• 中文核心期刊
  • CSCD来源期刊
  • 中国科技核心期刊
  • CA、CABI、ZR收录期刊

武夷岩茶副产品“黄片”对高血糖大鼠肠道菌群的影响

Effect of Wuyi Rock Tea Byproduct on Serum Glucose and Gut Microbiota in Hyperglycemic Rats

  • 摘要:
    目的 为了探讨武夷岩茶加工副产品“黄片”对高血糖大鼠血糖和肠道菌群的影响。
    方法 通过脲佐菌素诱导形成2型糖尿病大鼠模型,分析“黄片”茶汤对高血糖大鼠血糖、血清胰岛素和肠道菌群的影响。
    结果 与模型组相比,饮茶组大鼠空腹血糖、血清胰岛素、HOMA-IR水平均均降低。HE染色显示肝脏、胰腺细胞形态均呈改善趋势。肠道菌群检测结果显示,造模后糖尿病大鼠肠道内厚壁菌门相对丰度显著降低,拟杆菌门相对丰度显著升高。武夷岩茶“黄片”可有效干预该菌群结构变化。在菌属水平上,模型组(DC 组)异杆菌属、狭窄梭菌属 1、毛螺菌科 NK4A136 群丰度显著上升,乳杆菌属、瘤胃球菌属丰度显著下降;乳杆菌属、瘤胃球菌属丰度则明显下调;武夷岩茶“黄片”干预后,上述菌属的相对丰度均得到良性调控。
    结论 武夷岩茶“黄片”具有调节高血糖大鼠血糖和肠道菌群结构的作用,使其趋向空白对照组恢复,推测其可能是通过肠道菌群干预糖代谢途径发挥降血糖功效。

     

    Abstract:
    Objective Effect of feeding hyperglycemic rats the decoction of discarded yellowing Wuyi rock tea leaves on serum glucose and gut microbiota of the animals was investigated for possible utilization of the byproduct.
    Methods Model type 2 diabetic rats (DC) were created by streptozotocin induction to be fed with decoction of yellowing leaves rejected in the Wuyi rock tea making process. Serum glucose and insulin as well as gut microbiota in the hyperglycemic rats were determined.
    Results The fasting glucose, insulin, and HOMA-IR in blood of the treatment rats were lower than those of DC. The HE-stained rat liver and pancreatic cells showed steady improvements by the treatments. And in the guts, the relative abundance of Firmicutes significantly decreased, while Bacteroidetes increased. For comparison, the microbiota in the guts of DC at genus level were upregulated on Allobaculum, Clostridium_sensu_stricto_1, and Lachnospiraceae_NK4A136, whereas downregulated on Lactobacillus and Ruminococcus. In contrast, the microbial communities were positively changed in the treatment rats.
    Conclusion The discarded old rock tea leaves seemed to contain functional ingredients therapeutic for diabetes in hyperglycemic rats. By feeding the rats with decoction of the leaves, serum glucose and gut microbiota were restored to the normal levels. The hypoglycemic effect was speculated to come from microbial modulation through glucose metabolism pathways.

     

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