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中国精品科技期刊2020
付永霞,王晗,刘振宇,等. 基于肠道菌群和转录组学分析生小米醇溶蛋白对高脂膳食联合STZ诱导的糖尿病小鼠的改善机制J. 食品工业科技,2026,47(8):1−10. doi: 10.13386/j.issn1002-0306.2025030396.
引用本文: 付永霞,王晗,刘振宇,等. 基于肠道菌群和转录组学分析生小米醇溶蛋白对高脂膳食联合STZ诱导的糖尿病小鼠的改善机制J. 食品工业科技,2026,47(8):1−10. doi: 10.13386/j.issn1002-0306.2025030396.
FU Yongxia, WANG Han, LIU Zhenyu, et al. Improvement Mechanism of Raw Foxtail Millet Prolamin on High-Fat Diet Combined with STZ Induced Diabetic Mice Based on Gut Microbiota and Hepatic TranscriptomicsJ. Science and Technology of Food Industry, 2026, 47(8): 1−10. (in Chinese with English abstract). doi: 10.13386/j.issn1002-0306.2025030396.
Citation: FU Yongxia, WANG Han, LIU Zhenyu, et al. Improvement Mechanism of Raw Foxtail Millet Prolamin on High-Fat Diet Combined with STZ Induced Diabetic Mice Based on Gut Microbiota and Hepatic TranscriptomicsJ. Science and Technology of Food Industry, 2026, 47(8): 1−10. (in Chinese with English abstract). doi: 10.13386/j.issn1002-0306.2025030396.

基于肠道菌群和转录组学分析生小米醇溶蛋白对高脂膳食联合STZ诱导的糖尿病小鼠的改善机制

Improvement Mechanism of Raw Foxtail Millet Prolamin on High-Fat Diet Combined with STZ Induced Diabetic Mice Based on Gut Microbiota and Hepatic Transcriptomics

  • 摘要: 生和熟小米醇溶蛋白均具有显著的糖代谢改善功能。与生小米醇溶蛋白相比,熟小米醇溶蛋白的蛋白质质量显著下降。因此,生小米醇溶蛋白作为潜在的食源性降糖功能物质更有价值。为了研究生小米醇溶蛋白对2型糖尿病(Type 2 diabetes, T2D)小鼠肠道菌群及肝脏的影响,通过高脂膳食+链脲佐菌素注射构建T2D模型,采用生小米醇溶蛋白对T2D小鼠连续干预5周,并利用16S rRNA 测序和转录组学技术分别对小鼠肠道菌群组成和肝脏基因表达进行分析。结果显示:结果表明,RFMP可通过缓解糖尿病引起的肠道菌群紊乱来改善葡萄糖代谢。生小米醇溶蛋白干预显著增加了T2D小鼠中乳酸杆菌属(Lactobacillus)、未分类穆里氏菌属(norank_f_Muribaculaceae)和毛螺菌科_NK4A136_group属(Lachnospiraceae_NK4A136_group)丰度。肝脏转录组学分析发现,生小米醇溶蛋白干预后,成纤维细胞生长因子21(Fgf21)、双特异性磷酸酶1(Dusp1)、Ras鸟嘌呤核苷酸释放蛋白1(Rasgrp1)和己糖激酶3(HK3)表达量上调,磷酸烯醇式丙酮酸羧激酶1(Pck1)表达量下调,这些均为其调控糖代谢的关键基因。研究结果完善了生小米醇溶蛋白改善糖代谢的机制,为开发功能性小米醇溶蛋白产品提供了理论依据。

     

    Abstract: Both raw and cooked millet prolamin (RFMP and CFMP) exhibited significant functions in improving glucose metabolism. Compared to RFMP, the protein quality of CFMP significantly decreased. Therefore, RFMP is more valuable as a potential food-derived hypoglycemic functional substance. In order to study the effects of RFMP on the intestinal flora and liver of type 2 diabetes (T2D) mice, C57BL/6J mice were used as the objects, and T2D models were established by high-fat diet combined with streptozotocin. The T2D mice were continuously intervened with RFMP for five weeks. Subsequently, 16S rRNA sequencing and transcriptomics technology were employed to analyze the composition of the gut microbiota and liver gene expression, respectively. The results showed that RFMP could improve glucose metabolism by alleviating the intestinal flora disorder induced by diabetes. At the genus level, RFMP intervention significantly increased the abundance of Lactobacillus, norank_f_Muribaculaceae, and Lachnospiraceae_NK4A136_group in T2D mice. Liver transcriptome results showed that the intervention of RFMP upregulated the expression levels of Fgf21, Dusp1, Rasgrp1, and HK3, while downregulated the expression level of Pck1, which were the key genes for regulating glucose metabolism. This study improved the mechanism of improving glucose metabolism with RFMP, providing a theoretical basis for the development of functional FMP product.

     

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