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Understanding molecular mechanisms of Rhodiola rosea for the treatment of acute mountain sickness through computational approaches (a STROBE-compliant article)

机译:通过计算方法了解玫瑰红景天治疗急性山区疾病的分子机制(符合STROBE的文章)

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Rhodiola rosea has been used in the treatment of acute mountain sickness (AMS) for a long time, but the mechanism of its action is not still completely clear. In this paper, the therapeutic mechanism of R rosea for AMS was investigated by analysis of the relationship between R rosea compositions and hypoxia-inducible factor 1 (HIF-1) degradation pathway. System biology and network biology, computational approaches were used to explore the molecular mechanisms of traditional Chinese medicine (TCM). Our results showed that chemical compositions of R rosea could inhibit the targets of HIF-1 degradation pathway in multi-composition/multi-target ways. We conclude that the 18 components with more than 2 targets and 5 targets (arrest-defective-1 [ARD1], forkhead transcription factor [FOXO4], osteosarcoma-9 [OS-9], prolyl hydroxylase 2 [PHD2], human double minute 2 [Hdm2]) deserve to be noticed, and PHD2, receptor for activated C-kinase1 (RACK1) and spermidine/spermine-N1-acetyltransferase-1 (SSAT1) may be the targets of active ingredients of rhodionin, rhodiosin, and rhodiolatuntoside, respectively.
机译:红景天已被用于治疗急性高山病(AMS)了很长一段时间,但其作用机理仍不完全清楚。本文通过分析R rosea组成与缺氧诱导因子1(HIF-1)降解途径之间的关系,研究了R rosea对AMS的治疗机制。系统生物学和网络生物学,计算方法被用于探索中药的分子机制。我们的结果表明,玫瑰蔷薇的化学成分可以通过多组分/多靶点的方式抑制HIF-1降解途径的靶点。我们得出的结论是,具有超过2个靶标和5个靶标的18个组分(逮捕缺陷1 [ARD1],叉头转录因子[FOXO4],骨肉瘤9 [OS-9],脯氨酰羟化酶2 [PHD2],人双分2 [Hdm2])值得关注,活化的C激酶1(RACK1)和亚精胺/亚精胺-N1-乙酰基转移酶-1(SSAT1)的受体PHD2可能是红景素,红景天苷和红景天糖苷活性成分的靶标,分别。

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