|本期目录/Table of Contents|

[1]曹江晨,雷军平,李路军,等.辛伐他汀对变态反应性脑脊髓炎小鼠INF-γ 和IL-10表达的影响[J].医学研究与战创伤救治(原医学研究生学报),2011,13(01):24-27.
 CAO Jiang-chen,LEI Jun-ping,LI Lu-jun,et al.Effect of simvastatin on expression of INF-γ and IL-10 in mice with allergic encephalomyelitis[J].JOURNAL OF MEDICALRESEARCH —COMBAT TRAUMA CARE,2011,13(01):24-27.
点击复制

辛伐他汀对变态反应性脑脊髓炎小鼠INF-γ 和IL-10表达的影响()

《医学研究与战创伤救治》(原医学研究生学报)[ISSN:1672-271X/CN:32-1713/R]

卷:
第13卷
期数:
2011年01期
页码:
24-27
栏目:
出版日期:
2011-01-20

文章信息/Info

Title:
Effect of simvastatin on expression of INF-γ and IL-10 in mice with allergic encephalomyelitis
文章编号:
1672-271X(2011)01-0024-04
作者:
曹江晨1雷军平2李路军3陈光勇4
1.214063 江苏无锡, 解放军73801部队门诊部;2.200433 上海,第二军医大学附属长海医院心内科;3.214063 江苏无锡,南京军区联勤部无锡干休所卫生所;4.351100 福建莆田,南京军区福州总医院第一附属医院
Author(s):
CAO Jiang-chen1 LEI Jun-ping2 LI Lu-jun3 CHEN Guang-yong4
1.Out-patient Department of 73801 army, PLA, Wuxi, Jiangsu 214063,China;2.Department of Cardiology, Changhai Hospital Affiliated to the Second Military Medical University, Shanghai 200433,China;3. Joint Logistics Department of the Nanjing Military Area Command,retired cadres health center,wuxi,Jiangsu 214063,China;4. The First Affiliated Hospital of Fuzhou General Hospital, Nanjing Military Area Command, Putian,Fujian 351100,China
关键词:
多发性硬化实验性变态反应性脑脊髓炎(EAE)辛伐他汀INF-γIL-10
Keywords:
multiple sclerosisexperiment allergic encephalomyelitissimvastatinINF-γIL-10
分类号:
R744.5
DOI:
-
文献标志码:
A
摘要:
目的 研究辛伐他汀(Simvastatin)对实验性变态反应性脑脊髓炎(experiment allergic encephalomyelitis,EAE)小鼠肿瘤坏死因子-γ(INF-γ)和白细胞介素-10(IL-10)表达的影响,探讨该药物对EAE保护作用的免疫调节机制。方法 通过皮下注射MOG33-55肽段诱导小鼠急性EAE模型,实验分为EAE给药组、EAE对照组和正常对照组。观察各组小鼠体重等变化,测定EAE发病高峰期血清、培养的单核细胞及脾细胞培养上清液的INF-γ和IL-10水平。结果 辛伐他汀能降低EAE小鼠的发病率,减轻了症状的严重程度,并能显著降低EAE小鼠血清、单个核细胞及脾细胞培养上清中INF-γ水平,升高IL-10水平。结论 辛伐他汀可能通过其抑制INF-γ和上调IL-10的表达,调节免疫状态,从而对小鼠EAE起到保护作用。
Abstract:
Objective To investigate the effect of simvastatin on expression of INF- and IL-10 in mice with experiment allergic encephalomyelitis (EAE), and the immunomodulatory mechanism for protection of allergic encephalomyelitis. Methods EAE was induced in C57BL/6J mice by immunization with MOG33-55. Mice were randomly divided into three groups: EAE simvastatin treatment group, EAE sham treatment group, and normal control group. The clinical assessment of EAE was performed daily. The levels of INF-γ and IL-10 in the serum, and the cell suspension of cultured mononuclear cell (MNC) or spleen cell were analyzed by ELISA. Results Simvastatin reduced the incidence and severity of EAE, which was accomplished by the inhibited expression of INF-γ and enhanced expression of IL-10. Conclusions Simvastatin might ameliorated EAE through an immunomodulatory effect that inhibits the expression of INF-γ and enhances the expression of IL-10.

参考文献/References:

[1]Confavreux C, Vukusic S.Natural history of multiple sclerosis: a unifying concept [J].Brain, 2006,129(3):606-616.
[2]Steinman L.Immune therapy for autoimmune diseases [J].Science, 2004, 305(5681): 212-216.
[3]Weber MS, Youssef S, Dunn SE, et al.Statins in the treatment of central nervous system autoimmune disease[J].J Neuroimmunol,2006, 178(1-2):140-148.
[4]Luccarini I,Ballerini C,Biagioli T,et al.Combined treatment with atorvastatin and minocycline suppresses severity of EAE [J].Exp Neurol, 2008, 211(1): 214-226.
[5] Paintlia AS, Paintlia MK, Singh AK, et al.Inhibition of rho family functions by lovastatin promotes myelin repair in ameliorating experimental autoimmune encephalomyelitis [J].Mol Pharmacol, 2008,73(5):1381-1393.
[6]Fu YF,Wang JX,Zhao Y,et al.S-Adenosyl-l-homocysteine hydrolase inactivation curtails ovalbumininduced immune responses [J].J Pharmacol Exp Ther, 2006, 316(3):1229-1237.
[7]Peterson JW,Trapp BD.Neuropathobiology of multiple sclerosis [J].Neurologic Clin, 2005,23(1):107-129.
[8]Gold R,Linington C,Lassmann H.Understanding pathogenesis and therapy of multiple sclerosis via animal models: 70 years of merits and culprits in experimental autoimmune encephalomyelitis research [J].Brain, 2006, 129(8):1953-1971.
[9]Bettelli E,Das MP,Howard ED,et al.IL-10 is critical in the regulation of autoimmune encephalomyelitis as demonstrated by studies of IL-10- and IL-4-deficient and transgenic mice [J].J Immunol, 1998, 161(7): 3299-3306.
[10]Yang JX, Jiang ZL, Fitzgerald DC, et al.Adult neural stem cells expressing IL-10 confer potent immunomodulation and remyelination in experimental autoimmune encephalitis [J].J Clin Invest, 2009, 119(12): 3678-3691.
[11]Wang Y, Mei YH, Feng DC, et al.Triptolide modulates T-cell inflammatory responses and ameliorates experimental autoimmune encephalomyelitis [J].J Neurosci Res, 2008, 86 (11): 2441-2449.
[12]Fu FY, Zhu NY, Ni J, et al.(5R)-5-Hydroxytriptolide (LLDT-8), a novel triptolide derivative, prevents experimental autoimmune encephalomyelitis via inhibiting T cell activation [J].J Neuroimmunol, 2006, 175(1-2):142-151.
[13]Stuve O, Prod’homme T, Youssef  S, et al.Statins as potential therapeutic agents in multiple sclerosis [J].Curr Neurol Neurosci Rep,2004, 4(3):237-244.
[14]陈卫兵,蒲 红,黄丽娜.早期应用辛伐他汀治疗急性冠状动脉综合征临床观察及对炎症因子的影响[J].东南国防医药,2003,5(5):330-332.
[15]丁雪燕,罗助荣.急性冠脉综合征血清脑钠肽水平及阿托伐他汀对其影响[J].东南国防医药,2009,11(1):37-39.

相似文献/References:

备注/Memo

备注/Memo:
-
更新日期/Last Update: 2011-01-20