山东大学学报(医学版) ›› 2015, Vol. 53 ›› Issue (2): 1-5.doi: 10.6040/j.issn.1671-7554.0.2014.639
• 基础医学 • 下一篇
张蓬1, 岳龙涛2, 李亨1, 张民1, 王聪聪1, 段瑞生1, 窦迎春3
ZHANG Peng1, YUE Longtao2, LI Heng1, ZHANG Min1, WANG Congcong1, DUAN Ruisheng1, DOU Yingchun3
摘要: 目的 探讨传统中药血脂康对实验性自身免疫性神经炎(EAN)大鼠的治疗潜能及免疫调节机制.方法 应用周围髓鞘蛋白(P0)抗原180~199肽段免疫雌性Lewis大鼠建立EAN模型,将15只EAN大鼠随机、平均分为大剂量治疗组[1 000 mg/(kg·d)]、小剂量治疗组[200 mg/(kg·d)]和对照组(每组n=5),采用双盲法每日观察大鼠临床症状并评分;流式细胞技术检测淋巴结单个核细胞悬液细胞因子TNF-α、IFN-γ、IL-10和 IL-17的分泌情况以及调节性T细胞在淋巴结单个核细胞及CD4+T细胞中所占百分比.结果 与对照组相比,血脂康大、小剂量治疗组的临床评分均降低,TNF-α的分泌均减少(P均< 0.01);IL-10的分泌量均明显受到抑制(P<0.001和P<0.01);大剂量治疗组IL-17的分泌较对照组减少(P<0.01).与对照组相比,小剂量治疗组CD4+CD25+ T细胞占淋巴结单个核细胞的百分比、大剂量治疗组CD4+CD25+ T细胞和CD4+Foxp3+ T细胞占淋巴结单个核细胞及CD4+T细胞的比例均明显降低(P均<0.05).与对照组比较,大剂量治疗组CD4+CD25+Foxp3+Treg占淋巴结单个核细胞及CD4+T细胞的比例降低(P值分别为0.075和0.066).结论 血脂康通过抑制TNF-α、IL-10和 IL-17细胞因子产生,缓解了EAN大鼠病情,但同时抑制了CD4+T细胞向Treg的分化.
中图分类号:
| [1] Xia RH, Yosef N, Ubogu EE. Clinical, electrophysiological and pathologic correlations in a severe murine experimental autoimmune neuritis model of Guillain-Barre syndrome[J]. J Neuroimmunol, 2010, 219(1-2):54-63. [2] Li H, Li XL, Zhang M, et al. Berberine ameliorates experimental autoimmune neuritis by suppressing both cellular and humoral immunity[J]. Scand J Immunol, 2014, 79(1):12-19. [3] Li XL, Dou YC, Liu Y, et al. Atorvastatin ameliorates experimental autoimmune neuritis by decreased Th1/Th17 cytokines and up-regulated T regulatory cells[J]. Cell Immunol, 2011, 271(2):455-461. [4] Yang CW, Mousa SA. The effect of red yeast rice (Monascus purpureus) in dyslipidemia and other disorders[J]. Complement Ther Med, 2012, 20(6):466-474. [5] Nicholls SJ, Pisaniello AD, Kataoka Y, et al. Lipid pharmacotherapy for treatment of atherosclerosis[J]. Expert Opin Pharmacother, 2014, 15(8):1119-1125. [6] Zhang X, Jin J, Peng X, et al. Simvastatin inhibits IL-17 secretion by targeting multiple IL-17-regulatory cytokines and by inhibiting the expression of IL-17 transcription factor RORC in CD4+ lymphocytes[J]. J Immunol, 2008, 180(10):6988-6996. [7] Zhang X, Tao Y, Wang J, et al. Simvastatin inhibits secretion of Th17-polarizing cytokines and antigen presentation by DCs in patients with relapsing remitting multiple sclerosis[J]. Eur J Immunol, 2013, 43(1):281-289. [8] Tang TT, Song Y, Ding YJ, et al. Atorvastatin upregulates regulatory T cells and reduces clinical disease activity in patients with rheumatoid arthritis[J]. J Lipid Res, 2011, 52(5):1023-1032. [9] Xiao Y, Liang L, Pan Y, et al. Inhibitory effects of simvastatin on migration and invasion of rheumatoid fibroblast-like synoviocytes by preventing geranylgeranylation of RhoA[J]. Rheumatol Int, 2013, 33(2):389-399. [10] 王慧力, 唐长华, 王芳. 血脂康不良反应[J]. 中国误诊学杂志, 2010, 10(6):1496-1501. [11] 蓝晓红, 周永刚. 血脂康胶囊致横纹肌溶解症1例[J]. 中国药物警戒, 2010, 7(4):255-256. [12] Zhang HL, Zheng XY, Zhu J. Th1/Th2/Th17/Treg cytokines in Guillain-Barre syndrome and experimental autoimmune neuritis[J]. Cytokine Growth Factor Rev, 2013, 24(5):443-453. [13] Deng H, Yang X, Jin T, et al. The role of IL-12 and TNF-alpha in AIDP and AMAN[J]. Eur J Neurol, 2008, 15(10):1100-1105. [14] Bao L, Lindgren JU, Zhu Y, et al. Exogenous soluble tumor necrosis factor receptor type I ameliorates murine experimental autoimmune neuritis[J]. Neurobiol Dis, 2003, 12(1):73-81. [15] Sabat R, Grutz G, Warszawska K, et al. Biology of interleukin-10[J]. Cytokine Growth Factor Rev, 2010, 21(5):331-344. [16] O'Garra A, Barrat FJ, Castro AG, et al. Strategies for use of IL-10 or its antagonists in human disease[J]. Immunol Rev, 2008, 223:114-131. [17] Myhr KM, Vagnes KS, Maroy TH, et al. Interleukin-10 promoter polymorphisms in patients with Guillain-Barre syndrome[J]. J Neuroimmunol, 2003, 139(1-2):81-83. [18] Doreau A, Belot A, Bastid J, et al. Interleukin 17 acts in synergy with B cell-activating factor to influence B cell biology and the pathophysiology of systemic lupus erythematosus[J]. Nat Immunol, 2009, 10(7):778-785. [19] Li S, Yu M, Li H, et al. IL-17 and IL-22 in cerebrospinal fluid and plasma are elevated in Guillain-Barre syndrome[J]. Mediators Inflamm, 2012, 2012:260473. doi: 10.1155/2012/260473. [20] Hofstetter HH, Ibrahim SM, Koczan D, et al. Therapeutic efficacy of IL-17 neutralization in murine experimental autoimmune encephalomyelitis[J]. Cell Immunol, 2005,237(2):123-130. [21] Reise Sousa C. Dendritic cells in a mature age[J]. Nat Rev Immunol, 2006, 6(6):476-483. [22] Li XL, Liu Y, Cao LL, et al. Atorvastatin-modified dendritic cells in vitro ameliorate experimental autoimmune myasthenia gravis by up-regulated Treg cells and shifted Th1/Th17 to Th2 cytokines[J]. Mol Cell Neurosci, 2013, 56:85-95. |
| [1] | 张锦涛,董亮. 气道上皮及其源性细胞因子与哮喘:思考与展望[J]. 山东大学学报 (医学版), 2024, 62(5): 1-6. |
| [2] | 田欣鑫,王立俊,李琳,孙正达,刘海燕. CD300c-Ig对小鼠关节损伤的影响及机制[J]. 山东大学学报 (医学版), 2024, 62(2): 29-35. |
| [3] | 吴飞,李清丽,肖振卫. 孟德尔随机化探究细胞因子与慢性肾脏病的因果关系[J]. 山东大学学报 (医学版), 2024, 62(11): 85-95. |
| [4] | 祁少俊,唐延金,张正铎,吴虹,张佳程,秦川,刘锐,高希宝. 补充多种微量元素对高糖饮食大鼠的保护作用[J]. 山东大学学报 (医学版), 2023, 61(7): 19-26. |
| [5] | 王园园,孙云. 合并新型冠状病毒肺炎的维持性血液透析患者死亡危险因素[J]. 山东大学学报 (医学版), 2023, 61(11): 68-73. |
| [6] | 王福立,孙银萍,秦杰,荣建胜. DC-CIK细胞联合EGFR-TKI治疗35例老年晚期EGFR突变肺癌的效果[J]. 山东大学学报 (医学版), 2022, 60(7): 110-117. |
| [7] | 高惠茹,杜甜甜,王允山,杜鲁涛,王传新. 基于单细胞转录组测序数据分析胃癌调节性T细胞特征[J]. 山东大学学报 (医学版), 2022, 60(5): 43-49. |
| [8] | 李华玉,时萧寒,张新蕊,李峰. 203例胶质瘤患者睡眠障碍与炎症细胞因子的关联分析[J]. 山东大学学报 (医学版), 2022, 60(12): 26-30. |
| [9] | 张阿敏,李国盛,李福海. 儿童支原体大叶性肺炎肺泡灌洗液细胞因子与局部炎症的相关性[J]. 山东大学学报 (医学版), 2022, 60(11): 82-88. |
| [10] | 葛少华,丁田,刘红蕊. 2型免疫在组织修复中的作用及调控机制[J]. 山东大学学报 (医学版), 2021, 59(9): 51-56. |
| [11] | 周溪,黄霂晗,任玉洁,邱洋. 新型冠状病毒感染与天然免疫及炎症反应[J]. 山东大学学报 (医学版), 2021, 59(5): 15-21. |
| [12] | 李湘青,殷欣,赵雪莲,赵培庆. NK细胞亚群CD56bright在帕金森患者外周血中的表达及临床意义[J]. 山东大学学报 (医学版), 2021, 59(2): 34-40. |
| [13] | 鞠秀丽. 间充质干细胞治疗新型冠状病毒肺炎的潜在机制和研究进展[J]. 山东大学学报 (医学版), 2020, 58(3): 32-37. |
| [14] | 李雪,李栋,时庆,周盼盼,鞠秀丽. Helios在儿童急性淋巴细胞性白血病调节性T细胞中的表达及功能[J]. 山东大学学报(医学版), 2017, 55(4): 76-81. |
| [15] | 余桂芳,陈树娣,陈雪竹,侯开连,梁敏. miR-916a调控SOCS6促进HBx-HepG2细胞生长[J]. 山东大学学报(医学版), 2016, 54(12): 14-19. |
|
||