Anti-inflammatory germacrane-type sesquiterpene lactones from Vernonia sylvatica

Min WANG , Han LI , Bintao HU , Chunping TANG , Hui XU , Changqiang KE , Zuoquan XIE , Yang YE , Sheng YAO

Chinese Journal of Natural Medicines ›› 2024, Vol. 22 ›› Issue (6) : 568 -576.

PDF (1122KB)
Chinese Journal of Natural Medicines ›› 2024, Vol. 22 ›› Issue (6) :568 -576. DOI: 10.1016/S1875-5364(24)60656-4
Original article
research-article
Anti-inflammatory germacrane-type sesquiterpene lactones from Vernonia sylvatica
Author information +
History +
PDF (1122KB)

Abstract

Nine new germacranolides, sylvaticalides A−H (1-9), and three known analogues (10-12) were isolated from the aerial part of Vernonia sylvatica. Their structures were established using comprehensive spectroscopic analysis, including high-resolution electrospray ionization mass spectroscopy (HR-ESI-MS) and 1D and 2D nuclear magnetic resonance (NMR) spectra. Their absolute configurations were determined by X-ray diffraction experiments. The anti-inflammatory activities of all isolated compounds were assessed by evaluating their inhibitory effects on the nuclear factor kappa B (NF-κB) pathway, which was activated by lipopolysaccharide (LPS)-stimulated human THP1-Dual cells, and the interferon-stimulated gene (ISG) pathway, activated by STING agonist MSA-2 in the same cell model. Compounds 1, 2 and 6 showed inhibitory effects on the NF-κB and ISG signaling pathways, with IC50 values ranging from 4.12 to 10.57 μmol·L−1.

Keywords

Vernonia sylvatica / Germacrane-type sesquiterpene lactone / Sylvaticalides A−H / Anti-inflammatory / NF-κB pathway / ISG pathway

Cite this article

Download citation ▾
Min WANG, Han LI, Bintao HU, Chunping TANG, Hui XU, Changqiang KE, Zuoquan XIE, Yang YE, Sheng YAO. Anti-inflammatory germacrane-type sesquiterpene lactones from Vernonia sylvatica. Chinese Journal of Natural Medicines, 2024, 22(6): 568-576 DOI:10.1016/S1875-5364(24)60656-4

登录浏览全文

4963

注册一个新账户 忘记密码

References

[1]

Zhu L, Liu XQ, Lin YL, et al. Cytotoxic germacranolides from the whole plant of Carpesium minus[J]. J Nat Prod, 2020, 83(11): 3230-3238.

[2]

Zhu NL, Tang C, Xu C, et al. Cytotoxic germacrane-Ttype sesquiterpene lactones from the whole plant of Carpesium lipskyi[J]. J Nat Prod, 2019, 82(4): 919-927.

[3]

Thongnest S, Chawengrum P, Keeratichamroen S, et al. Vernodalidimer L, a sesquiterpene lactone dimer from Vernonia extensa and anti-tumor effects of vernodalin, vernolepin, and vernolide on HepG2 liver cancer cells[J]. Bioorg Chem, 2019, 92: 103197.

[4]

Kuo LY, Tseng PY, Lin YC, et al. New hirsutinolide-type sesquiterpenoids from Vernonia cinerea inhibit nitric oxide production in LPS-stimulated RAW264.7 cells[J]. Planta Med, 2018, 84(18): 1348-1354.

[5]

Wu JW, Tang CP, Cai YY, et al. Cytotoxic germacrane-type sesquiterpene lactones from the whole plant of Inula cappa[J]. Chinese Chem Lett, 2017, 28(5): 927-930.

[6]

Xu W, Bai M, Liu DF, et al. MS/MS-based molecular networking accelerated discovery of germacrane-type sesquiterpene lactones from Elephantopus scaber L.[J]. Phytochemistry, 2022, 198: 113136.

[7]

Jang H, Lee JW, Kim JG, et al. Nitric oxide inhibitory constituents from Siegesbeckia pubescens[J]. Bioorg Chem, 2018, 80: 81-85.

[8]

Mofidi TS, Nejad ES, Salehi P, et al. Antiprotozoal germacranolide sesquiterpene lactones from Tanacetum sonbolii[J]. Planta Med, 2019, 85(5): 424-430.

[9]

Kimani NM, Matasyoh JC, Kaiser M, et al. Antiprotozoal sesquiterpene lactones and other constituents from Tarchonanthus camphoratus and Schkuhria pinnata[J]. J Nat Prod, 2018, 81(1): 124-130.

[10]

Yu X, Zhang Q, Tian L, et al. Germacrane-type sesquiterpenoids with antiproliferative activities from Eupatorium chinense[J]. J Nat Prod, 2018, 81(1): 85-91.

[11]

Freund RRA, Gobrecht P, Fischer D, et al. Advances in chemistry and bioactivity of parthenolide[J]. Nat Prod Rep, 2020, 37(4): 541-565.

[12]

Long J, Zhang SF, Wang PP, et al. Total syntheses of parthenolide and its analogues with macrocyclic stereocontrol[J]. J Med Chem, 2014, 57(16): 7098-7112.

[13]

Dogra NK, Kumar S, Kumar D. Vernonia anthelmintica (L. ) Willd. : an ethnomedicinal, phytochemical, pharmacological and toxicological review[J]. J Ethnopharmacol, 2020, 256: 112777.

[14]

Zhang M, Yang X, Wei Y, et al. Bioactive sesquiterpene lactones isolated from the whole plants of Vernonia cinerea[J]. J Nat Prod, 2019, 82(8): 2124-2131.

[15]

Sinisi A, Millan E, Abay SM, et al. Poly-electrophilic sesquiterpene lactones from Vernonia amygdalina: new members and differences in their mechanism of thiol trapping and in bioactivity[J]. J Nat Prod, 2015, 78(7): 1618-1623.

[16]

Youn UJ, Miklossy G, Chai X, et al. Bioactive sesquiterpene lactones and other compounds isolated from Vernonia cinerea[J]. Fitoterapia, 2014, 93: 194-200.

[17]

Editor committee. Flora of China[M]. Science Press, Beijing, 1985: 18.

[18]

Alicia B, Cesar A, Alicia B, et al. Glaucolides and related sesquiterpene lactones from Vernonia incana[J]. Phytochemistry, 1990, 29: 313-315.

[19]

Patricia LC, John MC, Ching C, et al. Isolation and structure determination of Piptocarphins A-F, cytotoxic germacranolide lactones from Piptocarpha chontalensis[J]. J Org Chem, 1981, 46: 1108-1114.

[20]

Susana B, Alicia B, Cesar AN, et al. Glaucolides, hirsutinolides and other sesquiterpene lactones from Vernonanthura pinguis[J]. Phytochemistry, 1997, 44: 465-470.

[21]

Guha M, Mackman N. LPS induction of gene expression in human monocytes[J]. Cell Signal, 2001, 13: 85-94.

[22]

Pan BS, Perera SA, Piesvaux JA, et al. An orally available non-nucleotide STING agonist with antitumor activity[J]. Science, 2020, 369: 935.

PDF (1122KB)

0

Accesses

0

Citation

Detail

Sections
Recommended

/