Sasaki Geoffrey Y, Vodovotz Yael, Yu Zhongtang, Bruno Richard S
Human Nutrition Program, The Ohio State University, Columbus, OH 43210, USA.
Department of Food Science and Technology, The Ohio State University, Columbus, OH 43210, USA.
Antioxidants (Basel). 2022 Dec 18;11(12):2490. doi: 10.3390/antiox11122490.
Obesity-related cardiometabolic disorders are driven by inflammation, oxidative stress, and gut dysbiosis. Green tea catechins protect against cardiometabolic disorders by anti-inflammatory, antioxidant, and prebiotic activities. However, whether obesity alters catechin bioavailability remains unknown. We hypothesized that obesity would decrease catechin bioavailability due to altered gut microbiota composition. Obese and healthy persons completed a pharmacokinetics trial in which a confection formulated with green tea extract (GTE; 58% epigallocatechin gallate, 17% epigallocatechin, 8% epicatechin, 6% epicatechin gallate) was ingested before collecting plasma and urine at timed intervals for up to 24 h. Stool samples were collected prior to confection ingestion. Catechins and γ-valerolactones were assessed by LC-MS. Obesity reduced plasma area under the curve (AUC) by 24-27% and maximum plasma concentrations by 18-36% for all catechins. Plasma AUC for 5'-(3',4'-dihydroxyphenyl)-γ-valerolactone and 5'-(3',4',5'-trihydroxyphenyl)-γ-valerolactone, as well as total urinary elimination of all catechins and valerolactones, were unaffected. ⍺-Diversity in obese persons was lower, while was the only catechin-metabolizing bacteria that was altered by obesity. Ascorbic acid and diversity metrics were correlated with catechin/valerolactone bioavailability. These findings indicate that obesity reduces catechin bioavailability without affecting valerolactone generation, urinary catechin elimination, or substantially altered gut microbiota populations, suggesting a gut-level mechanism that limits catechin absorption.
肥胖相关的心脏代谢紊乱是由炎症、氧化应激和肠道菌群失调引起的。绿茶儿茶素通过抗炎、抗氧化和益生元活性来预防心脏代谢紊乱。然而,肥胖是否会改变儿茶素的生物利用度仍不清楚。我们假设肥胖会由于肠道微生物群组成的改变而降低儿茶素的生物利用度。肥胖者和健康者完成了一项药代动力学试验,试验中在摄入一种用绿茶提取物(GTE;58%表没食子儿茶素没食子酸酯、17%表没食子儿茶素、8%表儿茶素、6%表儿茶素没食子酸酯)配制的糖果后,在长达24小时的时间间隔内采集血浆和尿液。在摄入糖果之前采集粪便样本。通过液相色谱-质谱法评估儿茶素和γ-戊内酯。肥胖使所有儿茶素的血浆曲线下面积(AUC)降低了24 - 27%,血浆最大浓度降低了18 - 36%。5'-(3',4'-二羟基苯基)-γ-戊内酯和5'-(3',4',5'-三羟基苯基)-γ-戊内酯的血浆AUC,以及所有儿茶素和戊内酯的总尿排泄量均未受影响。肥胖者的α多样性较低,而[具体细菌名称未给出]是唯一因肥胖而改变的儿茶素代谢细菌。抗坏血酸和多样性指标与儿茶素/戊内酯的生物利用度相关。这些发现表明,肥胖会降低儿茶素的生物利用度,而不影响戊内酯的生成、尿儿茶素排泄或肠道微生物群数量的大幅改变,提示了一种限制儿茶素吸收的肠道水平机制。