Department of Pharmaceutical Sciences, University of Arkansas for Medical Sciences, Little Rock, AR 72205-7199, USA.
Center for Dietary Supplements Research, University of Arkansas for Medical Sciences, Little Rock, AR 72205-7199, USA.
Nutrients. 2019 Apr 3;11(4):776. doi: 10.3390/nu11040776.
The main purpose of this study was to investigate the hepatotoxic potential and effects on the gut microbiome of decaffeinated green tea extract (dGTE) in lean B6C3F₁ mice. Gavaging dGTE over a range of 1X-10X mouse equivalent doses (MED) for up to two weeks did not elicit significant histomorphological, physiological, biochemical or molecular alterations in mouse livers. At the same time, administration of dGTE at MED comparable to those consumed by humans resulted in significant modulation of gut microflora, with increases in . being most pronounced. Results of this study demonstrate that administration of relevant-to-human-consumption MED of dGTE to non-fasting mice does not lead to hepatotoxicity. Furthermore, dGTE administered to lean mice, caused changes in gut microflora comparable to those observed in obese mice. This study provides further insight into the previously reported weight management properties of dGTE; however, future studies are needed to fully evaluate and understand this effect.
本研究的主要目的是研究去咖啡因绿茶提取物(dGTE)在 lean B6C3F₁ 小鼠中的肝毒性潜力及其对肠道微生物组的影响。灌胃 dGTE 的范围为 1X-10X 小鼠等效剂量(MED),长达两周,未引起小鼠肝脏明显的组织形态学、生理、生化或分子改变。与此同时,给予 MED 剂量的 dGTE 与人类摄入的剂量相当,导致肠道微生物群发生显著调节,其中增加最为明显。本研究结果表明,给予非禁食小鼠与人类摄入 MED 相当的 dGTE 不会导致肝毒性。此外,给予 lean 小鼠 dGTE 会导致肠道微生物群发生类似于肥胖小鼠观察到的变化。本研究进一步深入了解了 dGTE 先前报道的体重管理特性;然而,需要进一步的研究来全面评估和理解这种效果。