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Zhonghua Liu

Researcher at Hunan Agricultural University

Publications -  9
Citations -  232

Zhonghua Liu is an academic researcher from Hunan Agricultural University. The author has contributed to research in topics: Insulin receptor & Protein aggregation. The author has an hindex of 5, co-authored 9 publications receiving 162 citations. Previous affiliations of Zhonghua Liu include Tsinghua University.

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Anti-obesity and hypolipidemic effects of Fuzhuan brick tea water extract in high-fat diet-induced obese rats

TL;DR: It is demonstrated that FTEs have anti-obesity and hypolipidemic functions, suggesting that it might be effective for treatment of obesity and hyperlipemia.
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Biochemical Components Associated With Microbial Community Shift During the Pile-Fermentation of Primary Dark Tea

TL;DR: In this article, the changes of major chemical compounds, enzyme activities, microbial diversity, and their correlations were explored during the pile-fermentation process, and the amino acid was identified as the important abiotic factor in shaping the microbial community structure of primary dark tea ecosystem.
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Comparative proteomic analysis using 2DE-LC-MS/MS reveals the mechanism of Fuzhuan brick tea extract against hepatic fat accumulation in rats with nonalcoholic fatty liver disease

TL;DR: The reduced lipogenesis and enhanced β‐oxidation, tricarboxylic acid cycle and respiratory chain in HFD + HFTE‐fed rats, which mainly contributed to ameliorate hepatic fat accumulation and associated NAFLD.
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Proteomic analysis of the inhibitory effect of epigallocatechin gallate on lipid accumulation in human HepG2 cells

TL;DR: The proteomic analysis hypothesized that EGCG reduced cellular lipid accumulation in FFA-induced HepG2 cells through the activation of AMP-activated protein kinase (AMPK) resulting from the generation of reactive oxygen species (ROS).
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Blockade of the formation of insoluble ubiquitinated protein aggregates by EGCG3"Me in the alloxan-induced diabetic kidney.

TL;DR: Methylated derivative EGCG3”Me exhibiting anti-β-sheet-rich IUP aggregate properties may represent a new strategy to impede the progression of diabetic nephropathy and other diabetic complications.