Generic placeholder image

Current Analytical Chemistry

Editor-in-Chief

ISSN (Print): 1573-4110
ISSN (Online): 1875-6727

General Research Article

Characterization of Flavonoid Constituents in Stems of Lithocarpus litseifolius (Hance) Chun by UHPLC-Q-Exactive Orbitrap MS

Author(s): Liang-Hong Liu, Jie Peng, Si-lin Shi, Kai-Lin Li, Pei Xiong and Wei Cai*

Volume 17, Issue 4, 2021

Published on: 19 June, 2020

Page: [521 - 527] Pages: 7

DOI: 10.2174/1573411016999200619184952

Price: $65

Abstract

Background: Lithocarpus litseifolius (Hance) Chun (L. litseifolius) has been used for treating diabetes, allergic and inflammatory diseases, and hyperlipidemia in folk medicine. Previous studies have shown that the main active ingredients of its leaves are flavonoids. However, to the best of our knowledge, the stem of L. litseifolius has not been investigated for its constituents yet. The stems of the decaying plants fall every year. It is considered as a waste due to limited knowledge of the benefits of these stems, which is a sheer waste of the plant resource. Therefore, it is necessary to investigate the chemical constituents of the stem, which will be beneficial for the treatment of many diseases and help utilize the stem in a better way instead of wasting the plant resource.

Methods: In this study, the dry twigs of L. litseifolius were collected, powdered, and extracted. Then, the extracted sample was subjected to UHPLC-Q-Exactive Orbitrap MS in negative mode combined with Parallel reaction monitoring scanning to gain the high-resolution mass spectrum, which was processed by the Compound Discover version 3.0 using high resolution extracted ion chromatography to predict the constituent compounds.

Results: A total of 35 flavonoids including flavone, flavonol, dihydroflavone, isoflavone, and dihydrochalcone were putatively identified based on their accurate mass measurement, chromatographic retention, MSn spectra, and bibliography data.

Conclusion: In this study, a total of 35 flavonoids were identified in the stem of L. litseifolius, among which 5 flavonoids were the first to be reported from this plant, which will be very helpful for the development of medicines for the treatment of many diseases and utilization of the stem of L. litseifolius.

Keywords: Flavonoid, folk medicine, Lithocarpus litseifolius (Hance) Chun, Lithocarpus polystachyus Rehder, traditional chinese medicine, UHPLC-Q-Excative Orbitrap MS.

Graphical Abstract

[1]
Editorial Board of Flora of China. Flora of China, 1st Ed.; Bei Jing: Science Press, 1999, 4, p. 59.
[2]
Sun, Y.; Li, W.; Liu, Z. Preparative isolation, quantification and antioxidant activity of dihydrochalcones from Sweet Tea (Lithocarpus polystachyus Rehd.). J. Chromatogr. B Analyt. Technol. Biomed. Life Sci., 2015, 1002, 372-378.
[http://dx.doi.org/10.1016/j.jchromb.2015.08.045] [PMID: 26363372]
[3]
Cheng, J.; Lyu, L.S.; Shen, Y.B.; Li, K.X.; Liu, Z.H.; Wang, W.X.; Xie, L. Population structure and genetic diversity of Lithocarpus litseifolius (Fagaceae) assessed using microsatellite markers. Nord. J. Bot., 2016, 34, 752-760.
[http://dx.doi.org/10.1111/njb.01111]
[4]
Li, A.M.; Li, S.H.; Wu, X.J.; Zhang, J.; He, A.N.; Zhao, G.; Yang, X. Effect of light intensity on leaf photosynthetic characteristics and accumulation of flavonoids in Lithocarpus litseifolius (Hance) Chun. (Fagaceae). Open J. For., 2016, 6, 445-459.
[http://dx.doi.org/10.4236/ojf.2016.65034]
[5]
Meng, Y.; Ding, L.; Wang, Y.; Nie, Q.; Xing, Y.; Ren, Q. Phytochemical identification from Lithocarpus polystachyus by UHPLC-Q-TOF-MS and its protein tyrosine phosphatase 1B and α-glucosidase activities. Biomed. Chromatogr., 2019, 2019e4705
[PMID: 31629370]
[6]
Dong, H.Q.; Li, M.; Zhu, F.; Liu, F.L.; Huang, J.B. Inhibitory potential of trilobatin from Lithocarpus polystachyus Rehd against α-glucosidase and α-amylase linked to type 2 diabetes. Food Chem., 2012, 130, 261-266.
[http://dx.doi.org/10.1016/j.foodchem.2011.07.030]
[7]
Zhou, C.J.; Huang, S.; Liu, J.Q.; Qiu, S.Q.; Xie, F.Y.; Song, H.P.; Li, Y.S.; Hou, S.Z.; Lai, X.P. Sweet tea leaves extract improves leptin resistance in diet-induced obese rats. J. Ethnopharmacol., 2013, 145(1), 386-392.
[http://dx.doi.org/10.1016/j.jep.2012.09.057] [PMID: 23147498]
[8]
Hou, S.Z.; Chen, S.X.; Huang, S.; Jiang, D.X.; Zhou, C.J.; Chen, C.Q.; Liang, Y.M.; Lai, X.P. The hypoglycemic activity of Lithocarpus polystachyus Rehd. leaves in the experimental hyperglycemic rats. J. Ethnopharmacol., 2011, 138(1), 142-149.
[http://dx.doi.org/10.1016/j.jep.2011.08.067] [PMID: 21924344]
[9]
Lin, C.; Wang, L.; Wang, H.; Fang, S.; Zhang, Q.; Yang, L.; Guo, H.; Lin, P.; Zhang, J.; Wang, X. Lithocarpus polystachyus REHD leaf aqueous extract inhibits human breast cancer growth in vitro and in vivo. Nutr. Cancer, 2014, 66(4), 613-624.
[http://dx.doi.org/10.1080/01635581.2014.894094] [PMID: 24660968]
[10]
Li, S.H.; Zeng, J.Y.; Tan, J.; Zhang, J.; Wu, Q.F.; Wang, L.P.; Wu, X.J. Antioxidant and hepatoprotective effects of Lithocarpus polystachyus against carbon tetrachloride-induced injuries in rat. Bangladesh J. Pharmacol., 2013, 8, 420-427.
[11]
Koprivica, M.R.; Trifković, J.Đ.; Dramićanin, A.M. Gašić, U. M. Fotirić Akšić, M. M. Milojković-Opsenica, D. M. Determination of the phenolic profile of peach (Prunus persica L.) kernels using UHPLC-LTQ OrbiTrap MS/MS technique. Eur. Food Res. Technol., 2018, 244, 2051-2064.
[http://dx.doi.org/10.1007/s00217-018-3116-2]
[12]
Chen, X.; Xu, L.; Guo, S.; Wang, Z.; Jiang, L.; Wang, F.; Zhang, J.; Liu, B. Profiling and comparison of the metabolites of diosmetin and diosmin in rat urine, plasma and feces using UHPLC-LTQ-Orbitrap MSn. J. Chromatogr. B Analyt. Technol. Biomed. Life Sci., 2019, 1124, 58-71.
[http://dx.doi.org/10.1016/j.jchromb.2019.05.030] [PMID: 31177049]
[13]
Lv, X.; Sun, J.Z.; Xu, S.Z.; Cai, Q.; Liu, Y.Q. Rapid characterization and identification of chemical constituents in gentiana radix before and after wine-processed by UHPLC-LTQ-Orbitrap MSn. Molecules, 2018, 23(12), 3222.
[http://dx.doi.org/10.3390/molecules23123222] [PMID: 30563266]
[14]
Jiao, Q.; Xu, L.; Jiang, L.; Jiang, Y.; Zhang, J.; Liu, B. Metabolism study of hesperetin and hesperidin in rats by UHPLC-LTQ-Orbitrap MSn. Xenobiotica, 2019, 2019, 1-27.
[http://dx.doi.org/10.1080/00498254.2019.1567956 PMID: 30654682]
[15]
Liu, L.; Zhang, J.; Zheng, B.; Guan, Y.; Wang, L.; Chen, L.; Cai, W. Rapid characterization of chlorogenic acids in Duhaldea nervosa based on ultra-high-performance liquid chromatography-linear trap quadropole-Orbitrap-mass spectrometry and mass spectral trees similarity filter technique. J. Sep. Sci., 2018, 41(8), 1764-1774.
[http://dx.doi.org/10.1002/jssc.201701047] [PMID: 29327507]
[16]
Dahibhate, N.L.; Kumar, D.; Kumar, K. Simultaneous analysis of vanillin and coumarin in mangrove plants and commercial food products using UPLC-ESI-MS/MS. Curr. Anal. Chem., 2019, 15, 1-10.
[http://dx.doi.org/10.2174/1573411015666190828185647]
[17]
Wang, M.; Liu, X.; Zhang, Z.; Yu, J.; Liu, J.; Wu, Y. Phytochemicals and bioactive analysis of different sweet tea (Lithocarpus litseifolius [Hance] Chun) varieties. J. Food Biochem., 2020, 8e13183
[http://dx.doi.org/10.1111/jfbc.13183] [PMID: 32180255]
[18]
Cai, W.; Li, K.L.; Xiong, P.; Gong, K.Y.; Zhu, L.; Yang, J.B. Wu. W. H. A systematic strategy for rapid identification of chlorogenic acids derivatives in Duhaldea nervosa using UHPLC-Q-Exactive Orbitrap mass spectrometry. Arab. J. Chem., 2020, 13, 3751-3761.
[http://dx.doi.org/10.1016/j.arabjc.2020.01.007]
[19]
Zhao, Y.; Li, X.; Zeng, X.; Huang, S.; Hou, S.Z.; Lai, X.P. Characterization of phenolic constituents in Lithocarpus polystachyus. Anal Methods-UK, 2014, 6, 1359-1363.
[http://dx.doi.org/10.1039/c3ay41288a]
[20]
Yang, J.; Huang, Y.Y.; Yang, Z.; Zhou, C.; Hu, X.J. Identification and quantitative evaluation of major sweet ingredients in sweet tea (Lithocarpus polystachyus Rehd.) Based upon location, harvesting time, leaf age. J. Chem. Soc. Pakistan, 2018, 40, 158-164.
[21]
Kachlicki, P.; Piasecka, A.; Stobiecki, M.; Marczak, Ł. Structural characterization of flavonoid glycoconjugates and their derivatives with mass spectrometric techniques. Molecules, 2016, 21(11), 1494.
[http://dx.doi.org/10.3390/molecules21111494] [PMID: 27834838]

Rights & Permissions Print Cite
© 2024 Bentham Science Publishers | Privacy Policy