TY - JOUR
T1 - Phytochemical investigation and anti-inflammatory activity of the leaves of Machilus japonica var. kusanoi
AU - Li, Shiou Ling
AU - Wu, Ho Cheng
AU - Hwang, Tsong Long
AU - Lin, Chu Hung
AU - Yang, Shuen Shin
AU - Chang, Hsun Shuo
N1 - Funding Information:
This study was supported by the Ministry of Science and Technology, R.O.C. (MOST 109-2628-B-037-015), and a Kaohsiung Medical University grant (KMU-TC108A03-8 and KMU-TC108A03-9). We thank the Center for Research Resources and Development of Kaohsiung Medical University for providing a nuclear magnetic resonance (NMR) spectrometer, and also senior technician Chyi-Jia Wang for measuring the 2D NMR data.
Funding Information:
Funding: This study was supported by the Ministry of Science and Technology, R.O.C. (MOST 109-2628-B-037-015), and a Kaohsiung Medical University grant (KMU-TC108A03-8 and KMU-TC108A03-9).
Publisher Copyright:
© 2020 by the authors. Licensee MDPI, Basel, Switzerland.
PY - 2020/9
Y1 - 2020/9
N2 - In a series of anti-inflammatory screenings of lauraceous plants, the methanolic extract of the leaves of Machilus japonica var. kusanoi (Hayata) J.C. Liao showed potent inhibition on both superoxide anion generation and elastase release in human neutrophils. Bioassay-guided fractionation of the leaves of M. japonica var. kusanoi led to the isolation of twenty compounds, including six new butanolides, machinolides A–F (1–6), and fourteen known compounds (7–20). Their structures were characterized by 1D and 2D NMR, UV, IR, CD, and MS data. The absolute configuration of the new compounds were unambiguously confirmed by single-crystal X-ray diffraction analyses (1, 2, and 3) and Mosher’s method (4, 5, and 6). In addition, lignans, (+)-eudesmin (11), (+)-methylpiperitol (12), (+)-pinoresinol (13), and (+)-galbelgin (16) exhibited inhibitory effects on N-formyl-methionyl-leucyl-phenylalanine/cytochalasin B (fMLP/CB)-induced superoxide anion generation in human neutrophils with IC50 values of 8.71 ± 0.74 µM, 2.23 ± 0.92 µM, 6.81 ± 1.07 µM, and 7.15 ± 2.26 µM, respectively. The results revealed the anti-inflammatory potentials of Formosan Machilus japonica var. kusanoi.
AB - In a series of anti-inflammatory screenings of lauraceous plants, the methanolic extract of the leaves of Machilus japonica var. kusanoi (Hayata) J.C. Liao showed potent inhibition on both superoxide anion generation and elastase release in human neutrophils. Bioassay-guided fractionation of the leaves of M. japonica var. kusanoi led to the isolation of twenty compounds, including six new butanolides, machinolides A–F (1–6), and fourteen known compounds (7–20). Their structures were characterized by 1D and 2D NMR, UV, IR, CD, and MS data. The absolute configuration of the new compounds were unambiguously confirmed by single-crystal X-ray diffraction analyses (1, 2, and 3) and Mosher’s method (4, 5, and 6). In addition, lignans, (+)-eudesmin (11), (+)-methylpiperitol (12), (+)-pinoresinol (13), and (+)-galbelgin (16) exhibited inhibitory effects on N-formyl-methionyl-leucyl-phenylalanine/cytochalasin B (fMLP/CB)-induced superoxide anion generation in human neutrophils with IC50 values of 8.71 ± 0.74 µM, 2.23 ± 0.92 µM, 6.81 ± 1.07 µM, and 7.15 ± 2.26 µM, respectively. The results revealed the anti-inflammatory potentials of Formosan Machilus japonica var. kusanoi.
KW - Anti-inflammatory activity
KW - Butanolide
KW - Lauraceae
KW - Lignan
KW - Machilus japonica var. kusanoi
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U2 - 10.3390/molecules25184149
DO - 10.3390/molecules25184149
M3 - Article
C2 - 32927887
AN - SCOPUS:85090825427
SN - 1420-3049
VL - 25
JO - Molecules
JF - Molecules
IS - 18
M1 - 4149
ER -