Back to Search
Start Over
A green tea extract confection decreases circulating endotoxin and fasting glucose by improving gut barrier function but without affecting systemic inflammation: A double-blind, placebo-controlled randomized trial in healthy adults and adults with metabolic syndrome
- Source :
-
Nutrition Research . Apr2024, Vol. 124, p94-110. 17p. - Publication Year :
- 2024
-
Abstract
- 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 years) and adults with MetS (n = 21, 40 ± 3 years) examined 4-week 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 =.023) in both healthy persons and those with MetS, while increasing concentrations of circulating catechins (P <.0001) and γ-valerolactones (P =.0001). Fecal calprotectin (P =.029) and myeloperoxidase (P =.048) concentrations were decreased by GTE regardless of health status. Following the ingestion of gut permeability probes, urinary lactose/mannitol (P =.043) but not sucralose/erythritol (P >.05) was decreased by GTE regardless of health status. No between-treatment differences (P >.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 =.029) by the GTE confection compared with 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. • A novel green tea extract (GTE) confection was provided to healthy adults and adults with metabolic syndrome. • GTE increased circulating catechins and valerolactones regardless of health status. • GTE decreased intestinal inflammation and small intestinal permeability. • GTE decreased circulating endotoxin. • GTE decreased fasting glucose without affecting systemic inflammation. • Gut-level benefits by GTE support research translation for cardioprotection by green tea. Healthy adults and adults with metabolic syndrome were randomized to a placebo or GTE (1 g; 890 mg catechins) confection for 1 month and then crossed-over to the alternative treatment following a 1-month washout. Regardless of health status, the GTE confection decreased fecal biomarkers of intestinal inflammation (calprotectin and myeloperoxidase) and small intestinal permeability based on a differential sugar absorption test while decreasing serum endotoxin. Abbreviations: GTE, green tea extract; MetS, metabolic syndrome [Display omitted] [ABSTRACT FROM AUTHOR]
- Subjects :
- *ANTIGEN analysis
*ENDOTOXEMIA prevention
*FECAL analysis
*BLOOD sugar analysis
*ANTI-inflammatory agents
*PLACEBOS
*MANNITOL
*BODY mass index
*CARRIER proteins
*GREEN tea
*INTESTINAL barrier function
*BLIND experiment
*STATISTICAL sampling
*CALCIUM-binding proteins
*LIPIDS
*RANDOMIZED controlled trials
*DESCRIPTIVE statistics
*PLANT extracts
*CANDY
*CROSSOVER trials
*NERVE tissue proteins
*LACTOSE
*SUGAR alcohols
*PRE-tests & post-tests
*ENTERITIS
*METABOLIC syndrome
*DRUG efficacy
*OXIDOREDUCTASES
*LIPOPOLYSACCHARIDES
*COMPARATIVE studies
*LACTONES
*BLOOD pressure
*ENDOTOXINS
*FASTING
*AMINOTRANSFERASES
*TUMOR necrosis factors
*INTERLEUKINS
*BIOMARKERS
*EVALUATION
*ADULTS
Subjects
Details
- Language :
- English
- ISSN :
- 02715317
- Volume :
- 124
- Database :
- Academic Search Index
- Journal :
- Nutrition Research
- Publication Type :
- Academic Journal
- Accession number :
- 176900502
- Full Text :
- https://doi.org/10.1016/j.nutres.2024.02.001