AI Article Synopsis

  • Shaoyao-Gancao Decoction (SGD) is a traditional Chinese medicine commonly used to manage conditions like adenomyosis, but its mechanisms of action were not well understood.
  • This study evaluated the effects of SGD and its key components (paeoniflorin and liquiritin) on human adenomyosis-derived cells, focusing on cell growth and apoptosis.
  • Findings revealed that SGD and its components can inhibit cell proliferation, promote apoptosis, and reduce inflammation-related factors, suggesting potential therapeutic pathways for treating adenomyosis.

Article Abstract

Background. Shaoyao-Gancao Decoction (SGD), a well-known traditional Chinese medicine prescription, has been widely used to treat adenomyosis, dysmenorrhea, abdominal pain, and inflammation in Asia. However, the mechanism underlying the effectiveness of SGD in the treatment of adenomyosis still remains elusive. The present study aimed to investigate the bioactivity of SGD and its underlying molecular mechanisms using cultured human adenomyosis-derived cells. Methods. Human adenomyosis-derived cells were treated with SGD and its major constituents (paeoniflorin and liquiritin) in vitro. Effects of SGD, paeoniflorin, and liquiritin on cell proliferation and apoptosis were examined by MTT assay and flow cytometry analyses. The effects of SGD, paeoniflorin, and liquiritin on the production of PGE2 and PGF2α were assayed using ELISA. ER-α and OTR mRNA expression levels were also evaluated by real-time qRT-PCR. Results. SGD, paeoniflorin, and liquiritin inhibited proliferation and induced apoptosis of human adenomyosis-derived cells in a dose-dependent manner. SGD and paeoniflorin significantly reduced the PGE2 and PGF2α production. Furthermore, they remarkably decreased the mRNA levels of ER-α and OTR. Conclusions. The results of this study provide possible mechanisms for the bioactivity of SGD for treating adenomyosis and contribute to the ethnopharmacological knowledge about this prescription.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4243767PMC
http://dx.doi.org/10.1155/2014/982913DOI Listing

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