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首页> 外文期刊>Neuroscience Letters: An International Multidisciplinary Journal Devoted to the Rapid Publication of Basic Research in the Brain Sciences >Acyclovir treatment of experimentally induced herpes simplex virus encephalitis: monitoring the changes in immunologic NO synthase expression and viral load within brain tissue of SJL mice.
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Acyclovir treatment of experimentally induced herpes simplex virus encephalitis: monitoring the changes in immunologic NO synthase expression and viral load within brain tissue of SJL mice.

机译:阿昔洛韦治疗实验性单纯疱疹病毒性脑炎的方法:监测SJL小鼠脑组织中免疫NO合酶表达和病毒载量的变化。

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The effect of acyclovir treatment on viral burden and the expression of immunologic nitric oxide synthase (iNOS) within brains of 42 HSV-1 F infected mice was studied by using a titration PCR assay for HSV-1 DNA and a semiquantitative RT-PCR for iNOS mRNA. iNOS mediated NO-production may possibly be involved in secondary mechanisms of brain injury following virus infection, which may account for treatment failures in human herpes simplex virus encephalitis (HSVE). Following infection, a parallel increase of iNOS mRNA and HSV-1F-DNA occurred with peaks after 7 days that were both significantly lower under acyclovir treatment. Six months post infection viral load had declined, but iNOS mRNA expression in both treated and untreated mice was still enhanced as compared with mock infected controls. This suggests that acyclovir decreases iNOS expression via inhibition of viral replication shortly after infection but fails to influence elevated iNOS within the brain late in the course of experimental HSVE.
机译:使用滴定PCR检测HSV-1 DNA和半定量RT-PCR研究无环鸟苷治疗对42例HSV-1 F感染小鼠的病毒载量和免疫性一氧化氮合酶(iNOS)表达的影响mRNA。 iNOS介导的NO产生可能与病毒感染后脑损伤的继发机制有关,这可能是人类单纯疱疹病毒性脑炎(HSVE)治疗失败的原因。感染后,iNOS mRNA和HSV-1F-DNA平行增加,并在7天后出现峰值,在阿昔洛韦治疗下均明显降低。感染后六个月病毒载量下降,但与模拟感染的对照组相比,治疗和未治疗小鼠中iNOS mRNA的表达仍得到增强。这表明阿昔洛韦在感染后不久就通过抑制病毒复制而降低了iNOS的表达,但在实验性HSVE过程的后期却无法影响脑内升高的iNOS。

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