College of Veterinary Medicine, Huazhong Agricultural University, Wuhan 430070, China.
Int J Mol Sci. 2020 Jan 31;21(3):968. doi: 10.3390/ijms21030968.
Numerous studies have verified that electroacupuncture (EA) can relieve neuropathic pain through a variety of mechanisms. Synaptotagmin 1 (Syt-1), a synaptic vesicle protein for regulating exocytosis of neurotransmitters, was found to be affected by EA stimulation. However, the roles of Syt-1 in neuropathic pain and EA-induced analgesic effect remain unclear. Here, the effect of Syt-1 on nociception was assessed through an antibody blockade, siRNA silencing, and lentivirus-mediated overexpression of spinal Syt-1 in rats with spared nerve injury (SNI). EA was used for stimulating bilateral "Sanjinjiao" and "Zusanli" acupoints of the SNI rats to evaluate its effect on nociceptive thresholds and spinal Syt-1 expression. The mechanically and thermally nociceptive behaviors were assessed with paw withdrawal threshold (PWT) and paw withdrawal latency (PWL) at different temperatures, respectively, at day 0, 7, 8, 14, and 20. Syt-1 mRNA and protein levels were determined with qRT-PCR and Western blot, respectively, and its distribution was observed with the immunohistochemistry method. The results demonstrated Syt-1 antibody blockade and siRNA silencing increased ipsilateral PWTs and PWLs of SNI rats, while Syt-1 overexpression decreased ipsilateral PWTs and PWLs of rats. EA significantly attenuated nociceptive behaviors and down-regulated spinal Syt-1 protein levels (especially in laminae I-II), which were reversed by Syt-1 overexpression. Our findings firstly indicate that Syt-1 is involved in the development of neuropathic pain and that EA attenuates neuropathic pain, probably through suppressing Syt-1 protein expression in the spinal cord.
大量研究证实电针(EA)通过多种机制缓解神经性疼痛。突触结合蛋白 1(Syt-1)作为一种调节神经递质释放的突触小泡蛋白,其表达受 EA 刺激影响。然而,Syt-1 在神经性疼痛和 EA 诱导的镇痛作用中的作用仍不清楚。本研究通过抗体阻断、siRNA 沉默和脊髓 Syt-1 的慢病毒过表达,评估 Syt-1 在 spared nerve injury(SNI)大鼠伤害感受中的作用。采用 EA 刺激 SNI 大鼠双侧“三阴交”和“足三里”穴位,评估其对痛觉阈值和脊髓 Syt-1 表达的影响。采用机械和热痛觉行为评估,分别于第 0、7、8、14 和 20 天检测大鼠的足底缩足反射阈值(PWT)和足底回缩潜伏期(PWL)。采用 qRT-PCR 和 Western blot 分别检测 Syt-1 mRNA 和蛋白水平,免疫组织化学方法观察其分布。结果显示,Syt-1 抗体阻断和 siRNA 沉默增加了 SNI 大鼠的同侧 PWT 和 PWL,而过表达 Syt-1 则降低了大鼠的同侧 PWT 和 PWL。EA 显著减轻痛觉行为,并下调脊髓 Syt-1 蛋白水平(尤其在 I-II 层),而过表达 Syt-1 则逆转了这一效应。本研究首次表明,Syt-1 参与神经性疼痛的发生,EA 减轻神经性疼痛,可能是通过抑制脊髓 Syt-1 蛋白表达。