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Epigallocatechin-3-Gallate-Rich Green Tea Extract Ameliorates Fatty Liver and Weight Gain in Mice Fed a High Fat Diet by Activating the Sirtuin 1 and AMP Activating Protein Kinase Pathway.

Abstract
The prevalence of metabolic diseases has risen globally in parallel with the obesity epidemic over the past few decades. Green tea has been reported to have metabolically beneficial effects on obesity; however, the mechanism by which green tea regulates lipid metabolism is not clearly understood. Male c57BL/6 mice were fed a normal chow diet, a high-fat diet (HFD), or an HFD supplemented with various doses of epigallocatechin gallate-rich green tea extract (GTE) for 12 weeks. GTE supplementation reduced body weight gain, prevented hepatic fat accumulation, decreased hypertriglyceridemia, and improved hyperglycemia and insulin resistance in HFD-fed mice. The underlying mechanisms of these beneficial effects of GTE might involve the upregulation of sirtuin 1 and AMP activated protein kinase (AMPK) and the downregulation of enzymes related to de novo lipogenesis. Consistent with the in vivo findings, GTE increased the expression and activity of sirtuin 1, enhanced the binding of sirtuin 1 to liver kinase B1 (LKB1) and subsequent deacetylation of LKB1, and reduced triglyceride accumulation in HepG2 cells. These results suggest the possible therapeutic potential of dietary epigallocatechin gallate-rich GTE supplementation for preventing the development and progression of hepatic steatosis and obesity.
AuthorsUi-Jin Bae, John Park, Il Woon Park, Byung Min Chae, Mi-Ra Oh, Su-Jin Jung, Geon-Seek Ryu, Soo-Wan Chae, Byung-Hyun Park
JournalThe American journal of Chinese medicine (Am J Chin Med) Vol. 46 Issue 3 Pg. 617-632 ( 2018) ISSN: 1793-6853 [Electronic] Singapore
PMID29595075 (Publication Type: Journal Article)
Chemical References
  • Plant Extracts
  • Tea
  • Catechin
  • epigallocatechin gallate
  • SIRT1 protein, human
  • Sirtuin 1
Topics
  • Animals
  • Catechin (administration & dosage, analogs & derivatives, pharmacology)
  • Cell Survival (drug effects)
  • Diet, High-Fat (adverse effects)
  • Fatty Liver (etiology, prevention & control)
  • Hep G2 Cells
  • Humans
  • Hyperglycemia (prevention & control)
  • Hypertriglyceridemia (prevention & control)
  • Insulin Resistance
  • MAP Kinase Signaling System (drug effects)
  • Male
  • Mice, Inbred C57BL
  • Obesity (etiology, prevention & control)
  • Phytotherapy
  • Plant Extracts (administration & dosage, pharmacology)
  • Sirtuin 1 (metabolism)
  • Tea (chemistry)
  • Weight Gain (drug effects)

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