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熟化普洱茶改善昼夜节律紊乱小鼠模型的肠肝循环。

Ripened Pu-Erh Tea Improved the Enterohepatic Circulation in a Circadian Rhythm Disorder Mice Model.

机构信息

College of Food Science, Southwest University, Beibei, Chongqing 400715, People's Republic of China.

出版信息

J Agric Food Chem. 2021 Nov 17;69(45):13533-13545. doi: 10.1021/acs.jafc.1c05338. Epub 2021 Nov 2.

Abstract

Glucolipid metabolism, nitrogen metabolism, and inflammation are closely related to circadian rhythm disorder (CRD). Ripened Pu-erh tea (RPT) shows significant antidyslipidemic, antihyperurecemic, and anti-inflammatory effects. However, it is unclear whether healthy population are affected by CRD and whether long-term consumption of RPT can alleviate it. To investigate this problem, healthy mice were pretreated with RPT (0.25%, w/v) for 60 days and then subjected to CRD for 40 days. Our results indicated that healthy mice showed obesity, and the intestinal and liver inflammation increased after CRD, which were associated with the development of a metabolic disorder syndrome. RPT effectively reversed this trend by increasing the production and excretion rates of bile acid. RPT reshaped the disorder of gut microbiota caused by CRD and promoted the change of archaeal intestinal types from -dominant type to -dominant type. In addition, by repairing the intestinal barrier function, RPT inhibited the infiltration of harmful microorganisms or metabolites through enterohepatic circulation, thus reducing the risk of chronic liver inflammation. In conclusion, RPT may reduce the risk of CRD-induced obesity in mice by increasing bile acid metabolism. The change of bile acid pool contributes to the reshaping of gut microflora, thus reducing intestinal inflammation and oxidative stress induced by CRD. Therefore, we speculated that the weakening of CRD damage caused by RPT is due to the improvement of bile acid-mediated enterohepatic circulation. It was found that 0.25% RPT (a human equivalent dose of 7 g/60 kg/day) has potential for regulating CRD.

摘要

糖脂代谢、氮代谢和炎症与昼夜节律紊乱(CRD)密切相关。陈化普洱茶(RPT)具有显著的抗血脂异常、抗高尿酸血症和抗炎作用。然而,目前尚不清楚健康人群是否会受到 CRD 的影响,以及长期饮用 RPT 是否可以缓解 CRD。为了研究这个问题,我们将健康小鼠用 RPT(0.25%,w/v)预处理 60 天,然后进行 40 天的 CRD。结果表明,CRD 后健康小鼠出现肥胖,肠道和肝脏炎症增加,这与代谢紊乱综合征的发展有关。RPT 通过增加胆汁酸的产生和排泄率有效地逆转了这一趋势。RPT 重塑了 CRD 引起的肠道微生物群紊乱,并促进了古菌肠道类型从 -dominant 型向 -dominant 型的改变。此外,通过修复肠道屏障功能,RPT 抑制了有害物质或代谢物通过肠肝循环的渗透,从而降低了慢性肝炎症的风险。总之,RPT 通过增加胆汁酸代谢可能降低 CRD 诱导的肥胖风险。胆汁酸库的变化有助于重塑肠道微生物群,从而减少 CRD 引起的肠道炎症和氧化应激。因此,我们推测 RPT 减弱 CRD 损伤的原因是由于改善了胆汁酸介导的肠肝循环。研究发现,0.25%的 RPT(相当于人类 7 g/60 kg/天的剂量)具有调节 CRD 的潜力。

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