Sulfur-containing spiroketals from Breynia disticha and evaluations of their anti-inflammatory effect.
Ken-Ichi NakashimaNaohito AbeMasayoshi OyamaHiroko MurataMakoto InouePublished in: Beilstein journal of organic chemistry (2023)
Breynia spp. are a key source of sulfur-containing spiroketal glycosides with potential anti-inflammatory activity. In this study, three new sulfur-containing spiroketals - breynin J ( 1 ), epibreynin J ( 2 ), and probreynogenin ( 3 ) - along with four known compounds - probreynin I ( 4 ), phyllaemblic acid ( 5 ), breynin B ( 6 ), and epibreynin B ( 7 ) - were isolated from the roots of Breynia disticha . The structures of compounds 1 - 7 were elucidated by extensive 1D and 2D NMR spectroscopic analyses, including 1D total correlation spectroscopy (TOCSY), HSQC, HMBC, double quantum-filtered (DQF)-COSY, heteronuclear two-bond correlation (H2BC), and HSQC-TOCSY experiments, as well as high-resolution electrospray ionization HRESIMS analysis, and quantum chemical electronic CD calculations. Furthermore, the absolute configurations of sugar residues were determined by derivatization of the hydrolysates with ʟ-cysteine methyl ester and o -tolyl isothiocyanate followed by HPLC analysis. The anti-inflammatory effects of the isolated compounds were evaluated based on the mRNA levels of proinflammatory cytokines in lipopolysaccharide (LPS)-stimulated RAW 264.7 murine macrophage cells. Compounds 1 , 2 , 6 , and 7 inhibited the increase in interleukin (IL)-1β and IL-6 mRNA levels stimulated by LPS. Moreover, the most potent compound 7 was found to significantly inhibit the production of IL-1β and IL-6 proteins, as revealed by the analysis of culture supernatants.
Keyphrases
- anti inflammatory
- high resolution
- molecular dynamics
- inflammatory response
- ms ms
- simultaneous determination
- induced apoptosis
- tandem mass spectrometry
- high performance liquid chromatography
- mass spectrometry
- toll like receptor
- molecular docking
- adipose tissue
- cell death
- liquid chromatography tandem mass spectrometry
- binding protein
- solid state
- cell cycle arrest
- oxidative stress
- magnetic resonance imaging
- endoplasmic reticulum stress
- monte carlo
- risk assessment
- high speed
- climate change
- cell proliferation
- signaling pathway