Weldon School of Biomedical Engineering, Purdue University, West Lafayette, IN, USA.
Department of Electrical and Computer Engineering, Johns Hopkins University, Baltimore, MD, USA.
Epilepsy Behav. 2022 Nov;136:108918. doi: 10.1016/j.yebeh.2022.108918. Epub 2022 Oct 3.
To investigate carotid body (CB) mechanisms related to sudden death during seizure. Ictal activation of oxygen-conserving reflexes (OCRs) can trigger fatal cardiorespiratory collapse in seizing rats, which presents like human sudden unexpected death in epilepsy (SUDEP). The CB is strongly implicated in OCR pathways; we hypothesize that modulating CB activity will provide insight into these mechanisms of death.
Long-Evans rats were anesthetized with urethane. Recordings included: electrocorticography, electrocardiography, respiration via nasal thermocouple, and blood pressure (BP). The mammalian diving reflex (MDR) was activated by cold water delivered through a nasal cannula. Reflex and stimulation trials were repeated up to 16 times (4 pre-intervention, 12 post-intervention) or until death. In some animals, one or both carotid bodies were denervated. In some animals, the CB was electrically stimulated, both with and without MDR. Seizures were induced with kainic acid (KA).
Animals without seizure and with no CB modulation survived all reflexes. Non-seizing animals with CB denervation survived 7.1 ± 5.4 reflexes before death, and only 1 of 7 survived past the 12-trial threshold. Electrical CB stimulation without seizure and without reflex caused significant tachypnea and hypotension. Electrical CB stimulation with seizure and without reflex required higher amplitudes to replicate the physiological responses seen outside seizure. Seizing animals without CB intervention survived 3.2 ± 3.6 trials (per-reflex survival rate 42.0% ± 44.4%), and 0 of 7 survived past the 12-trial threshold. Seizing animals with electrical CB stimulation survived 10.5 ± 4.7 ictal trials (per-reflex survival rate 86.3% ± 35.0%), and 6 of 8 survived past the 12-trial threshold.
These results suggest that, during seizure, the ability of the CB to stimulate a restart of respiration is impaired. The CB and its afferents may be relevant to fatal ictal apnea and SUDEP in humans, and CB stimulation may be a relevant intervention technique in these deaths.
研究与癫痫发作期间猝死相关的颈动脉体 (CB) 机制。发作期间氧合反射 (OCR) 的即刻激活可引发发作大鼠致命的心肺衰竭,类似于人类癫痫猝死 (SUDEP)。CB 强烈参与 OCR 通路;我们假设调节 CB 活性将为这些死亡机制提供深入了解。
长爪沙鼠用氨基甲酸乙酯麻醉。记录包括:皮层电图、心电图、通过鼻腔热电偶的呼吸以及血压 (BP)。通过鼻腔套管输送冷水来激活哺乳动物潜水反射 (MDR)。反射和刺激试验重复进行多达 16 次(4 次预处理,12 次后处理)或直至死亡。在一些动物中,一侧或两侧颈动脉体被去神经支配。在一些动物中,电刺激 CB,同时进行和不进行 MDR。用海人酸 (KA) 诱导癫痫发作。
无癫痫发作且无 CB 调节的动物在所有反射中均存活。无 CB 去神经支配且无癫痫发作的非发作动物在死亡前存活了 7.1±5.4 次反射,只有 7 只动物中的 1 只存活过 12 次试验阈值。无癫痫发作和无反射的电刺激 CB 引起明显的呼吸急促和低血压。有癫痫发作和无反射的电刺激 CB 需要更高的振幅才能复制发作外观察到的生理反应。无 CB 干预的癫痫发作动物存活了 3.2±3.6 次试验(每次反射存活率为 42.0%±44.4%),只有 7 只动物中的 0 只存活过 12 次试验阈值。有电刺激 CB 的癫痫发作动物存活了 10.5±4.7 次癫痫发作(每次反射存活率为 86.3%±35.0%),8 只动物中有 6 只存活过 12 次试验阈值。
这些结果表明,在癫痫发作期间,CB 刺激呼吸恢复的能力受损。CB 及其传入神经可能与人类致命性癫痫发作性呼吸暂停和 SUDEP 相关,CB 刺激可能是这些死亡的相关干预技术。