| Literature DB >> 24239847 |
Jae-Kyeong Byun1, Bo-Young Yoon2, Joo-Yeon Jhun1, Hye-Joa Oh1, Eun-kyoung Kim1, Jun-Ki Min1, Mi-La Cho3.
Abstract
Epigallocatechin-3-gallate (EGCG) is the most biologically active catechin in green tea. EGCG has been shown to have therapeutic effects in autoinflammatory diseases and obesity. Obesity is currently regarded-partly-as an inflammatory condition because of the inflammatory cytokines and higher Th1 cell differentiation detected in obese animal models and human cohort studies. In this work, the effects of EGCG on diet-induced obesity (DIO) mice and obese collagen-induced arthritis (CIA) mice were investigated. EGCG reduced the body weight and fat infiltration in liver tissue while improving serum lipid profiles in DIO mice. EGCG also induced a higher Treg/Th17 cell ratio in CD4(+) T-cell differentiation by decreasing the ratio of STAT3/STAT5 expression in DIO mice. EGCG was also effective in obese CIA mice. Reducing Th17 cells and increasing regulatory T (Treg) cells by affecting the STAT protein ratio were important effects of EGCG that might result in improved arthritic scores and levels of several inflammatory indicators. Thus, EGCG has an anti-inflammatory effect by suppressing STAT3 proteins and Th17-cell differentiation. EGCG thus shows promise for treating autoimmune conditions related to STAT3 or Th17 cells, such as metabolic syndrome, inflammatory arthritis, and some neoplastic diseases.Entities:
Keywords: Autoinflammatory; EGCG; Obese; Obese CIA; Th17/Treg balance
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Year: 2013 PMID: 24239847 DOI: 10.1016/j.imlet.2013.11.006
Source DB: PubMed Journal: Immunol Lett ISSN: 0165-2478 Impact factor: 3.685