna1 mice approached SD. MCh-induced seizures experienced by a subset of younger Kcna1 mice triggered death. Respiratory parameters of these younger Kcna1 mice resembled older near-SD Kcna1 mice. Kcna1 gene and protein were not expressed in Kcna1 and Kcna1 lungs, and MCh-mediated airway smooth muscle contractions exhibited similar half-maximal effective concentration( EC ) in isolated Kcna1 and Kcna1 trachea.

SIGNIFICANCE

The Kcna1 model of SUDEP exhibits progressive respiratory dysfunction, which suggests a potential increased susceptibility for respiratory failure during severe seizures that may result in sudden death.

摘要

目的

呼吸频率加快、呼吸暂停和呼吸衰竭与癫痫猝死(SUDEP)有关。我们最近证明了 Kcna1 小鼠(颞叶癫痫和 SUDEP 的模型)癫痫和死亡率的进行性特征。在这里,我们测试了这样一个假设,即在 Kcna1 小鼠中,呼吸功能障碍随年龄的增长而进展,从而增加呼吸衰竭和突然死亡(SD)的风险。

方法

使用非侵入性气道力学(NAM)系统,在清醒的小鼠中,在基线时和给予越来越多的乙酰甲胆碱(MCh)后,确定呼吸参数。在 Kcna1 、 Kcna1 和 Kcna1 同窝仔鼠分别经历高达约 30%、约 55%和约 90%的 SUDEP 时,评估了 3 个年龄范围的呼吸参数:出生后第 32-36 天、第 40-46 天和第 48-56 天。用脉搏血氧仪测定动脉血氧饱和度(SaO )。分离肺和脑组织,通过逆转录定量聚合酶链反应(RT-qPCR)和 Western blot 技术评估 Kcna1 基因和蛋白表达。用 MCh 暴露分离的气管,评估气道平滑肌的反应性。

结果

Kcna1 小鼠的基础呼吸驱动力增加、慢性氧饱和度降低、频繁的呼吸暂停-低通气(A-H)、A-H-呼吸急促-A-H 的异常呼吸序列、潮气量增加和 MCh 诱导的过度通气。随着年龄的增长,MCh 引起的过度通气明显减弱。有趣的是,只有 Kcna1 小鼠在暴露于 MCh 后才会出现癫痫发作。随着 Kcna1 小鼠接近 SD,较低浓度的 MCh 就可以引发癫痫发作。一小部分较年轻的 Kcna1 小鼠在经历 MCh 诱导的癫痫发作后死亡。这些年轻的 Kcna1 小鼠的呼吸参数与接近 SD 的年长的 Kcna1 小鼠相似。Kcna1 基因和蛋白在 Kcna1 和 Kcna1 肺中均不表达,MCh 介导的气道平滑肌收缩在分离的 Kcna1 和 Kcna1 气管中的半最大有效浓度(EC )相似。

意义

SUDEP 的 Kcna1 模型表现出进行性呼吸功能障碍,这表明在严重癫痫发作期间呼吸衰竭的易感性增加,可能导致突然死亡。

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本文引用的文献

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Genetic Basis of Sudden Unexpected Death in Epilepsy.癫痫性猝死的遗传基础
Front Neurol. 2017 Jul 20;8:348. doi: 10.3389/fneur.2017.00348. eCollection 2017.
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Functional hemodynamic monitoring.功能性血流动力学监测
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