The Antimutagenic Effects and Cytotoxic Activities of Agaricus blazei Murill Mycelium Extracts and Fractions

아가리쿠스 버섯 균사체 추출물 및 분획물의 항돌연변이원성 및 세포 독성 효과

  • Oh, Hyun-Taek (School of Bioscience and Biotechnology, Kangwon National University) ;
  • Kim, Soo-Hyun (School of Bioscience and Biotechnology, Kangwon National University) ;
  • Yoo, Su-Jung (School of Bioscience and Biotechnology, Kangwon National University) ;
  • Ham, Seung-Shi (School of Bioscience and Biotechnology, Kangwon National University)
  • 오현택 (강원대학교 바이오산업공학부 식품생명공학과) ;
  • 김수현 (강원대학교 바이오산업공학부 식품생명공학과) ;
  • 유수정 (강원대학교 바이오산업공학부 식품생명공학과) ;
  • 함승시 (강원대학교 바이오산업공학부 식품생명공학과)
  • Published : 2007.08.31

Abstract

This study was performed to observe the antioxidative effects, antimutagenic capacity, and cytotoxic activity of the 70% ethanol extract, and fractions, of Agaricus blazei Murill mycelium, using DPPH free radical scavenging ability, the Ames test, and SRB assay, respectively. Among the fractions, ethyl acetate showed the most effective antioxidative capacity according to the $RC_{50}$(73.6 $\mu$g/mL) of the scavenging effect on the DPPH radical. The inhibition rate of both the aqueous fraction and 70% ethanol extract(200 $\mu$g/plate) toward the Salmonella typhimurium TA100 strain was 94.6%, and it was 89.4% against the mutagenesis induced by MNNG(0.4 $\mu$g/plate). In addition, an identical concentration of the 70% ethanol extract in the TA98 strain, and the ethyl acetate fraction in the TA100 strain, showed inhibition rates of 80.3% and 76.9%, respectively, the highest activities against the mutagenesis induced by 4NQO(0.15 $\mu$g/plate). The cytotoxic effects of the 70% ethanol extract and its fractions increased with increasing sample concentration against human cervical adenocarcinoma(HeLa), human hepatocellular carcinoma(Hep3B), human breast adenocarcinoma(MCF-7), human stomach adenocarcinoma(AGS), and human lung carcinoma (A549). A 1 mg/mL concentration of the ethyl acetate fraction showed cytotoxicities of 77%, 83.8%, 82.1%, 83.1%, and 92.6% against HeLa, Hep3B, MCF-7, AGS and A549, respectively.

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