Central Laboratory, Nanjing Municipal Hospital of Chinese Medicine, The Third Affiliated Hospital of Nanjing University of Chinese Medicine, Nanjing, 210001, China.
Department of pediatrics, Nanjing Municipal Hospital of Chinese Medicine, The Third Affiliated Hospital of Nanjing University of T.C.M, Nanjing, 210001, China.
Metab Brain Dis. 2017 Dec;32(6):1929-1934. doi: 10.1007/s11011-017-0084-3. Epub 2017 Aug 9.
Tourette syndrome (TS) is a neurological disorder characterized by highest familial recurrence rate among neuropsychiatric diseases with complicated inheritance. Recurrence of Tourette syndrome was frequently observed in clinical. Unexpectedly, the mechanism of recurrence of Tourette syndrome was failure to elucidate. Here, we first shown that lipopolysaccharide(LPS) may played an important role in the recurrence of Tourette syndrome. The TS model in rats was induced by DOI (the selective 5-HT2A/2C agonist 1-(2, 5-dimethoxy-4-iodophenyl) -2- aminopropane). The rats were randomly divided into 4 groups:(1)Control;(2) Control + LPS; (2)TS; (3)TS + LPS. The results demonstrated that the LPS treatment significantly increased stereotypic score and autonomic activity. LPS treatment also significantly increased inflammatory cytokines such as interleukin-6 (IL-6), interleukin-1β (IL-1β) and tumor necrosis factor-α (TNF-α) in serum and striatum. Also, highly expressed TLR4, MyD88, P-NF-κBp65, P-IκBα in TS rats were increased respectively by LPS treatment as indicted in western blot analysis and immunohistochemistry analysis. Thus, it was supposed that lipopolysaccharide(LPS) may played an important role in the recurrence of Tourette syndrome and its mechanism was related to TLR/NF-κB pathway.
妥瑞氏症候群(TS)是一种神经系统疾病,具有神经精神疾病中最高的家族复发率,其遗传方式复杂。在临床中经常观察到妥瑞氏症候群的复发。出乎意料的是,妥瑞氏症候群复发的机制尚未阐明。在这里,我们首次表明脂多糖(LPS)可能在妥瑞氏症候群的复发中起重要作用。通过使用 DOI(5-羟色胺 2A/2C 受体选择性激动剂 1-(2,5-二甲氧基-4-碘苯基)-2-氨基丙烷)诱导大鼠 TS 模型。大鼠被随机分为 4 组:(1)对照组;(2)对照组+LPS;(3)TS 组;(4)TS+LPS 组。结果表明,LPS 处理显著增加刻板评分和自主活动。LPS 处理还显著增加了血清和纹状体中炎症细胞因子,如白细胞介素-6(IL-6)、白细胞介素-1β(IL-1β)和肿瘤坏死因子-α(TNF-α)。此外,Western blot 分析和免疫组织化学分析表明,LPS 处理还分别增加了 TS 大鼠中 TLR4、MyD88、P-NF-κBp65、P-IκBα 的高表达。因此,推测脂多糖(LPS)可能在妥瑞氏症候群的复发中起重要作用,其机制与 TLR/NF-κB 通路有关。