Identifying panaxynol, a natural activator of nuclear factor erythroid-2 related factor 2 (Nrf2) from American ginseng as a suppressor of inflamed macrophage-induced cardiomyocyte hypertrophy

J Ethnopharmacol. 2015 Jun 20:168:326-36. doi: 10.1016/j.jep.2015.04.004. Epub 2015 Apr 14.

Abstract

Ethnopharmacological relevance: American ginseng is capable of ameliorating cardiac dysfunction and activating Nrf2, a master regulator of antioxidant defense, in the heart. This study was designed to isolate compounds from American ginseng and to determine those responsible for the Nrf2-mediated resolution of inflamed macrophage-induced cardiomyocyte hypertrophy.

Materials and methods: A standardized crude extract of American ginseng was supplied by the National Research Council of Canada, Institute for National Measurement Standards. A bioassay-based fractionization of American ginseng was performed to identify the putative substances which could activate Nrf2-mediated suppression of pro-inflammatory cytokine expression in macrophages and macrophage-mediated pro-hypertrophic growth in cardiomyocytes.

Results: A hexane fraction of an anti-inflammatory crude extract of American ginseng was found to be most effective in suppressing the inflammatory responses in macrophages. Preparative, reverse-phase HPLC and a comparative analysis by analytical scale LC-UV/MS revealed the hexane fraction contains predominantly C17 polyacetylenes and linolenic acid. Panaxynol, one of the major polyacetylenes, was found to be a potent Nrf2 activator. Panaxynol posttranscriptionally activated Nrf2 by inhibiting Kelch-like ECH-associated protein (Keap) 1-mediated degradation without affecting the binding of Keap1 and Nrf2. Moreover, panaxynol suppressed a selected set of cytokine expression via the activation of Nrf2 while minimally regulating nuclear factor-kappa B (NF-κB)-mediated cytokine expression in macrophages. It also dramatically inhibited the inflamed macrophage-mediated cardiomyocyte death and hypertrophy by activating Nrf2 in macrophages.

Conclusions: These results demonstrate that American ginseng-derived panaxynol is a specific Nrf2 activator and panaxynol-activated Nrf2 signaling is at least partly responsible for American ginseng-induced health benefit in the heart.

Keywords: American ginseng; Cardiomyocytes; Inflammation; Macrophages; Nrf2; Panaxynol.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Anti-Inflammatory Agents / isolation & purification
  • Anti-Inflammatory Agents / pharmacology
  • Cell Line
  • Cytokines / metabolism
  • Diynes / isolation & purification
  • Diynes / pharmacology*
  • Fatty Alcohols / isolation & purification
  • Fatty Alcohols / pharmacology*
  • Female
  • Hypertrophy / drug therapy
  • Hypertrophy / metabolism
  • Macrophages / drug effects*
  • Macrophages / metabolism
  • Male
  • Mice, Knockout
  • Myocytes, Cardiac / drug effects*
  • Myocytes, Cardiac / pathology
  • NF-E2-Related Factor 2 / metabolism*
  • Nitric Oxide Synthase Type II / metabolism
  • Panax*
  • Plant Extracts / chemistry
  • Plant Extracts / pharmacology
  • Rats

Substances

  • Anti-Inflammatory Agents
  • Cytokines
  • Diynes
  • Fatty Alcohols
  • NF-E2-Related Factor 2
  • Plant Extracts
  • falcarinol
  • Nitric Oxide Synthase Type II
  • Nos2 protein, mouse