4.3 Article

The Toxicity and Metabolism Properties of Herba Epimedii Flavonoids on Laval and Adult Zebrafish

Journal

Publisher

HINDAWI LTD
DOI: 10.1155/2019/3745051

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Funding

  1. National Natural Science Foundation of China [81573833, 81303275, 81503253, 81603500, 30973978, 81873055]
  2. 2015 Annual Traditional Chinese Medicine for Public Interest Research from Ministry of Finance of China [201507004-10]
  3. National Major Scientific and Technological Special Project for Significant New Drugs Development [2017ZX09301-056, 2017ZX09301-051]
  4. Natural Science Foundation of Jiangsu Province of China [BK20141507]
  5. 333 Project of Jiangsu Province [BRA2014348]
  6. Foundation for High-Level Talent in Six Areas of Jiangsu Province [2013-YY006]

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Zebrafish is being increasingly used for metabolism and toxicity assessment. The drugs consumed in zebrafish metabolism studies are far less than those used in rat studies. In our study, zebrafish embryos were exposed to icariin, Baohuoside I (BI), Epimedin A (EA), Epimedin B (EB), Epimedin C (EC), Sagittatoside A (SA), Sagittatoside B (SB), and 2-O-rhamnosylicariside II (SC), respectively, to examine the toxicity and metabolic profiles of these flavonoids. The order of toxicity was SC, SB > EC, SA > BI, icariin, EA, EB. After 24 h exposure to SB and SC, the mortality of zebrafish larvae reached 100% and yolk sac swollen was obvious. Both SC and SB caused severe hepatocellular vacuolization and liver cells degeneration in adult zebrafish after 15 consecutive days' treatment. The metabolic profiles of these flavonoids with trace amount were also monitored in larvae. BI was the common metabolite shared by icariin, EA, EB, SA, and SB, via deglycosylation. Both BI and SC remained as the prototype in the medium, suggesting that it is hard for BI and SC to cleave the rhamnose residue. EC was metabolized into SC and BI in zebrafish, inferring that SC might be responsible for the toxicity observed in EC group. The metabolites of icariin, EA, EB, EC, and BI in zebrafish larvae coincided with results from rats and intestinal flora. These data support the use of this system as a surrogate in predicting metabolites and hepatotoxicity risk, especially for TCM compound with trace amount.

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