Potential mechanism of kaempferol against Cu²+-induced oxidative stress through chelating activity and regulation of nuclear factorerythroid-2-related factor 2 signaling

Metal ions play important roles in various biological processes of living systems. However, the generation of reactive oxygen species (ROS) is also closely linked with the participation of redox-active metal ions such as copper, iron, chromium, and cobalt ions. Excessive production of ROS by redox-a...

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Published inFood science and biotechnology Vol. 21; no. 5; pp. 1469 - 1475
Main Authors Kim, G.N., Kyungnam University, Changwon, Republic of Korea, Kim, E.S., Hannam University, Daejeon, Republic of Korea, Kwon, Y.I., Hannam University, Daejeon, Republic of Korea, Jang, H.D., Hannam University, Daejeon, Republic of Korea
Format Journal Article
LanguageEnglish
Published Heidelberg The Korean Society of Food Science and Technology 01.10.2012
한국식품과학회
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ISSN1226-7708
2092-6456
DOI10.1007/s10068-012-0194-y

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Summary:Metal ions play important roles in various biological processes of living systems. However, the generation of reactive oxygen species (ROS) is also closely linked with the participation of redox-active metal ions such as copper, iron, chromium, and cobalt ions. Excessive production of ROS by redox-active metal ions can cause oxidative stress and further oxidative stress-related diseases. This study shows the results of the antioxidant activity of kaempferol in both ORAC∧OH center dot and Cu²+-treated HepG2 cells. Preventive mechanism of kaempferol in Cu²+-treated HepG2 cells is also elucidated. These results suggest that both cellular Cu²+-chelating activity and expression of phase Ⅱ detoxifying enzymes such as HO-1 and GSTA2 through activating Nrf2 are required for cellular antioxidant activity of kaempferol in Cu²+-treated HepG2 cells. Our findings provide the scientific evidence for the development of Nrf2 targeting dietary antioxidant to prevent oxidative stress-related conditions.
Bibliography:2013002681
Q01
G704-000139.2012.21.5.033
ISSN:1226-7708
2092-6456
DOI:10.1007/s10068-012-0194-y