Sahai Nikhil, Bard Angela M, Devinsky Orrin, Kalume Franck
Center for Integrative Brain Research, Seattle Children's Research Institute, Seattle, WA 98101, USA.
Department of Neurology, NYU Langone Medical Center, New York, NY 10016, USA.
Neurobiol Dis. 2021 Jan;147:105154. doi: 10.1016/j.nbd.2020.105154. Epub 2020 Nov 2.
To examine autonomic regulation of core body temperature, heart rate (HR), and breathing rate (BR) in response to moderately elevated ambient temperature or moderate physical exercise in a mouse model of Dravet syndrome (DS).
We studied video-EEG, ECG, respiration, and temperature in mice with global heterozygous Scn1a knockout (KO) (DS mice), interneuron specific Scn1a KO, and wildtype (WT) mice during exposure to increased environmental temperature and moderate treadmill exercise.
Core body temperatures of WT and DS mice were similar during baseline. After 15 mins of heat exposure, the peak value was lower in DS than WT mice. In the following mins of heat exposure, the temperature slowly returned close to baseline level in WT, whereas it remained elevated in DS mice. KO of Scn1a in GABAergic neurons caused similar thermoregulatory deficits in mice. During exercise, the HR increase was less prominent in DS than WT mice. After exercise, the HR was significantly more suppressed in DS. The heart rate variability (HRV) was lower in DS than WT mice during baseline and higher in DS during exercise-recovery periods.
We found novel abnormalities that expand the spectrum of interictal, ictal, and postictal autonomic dysregulation in DS mice. During mild heat stress, there was a significantly blunted correction of body temperature, and a less suppression of both HR and respiration rate in DS than WT mice. These effects were seen in mice with selective KO of Scn1A in GABAergic neurons. During exercise stress, there was diminished increase in HR, followed by an exaggerated HR suppression and HRV elevation during recovery in DS mice compared to controls. These findings suggest that different environmental stressors can uncover distinct autonomic disturbances in DS mice. Interneurons play an important role in thermoregulation. Understanding the spectrum and mechanisms of autonomic disorders in DS may help develop more effective strategies to prevent seizures and SUDEP.
在Dravet综合征(DS)小鼠模型中,研究核心体温、心率(HR)和呼吸频率(BR)对适度升高的环境温度或适度体育锻炼的自主调节情况。
我们在环境温度升高和适度跑步机运动期间,研究了全球杂合Scn1a基因敲除(KO)小鼠(DS小鼠)、中间神经元特异性Scn1a基因敲除小鼠和野生型(WT)小鼠的视频脑电图、心电图、呼吸和体温。
基线时WT和DS小鼠的核心体温相似。热暴露15分钟后,DS小鼠的峰值低于WT小鼠。在接下来的热暴露分钟内,WT小鼠的温度缓慢恢复到接近基线水平,而DS小鼠的温度仍保持升高。GABA能神经元中Scn1a基因敲除在小鼠中导致类似的体温调节缺陷。运动期间,DS小鼠的心率增加不如WT小鼠明显。运动后,DS小鼠的心率受到更明显的抑制。在基线时,DS小鼠的心率变异性(HRV)低于WT小鼠,在运动恢复期间DS小鼠的HRV较高。
我们发现了新的异常情况,扩展了DS小鼠发作间期、发作期和发作后期自主神经调节障碍的范围。在轻度热应激期间,DS小鼠的体温校正明显减弱,心率和呼吸频率的抑制均低于WT小鼠。在GABA能神经元中选择性敲除Scn1A的小鼠中也观察到了这些效应。在运动应激期间,DS小鼠的心率增加减少,随后在恢复期间与对照组相比,心率抑制过度且HRV升高。这些发现表明,不同的环境应激源可揭示DS小鼠不同的自主神经紊乱。中间神经元在体温调节中起重要作用。了解DS自主神经障碍的范围和机制可能有助于制定更有效的策略来预防癫痫发作和不明原因的癫痫猝死(SUDEP)。