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Polysaccharide peptides from Ganoderma lucidum ameliorate lipid metabolic disorders and gut microbiota dysbiosis in high-fat diet-fed rats

机译:来自Ganoderma Lucidum的多糖肽改善脂质代谢障碍和高脂饮食喂养大鼠的肠道微生物症脱蛋白酶

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This study aimed to investigate the effects of polysaccharide peptides from Ganoderma lucidum (GLPP) on hyperlipidaemia and gut microbiota dysbiosis in high-fat diet (HFD)-exacerbated hypercholesterolemic rats. Results showed that oral administrations of GLPP markedly alleviated the dyslipidaemia through decreasing the serum levels of triglyceride (TG), cholesterol (TC), free fatty acids (FFA) and low-density lipoprotein cholesterol (LDL-C), and significantly suppressing hepatic lipid accumulation and steatosis. Metagenomic analysis revealed that GLPP supplementation produced significant structure changes on the intestinal microbiota in HFD-fed rats, in particular modulating the relative abundance of functionally relevant microbial phylotypes compared with the HFD group. The Spearman's correlation analysis revealed that the serum and hepatic lipid profiles were negatively correlated with Jeotgalicoccus, Ignavigranum, Sporosarcina, Bacteroides, Anaerovorax, Parasutterella, Alistipes and Alloprevotella, but positively correlated with Allobaculum, Phascolarctobacterium, Psychrobacter, Enterorhabdus, Blautia and Roseburia. Meanwhile, the GLPP treatment regulated the mRNA expression responsible for hepatic lipid metabolism and promoted fecal excretion of total bile acids (BAs). These findings indicated that GLPP ameliorate lipid metabolic disorders through modulating gut microbiota structure and regulating the genes involved in hepatic lipid and cholesterol metabolism.
机译:本研究旨在探讨多糖肽从灵芝(GLPP)对高脂饮食(HFD)的高脂血症和肠道微生物症失育症的影响。结果表明,通过降低甘油三酯(Tg),胆固醇(Tc),游离脂肪酸(FFA)和低密度脂蛋白胆固醇(LDL-C),并显着抑制肝脂质,并且通过降低血清水平,GLPP的口腔脂肪血症显着减轻了血清水平,并显着抑制了肝脂质积累和脂肪化。 Metagenomic分析表明,GLPP补充在HFD喂养大鼠中产生了显着的结构变化,特别是调节与HFD组相比的功能相关的微生物型的相对丰度。 Spearman的相关性分析表明,血清和肝脂肪曲线与JeoTgalicccus,Ignavigranum,Sporosarcina,Bragodes,Anaerovorax,Parasuctella,Alistipes和Alloprevotella负相关,但与Allobaculum,Phascolaracterium,心理杆菌,肠杆菌,Blautia和Roseburia呈正相关。同时,GLPP处理调节负责肝脂代谢的mRNA表达,促进总胆汁酸的粪便排泄(BAS)。这些发现表明GLPP通过调节肠道微生物群结构和调节肝脂质和胆固醇代谢的基因来改善脂质代谢紊乱。

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