Zhang Wei, Bai Yang, Qiao Yu, Wang Jian, Li Meng-Ying, Wang Jing-Wen, Jia Na, Chen Tao, Li Yun-Qing, Wen Ai-Dong
Department of Pharmacy, Xijing Hospital, The Fourth Military Medical University, Xi'an, China.
Department of Anatomy and K. K. Leung Brain Research Centre, The Fourth Military Medical University, Xi'an, China.
Front Cell Neurosci. 2018 Mar 8;12:54. doi: 10.3389/fncel.2018.00054. eCollection 2018.
(; Benth.) Kudo is an effective traditional herb in the clinical treatment of chronic pain syndromes in China. 8-O-acetyl shanzhiside methylester (8-OaS), a chief component in , possesses potent immunosuppressive activities and favorable analgesic effects. This study was proposed to compare the analgesic effects of 8-OaS with those of lidocaine and ketamine in a spinal nerve ligation (SNL) model by behavioral tests, and then investigated its effects upon the expression of spinal glial fibrillary acidic protein (GFAP), phosphorylated extracellular regulated protein kinases (pERK) and tumor necrosis factor-alpha (TNF-α) via immunofluorescence staining and western blot analyses. The data showed consecutive intrathecal injection of 8-OaS for 2 weeks brought about remarkable palliation of neuropathic pain (NP), possessing similar anti-allodynia effects with those of lidocaine and ketamine. Two weeks after surgery, pERK within the spinal dorsal horn was mainly expressed in astrocytes more than neurons and microglia, and 8-OaS inhibited spinal astrocytic activation and TNF-α expression. Finally, co-treatment of 8-OaS and PD98059 (an Extracellular signal-regulated kinase, ERK inhibitor) did not lead to remarkable increase in pain relief or TNF-α expression comparing to rats treated with 8-OaS or PD98059 alone. In conclusion, the anti-nociceptive effects of 8-OaS in the condition of NP relied on the inhibition of SNL-induced astrocyte activation, probably via the down-regulation of the ERK/TNF-α pathway.
(; 本特。) 苦豆是中国临床治疗慢性疼痛综合征的一种有效传统草药。8-O-乙酰山栀苷甲酯(8-OaS)是苦豆中的主要成分,具有强大的免疫抑制活性和良好的镇痛作用。本研究旨在通过行为学测试比较8-OaS与利多卡因和氯胺酮在脊髓神经结扎(SNL)模型中的镇痛效果,然后通过免疫荧光染色和蛋白质免疫印迹分析研究其对脊髓胶质纤维酸性蛋白(GFAP)、磷酸化细胞外调节蛋白激酶(pERK)和肿瘤坏死因子-α(TNF-α)表达的影响。数据显示,连续鞘内注射8-OaS 2周可显著减轻神经性疼痛(NP),其抗痛觉过敏作用与利多卡因和氯胺酮相似。手术后2周,脊髓背角内的pERK主要在星形胶质细胞中表达,而非神经元和小胶质细胞,且8-OaS可抑制脊髓星形胶质细胞活化和TNF-α表达。最后,与单独使用8-OaS或PD98059(一种细胞外信号调节激酶,ERK抑制剂)治疗的大鼠相比,8-OaS与PD98059联合治疗并未导致疼痛缓解或TNF-α表达显著增加。总之,8-OaS在NP条件下的抗伤害感受作用可能依赖于通过下调ERK/TNF-α途径抑制SNL诱导的星形胶质细胞活化。