Lei Liu

Dr. Lei Liu


Research Focus & Metrics

Academic Career Length

10Years (2017-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 January 2017 in Food Chemistry
Verified
Journal Article
Closed access
LLLei Liu
Lei Liu
WWWei Wen
Wei Wen
RZRuifen Zhang
Ruifen Zhang
ZWZhencheng Wei
Zhencheng Wei
YDYuanyuan Deng
Yuanyuan Deng
MZMingwei Zhang
Mingwei Zhang

7 July 2019 in Bioscience, Biotechnology, and Biochemistry
Verified
Journal Article
Closed access
YHYameng Han
Yameng Han
JCJianwei Chi
Jianwei Chi
MZMingwei Zhang
Mingwei Zhang
RZRuifen Zhang
Ruifen Zhang
SFSanhong Fan
Sanhong Fan
LLLei Liu
Lei Liu
This study investigated the contents of saponins and phenolic compounds in relation to their antioxidant activity and α-glucosidase inhibition activity of 7 colored quinoa varieties. The total saponin content was significantly different among 7 varieties and ranged from 7.51 to 12.12 mg OAE/g DW. Darker quinoa had a higher content of phenolic compounds, as well as higher flavonoids and antioxidant activity than that of light varieties. Nine individual phenolic compounds were detected in free and bound form, with gallic acid and ferulic acid representing the major compounds. The free and bound phenolic compounds (gallic acid and ferulic acid in particular) exhibited high linear correlation with their corresponding antioxidant values. In addition, the free phenolic extracts from colored quinoa exhibited higher inhibitory activity against α-glucosidase than the bound phenolic extracts. These findings imply that colored quinoa with abundant bioactive phytochemicals could be an important natural source for preparing functional food.

18 January 2018 in Molecules
Verified
Journal Article
Open access
PDF file
GZGuanghe Zhao
Guanghe Zhao
RZRuifen Zhang
Ruifen Zhang
LDLihong Dong
Lihong Dong
FHFei Huang
Fei Huang
LLLei Liu
Lei Liu
MZMingwei Zhang
Mingwei Zhang
The composition, in vitro bioaccessibility and antioxidant activities of the phenolic compounds in defatted rice bran (DRB) and its soluble and insoluble dietary fibres were systematically evaluated in this study. The total phenolic content of insoluble dietary fibre from DRB (IDFDRB) was much higher than that of the soluble dietary fibre from DRB (SDFDRB) but was 10% lower than that of DRB. Bound phenolics accounted for more than 90% of the total phenolics in IDFDRB, whereas they accounted for 34.2% and 40.5% of the total phenolics in DRB and SDFDRB, respectively. Additionally, the phenolic profiles and antioxidant activities were significantly different in DRB, SDFDRB and IDFDRB. The phenolic compounds in IDFDRB were much less bioaccessibility than those in DRB and SDFDRB due to the higher proportion of bound phenolics in IDFDRB. Considering that bound phenolics could be released from food matrices by bacterial enzymes in the large intestine and go on to exert significant beneficial health effects in vivo, further studies on IDFDRB are needed to investigate the release of the phenolics from IDFDRB via gut microbiota and the related health benefits.

17 March 2022 in Nutrients
Verified
Journal Article
Open access
PDF file
GZGuanghe Zhao
Guanghe Zhao
RZRuifen Zhang
Ruifen Zhang
FHFei Huang
Fei Huang
LDLihong Dong
Lihong Dong
LLLei Liu
Lei Liu
MZMingwei Zhang
Mingwei Zhang
It has been confirmed the lipid-lowering effect of rice bran free phenolics, but it is unknown whether rice bran bound phenolics, the phenolic profile of which differs from the free ones, have a similar effect. Thus, the hypolipidemic effect and potential mechanism of hydrolyzed bound phenolics (HBP) from rice bran was investigated in this study. The results showed that HBP supplementation significantly improved serum lipid profiles of high-fat-diet fed mice. HBP inhibited the activation of nuclear receptors liver X receptor-α (LXRα), sterol regulatory element binding protein 1c (SREBP-1c), and peroxisome proliferators-activated receptors-γ (PPARγ), and, therefore, changed the expressions of their downstream genes, including LDLR, CD36, ACC1, FAS, and DGAT2 in the liver. Moreover, HBP supplementation reversed the high-fat-diet induced gut microbiota dysbiosis. These findings suggest that HBP might alleviate the hyperlipidemia via inhibiting the hepatic de novolipogenesis, regulating the uptake of cholesterol and fatty acid in the liver and their absorption in the gut. The attenuation of microbiota dysbiosis might contribute to the above effects.