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病毒性心肌炎中的收缩功能抑制及促炎细胞因子和诱导型一氧化氮合酶的表达

Contractile depression and expression of proinflammatory cytokines and iNOS in viral myocarditis.

作者信息

Freeman G L, Colston J T, Zabalgoitia M, Chandrasekar B

机构信息

Division of Cardiology, University of Texas Health Science Center at San Antonio, USA.

出版信息

Am J Physiol. 1998 Jan;274(1):H249-58. doi: 10.1152/ajpheart.1998.274.1.H249.

Abstract

We assessed two strains of mice [CD-1 and C3H.HeJ (C3H)] with different responses to coxsackievirus B3 (CVB3) infection at 7, 14, and 21 days after inoculation with 10(5) pfu of CVB3. CD-1 mice developed inflammatory lesions at 7 days that nearly recovered by 21 days; C3H mice demonstrated persistence of infiltrates. Although there were differences in the baseline fractional shortening, it was further reduced at 7 and 14 days in both strains. It recovered in CD-1 mice but remained depressed at 21 days in C3H mice. Interleukin-6 and tumor necrosis factor-alpha transcripts were increased in both strains at 7 days. Levels dropped to near control in CD-1 mice at 21 days but remained elevated in C3H mice. Interleukin-1 beta was minimally elevated in CD-1 mice but increased progressively in C3H mice. mRNA for the inducible form of NO synthase (iNOS) was increased at 7 days in the CD-1 mice, returning to baseline by 14 days; it rose progressively in C3H mice, with a fivefold increase at 21 days. We conclude that mice infected with CVB3 show increased expression of proinflammatory cytokines as well as iNOS associated with reduced contractile performance. In more susceptible mice, contractile depression and cytokine and iNOS expression are more pronounced.

摘要

我们评估了两种对柯萨奇病毒B3(CVB3)感染有不同反应的小鼠品系[CD - 1和C3H.HeJ(C3H)],在接种10(5) 蚀斑形成单位(pfu)的CVB3后7天、14天和21天进行观察。CD - 1小鼠在7天时出现炎性病变,到21天时几乎恢复;C3H小鼠则表现出浸润持续存在。尽管基线缩短分数存在差异,但在7天和14天时两个品系的该指标均进一步降低。CD - 1小鼠的缩短分数恢复了,但C3H小鼠在21天时仍处于降低状态。白细胞介素 - 6和肿瘤坏死因子 - α转录本在两个品系的7天时均增加。CD - 1小鼠在21天时水平降至接近对照,但C3H小鼠仍保持升高。白细胞介素 - 1β在CD - 1小鼠中轻微升高,但在C3H小鼠中逐渐增加。诱导型一氧化氮合酶(iNOS)的mRNA在CD - 1小鼠的7天时增加,到14天时恢复至基线;在C3H小鼠中则逐渐升高,在21天时增加了五倍。我们得出结论,感染CVB3的小鼠表现出促炎细胞因子以及与收缩性能降低相关的iNOS表达增加。在更易感的小鼠中,收缩功能降低以及细胞因子和iNOS表达更为明显。

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