Hongwei Wang

Dr. Hongwei Wang

orcid

Research Focus & Metrics

Academic Career Length

12Years (2015-Present)

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

Representative Publications

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11 August 2020 in Antioxidants
Verified
Journal Article
Open access
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YZYixiu Zeng
Yixiu Zeng
Jiajia SongJiajia Song
Jiajia Song
MZMeimei Zhang
Meimei Zhang
HWHongwei Wang
Hongwei Wang
YZYu Zhang
Yu Zhang
HSHua-Yi Suo
Hua-Yi Suo
The in vitro and in vivo antioxidant activities of six flavonoids with similar structures, including epicatechin (EC), epigallocatechin (EGC), procyanidin B2 (P), quercetin (Q), taxifolin (T), and rutin (R) were compared. The structures of the six flavonoids and their scavenging activities for 2,2-diphenyl-1-picrylhydrazyl (DPPH•) and 2,2′-azino-bis-(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS+) radicals were closely related. The flavonoids decreased serum contents of malondialdehyde (MDA) and nitric oxide (NO), and increased serum total antioxidative capacity (T-AOC), superoxide dismutase (SOD), catalase (CAT), and glutathione peroxidase (GSH-Px) levels to different degrees in d-galactose-treated mice. The changes in mRNA expression of liver GSH-Px1, CAT, SOD1, and SOD2 by d-galactose were dissimilarly restored by the six flavonoids. Moreover, the six flavonoids differentially prevented the inflammatory response caused by oxidative stress by inhibiting interleukin (IL)-1β, IL-6, and tumor necrosis factor (TNF)-α levels, and restoring IL-10 levels. These six flavonoids from two subclasses revealed the following antioxidant capability: P > EC, EGC > EC, Q > T, Q > R. Our results indicate that (1) the pyrogallol, dimerization, and C2=C3 double bonds of flavonoids enhanced antioxidant activity and (2) the C3 glycosylation of flavonoids attenuated antioxidant capacity.

25 May 2017 in Nutrients
Verified
Journal Article
Open access
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XCXiaoyong Chen
Xiaoyong Chen
XZXin Zhao
Xin Zhao
HWHongwei Wang
Hongwei Wang
ZYZelin Yang
Zelin Yang
JLJian Li
Jian Li
HSHua-Yi Suo
Hua-Yi Suo
The aim of this study is to assess the preventive effects of Lactobacillus fermentum HY01 (LF-HY01) to dextran sulfate sodium induced-colitis. We observed the ratio of colon weight to its length, colon pathological changes, and the concentrations of pro-inflammatory factors (IFN-γ, IL-12, TNFα, and IL-6) in serum. We also took account of the protein levels of IκBα, NF-κB p65, iNOS, and COX-2, and we measured the best effects of different doses of Lactobacillus fermentum HY01 (low dose group was 109 CFU/kg·bw, high dose group was 1010 CFU/kg·bw) on dextran sulfate sodium-induced colitis mice. The results were remarkable, suggesting that Lactobacillus fermentum HY01 had significant preventive effects in dextran sulfate sodium induced-colitis; simultaneously, the high dose group showed the best results among other groups. It can effectively alleviate the shortened colon length, reduce the ratio of colon weight to its length, reduce edema, inflammatory cells infiltration, and colon mucosa injury, and play an important role in the down-regulation of concentrations of pro-inflammatory factors (IFN-γ, IL-12, TNFα, and IL-6). Above all, Lactobacillus fermentum HY01 shows promising prevention for IκBα degradation, inhibition of NF-κB p65 phosphorylation cascades, and decreases the protein levels of iNOS and COX-2 as well.

26 November 2018 in Journal of the Science of Food and Agriculture
Verified
Journal Article
Closed access
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XLXingyao Long
Xingyao Long
XZXin Zhao
Xin Zhao
WWWei Wang
Wei Wang
YZYu Zhang
Yu Zhang
HWHongwei Wang
Hongwei Wang
HSHua-Yi Suo
Hua-Yi Suo

28 March 2018 in Molecules
Verified
Journal Article
Open access
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HWHongwei Wang
Hongwei Wang
Edgar ChambersEdgar Chambers
Edgar Chambers
This research describes the sensory odor characteristics of 19 phenolic compounds (11 phenol derivatives, six guaiacol derivatives, and two syringol derivatives) that have been associated with smoked aroma in previous literature. Seven concentrations varying from 1 to 100,000 ppm of each chemical were examined. A highly trained descriptive panel used a recently published lexicon for smoky aroma and flavor and found that smoked aroma compounds have many different attributes that make up smokiness. Musty/dusty, musty/earthy, pungent, acid, smoky, woody, burnt, ashy, cedar, creosote or petroleum-like collectively imparted smoked aroma. Most of the phenolic compounds were described as having smoky characteristics at low concentrations, generally at 1 and 10 ppm, except 3,4-dimethylphenol at 5000 ppm. 2,6-Dimethylphenol was not associated with smoky characteristics. This research is the first to evaluate a set of phenolic compounds for their sensory characteristics using a professionally developed set of sensory attributes.

13 June 2017 in Journal of Sensory Studies
Verified
Journal Article
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TJTaylor R. Jaffe
Taylor R. Jaffe
HWHongwei Wang
Hongwei Wang
Edgar ChambersEdgar Chambers
Edgar Chambers

24 November 2019 in Journal of Food Science
Verified
Journal Article
Closed access
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YQYu Qian
Yu Qian
MLMingyue Li
Mingyue Li
WWWei Wang
Wei Wang
HWHongwei Wang
Hongwei Wang
YZYu Zhang
Yu Zhang
HSHua-Yi Suo
Hua-Yi Suo