10.3389/fphar.2019.01356.s001 Yi Ma Yi Ma Yi Wu Yi Wu Zhengchao Xia Zhengchao Xia Jingyi Li Jingyi Li Xiaorong Li Xiaorong Li Pingxiang Xu Pingxiang Xu Xuelin Zhou Xuelin Zhou Ming Xue Ming Xue DataSheet_1_Anti-Hypoxic Molecular Mechanisms of Rhodiola crenulata Extract in Zebrafish as Revealed by Metabonomics.docx Frontiers 2019 Rhodiola crenulata anti-hypoxia zebrafish metabonomics network analysis 2019-11-12 04:17:07 Dataset https://frontiersin.figshare.com/articles/dataset/DataSheet_1_Anti-Hypoxic_Molecular_Mechanisms_of_Rhodiola_crenulata_Extract_in_Zebrafish_as_Revealed_by_Metabonomics_docx/10287612 <p>The health supplement of Rhodiola crenulata (RC) is well known for its effective properties against hypoxia. However, the mechanisms of its anti-hypoxic action were still unclear. The objective of this work was to evaluate the molecular mechanisms of RC extract against hypoxia in a hypoxic zebrafish model through metabonomics and network pharmacology analysis. The hypoxic zebrafish model in the environment with low concentration (3%) of oxygen was constructed and used to explore the anti-hypoxic effects of RC extract, followed by detecting the changes of the metabolome in the brain through liquid chromatography–high resolution mass spectrometry. An in silico network for metabolite-protein interactions was further established to examine the potential mechanisms of RC extract, and the mRNA expression levels of the key nodes were validated by real-time quantitative PCR. As results, RC extract could keep zebrafish survive after 72-h hypoxia via improving lactate dehydrogenase, citrate synthase, and hypoxia-induced factor-1α in brains. One hundred and forty-two differential metabolites were screened in the metabonomics, and sphingolipid metabolism pathway was significantly regulated after RC treatment. The constructed protein-metabolites network indicated that the HIF-related signals were recovered, and the mRNA level of AMPK was elevated. In conclusion, RC extract had markedly anti-hypoxic effects in zebrafish via changing sphingolipid metabolism, HIF-related and AMPK signaling pathways.</p>