Preparation and characterization of fenugreek leaf flavonoids and their protective effects against oxidative damage to hepatocytes.
10.19540/j.cnki.cjcmm.20211029.402
- Author:
Rui-Nan WANG
1
;
Yang-Yang FU
2
;
Fang-Fang TIE
2
;
Na HU
2
;
Hong-Lun WANG
2
;
Yan-Feng HE
1
Author Information
1. College of Pharmacy, Qinghai Minzu University Xining 810007, China.
2. Key Laboratory of Tibetan Medicine Research, Northwest Institute of Plateau Biology, Chinese Academy of Sciences Xining 810001, China.
- Publication Type:Journal Article
- Keywords:
H_2O_2;
L02 cell;
MAPKs/Nrf2/HO-1;
fenugreek leaf;
flavonoids;
oxidative stress
- MeSH:
Antioxidants/pharmacology*;
Apoptosis;
Flavonoids/pharmacology*;
Hepatocytes/metabolism*;
NF-E2-Related Factor 2/metabolism*;
Oxidative Stress;
Plant Leaves/metabolism*;
Superoxide Dismutase/metabolism*;
Tandem Mass Spectrometry;
Trigonella/metabolism*
- From:
China Journal of Chinese Materia Medica
2022;47(8):2178-2186
- CountryChina
- Language:Chinese
-
Abstract:
The present study investigated the main components of fenugreek(Trigonella foenum-graecum L.) leaf flavonoids(FLFs) and their antioxidant activity. FLFs were prepared and enriched by solvent extraction, and the flavonoids were characterized by high-performance liquid chromatography-quadrupole-time-of-flight tandem mass spectrometry(HPLC-Q-TOF-MS/MS). The protective effect of FLFs against H_2O_2-induced stress damage to L02 hepatocytes was also investigated. Firstly, the cell viability was measured by MTT assay. The oxidative stress injury model was induced by H_2O_2 in L02 cells. The release of lactate dehydrogenase(LDH), the content of reduced glutathione(GSH) and malondialdehyde(MDA), and the activities of superoxide dismutase(SOD) and catalase(CAT) were measured by assay kits. Hoechst fluorescence staining was performed to observe the cell apoptosis. The expression levels of c-Jun N-terminal kinase(JNK), extracellular signal-regulated kinase 1/2(ERK1/2), nuclear factor erythroid-2 related factor 2(Nrf2), heme oxygenase 1(HO-1), and their phosphorylated proteins were detected by Western blot. Based on the MS fragment ion information and data in databases, FLFs contained eight flavonoids with quercetin and kaempferol as the main aglycons. The cell viabi-lity assay revealed that as compared with the conditions in the H_2O_2 treatment group, 3.125-25 μg·mL~(-1) FLFs could increase the viability of L02 cells, reduce LDH release and MDA content in a dose-dependent manner, potentiate the activities of SOD, CAT, and GSH, decrease the phosphorylation of JNK and ERK1/2 proteins, and up-regulate the expression of Nrf2 and HO-1. The results of fluorescence staining showed that the nucleus of the H_2O_2 treatment group showed concentrated and dense strong blue fluorescence, while the blue fluorescence intensity of the FLFs group decreased significantly. FLFs showed a protective effect against H_2O_2-induced oxidative damage in L02 cells, and the underlying mechanism is associated with the enhancement of cell capability in clearing oxygen free radicals and the inhibition of apoptosis by the activation of the MAPKs/Nrf2/HO-1 signaling pathway. The antioxidant effect of fenugreek leaf is related to its rich flavonoids.
