• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

氯苯扎利二钠通过抑制脾脏全T细胞增强小鼠柯萨奇病毒B3心肌炎

Enhancement of coxsackievirus B3 myocarditis in mice by lobenzarit disodium through inhibition of splenic pan T cells.

作者信息

Kishimoto C, Takada H, Kuroki Y, Matsushita I, Hiraoka Y, Kurokawa M, Ochiai H, Sasayama S

机构信息

Faculty of Medicine, Toyama Medical and Pharmaceutical University, Japan.

出版信息

Cardiovasc Res. 1993 Feb;27(2):243-8. doi: 10.1093/cvr/27.2.243.

DOI:10.1093/cvr/27.2.243
PMID:8386064
Abstract

OBJECTIVE

The aim was to test the efficacy of the immune system modulator lobenzarit disodium in the treatment of coxsackievirus B3 myocarditis.

METHODS

Two week old C3H/He mice were inoculated with 10(3) plaque forming units of coxsackievirus B3. Lobenzarit disodium, 25 mg.kg-1.d-1, was given subcutaneously daily on days 0-14 (experiment I; group 2) and days 14-28 (experiment II; group 4). Both treated groups were compared to infected controls for each experiment (groups 1 and 3). For the analysis of splenic lymphocyte subsets, additional mice in untreated and treated groups were killed on d 7, and the percentages of Thy 1.2 (CD3), L3T4 (CD4), Ly 2 (CD8) subsets were analysed by laser flow cytometry (experiment III).

RESULTS

In experiment I, the survival rate in the lobenzarit treated group was significantly lower than in the controls (2/11 v 8/11). Cellular infiltration and myocardial necrosis in the lobenzarit group were more severe. Myocardial virus titres and serum neutralising antibody titres did not differ significantly between the two groups. In experiment II, the survival rate (7/9 v 13/13) and cardiac pathology between the two groups did not differ significantly. In experiment III, the percentage of the Thy 1.2 subset (CD3) in the treated group was significantly lower (p < 0.05) than in the control group, at 36.0(SD 2.9)% v 42.8(5.8)%.

CONCLUSIONS

Lobenzarit disodium decreased splenic pan T cells and aggravated both clinical course and cardiac pathology in acute murine coxsackievirus B3 myocarditis.

摘要

目的

旨在测试免疫系统调节剂苯扎利特二钠治疗柯萨奇病毒B3心肌炎的疗效。

方法

给两周龄的C3H/He小鼠接种10³空斑形成单位的柯萨奇病毒B3。在第0 - 14天(实验I;第2组)和第14 - 28天(实验II;第4组)每天皮下给予苯扎利特二钠,剂量为25 mg·kg⁻¹·d⁻¹。将两个治疗组与每个实验的感染对照组(第1组和第3组)进行比较。为了分析脾脏淋巴细胞亚群,在第7天处死未治疗组和治疗组中的额外小鼠,通过激光流式细胞术分析Thy 1.2(CD3)、L3T4(CD4)、Ly 2(CD8)亚群的百分比(实验III)。

结果

在实验I中,苯扎利特治疗组的存活率显著低于对照组(2/11对8/11)。苯扎利特组的细胞浸润和心肌坏死更严重。两组之间的心肌病毒滴度和血清中和抗体滴度无显著差异。在实验II中,两组之间的存活率(7/9对13/13)和心脏病理学无显著差异。在实验III中,治疗组中Thy 1.2亚群(CD3)的百分比显著低于对照组(p < 0.)

相似文献

1
Enhancement of coxsackievirus B3 myocarditis in mice by lobenzarit disodium through inhibition of splenic pan T cells.氯苯扎利二钠通过抑制脾脏全T细胞增强小鼠柯萨奇病毒B3心肌炎
Cardiovasc Res. 1993 Feb;27(2):243-8. doi: 10.1093/cvr/27.2.243.
2
The effects of lobenzarit disodium, a novel immunomodulator, upon murine coxsackievirus B3 myocarditis.新型免疫调节剂氯苯扎利二钠对小鼠柯萨奇病毒B3心肌炎的影响。
Heart Vessels. 1993;8(2):59-66. doi: 10.1007/BF01744384.
3
Absence of effects of cyclosporine on myocardial lymphocyte subsets in Coxsackievirus B3 myocarditis in the aviremic stage.环孢素对柯萨奇病毒B3无病毒血症期心肌炎心肌淋巴细胞亚群无影响。
Circ Res. 1989 Oct;65(4):934-45. doi: 10.1161/01.res.65.4.934.
4
Serial immunologic identification of lymphocyte subsets in murine coxsackievirus B3 myocarditis: different kinetics and significance of lymphocyte subsets in the heart and in peripheral blood.小鼠柯萨奇病毒B3心肌炎中淋巴细胞亚群的系列免疫鉴定:心脏和外周血中淋巴细胞亚群的不同动力学及意义
Circulation. 1988 Mar;77(3):645-53. doi: 10.1161/01.cir.77.3.645.
5
Cytokine and murine coxsackievirus B3 myocarditis. Interleukin-2 suppressed myocarditis in the acute stage but enhanced the condition in the subsequent stage.细胞因子与小鼠柯萨奇病毒B3心肌炎。白细胞介素-2在急性期可抑制心肌炎,但在随后阶段会加重病情。
Circulation. 1994 Jun;89(6):2836-42. doi: 10.1161/01.cir.89.6.2836.
6
The effects of FK-506, a novel and potent immunosuppressant, upon murine Coxsackievirus B3 myocarditis.新型强效免疫抑制剂FK-506对小鼠柯萨奇B3病毒性心肌炎的影响。
J Pharmacol Exp Ther. 1992 Mar;260(3):1386-91.
7
Effects of polyethylene glycol conjugated superoxide dismutase on coxsackievirus B3 myocarditis in mice.聚乙二醇共轭超氧化物歧化酶对小鼠柯萨奇病毒B3心肌炎的影响。
Cardiovasc Res. 1992 Oct;26(10):956-61. doi: 10.1093/cvr/26.10.956.
8
Effects of granulocyte colony-stimulating factor upon coxsackievirus B3 myocarditis in mice.粒细胞集落刺激因子对小鼠柯萨奇病毒B3心肌炎的影响。
Eur Heart J. 1995 Dec;16(12):1900-6. doi: 10.1093/oxfordjournals.eurheartj.a060845.
9
Immunosuppression with high doses of cyclophosphamide reduces the severity of myocarditis but increases the mortality in murine Coxsackievirus B3 myocarditis.高剂量环磷酰胺进行免疫抑制可减轻小鼠柯萨奇病毒B3心肌炎的严重程度,但会增加死亡率。
Circulation. 1990 Sep;82(3):982-9. doi: 10.1161/01.cir.82.3.982.
10
Effects of naloxone, an opiate receptor antagonist, on coxsackievirus B3 myocarditis in the mouse.阿片受体拮抗剂纳洛酮对小鼠柯萨奇病毒B3心肌炎的影响。
Cardiovasc Res. 1995 Jan;29(1):80-4.

引用本文的文献

1
Coxsackievirus B3-induced myocarditis: perforin exacerbates disease, but plays no detectable role in virus clearance.柯萨奇病毒B3诱导的心肌炎:穿孔素会加重病情,但在病毒清除中未发挥可检测到的作用。
Am J Pathol. 1998 Aug;153(2):417-28. doi: 10.1016/S0002-9440(10)65585-X.
2
Effects of levamisole, an immunomodulator, upon murine encephalomyocarditis virus myocarditis.免疫调节剂左旋咪唑对小鼠脑心肌炎病毒心肌炎的影响。
Heart Vessels. 1997;12(2):67-73. doi: 10.1007/BF02820869.