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中国精品科技期刊2020
孟然,冯薇,李赵嘉,等. 基于肠道菌群探究金菊茶改善2型糖尿病大鼠的作用机制J. 食品工业科技,2026,47(16):1−12. doi: 10.13386/j.issn1002-0306.2025070212.
引用本文: 孟然,冯薇,李赵嘉,等. 基于肠道菌群探究金菊茶改善2型糖尿病大鼠的作用机制J. 食品工业科技,2026,47(16):1−12. doi: 10.13386/j.issn1002-0306.2025070212.
MENG Ran, FENG Wei, LI Zhaojia, et al. Mechanism of Jin-Ju Tea in Ameliorating Type 2 Diabetes in Rats through Gut MicrobiotaJ. Science and Technology of Food Industry, 2026, 47(16): 1−12. (in Chinese with English abstract). doi: 10.13386/j.issn1002-0306.2025070212.
Citation: MENG Ran, FENG Wei, LI Zhaojia, et al. Mechanism of Jin-Ju Tea in Ameliorating Type 2 Diabetes in Rats through Gut MicrobiotaJ. Science and Technology of Food Industry, 2026, 47(16): 1−12. (in Chinese with English abstract). doi: 10.13386/j.issn1002-0306.2025070212.

基于肠道菌群探究金菊茶改善2型糖尿病大鼠的作用机制

Mechanism of Jin-Ju Tea in Ameliorating Type 2 Diabetes in Rats through Gut Microbiota

  • 摘要: 目的:研究由金花葵、菊芋与蒲公英组成的药食同源复方——金菊茶(Jin-Ju Tea,JJT)对2型糖尿病(Type 2 diabetes mellitus,T2DM)大鼠的降糖降脂作用机制。方法:采用高脂饮食联合链脲佐菌素构建T2DM大鼠模型,将成功建模的大鼠分为糖尿病模型组(DM)、二甲双胍组(MET)、JJT低剂量组(JJTL,200 mg/kg)、JJT中剂量组(JJTM,400 mg/kg)、JJT高剂量组(JJTH,800 mg/kg),另设正常对照组(CON),连续灌胃给药8周,进行口服糖耐量试验,检测大鼠空腹血糖、血清糖化蛋白、空腹胰岛素、血脂四项、肝功能及促炎因子等指标。通过16S rRNA测序技术分析大鼠肠道菌群组成,并探讨菌群变化与代谢指标的相关性。结果:与DM组相比,JJTM组大鼠空腹血糖、血清糖化蛋白以及口服葡萄糖耐量试验-血糖曲线下面积显著降低(P<0.05),血清胰岛素水平显著升高(P<0.01);血清甘油三酯、总胆固醇、低密度脂蛋白胆固醇含量显著降低(P<0.001),高密度脂蛋白胆固醇含量显著升高(P<0.01);促炎因子白细胞介素-6、白细胞介素-1β和肿瘤坏死因子-α水平显著降低(P<0.001);谷草转氨酶、谷丙转氨酶活性分别显著下降47.64%和35.76%(P<0.001)。JJT可提高T2DM大鼠肠道菌群多样性、调节菌群结构,JJT上调了乳杆菌属(Lactobacillus)、芽孢杆菌属(Bacillus)、unclassified_Muribaculaceae、Prevotellaceae_UCG_001的相对丰度,下调了杜氏杆菌属(Dubosiella)、unclassified_Lachnospiraceae、Lachnospiraceae_NK4A136_group的相对丰度。相关性分析表明,Prevotella_UCG_001、双歧杆菌(Bifidobacterium)及杜氏杆菌(Dubosiella)与血糖血脂指标密切相关。结论:JJT能有效改善T2DM,其中JJTM组效果显著,其机制可能与缓解炎症反应、调节肠道菌群结构有关。

     

    Abstract: Objective: To investigate the mechanisms underlying the hypoglycemic and hypolipidemic effects of Jin-Ju tea (JJT), a medicinal and edible formula composed of Abelmoschus manihot, Helianthus tuberosus, and Taraxacum mongolicum, in rats with type 2 diabetes mellitus (T2DM). Methods: A T2DM rat model was established using a high-fat diet combined with streptozotocin injection. Successfully modeled rats were divided into the diabetic model (DM) group, metformin (MET) group, JJT low-dose (JJTL, 200 mg/kg), JJT medium-dose (JJTM, 400 mg/kg), and JJT high-dose (JJTH, 800 mg/kg) groups, with a normal control (CON) group also included. After 8 weeks of continuous intragastric administration, an oral glucose tolerance test was performed. Fasting blood glucose, glycated serum protein, fasting insulin, four lipid profile indicators, liver function, and pro-inflammatory cytokine levels were measured. The composition of the gut microbiota was analyzed via 16S rRNA sequencing, and correlations between microbial changes and metabolic indicators were explored. Results: Compared with the DM group, the JJTM group showed significant reductions in fasting blood glucose, glycated serum protein, and oral glucose tolerance test - area under the curve (P<0.05), along with a marked increase in fasting insulin levels (P<0.01). Serum levels of triglycerides, total cholesterol, and low-density lipoprotein cholesterol were significantly decreased (P<0.001), while high-density lipoprotein cholesterol were significantly increased (P<0.01). Levels of the pro-inflammatory cytokines interleukin-6, interleukin-1β, and tumor necrosis factor were significantly reduced (P<0.001). Aspartate aminotransferase and alanine aminotransferase activities decreased significantly by 47.64% and 35.76%, respectively (P<0.001). JJT increased the diversity of the gut microbiota and modulated its structure in T2DM rats, specifically upregulating the relative abundances of Lactobacillus, Bacillus, unclassified_Muribaculaceae, and Prevotellaceae_UCG_001, while downregulating Dubosiella, unclassified_Lachnospiraceae, and Lachnospiraceae_NK4A136_group. Correlation analysis indicated that Prevotellaceae_UCG_001, Bifidobacterium, and Dubosiella were closely associated with glycemic and lipid metabolic indicators. Conclusion: JJT effectively ameliorates T2DM, with the JJTM group exhibiting the most pronounced effects. The underlying mechanism may be related to the alleviation of inflammatory responses and modulation of the gut microbiota structure.

     

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