• 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

亚急性实验性病毒性心肌炎中心肌功能减退

Depressed myocardial function in subacute experimental viral myocarditis.

作者信息

Abelmann W H, Adesanya C O, Goldberg A H, Phear W P, Young N A

出版信息

Recent Adv Stud Cardiac Struct Metab. 1975;6:535-42.

PMID:1197901
Abstract

A model of experimental Coxsackie virus B3 myocarditis has been developed in the weaning Syrian golden hamster. The acute infection is characterized by extensive viral replication in the myocardium, associated with transient myocytolysis and leukocytic infiltration. At 2 weeks after inoculation, there is survival without evidence of cardiac hypertrophy or failure, and minimal residual light microscopic changes. In order to evaluate myocardial function during convalescence form this form of myocarditis, muscle mechanics were studied in left ventricular trabeculae careae in 10 infected and 7 control animals, 18 days after inoculation. Maximum developed tension of the infected animals was depressed by 25%, and there was a significant decrease in the time to peak tension. Furthermore, the infected muscles required less stretch to reach that length at which maximal developed tension was produced. These data indicate that myocardial function remains depressed during early convalescence from acute Coxsackie virus B3 myocarditis and suggest that this state is associated with decreased compliance. Studies of myocardial morphology and function at longer intervals after acute experimental viral myocarditis are indicated, to further test the hypothesis that viral myocarditis might be a precursor chronic isiopathic cardiomyopathy.

摘要

在断奶的叙利亚金黄地鼠中建立了实验性柯萨奇病毒B3心肌炎模型。急性感染的特征是心肌中广泛的病毒复制,伴有短暂的心肌细胞溶解和白细胞浸润。接种后2周,动物存活,无心脏肥大或衰竭的迹象,光镜下残留变化极小。为了评估这种心肌炎康复期的心肌功能,在接种后18天,对10只感染动物和7只对照动物的左心室乳头肌进行了肌肉力学研究。感染动物的最大舒张张力降低了25%,达到峰值张力的时间显著缩短。此外,感染的肌肉达到产生最大舒张张力的长度所需的拉伸较小。这些数据表明,急性柯萨奇病毒B3心肌炎早期康复期心肌功能仍受抑制,提示这种状态与顺应性降低有关。有必要对急性实验性病毒性心肌炎后更长时间的心肌形态和功能进行研究,以进一步验证病毒性心肌炎可能是慢性特发性心肌病先兆的假说。

相似文献

1
Depressed myocardial function in subacute experimental viral myocarditis.亚急性实验性病毒性心肌炎中心肌功能减退
Recent Adv Stud Cardiac Struct Metab. 1975;6:535-42.
2
Heart muscle performance after experimental viral myocarditis.实验性病毒性心肌炎后的心肌性能
J Clin Invest. 1976 Mar;57(3):569-75. doi: 10.1172/JCI108312.
3
Cytokine profiles in heart, spleen, and thymus during the acute stage of experimental coxsackievirus B3-induced chronic myocarditis.实验性柯萨奇病毒B3诱导的慢性心肌炎急性期心脏、脾脏和胸腺中的细胞因子谱
J Med Virol. 2000 Aug;61(4):518-26.
4
Experimental coxsackie B virus myocarditis in mice: 18 month histopathological and virological study.小鼠实验性柯萨奇B病毒心肌炎:18个月的组织病理学和病毒学研究
Jpn Circ J. 1981 Jul;45(7):747-62.
5
Enteroviral infection of mice with severe combined immunodeficiency. Evidence for direct viral pathogenesis of myocardial injury.严重联合免疫缺陷小鼠的肠道病毒感染。心肌损伤直接病毒发病机制的证据。
Lab Invest. 1992 Jan;66(1):24-31.
6
The viral genetic background determines the outcome of coxsackievirus B3 infection in outbred NMRI mice.病毒遗传背景决定了远交系NMRI小鼠中柯萨奇病毒B3感染的结果。
J Med Virol. 2007 Sep;79(9):1334-42. doi: 10.1002/jmv.20933.
7
[Patterns of acute and persistent infections in enteroviral heart diseases].[肠道病毒性心脏病中的急性和持续性感染模式]
Verh Dtsch Ges Pathol. 1990;74:404-8.
8
Temporal changes in stem cells in the circulation and myocardium of mice with Coxsackie virus B3-induced myocarditis.柯萨奇病毒B3诱导的心肌炎小鼠循环系统和心肌中干细胞的时间变化。
Microvasc Res. 2008 Apr;75(3):358-66. doi: 10.1016/j.mvr.2007.10.005. Epub 2007 Nov 9.
9
Trace element distribution in heart tissue sections studied by nuclear microscopy is changed in Coxsackie virus B3 myocarditis in methyl mercury-exposed mice.通过核显微镜研究发现,甲基汞暴露小鼠感染柯萨奇病毒B3引发心肌炎时,心脏组织切片中的微量元素分布发生了变化。
Biol Trace Elem Res. 2000 Winter;78(1-3):131-47. doi: 10.1385/BTER:78:1-3:131.
10
A mouse model of coxsackievirus myocarditis.柯萨奇病毒心肌炎的小鼠模型
Can J Cardiol. 1992 Mar;8(2):145-8.

引用本文的文献

1
Evaluation of the effects of low molecular weight heparin on inflammation and collagen deposition in chronic coxsackievirus B3-induced myocarditis in A/J mice.评估低分子量肝素对A/J小鼠慢性柯萨奇病毒B3诱导的心肌炎中炎症和胶原沉积的影响。
Am J Pathol. 1992 Jul;141(1):203-9.
2
Virological investigations in congestive cardiomyopathy.充血性心肌病的病毒学研究。
Postgrad Med J. 1978 Jul;54(633):505-9. doi: 10.1136/pgmj.54.633.505.