Multi-model Evaluation of Anti-glycation Effects of Sophora japonica Flowers Aqueous Extract and Its Active Components Analysis

被引:0
作者
Zhou H. [1 ]
Li T. [1 ,2 ]
Li B. [1 ,2 ]
机构
[1] Amway (Shanghai) Technology Development Co., Ltd, Shanghai
[2] Amway (China) Botanical R & D Center, Wuxi
关键词
active components; anti-glycation; fibroblast; non-enzymatic glycosylation; Sophora japonica; UPLC-Triple TOF/MS; zebrafish;
D O I
10.13386/j.issn1002-0306.2022050062
中图分类号
学科分类号
摘要
:Objective: To investigate and analyze anti-glycation effects of the aqueous extract of Sophora japonica flower (SJF) by using different models, as well as its active constitutes identification. Methods: BSA/reducing sugar reaction system, glycosylated fibroblast induced by methylglyoxal and AGEs-increased zebrafish model triggered by glucose solution were simultaneously established to comprehensively evaluate the anti-glycation effects of SJF aqueous extract from biochemical, cellular and zebrafish aspects, respectively. Identification of major components was performed by ultra-high performance liquid chromatography-high resolution mass spectrometry technique (UPLC-Triple TOF/MS). Biochemical system was subsequently adopted to further analyze anti-glycation effects of these primary components. Results: In the BSA/reducing sugar system, IC50 of AGEs inhibition of SJF aqueous extract was 53.93 μg/mL. 10 and 40 μg/mL of SJF aqueous extracts dramatically inhibited CML expressions in fibroblast model (P<0.0001), which decreased by 72.28% and 83.85%, respectively. Then, zebrafish model was also used to verify anti-glycation effects of SJF aqueous extract. When the concentration of SJF aqueous extract reached 2 mg/mL, the glycation inhibitory rate could be as high as 76.85%. Through analysis of UPLC-Triple-TOF/MS, a total of 14 chemical compounds, mainly flavonoids, were preliminarily identified. Seven compounds among them were selected for further anti-glycation evaluation by BSA/reducing sugar system. All of the seven compounds showed variable activities toward anti-AGEs production, notably, rutin, quercetin and kaempferol revealed a remarkable activity with a IC50 of 165.5, 133.0 and 42.9 μmol/L, respectively, which were better than that of positive control drugs. Conclusion: SJF aqueous extract shows remarkable anti-glycation activity. Flavonoids such as rutin, quercetin and kaempferol are its potential active compounds. © 2023, Editorial Department of Science and Technology of Food Science. All rights reserved.
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页码:371 / 379
页数:8
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共 49 条
[1]  
ELOSTA A, GHOUS T, AHMED N., Natural products as anti-glycation agents: Possible therapeutic potential for diabetic compli-cations[J], Current Diabetes Reviews, 8, 2, (2012)
[2]  
WEI Q, LIU T, SUN D, Et al., Advanced glycation end-pro-ducts (AGEs) in foods and their detecting techniques and methods: A review[J], Trends in Food Science & Technology, 82, pp. 32-45, (2018)
[3]  
DARIVA B, NAGARAJU G., Advanced glycation end products in diabetes, cancer and phytochemical therapy[J], Drug Discovery Today, 25, 9, pp. 1614-1623, (2020)
[4]  
BUSER W, ERBERSDOBLER H F, LIARDON R., Identification and determination of Nε-carboxymethyllysine by gas-liquid chromatography[J], Journal of Chromatography A, 387, pp. 515-519, (1987)
[5]  
HAN W F, TAN X H, LIN X L, Et al., Research progress on formation mechanism and inhibition pathway of carboxymethyl lysine in food[J], Modern Food Technology, 34, 1, (2018)
[6]  
EMEL V., Glycation, antiglycation, and deglycation: Their role in aging mechanisms and geroprotective effects (literature review) [J], Advances in Gerontology, 7, 1, pp. 1-9, (2017)
[7]  
OTT C, JACOBS K, HAUCKE E, Et al., Role of advanced gly-cation end products in cellular signaling[J], Redox Biology, 2, pp. 411-429, (2014)
[8]  
NEDIC O, RATTAN S, GRUNE T, Et al., Molecular effects of advanced glycation end products on cell signaling pathways, ageing and pathophysiology[J], Free Radical Research, 47, (2013)
[9]  
AHMED N., Advanced glycation end products role in patholo-gy of diabetic complications[J], Diabetes Research and Clinical Practice, 67, 1, (2005)
[10]  
FERREIRA C, PENNACCHI P C, ARAUJO T H, Et al., Aminoguanidine treatment increased NOX2 response in diabetic rats: Improved phagocytosis and killing of Candida albicans by neu-trophils[J], European Journal of Pharmacology, 772, (2016)