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肠道微生物-代谢轴深入了解高脂血症小鼠中莲子抗性淀粉的降脂作用。

Gut microbiota-metabolic axis insight into the hyperlipidemic effect of lotus seed resistant starch in hyperlipidemic mice.

机构信息

College of Food Science, Fujian Agriculture and Forestry University, Fuzhou 350002, China; Fujian Provincial Key Laboratory of Quality Science and Processing Technology in Special Starch, Fujian Agriculture and Forestry University, Fuzhou 350002, China.

College of Food Science, Fujian Agriculture and Forestry University, Fuzhou 350002, China; Fujian Provincial Key Laboratory of Quality Science and Processing Technology in Special Starch, Fujian Agriculture and Forestry University, Fuzhou 350002, China.

出版信息

Carbohydr Polym. 2023 Aug 15;314:120939. doi: 10.1016/j.carbpol.2023.120939. Epub 2023 Apr 27.

Abstract

We investigated the hyperlipidemic effect of different doses of lotus seed resistant starch (low-, medium and high-dose LRS, named as LLRS, MLRS and HLRS, respectively) in hyperlipidemic mice using gut microbiota-metabolic axis compared to high-fat diet mice (model control group, MC). Allobaculum was significantly decreased in LRS groups compared to MC group, while MLRS promoted the abundance of norank_f_Muribaculaceae and norank_f_Erysipelotrichaceae. Moreover, supplementation of LRS promoted cholic acid (CA) production and inhibited deoxycholic acid compared to MC group. Among, LLRS promoted formic acid, MLRS inhibited 20-Carboxy-leukotriene B4, while HLRS promoted 3, 4-Methyleneazelaic acid and inhibited Oleic acid and Malic acid. Finally, MLRS regulate microbiota composition, and this promoted cholesterol catabolism to form CA, which inhibited serum lipid index by gut microbiota-metabolic axis. In conclusion, MLRS can promote CA and inhibit medium chain fatty acids, so as to play the best role in lowering blood lipids in hyperlipidemia mice.

摘要

我们通过肠道微生物群-代谢轴研究了不同剂量的莲子抗性淀粉(低、中、高剂量 LRS,分别命名为 LLRS、MLRS 和 HLRS)对高脂血症小鼠的高脂血症作用,与高脂肪饮食组小鼠(模型对照组,MC)相比。与 MC 组相比,LRS 组中的 Allobaculum 明显减少,而 MLRS 促进了 norank_f_Muribaculaceae 和 norank_f_Erysipelotrichaceae 的丰度。此外,与 MC 组相比,补充 LRS 可促进胆酸(CA)的产生并抑制脱氧胆酸。其中,LLRS 促进甲酸,MLRS 抑制 20-羧基-白三烯 B4,而 HLRS 促进 3,4-亚甲基氮杂环庚酸并抑制油酸和苹果酸。最后,MLRS 调节微生物群落组成,这促进了胆固醇的分解代谢形成 CA,通过肠道微生物群-代谢轴抑制血清脂质指标。总之,MLRS 可以促进 CA 并抑制中链脂肪酸,从而在高脂血症小鼠中发挥最佳降血脂作用。

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