4.7 Article

Disordered autonomic function during exposure to moderate heat or exercise in a mouse model of Dravet syndrome

期刊

NEUROBIOLOGY OF DISEASE
卷 147, 期 -, 页码 -

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.nbd.2020.105154

关键词

Dravet syndrome; Dysautonomia; Scn1a; Exercise; Ambient temperature

资金

  1. NYU Finding A Cure for Epilepsy & Seizures (NYU/FACES)
  2. Ryan Murphy SUDEP Research Fund at UW
  3. NIH/NINDS Grant [R01 NS102796]
  4. CURE Epilepsy Research Grant
  5. Ellenbogen Chair UW Neurosurgery Research Funds
  6. FACES

向作者/读者索取更多资源

The study revealed that in response to mild heat stress, DS mice displayed significantly blunted correction of body temperature, with less suppression of heart rate and respiration rate compared to WT mice. During exercise stress, DS mice showed a diminished increase in heart rate, followed by an exaggerated HR suppression and HRV elevation during recovery, indicating the presence of autonomic disturbances in DS mice.
Objective: 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). Methods: 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. Results: 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. Significance: 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.

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