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反复发作的癫痫导致 SS 大鼠进行性通气功能障碍。

Repeated seizures lead to progressive ventilatory dysfunction in SS rats.

机构信息

Department of Physiology, Medical College of Wisconsin, Milwaukee, Wisconsin, United States.

Division of Nephrology, Department of Medicine, Medical University of South Carolina, Charleston, South Carolina, United States.

出版信息

J Appl Physiol (1985). 2023 Oct 1;135(4):872-885. doi: 10.1152/japplphysiol.00072.2023. Epub 2023 Aug 3.

Abstract

Patients with uncontrolled epilepsy experience repeated seizures putting them at increased risk for sudden unexpected death in epilepsy (SUDEP). Data from human patients have led to the hypothesis that SUDEP results from severe cardiorespiratory suppression after a seizure, which may involve pathological deficiencies in the brainstem serotonin (5-HT) system. Rats with a genomic mutation (SS rats) are susceptible to sound-induced generalized tonic-clonic seizures (GTCS) which, when repeated once daily for up to 10 days (10-day seizure protocol), increased mortality, particularly in male rats. Here, we test the hypothesis that repeated seizures across the 10-day protocol will cause a progressive ventilatory dysfunction due to time-dependent 5-HT deficiency. Initial severe seizures led to ictal and postictal apneas and transient decreases in breathing frequency, ventilatory drive, breath-to-breath variability, and brief hypoventilation. These seizure-induced effects on ventilation were exacerbated with increasing seizures and ventilatory chemoreflexes became further impaired after repeated seizures. Tissue analyses of key brainstem regions controlling breathing showed time-dependent 5-HT system suppression and increased immunoreactivity for IBA-1 (microglial marker) without changes in overall cell counts at 3, 7, and 10 days of seizures. Fluoxetine treatment in SS rats prevented repeated seizure-induced progressive respiratory suppression but failed to prevent seizure-related mortality. We conclude that repeated seizures cause a progressive compromise of ventilatory control in the immediate postictal period largely mediated by serotonin system suppression in brainstem regions of respiratory control. However, other unknown factors contribute to overall survival following repeated seizures in this model. This study demonstrated that repeated seizures in a novel rat model (SS rats) caused a progressively greater ventilatory dysfunction in the immediate postictal period associated with brainstem serotonin (5-HT) suppression. Augmenting brain 5-HT with a selective serotonin reuptake inhibitor prevented the progressive ventilatory dysfunction induced by repeated seizures but failed to prevent seizure-related mortality, suggesting that repeated seizures may lead to cardiorespiratory suppression and failure through multiple mechanisms.

摘要

患有未控制的癫痫的患者会反复出现癫痫发作,使他们面临癫痫猝死 (SUDEP) 的风险增加。来自人类患者的数据导致了这样的假设,即 SUDEP 是由于癫痫发作后严重的心肺抑制引起的,这可能涉及脑干 5-羟色胺(5-HT)系统的病理性缺乏。具有基因组 突变的大鼠(SS 大鼠)易患声音诱导的全身强直阵挛性癫痫发作(GTCS),当每天重复一次,持续 10 天(10 天癫痫发作方案)时,死亡率增加,特别是雄性大鼠。在这里,我们测试了这样的假设,即在 10 天方案中反复的癫痫发作将由于时间依赖性 5-HT 缺乏而导致进行性通气功能障碍。最初的严重癫痫发作导致癫痫发作期和发作后期的呼吸暂停以及呼吸频率、通气驱动、呼吸间变异性和短暂的低通气短暂降低。随着癫痫发作次数的增加,这些癫痫发作引起的通气效应加剧,并且重复癫痫发作后通气化学反射进一步受损。控制呼吸的关键脑干区域的组织分析显示,5-HT 系统的抑制随时间推移而增加,并且在 3、7 和 10 天癫痫发作后,IBA-1(小胶质细胞标志物)的免疫反应性增加,而总体细胞计数没有变化。SS 大鼠中的氟西汀治疗可预防重复癫痫发作引起的进行性呼吸抑制,但未能预防与癫痫发作相关的死亡率。我们得出结论,重复的癫痫发作会导致在即刻癫痫发作后期呼吸控制的进行性损害,主要由呼吸控制的脑干区域中 5-HT 系统的抑制介导。然而,在这种模型中,其他未知因素导致重复癫痫发作后的总体存活。本研究表明,在新型大鼠模型(SS 大鼠)中,重复癫痫发作会导致即刻癫痫发作后期呼吸功能障碍进行性加重,与脑干 5-HT(5-HT)抑制有关。用选择性 5-羟色胺再摄取抑制剂增强脑 5-HT 可预防重复癫痫发作引起的进行性通气功能障碍,但未能预防与癫痫发作相关的死亡率,这表明重复癫痫发作可能通过多种机制导致心肺抑制和衰竭。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0447/10642517/3ddf9c704498/jappl-00072-2023r01.jpg

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