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Pathway-focused bioassays and transcriptome analysis contribute to a better activity monitoring of complex herbal remedies

机译:以途径为重点的生物测定和转录组分析有助于更好地监测复杂草药的活性

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Background 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. Results 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. Conclusions 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.
机译:背景转录组分析与以途径为重点的生物测定相结合,被认为是一种有用的方法,可用于深入了解草药多组分制剂在活细胞中的复杂作用机理。基于多草药疗法的藏药和阿育吠陀医学概念通过多目标效应来考虑疗效。瑞士药物管理局(Swissmedic Nr。58436)批准了一种多草药印度-西藏制剂Padma 28(Swissmedic Nr。58436),用于更详细地分析人肝癌HepG2细胞的作用机理。采用无细胞和基于细胞的测定法评估抗氧化能力。全基因组表达谱分析是通过应用人类基因组U133 Plus 2.0 Affymetrix阵列完成的。面向路径和网络的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验证了结果。结果为揭示印度-藏族多方草药Padma 28乙醇提取物的直接自由基清除作用,采用了体外氧自由基吸收能力测定(ORAC),其过氧自由基清除活性为2006±235μmol TE /克此外,通过测量其对自由基诱导的ROS的清除能力,分析了Padma 28在活HepG2细胞中的抗氧化能力。该制剂通过以剂量依赖性方式显着降低ROS水平而显示出相当大的抗氧化剂能力。整合的转录组分析揭示了对I和II期解毒和氧化应激反应的主要影响。在qPCR实验中验证了选定的靶基因,例如血红素加氧酶1。网络分析显示,有18个相互关联的网络参与了重要的生物学功能,例如药物和生物分子的代谢,分子运输和细胞通讯。一些分子是信号级联反应的一部分,在发育和形态发生过程中是活跃的,或者参与病理状况和炎症反应。结论鉴定出的分子靶标和途径表明了该制剂生物学活性的几种机理。尽管不可能将这些发现推论到体内情况,但是获得的结果可能是进一步研究和检验新假设的基础。这项研究表明,在多组分草药混合物的作用分析模式中,结合重点研究和无偏见研究策略的潜力。

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