Division of Medical Biochemistry, Innsbruck Medical University, Center for Chemistry and Biomedicine, Innrain 80-82, Innsbruck, Austria.
BMC Genomics. 2013 Feb 27;14:133. doi: 10.1186/1471-2164-14-133.
Transcriptome analysis in combination with pathway-focused bioassays is suggested to be a helpful approach for gaining deeper insights into the complex mechanisms of action of herbal multicomponent preparations in living cells. The polyherbalism based concept of Tibetan and Ayurvedic medicine considers therapeutic efficacy through multi-target effects. A polyherbal Indo-Tibetan preparation, Padma 28, approved by the Swiss drug authorities (Swissmedic Nr. 58436), was applied to a more detailed dissection of mechanism of action in human hepatoma HepG2 cells. Cell-free and cell-based assays were employed to evaluate the antioxidant capacity. Genome-wide expression profiling was done by applying Human Genome U133 Plus 2.0 Affymetrix arrays. Pathway- and network-oriented analysis elucidated the affected biological processes. The results were validated using reporter gene assays and quantitative real-time PCR.
To reveal the direct radical scavenging effects of the ethanolic extract of the Indo-Tibetan polyherbal remedy Padma 28, an in vitro oxygen radical absorbance capacity assay (ORAC) was employed, which resulted in a peroxyl-radical scavenging activity of 2006 ± 235 μmol TE/g. Furthermore, the antioxidant capacity of Padma 28 was analysed in living HepG2 cells, by measuring its scavenging potential against radical induced ROS. This formulation showed a considerable antioxidant capacity by significantly reducing ROS levels in a dose-dependent manner.Integrated transcriptome analysis revealed a major influence on phase I and phase II detoxification and the oxidative stress response. Selected target genes, such as heme oxygenase 1, were validated in qPCR experiments. Network analysis showed 18 interrelated networks involved in important biological functions such as drug and bio-molecule metabolism, molecular transport and cellular communication. Some molecules are part of signaling cascades that are active during development and morphogenesis or are involved in pathological conditions and inflammatory response.
The identified molecular targets and pathways suggest several mechanisms that underlie the biological activity of the preparation. Although extrapolation of these findings to the in vivo situation is not possible, the results obtained might be the basis for further investigations and new hypotheses to be tested. This study demonstrates the potential of the combination of focused and unbiased research strategies in the mode of action analysis of multicomponent herbal mixtures.
转录组分析结合通路聚焦的生物测定被认为是深入了解草药多成分制剂在活细胞中复杂作用机制的有用方法。藏医和阿育吠陀医学的多草药理念通过多靶点效应来考虑治疗效果。一种基于多草药的藏印草药制剂 Padma 28 已被瑞士药物管理局(Swissmedic Nr. 58436)批准,用于更详细地剖析其在人肝癌 HepG2 细胞中的作用机制。采用无细胞和基于细胞的测定法来评估抗氧化能力。通过应用人类基因组 U133 Plus 2.0 Affymetrix 阵列进行全基因组表达谱分析。通路和网络导向分析阐明了受影响的生物过程。使用报告基因测定和定量实时 PCR 对结果进行了验证。
为了揭示藏印多草药复方 Padma 28 的乙醇提取物的直接清除自由基作用,采用体外氧自由基吸收能力测定法(ORAC)进行测定,结果表明其对过氧自由基的清除活性为 2006±235μmol TE/g。此外,通过测量其对自由基诱导的 ROS 的清除潜力,在活 HepG2 细胞中分析了 Padma 28 的抗氧化能力。该制剂通过显著降低 ROS 水平呈剂量依赖性方式显示出相当大的抗氧化能力。综合转录组分析表明,它对 I 相和 II 相解毒以及氧化应激反应有重大影响。在 qPCR 实验中验证了血红素加氧酶 1 等选定的靶基因。网络分析显示,涉及重要生物学功能的 18 个相互关联的网络,如药物和生物分子代谢、分子转运和细胞通讯。一些分子是发育和形态发生过程中活性的信号级联的一部分,或者参与病理状况和炎症反应。
鉴定的分子靶标和途径表明了几种机制,这些机制构成了制剂的生物学活性基础。虽然无法将这些发现推断到体内情况,但获得的结果可能为进一步研究和新假说提供基础,以进行测试。本研究证明了集中和无偏研究策略相结合在多成分草药混合物作用机制分析中的潜力。