A novel combination of four flavonoids derived from Astragali Radix relieves the symptoms of cyclophosphamide‐induced anemic rats
By using a feedback system control scheme, the best combination of formononetin, ononin, calycosin, and calycosin‐7‐O‐β‐d‐glucoside derived from Astragali Radix was shown to activate a hypoxia response element, a regulator for erythropoietin (EPO) transcription, in kidney fibroblast. In cyclophospha...
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Published in | FEBS open bio Vol. 7; no. 3; pp. 318 - 323 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
England
John Wiley & Sons, Inc
01.03.2017
John Wiley and Sons Inc |
Subjects | |
Online Access | Get full text |
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Summary: | By using a feedback system control scheme, the best combination of formononetin, ononin, calycosin, and calycosin‐7‐O‐β‐d‐glucoside derived from Astragali Radix was shown to activate a hypoxia response element, a regulator for erythropoietin (EPO) transcription, in kidney fibroblast. In cyclophosphamide‐induced anemic rats, the treatment of combined flavonoids, or EPO, improved the levels of red blood cells, white blood cells, hemoglobin, and hematocrit. In addition, the altered levels of antioxidant capacity, super oxidase dismutase, and malondialdehyde, triggered in anemic rats, were restored to control levels by the treatment of flavonoids. Here, we proposed a possible therapy by using the common flavonoids in treating anemia.
An engineering approach—feedback system control—was used to screen for the best combination of flavonoids from Astragali Radix, a traditional Chinese medicine, to treat anemia. The screen tested for the most effective combination of formononetin, ononin, calycosin, and calycosin‐7‐O‐β‐d‐glucoside in activating the transcriptional activity of erythropoietin gene. This combination was then verified in a rat model of anemia. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 These authors contributed equally to this work. |
ISSN: | 2211-5463 2211-5463 |
DOI: | 10.1002/2211-5463.12146 |