急性睡眠不足会加重硝酸甘油诱发的小鼠痛觉减退。

IF 2.8 3区 医学 Q2 NEUROSCIENCES
Zhe Yu, Bozhi Li, Wenjing Tang, Zhao Dong, Ruozhuo Liu, Shengyuan Yu
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引用次数: 0

摘要

睡眠不足会诱发偏头痛,偏头痛患者在急性偏头痛期间往往会选择睡眠来缓解头痛。本研究旨在探讨急性睡眠剥夺对硝酸甘油诱发小鼠痛觉减退的影响。在第一部分中,小鼠被剥夺睡眠6小时或正常睡眠6小时后,腹腔注射硝酸甘油或生理盐水。接下来,对新的小鼠进行同样的睡眠剥夺和注射程序,并在注射后 4.5 小时将小鼠处死。取三叉神经尾核和上颈椎段进行免疫荧光 Fos 染色。在第二部分中,注射生理盐水或硝酸甘油后,剥夺小鼠睡眠 6 小时或让小鼠在不受干扰的情况下睡眠。第三部分比较了小鼠腹腔注射生理盐水或硝酸甘油后的睡眠时间。剥夺睡眠 6 小时不会导致小鼠的基线痛阈值发生任何变化。然而,剥夺睡眠 6 小时可显著延长硝酸甘油诱导的痛觉减退持续时间。此外,6 小时睡眠剥夺和硝酸甘油组小鼠在 4.5 小时时的 Fos 表达明显高于其他三组。如果先进行腹腔注射,硝酸甘油组和剥夺睡眠6小时组的后爪机械痛阈值明显低于其他组。与注射生理盐水相比,一次性注射硝酸甘油会导致正常小鼠的睡眠潜伏期明显延长,睡眠时间明显缩短。急性睡眠剥夺会明显加重硝酸甘油诱导的小鼠痛觉减退,这凸显了睡眠障碍对偏头痛的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Acute sleep deprivation aggravates nitroglycerin-evoked hyperalgesia in mice.

Acute sleep deprivation aggravates nitroglycerin-evoked hyperalgesia in mice.

Acute sleep deprivation aggravates nitroglycerin-evoked hyperalgesia in mice.

Acute sleep deprivation aggravates nitroglycerin-evoked hyperalgesia in mice.

Sleep deprivation can trigger migraine, and migraineurs often choose to sleep to relieve headaches during acute migraine. This study aimed to explore the effect of acute sleep deprivation on hyperalgesia induced by nitroglycerin in mice. In part one, after either 6-h sleep deprivation or 6-h normal sleep, mice were intraperitoneally injected with nitroglycerin or saline. The mechanical pain threshold and withdrawal latency of the hindpaw were measured every 30 min for 6 h. Next, the same sleep deprivation and injection procedure was performed with new mice, and mice were sacrificed 4.5 h after injection. The trigeminal nucleus caudalis and upper cervical spinal segments were taken for immunofluorescence Fos staining. In part two, after injection of saline or nitroglycerin, the mice were either deprived of sleep for 6 h or allowed to sleep without interference. The mechanical and thermal pain threshold were measured after 6 h. In part three, we compared the sleep time of mice after intraperitoneal injection of saline or nitroglycerin without interference. Sleep deprivation for 6 h did not cause any changes in the baseline pain thresholds in mice. However, pretreatment with 6-h sleep deprivation significantly prolonged the duration of hyperalgesia induced by nitroglycerin. Additionally, the expression of Fos at 4.5 h was significantly higher in the 6-h sleep deprivation and nitroglycerin group than in the other three groups. When intraperitoneal injection was given first, the mechanical pain threshold of the hind paw was significantly lower in the group that received nitroglycerin with 6-h sleep deprivation than in the other groups. Compared to the saline injection, one-time nitroglycerin injection would result in a significant increase in sleep latency and decrease in sleep duration for the normal mice. Acute sleep deprivation significantly aggravated the hyperalgesia induced by nitroglycerin in mice, which highlights the importance of sleep disorders for migraine.

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来源期刊
Molecular Pain
Molecular Pain 医学-神经科学
CiteScore
5.60
自引率
3.00%
发文量
56
审稿时长
6-12 weeks
期刊介绍: Molecular Pain is a peer-reviewed, open access journal that considers manuscripts in pain research at the cellular, subcellular and molecular levels. Molecular Pain provides a forum for molecular pain scientists to communicate their research findings in a targeted manner to others in this important and growing field.
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