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褪黑素对腰椎间盘突出症大鼠模型神经根性疼痛的影响

The Effect of Melatonin on Radicular Pain in a Rat Model of Lumbar Disc Herniation.

作者信息

Tang Qian, Huang YangLiang, Zhu LiRong, Zhang WeiLi, Zhao YuanShu, Zhong Yi

机构信息

Key Laboratory of Neuroscience, School of Basic Medical Science, Guangzhou Medical University, Guangzhou, China.

Institute of Neuroscience and Department of Neurology of the Second Affiliated Hospital of Guangzhou Medical University; Guangzhou, China.

出版信息

Spine (Phila Pa 1976). 2022 May 15;47(10):754-763. doi: 10.1097/BRS.0000000000004329. Epub 2022 Jan 31.

Abstract

STUDY DESIGN

Controlled, randomized, animal study.

OBJECTIVE

To investigate the effect of melatonin and its receptors on radicular pain and the possible mechanisms.

SUMMARY OF BACKGROUND DATA

Lumbar disc herniation (LDH) may induce radicular pain, but the mechanism is not clear and therapeutic effect is still poor. Previously we report central sensitization meaning potentiation of spinal nociceptive synaptic transmission is the critical cause of radicular pain. Melatonin (Mel) has been reported to promote hippocampal synaptic transmission and thus improve learning ability. But the effect of Mel on spinal synaptic transmission and radicular pain are not clear.

METHODS

Rat LDH model was induced by autologous nucleus pulposus (NP) implantation. Melatonin was delivered intraperitoneally four times a day, from day 1 to day 3 after surgery. Melatonin receptor agonist and antagonists were delivered intrathecally for 3 days as well. Mechanical and thermal pain thresholds were assessed by von Frey filaments and hotplate test respectively. Electrophysiological recording was employed for survey C-fiber evoked field potentials. The protein level of N- methyl-D-aspartate submit 2A (NR2A), NR2B, melatonin receptor 1 (MT1), and receptor 2 (MT2) was evaluated by western blotting. Spinal expression of calcitonin gene related peptides (CGRP), isolectin b4 (IB4), and neurofilament-200 (NF200) was displayed by immunofluorescence staining.

RESULTS

Melatonin significantly increased mechanical and thermal pain thresholds, lasting at least to day 5 after surgery. Melatonin decreased C-fiber evoked field potentials; decreased spinal NR2B protein level; reduced spinal CGRP, and IB4 expression. MT2 was upregulated after NP implantation and was co-localized with neuron and microglia. MT2 receptor agonist simulated the effect of Mel, and both MT receptor broadspectrum antagonist and MT2 specific antagonist abolished the effect of MT2 receptor agonist.

CONCLUSION

Melatonin alleviates radicular pain from LDH by inhibiting central sensitization via binding with its receptor 2, decreasing spinal CGRP, IB4, and NR2B expression.

摘要

研究设计

对照、随机动物研究。

目的

探讨褪黑素及其受体对神经根性疼痛的影响及可能机制。

背景资料总结

腰椎间盘突出症(LDH)可诱发神经根性疼痛,但其机制尚不清楚,治疗效果仍欠佳。此前我们报道中枢敏化即脊髓伤害性突触传递的增强是神经根性疼痛的关键原因。据报道,褪黑素(Mel)可促进海马突触传递,从而提高学习能力。但Mel对脊髓突触传递和神经根性疼痛的影响尚不清楚。

方法

通过自体髓核(NP)植入诱导大鼠LDH模型。术后第1天至第3天,每天腹腔注射褪黑素4次。褪黑素受体激动剂和拮抗剂也鞘内注射3天。分别采用von Frey细丝和热板试验评估机械性和热痛阈值。采用电生理记录检测C纤维诱发场电位。通过蛋白质免疫印迹法评估N - 甲基 - D - 天冬氨酸亚基2A(NR2A)、NR2B、褪黑素受体1(MT1)和受体2(MT2)的蛋白水平。通过免疫荧光染色显示脊髓中降钙素基因相关肽(CGRP)、异凝集素b4(IB4)和神经丝200(NF200)的表达。

结果

褪黑素显著提高机械性和热痛阈值,至少持续至术后第5天。褪黑素降低C纤维诱发场电位;降低脊髓NR2B蛋白水平;减少脊髓CGRP和IB4表达。NP植入后MT2上调,并与神经元和小胶质细胞共定位。MT2受体激动剂模拟了Mel的作用,MT受体广谱拮抗剂和MT2特异性拮抗剂均消除了MT2受体激动剂的作用。

结论

褪黑素通过与其受体2结合抑制中枢敏化,降低脊髓CGRP、IB4和NR2B表达,从而减轻LDH引起的神经根性疼痛。

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