绿茶提取物
内科学
医学
钙蛋白酶
内分泌学
肠道通透性
安慰剂
代谢综合征
全身炎症
炎症
免疫学
炎症性肠病
化学
肥胖
食品科学
替代医学
疾病
病理
绿茶
作者
Min Zeng,Joanna K. Hodges,Avinash Pokala,Mona Khalafi,Geoffrey Y. Sasaki,Jillian Pierson,Sisi Cao,Guy Brock,Zhongtang Yu,Jiangjiang Zhu,Yael Vodovotz,Richard S. Bruno
标识
DOI:10.1016/j.nutres.2024.02.001
摘要
Anti-inflammatory activities of catechin-rich green tea extract (GTE) in obese rodents protect against metabolic endotoxemia by decreasing intestinal permeability and absorption of gut-derived endotoxin. However, translation to human health has not been established. We hypothesized that GTE would reduce endotoxemia by decreasing gut permeability and intestinal and systemic inflammation in persons with metabolic syndrome (MetS) compared with healthy persons. A randomized, double-blind, placebo-controlled, crossover trial in healthy adults(n=19, 34±2 y) and adults with MetS(n=21, 40±3 y) examined 4-wk administration of a decaffeinated GTE confection (890 mg/d total catechins) on serum endotoxin, intestinal permeability, gut and systemic inflammation, and cardiometabolic parameters. Compared with the placebo, the GTE confection decreased serum endotoxin(P=0.023) in both healthy persons and those with MetS, while increasing concentrations of circulating catechins(P<0.0001) and γ-valerolactones(P=0.0001). Fecal calprotectin(P=0.029) and myeloperoxidase(P=0.048) concentrations were decreased by GTE regardless of health status. Following the ingestion of gut permeability probes, urinary lactose/mannitol (P=0.043) but not sucralose/erythritol(P>0.05) was decreased by GTE regardless of health status. No between-treatment differences(P>0.05) were observed for plasma aminotransferases, blood pressure, plasma lipids, or body mass nor were plasma tumor necrosis factor-α, interleukin-6, or the ratio of lipopolysaccharide-binding protein/soluble cluster of differentiation-14 affected. However, fasting glucose in both study groups was decreased(P=0.029) by the GTE confection compared to within-treatment arm baseline concentrations. These findings demonstrate that catechin-rich GTE is effective to decrease circulating endotoxin and improve glycemic control in healthy adults and those with MetS, likely by reducing gut inflammation and small intestinal permeability but without affecting systemic inflammation.
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