脊髓
医学
坐骨神经
小胶质细胞
神经病理性疼痛
刺激
伤害
米诺环素
神经营养因子
腰脊髓
神经科学
麻醉
内分泌学
内科学
炎症
化学
生物
受体
抗生素
精神科
生物化学
作者
Bin Shu,Shao-Qiu He,Yun Guan
出处
期刊:Neuroscience Bulletin
[Springer Science+Business Media]
日期:2020-09-05
卷期号:36 (12): 1441-1453
被引量:29
标识
DOI:10.1007/s12264-020-00568-6
摘要
Microglia can modulate spinal nociceptive transmission. Yet, their role in spinal cord stimulation (SCS)-induced pain inhibition is unclear. Here, we examined how SCS affects microglial activation in the lumbar cord of rats with chronic constriction injury (CCI) of the sciatic nerve. Male rats received conventional SCS (50 Hz, 80% motor threshold, 180 min, 2 sessions/day) or sham stimulation on days 18-20 post-CCI. SCS transiently attenuated the mechanical hypersensitivity in the ipsilateral hind paw and increased OX-42 immunoreactivity in the bilateral dorsal horns. SCS also upregulated the mRNAs of M1-like markers, but not M2-like markers. Inducible NOS protein expression was increased, but brain-derived neurotrophic factor was decreased after SCS. Intrathecal minocycline (1 μg-100 μg), which inhibits microglial activation, dose-dependently attenuated the mechanical hypersensitivity. Pretreatment with low-dose minocycline (1 μg, 30 min) prolonged the SCS-induced pain inhibition. These findings suggest that conventional SCS may paradoxically increase spinal M1-like microglial activity and thereby compromise its own ability to inhibit pain.
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