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Antiviral Activity and Possible Mechanism of Action of Constituents Identified in Paeonia lactiflora Root toward Human Rhinoviruses

机译:e药根中鉴定出的成分对人鼻病毒的抗病毒活性及其可能的作用机理

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摘要

Human rhinoviruses (HRVs) are responsible for more than half of all cases of the common cold and cost billions of USD annually in medical visits and missed school and work. An assessment was made of the antiviral activities and mechanisms of action of paeonol (PA) and 1,2,3,4,6-penta-O-galloyl-β-D-glucopyranose (PGG) from Paeonia lactiflora root toward HRV-2 and HRV-4 in MRC5 cells using a tetrazolium method and real-time quantitative reverse transcription polymerase chain reaction and enzyme-linked immunosorbent assay. Results were compared with those of a reference control ribavirin. Based on 50% inhibitory concentration values, PGG was 13.4 and 18.0 times more active toward HRV-2 (17.89 μM) and HRV-4 (17.33 μM) in MRC5 cells, respectively, than ribavirin. The constituents had relatively high selective index values (3.3–>8.5). The 100 μg/mL PA and 20 μg/mL PGG did not interact with the HRV-4 particles. These constituents inhibited HRV-4 infection only when they were added during the virus inoculation (0 h), the adsorption period of HRVs, but not after 1 h or later. Moreover, the RNA replication levels of HRVs were remarkably reduced in the MRC5 cultures treated with these constituents. These findings suggest that PGG and PA may block or reduce the entry of the viruses into the cells to protect the cells from the virus destruction and abate virus replication, which may play an important role in interfering with expressions of rhinovirus receptors (intercellular adhesion molecule-1 and low-density lipoprotein receptor), inflammatory cytokines (interleukin (IL)-6, IL-8, tumor necrosis factor, interferon beta, and IL-1β), and Toll-like receptor, which resulted in diminishing symptoms induced by HRV. Global efforts to reduce the level of synthetic drugs justify further studies on P. lactiflora root-derived materials as potential anti-HRV products or lead molecules for the prevention or treatment of HRV.
机译:人类鼻病毒(HRV)占所有普通感冒病例的一半以上,每年因医疗看望,失学和工作而花费数十亿美元。评估了Pa药根中丹皮酚(PA)和1,2,3,4,6-戊-O-galloyl-β-D-吡喃葡萄糖(PGG)对HRV-2的抗病毒活性和作用机理MRC5细胞中的HRV-4和HRV-4使用四唑鎓法,实时定量逆转录聚合酶链反应和酶联免疫吸附测定。将结果与参考对照利巴韦林的结果进行比较。基于50%抑制浓度值,PGG对MRC5细胞中HRV-2(17.89μM)和HRV-4(17.33μM)的活性分别是利巴韦林的13.4和18.0倍。成分具有较高的选择指数值(3.3-> 8.5)。 100μg/ mL PA和20μg/ mL PGG不与HRV-4颗粒相互作用。这些成分只有在病毒接种(0小时),HRV吸附期(而不是在1小时或之后)添加时才抑制HRV-4感染。而且,在用这些成分处理的MRC5培养物中,HRV的RNA复制水平显着降低。这些发现表明,PGG和PA可能会阻止或减少病毒进入细胞,以保护细胞免受病毒破坏和减弱的病毒复制,这可能在干扰鼻病毒受体(细胞间粘附分子- 1和低密度脂蛋白受体),炎性细胞因子(白介素(IL)-6,IL-8,肿瘤坏死因子,干扰素β和IL-1β)和Toll样受体,导致HRV诱导的症状减轻。降低合成药物水平的全球努力证明,对乳酸假单胞菌根源材料作为潜在的抗HRV产品或预防或治疗HRV的先导分子的进一步研究是合理的。

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