Table 1.
Study Name | Author and Year | Methods | Result |
---|---|---|---|
Green tea, black tea, and epigallocatechin modify body composition, improve glucose tolerance, and differentially alter metabolic gene expression in rats fed a high-fat diet [119] |
Chen et al., 2009 | Rat models were fed a HFD for 6 months and were treated with either: EGCG, GT, BT or water control. | GT, BT, and EGCG all improved glocuse tolerance as compared to the control. GT, BT increased FA oxidation, but not EGCG. Only EGCG upregulated UCP-2 and PPAR- γ genes. |
Protective potential of epigallocatechin-3-gallate against benign prostatic hyperplasia in metabolic syndrome rats [122] |
Chen et al., 2016 | Rat models were fed a HFD for 12 weeks. Testosterone was injected at 10 mg/kg/d and EGCG was given orally for weeks 9–12 | EGCG significantly decreased measured glucose levels, total cholesterol, triglycerides, IGFs, and inflammatory cytokines |
The major green tea polyphenol, (-)-epigallocatechin-3-gallate, inhibits obesity, metabolic syndrome, and fatty liver disease in high-fat-fed mice [121] |
Bose et al., 2008 | Mice were fed a HFD and concurrently treated with EGCG supplementation or received no treatment for 16 weeks. Weight gain, percent body fat, and visceral fat were measured. | EGCG treated mice showed decreased insulin resistance, plasma cholesterol, and inflammatory cytokines. |
EGCG reduces obesity and white adipose tissue gain partly through AMPK activation in mice [123] |
Li et al., 2018 | Mouse model: mice were fed a HFD for 20 weeks and 100 mg/kg EGCG was administered intragastrically/d. A control group fed a HFD, but no EGCG was present. | EGCG treatment group showed improved serum lipids, increased excretion of free fatty acids in feces, and decreased adipose tissue. |