Cycloartane-type saponins from <i>Curculigo orchioides</i> and their anti-inflammatory activity

<i>Curculigo orchioides</i> is a traditional medicinal plant used in Asia for treating inflammation and related ailments. In this study, nine compounds were isolated, including six novel cycloartane-type saponins, namely curculigosaponins P-U (1-6) and three known compounds. Among the six new compounds, compound 1 exhibited moderate inhibition of NO production (IC<sub>50</sub> = 37.21 μM) in LPS-stimulated RAW 264.7 macrophages. It also suppressed the expression of TNF-α and IL-6, and downregulated iNOS and COX-2 protein levels, confirming its anti-inflammatory activity. Molecular docking analysis revealed favorable binding interactions of compound 1 with key inflammatory targets (iNOS, IL-6, TNF-α, and COX-2), supporting its proposed mechanism of action. These results suggest that compound 1 (curculigosaponins P) is a promising anti-inflammatory lead compound from <i>C. orchioides</i> and deserves further investigation.

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Publication Details

Journal
RSC Advances
Published
2025-01-01
DOI
https://doi.org/10.1039/d5ra04849d
Primary Topic
Natural product bioactivities and synthesis
Type
article
Field-Weighted Citation Impact
0.00

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article

Cycloartane-type saponins from Curculigo orchioides and their anti-inflammatory activity

Vu N. Bach, Vu Mai Thao, Nguyễn Xuân Nhiệm, Nguyen Hai Dang et al.
RSC Advances
Natural product bioactivities and synthesis
article

Cycloartane-type saponins from Curculigo orchioides and their anti-inflammatory activity

Vu N. Bach, Vu Mai Thao, Nguyễn Xuân Nhiệm, Nguyen Hai Dang, Lê Thanh Hương, Hai Pham‐The
article en

Abstract

<i>Curculigo orchioides</i> is a traditional medicinal plant used in Asia for treating inflammation and related ailments. In this study, nine compounds were isolated, including six novel cycloartane-type saponins, namely curculigosaponins P-U (1-6) and three known compounds. Among the six new compounds, compound 1 exhibited moderate inhibition of NO production (IC<sub>50</sub> = 37.21 μM) in LPS-stimulated RAW 264.7 macrophages. It also suppressed the expression of TNF-α and IL-6, and downregulated iNOS and COX-2 protein levels, confirming its anti-inflammatory activity. Molecular docking analysis revealed favorable binding interactions of compound 1 with key inflammatory targets (iNOS, IL-6, TNF-α, and COX-2), supporting its proposed mechanism of action. These results suggest that compound 1 (curculigosaponins P) is a promising anti-inflammatory lead compound from <i>C. orchioides</i> and deserves further investigation.

RSC AdvancesVol. 15(49)
Vietnam Academy of Science and Technology (VN), Hanoi University of Science and Technology (VN)
Heilongjiang University of Science and Technology
Openalex Percentile: Top 72%
Natural product bioactivities and synthesis
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