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In vitro evaluation of Cordyceps militaris as a potential radioprotective agent.

Authors :
Jeong MH
Park YS
Jeong DH
Lee CG
Kim JS
Oh SJ
Jeong SK
Yang K
Jo WS
Source :
International journal of molecular medicine [Int J Mol Med] 2014 Nov; Vol. 34 (5), pp. 1349-57. Date of Electronic Publication: 2014 Aug 18.
Publication Year :
2014

Abstract

Radiation is an important component of therapy for a wide range of malignant conditions. However, it triggers DNA damage and cell death in normal cells and results in adverse side-effects. Cordyceps militaris (C. militaris), a traditional medicinal mushroom, produces the bioactive compound, cordycepin (3'-deoxyadenosine) and has multiple pharmacological activities, such as antitumor, antimetastatic, antioxidant and immunomodulatory effects. The present study was undertaken to investigate whether CM-AE, an extract obtained from C. militaris exerts protective effects against radiation-induced DNA damage. The protective effects of CM-AE were compared with those of cordycepin. CM-AE effectively increased free radical scavenging activity and decreased radiation-induced plasmid DNA strand breaks in in vitro assays. CM-AE significantly inhibited the generation of reactive oxygen species (ROS) and cellular DNA damage in 2 Gy irradiated Chinese hamster ovary (CHO)-K1 cells. Moreover, treatment with CM-AE induced similar levels of phosphorylated H2AX in the cells, which reflects the initial DNA double-strand breaks in the irradiated cells compared with the non-irradiated CHO-K1 cells. However, cordycepin did not show free radical scavenging activity and did not protect against radiation-induced plasmid DNA or cellular DNA damage. These results suggest that the free radical scavenging activity of CM-AE contributes towards its DNA radioprotective effects and that the protective effects of CM-AE are much more potent to those of cordycepin. The data presented in this study may provide useful information for the screening of potent radioprotective materials.

Details

Language :
English
ISSN :
1791-244X
Volume :
34
Issue :
5
Database :
MEDLINE
Journal :
International journal of molecular medicine
Publication Type :
Academic Journal
Accession number :
25176413
Full Text :
https://doi.org/10.3892/ijmm.2014.1901