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紫锥菊提取物对巨噬细胞抗病毒活性的影响。

Effects of Echinacea extracts on macrophage antiviral activities.

机构信息

Biology Department, Drake University, Des Moines, IA, USA.

出版信息

Phytother Res. 2010 Jun;24(6):810-6. doi: 10.1002/ptr.2991.

Abstract

Type I interferons are a class of cytokines synthesized by leukocytes such as macrophages that limit viral replication. We hypothesized that one mechanism whereby Echinacea spp. extracts may enhance immunity is through modulating interferon-associated macrophage pathways. We used herpes simplex viral infection in the murine macrophage cell line RAW264.7 and monitored virus-induced cell death, interferon secretion, and two intracellular proteins that indicate activation of interferon pathways. Cells were incubated with control media or extracts from four different species (E. angustifolia, E. purpurea, E. tennesseensis, E. pallida). Cells incubated with extracts prior to infection showed very modest enhancement of viability, and no increase in the secretion of interferons alpha or beta as compared to control cells. Virus-infected macrophages treated with extracts from E. purpurea showed a small (<2-fold) induction of guanylate binding protein (GBP) production, but no effect of extracts from other species was observed. In virus-infected cells, all the extracts increased the amount of inducible nitric oxide synthase (iNOS) protein, and this effect varied by type of extraction preparation. Together, these results suggest that any potential antiviral activities of Echinacea spp. extracts are likely not mediated through large inductions of Type I interferon, but may involve iNOS.

摘要

I 型干扰素是一类由白细胞(如巨噬细胞)合成的细胞因子,可限制病毒复制。我们假设,紫锥菊属植物提取物增强免疫力的机制之一是通过调节干扰素相关的巨噬细胞途径。我们使用单纯疱疹病毒感染鼠巨噬细胞系 RAW264.7,并监测病毒诱导的细胞死亡、干扰素分泌以及两种表明干扰素途径激活的细胞内蛋白。细胞用对照培养基或来自四种不同物种(狭叶紫锥菊、紫松果菊、紫锥花、苍白紫锥菊)的提取物孵育。与对照细胞相比,感染前用提取物孵育的细胞显示出对活力的适度增强,并且干扰素 alpha 或 beta 的分泌没有增加。用紫锥菊提取物处理感染病毒的巨噬细胞显示出鸟苷酸结合蛋白 (GBP) 产生的小(<2 倍)诱导,但其他物种的提取物没有观察到这种作用。在感染病毒的细胞中,所有提取物均增加了诱导型一氧化氮合酶 (iNOS) 蛋白的量,并且这种作用因提取制剂的类型而异。综上所述,这些结果表明,紫锥菊属植物提取物的任何潜在抗病毒活性可能不是通过大量诱导 I 型干扰素介导的,而是可能涉及 iNOS。

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