Glycyrrhizin inhibits LPS-induced inflammatory mediator production in endometrial epithelial cells
Lab / animal
OA: closed
CC0
⤵ 7 in-corpus citations
AI-generated summary
Glycyrrhizin was found to inhibit the production of inflammatory mediators in endometrial epithelial cells stimulated by lipopolysaccharide.
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Abstract
Endometriosis is a continuous inflammation of uterine endometrium that usually affects women of reproductive age. Glycyrrhizin, a triterpene isolated from the roots and rhizomes of licorice (Glycyrrhiza glabra), has been known to have anti-inflammatory effect. The purpose of this study was to investigate the anti-inflammatory effect of glycyrrhizin on LPS-stimulated mouse endometrial epithelial cells (MEEC). The levels of TNF-α, IL-1β, and PGE2 were measured by ELISA. The expression of COX-2, iNOS, TLR4, and NF-ĸB were detected by western blot analysis. The results showed that glycyrrhizin significantly suppressed LPS-induced TNF-α, IL-1β, NO, and PGE2 production. Also, LPS-induced iNOS and COX-2 expression were attenuated by glycyrrhizin. Furthermore, glycyrrhizin significantly attenuated TLR4 expression and NF-κB activation induced by LPS in MEEC. In conclusion, the present study demonstrated that glycyrrhizin inhibited LPS-induced inflammatory response by inhibiting TLR4 signaling pathway in MEEC. Glycyrrhizin may be used as a potential agent for the treatment of endometriosis.
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Cited by (7)
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- Establishment of Immortalized Human Endometriotic Stromal Cell Line from Ectopic Lesion of a Patient with Endometriosis 2023
- Immunotherapy: A promising novel endometriosis therapy 2023
- An Update on the Multifaceted Role of NF-kappaB in Endometriosis 2022
- The impact of herbal medicine in regulating intestinal flora on female reproductive disorders 2022
- Cyclooxygenase-2 in Endometriosis 2019
- From Endometriosis to Cancer: Spotlight on Intracellular Signaling Cascades and MicroRNAs 2018
Source provenance
- europepmc
- last seen: 2026-10-09T06:09:53.026058+00:00
- openalex
- last seen: 2026-06-10T17:14:06.276822+00:00
- pubmed
- last seen: 2026-10-08T21:20:02.015990+00:00
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