Molecules (Feb 2023)

Comparison of In Vitro Estrogenic Activity of <i>Polygoni multiflori</i> Radix and <i>Cynanchi wilfordii</i> Radix via the Enhancement of ERα/β Expression in MCF7 Cells

  • Reshmi Akter,
  • Dong Uk Yang,
  • Jong Chan Ahn,
  • Muhammad Awais,
  • Jinnatun Nahar,
  • Zelika Mega Ramadhania,
  • Jong Yun Kim,
  • Gyong Jai Lee,
  • Gi-Young Kwak,
  • Dong Wook Lee,
  • Byoung Man Kong,
  • Deok Chun Yang,
  • Seok-Kyu Jung

DOI
https://doi.org/10.3390/molecules28052199
Journal volume & issue
Vol. 28, no. 5
p. 2199

Abstract

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Postmenopausal women experience several symptoms, including inflammation and a sharp rise in oxidative stress caused by estrogen deprivation. Although estrogen replacement therapy (ERT) is generally regarded as an effective treatment for menopause, it has been used less frequently due to some adverse effects and high costs. Therefore, there is an immediate need to develop an effective herbal-based treatment that is affordable for low-income populations. Acordingly, this study explored the estrogen-like properties of methanol extracts from Cynanchum wilfordii (CW) and Poligonum multiflorum (PM), two important medicinal plants in Republic of Korea, Japan, and China. Due to the similar names and morphologies of these two radixes, they are frequently confused in the marketplace. Our previous colleagues discriminated between these two plants. In this study, we investigated the estrogenic activity of PM and CW using several in vitro assays with their possible mechanism of action. First, their phytochemical contents, such as gallic acid, 2,3,5,4′-tetrahydroxystilbene-2-O-glucoside (TSG) and emodin, were quantified using high-performance liquid chromatography (HPLC). Secondly, estrogen-like activity was assessed utilizing the well-known E-screen test and gene expression analysis in estrogen receptor (ER)-positive MCF7 cells. ROS inhibition and anti-inflammatory effects were analyzed using HaCaT and Raw 264.7 cells, respectively. Our findings demonstrate that PM extracts significantly increased the expression of the estrogen-dependent genes (ERα, ERβ, pS2) and boosted MCF7 cell proliferation in comparison to CW extracts. Additionally, PM extract demonstrated a significant reduction in reactive oxygen species (ROS) production as well as an enhanced antioxidant profile compared to the CW extract. Further, the PM extract treatment significantly reduced the generation of nitric oxide (NO) in RAW 264.7 cells, a murine macrophage cell line, demonstrating the anti-inflammatory properties of the extract. Finally, this research offers an experimental foundation for the use of PM as a phytoestrogen to minimize menopausal symptoms.

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