Key Laboratory of Chinese Medicine on Viral Diseases, Ministry of Education, Microbiology and Immunology Department, Beijing University of Chinese Medicine, Beijing, China.
Chin J Integr Med. 2011 Jun;17(6):444-52. doi: 10.1007/s11655-011-0640-3. Epub 2011 Jun 10.
To explore the potential effects of berberine on influenza virus infection both in vitro and in vivo.
In vitro anti-influenza virus assays were performed by cytopathogenic effect and neuraminidase assays in Madin Darby canine kidney cells. In vivo anti-influenza virus assays were performed on the viral pneumonia model of mice. The numbers of mice that died within day 2 to day 14 postinfection were recorded to calculate the mortality. On days 2, 4, and 6, the viral titers in the lungs were determined by hemagglutination assay; hematoxylin/eosin staining was used to assess the pathogenic changes of lung tissues; the concentrations of tumor necrosis factor-alpha (TNF-α) and monocyte specific chemoattractant molecule (MCP-1) were measured by radio immunoassay or enzyme-linked immunosorbent assay; the concentrations of nitric oxide (NO) and inducible nitric oxide synthetase (iNOS) were detected by colorimetric method; reverse transcription polymerase chain reaction was used to detect the mRNA level of TNF-α and MCP-1.
Berberine showed inhibitory effects on cytopathogenic effects and neuraminidase activity of virus, with the therapeutic index 9.69. In vivo, berberine decreased mice mortality from 90% to 55%, reduced virus titers in the lungs on day 2 postinfection (P<0.05). The lung histology scores were 1.50 ± 0.67, 4.50 ± 1.00, and 5.50 ± 1.00 in the berberine group on days 2, 4, and 6, respectively, which were significantly reduced compared to 2.17 ± 0.22, 6.83 ± 0.44, and 8.50 ± 0.33 in the infected group (P<0.05). The productions of NO and iNOS were repressed by berberine compared with those in the infected group (P<0.01). The transcription and expression of TNF-α were inhibited by berberine on day 4 (P<0.01) and day 6 (P<0.05), and those of MCP-1 were inhibited on day 6 (P<0.01) compared with the infected group.
Berberine exhibited antiviral effects on the influenza virus both in vitro and in vivo. The possible therapeutic mechanism of berberine on influenza-induced viral pneumonia might be inhibiting the virus infection, as well as improving the pathogenic changes by repressing inflammatory substances release.
探讨小檗碱在体外和体内抗流感病毒的潜在作用。
采用细胞病变效应和神经氨酸酶试验,在 Madin Darby 犬肾细胞中进行体外抗流感病毒试验。采用小鼠病毒性肺炎模型进行体内抗流感病毒试验。记录感染后第 2 至 14 天内死亡的小鼠数量,以计算死亡率。在第 2、4 和 6 天,通过血凝试验测定肺部的病毒滴度;采用苏木精/伊红染色评估肺组织的病变变化;通过放射免疫或酶联免疫吸附试验测定肿瘤坏死因子-α(TNF-α)和单核细胞趋化因子-1(MCP-1)的浓度;通过比色法检测一氧化氮(NO)和诱导型一氧化氮合酶(iNOS)的浓度;采用逆转录聚合酶链反应检测 TNF-α和 MCP-1 的 mRNA 水平。
小檗碱对病毒的细胞病变效应和神经氨酸酶活性均有抑制作用,治疗指数为 9.69。体内,小檗碱使小鼠死亡率从 90%降至 55%,并降低感染后第 2 天肺部的病毒滴度(P<0.05)。小檗碱组在第 2、4 和 6 天的肺组织学评分分别为 1.50±0.67、4.50±1.00 和 5.50±1.00,与感染组的 2.17±0.22、6.83±0.44 和 8.50±0.33相比明显降低(P<0.05)。与感染组相比,小檗碱抑制了 NO 和 iNOS 的产生(P<0.01)。小檗碱在第 4 天(P<0.01)和第 6 天(P<0.05)抑制了 TNF-α的转录和表达,在第 6 天(P<0.01)抑制了 MCP-1的表达,与感染组相比。
小檗碱在体外和体内均具有抗流感病毒作用。小檗碱治疗流感病毒诱导的病毒性肺炎的可能机制可能是抑制病毒感染,以及通过抑制炎症物质的释放来改善病变变化。