Extraction, isolation and identification of four phenolic compounds from Pleioblastus amarus shoots and their antioxidant and anti-inflammatory properties in vitro

[Display omitted] •Four phenolic compounds of the shoots of Pleioblastus amarus were isolated and identified for the first time.•All the four compounds showed significant antioxidant capacity.•Compound 2 (3-O-feruloyquinic acid) had strongest antioxidant capacity, but was unstable.•Compound 2 inhibi...

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Veröffentlicht in:Food chemistry 2022-04, Vol.374, p.131743-131743, Article 131743
Hauptverfasser: Ao, Xiaolin, Yan, Junling, Liu, Shuliang, Chen, Shujuan, Zou, Likou, Yang, Yong, He, Li, Li, Shanshan, Liu, Aiping, Zhao, Ke
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Sprache:eng
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Zusammenfassung:[Display omitted] •Four phenolic compounds of the shoots of Pleioblastus amarus were isolated and identified for the first time.•All the four compounds showed significant antioxidant capacity.•Compound 2 (3-O-feruloyquinic acid) had strongest antioxidant capacity, but was unstable.•Compound 2 inhibit IL-6, 1L-1β, iNOS, COX-2 and NF-κB production by RAW264.7 cells. Pleioblastus amarus (P. amarus) shoots, belong to the grass family Gramineae, a traditional green vegetable in China, are rich in nutritional properties, and can provide various health benefits. This study isolated four compounds, namely (1–4), 3-O-coumaroylquinic acid (1), 3-O-feruloylquinic acid (2), 4-O-feruloylquinic acid (3), and 5-O-feruloylquinic acid (4) from Pleioblastus amarus shoots for the first time. The structures of the extracted compounds were determined using detailed spectroscopic (1D/2D NMR), high resolution electrospray ionization mass spectrometry (HR-ESI-MS), and infrared (IR) spectroscopy. The antioxidant capacity of 3-O-feruloylquinic acid (2) was stronger than that of the other compounds, while it also exhibited anti-inflammatory activity, significantly restricting the release of nitric oxide (NO) by lipopolysaccharide (LPS)-induced RAW 264.7 cells, displaying an inhibitory rate of 60.92 percent at a concentration of 400 μg/mL. Furthermore, 3-O-feruloylquinic acid (2) inhibited interleukin-1β (IL-1β), interleukin-6 (IL-6), inducible nitric oxide synthase (iNOS), cyclooxygenase-2 (COX-2), and nuclear factor-κB (NF-κB) expression and may be useful for developing novel antioxidant and anti-inflammatory substances.
ISSN:0308-8146
1873-7072
DOI:10.1016/j.foodchem.2021.131743