Genistein From Fructus sophorae Protects Mice From Radiation-Induced Intestinal Injury
The development of an effective pharmacological countermeasure is needed to reduce the morbidity and mortality in high-dose ionizing radiation-induced acute damage. Genistein has shown bioactivity in alleviating radiation damage and is currently synthesized by chemosynthetic methods. Due to concerns...
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Veröffentlicht in: | Frontiers in pharmacology 2021-05, Vol.12, p.655652-655652 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | The development of an effective pharmacological countermeasure is needed to reduce the morbidity and mortality in high-dose ionizing radiation-induced acute damage. Genistein has shown bioactivity in alleviating radiation damage and is currently synthesized by chemosynthetic methods. Due to concerns about chemical residues and high costs, the clinical application of genistein is still a major challenge. In this study, we aimed to establish an efficient method for the extraction of genistein from
Fructus sophorae
. The effects of extracted genistein (FSGen) on preventing intestinal injury from radiation were further investigated in this study. C57/BL mice were exposed to 7.5 Gy whole body irradiation with and without FSGen treatments. Histological analysis demonstrated significant structural and functional restitution of the intestine and bone marrow in FSGen-pretreated cohorts after irradiation. Through mRNA expression, protein expression, and small interfering RNA analyses, we demonstrated that FSGen protects IEC-6 cells against radiation damage by upregulating the
Rassf1a
and
Ercc1
genes to effectively attenuate DNA irradiation damage. Together, our data established an effective method to extract genistein from the
Fructus sophorae
plant with high purity, and validated the beneficial roles of the FSGen in protecting the radiation damage. These results promise the future applications of
Fructus sophorae
extracted genistein in the protection of radiation related damages. |
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ISSN: | 1663-9812 1663-9812 |
DOI: | 10.3389/fphar.2021.655652 |