An essential role of Nrf2 in American ginseng-mediated anti-oxidative actions in cardiomyocytes

被引:73
作者
Li, Jinqing [1 ]
Ichikawa, Tomonaga [1 ]
Jin, Yu [2 ]
Hofseth, Lorne J. [2 ]
Nagarkatti, Prakash [3 ]
Nagarkatti, Mitzi [3 ]
Windust, Anthony [4 ]
Cui, Taixing [1 ]
机构
[1] Univ S Carolina, Dept Cell Biol & Anat, Columbia, SC 29208 USA
[2] Univ S Carolina, Dept Pharmaceut & Biomed Sci, Columbia, SC 29208 USA
[3] Univ S Carolina, Dept Pathol Microbiol & Immunol, Columbia, SC 29208 USA
[4] Natl Res Council Canada, Ottawa, ON, Canada
关键词
Panax quinquefolius; American ginseng; Nrf2; Oxidative stress; Cardiomyocytes; Cell death; CARDIAC-HYPERTROPHY; OXIDATIVE STRESS; CARDIOVASCULAR-DISEASE; OXIDANT STRESS; HEART-FAILURE; LIPOPOLYSACCHARIDE; CONSTITUENTS; MACROPHAGES; TRILINOLEIN; PROTECTION;
D O I
10.1016/j.jep.2010.03.040
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Aim of the study: Ginseng has been used as a folk medicine for thousands of years in Asia, and has become a popular herbal medicine world-wide. Recent studies have revealed that ginseng, including American ginseng, exerts antioxidant effects in the cardiovascular system; however, the underlying mechanisms are not fully understood. Thus, we investigated role of Nrf2, a master transcription factor of endogenous anti-oxidative defense systems, in the regulation of American ginseng-mediated anti-oxidative actions in cardiomyocytes. Materials and methods: A standardized crude extract of American ginseng was supplied by the National Research Council of Canada, Institute for National Measurement Standards. H9C2 cells, a rat cardiomyocyte cell line, were exposed to angiotensin II (Ang II) or tumor necrosis factor alpha (TNF alpha) to induce oxidative stress that was examined by measuring formation of reactive oxygen and nitrogen species. Oxidative stress-induced cell death was induced by exogenous addition of hydrogen peroxide (H2O2). Proteins were measured by Western blot and mRNA expression was determined by quantitative real time PCR. Nrf2-driven transcriptional activity was assessed by antioxidant response element (ARE)-luciferase reporter assay. Direct Nrf2 binding to its target gene promoters was determined by chromatin immunoprecipitation assay. Adenoviral over-expression of Nrf2 shRNA was utilized to knock down Nrf2 in H9C2 cells. Immunochemical staining was applied for Nrf2 expression in the heart. Results: American ginseng induced dramatic increases in Nrf2 protein expression, Nrf2 nuclear translocation, Nrf2 transcriptional activity, direct Nrf2 binding to its target gene promoters, and expression of a group of anti-oxidative genes driven by Nrf2 in H9C2 cells. In addition, American ginseng inhibited Ang II- or TNF alpha-induced free radical formation and H2O2-induced cell death in H9C2 cells over-expressed with control shRNA but not in the cells over-expressed with Nrf2 shRNA. Finally, oral administration of American ginseng markedly increased Nrf2 activity in murine hearts. Conclusion: These results demonstrate that American ginseng suppresses oxidative stress and oxidative stress-induced cell death in cardiomyocytes through activating the Nrf2 pathway, thereby providing cardioprotection against pathological cardiac remodeling. (C) 2010 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:222 / 230
页数:9
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