Dietary γ-Aminobutyric Acid Supplementation Inhibits High-Fat Diet-Induced Hepatic Steatosis via Modulating Gut Microbiota in Broilers

被引:11
作者
Chen, Qu [1 ,2 ]
Hu, Dan [1 ,2 ]
Wu, Xiaoting [1 ,2 ]
Feng, Yuyan [1 ,2 ]
Ni, Yingdong [1 ,2 ]
机构
[1] Nanjing Agr Univ, Key Lab Anim Physiol & Biochem, Nanjing 210095, Peoples R China
[2] MOE Joint Int Res Lab Anim Hlth & Food Safety, Nanjing 210095, Peoples R China
基金
国家重点研发计划;
关键词
broilers; gamma-aminobutyric acid; lipid metabolism; gut microbiota; LIVER HEMORRHAGIC SYNDROME; INSULIN-RESISTANCE; OXIDATIVE STRESS; DISEASE; GABA; METABOLISM; MICE;
D O I
10.3390/microorganisms10071281
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The present study aims to investigate the effect of gamma-aminobutyric acid (GABA) on liver lipid metabolism and on AA broilers. Broilers were divided into three groups and fed with low-fat diets, high-fat diets, and high-fat diets supplemented with GABA. Results showed that GABA supplementation decreased the level of triglyceride (TG) in the serum and liver of broilers fed high-fat diets, accompanied by up-regulated mRNA expression of genes related to lipolysis and beta-oxidation in the liver (p < 0.05). Furthermore, GABA supplementation increased liver antioxidant capacity, accompanied by up-regulated mRNA expression of antioxidant genes (p < 0.05). 16S rRNA gene sequencing showed that GABA improved high-fat diet-induced dysbiosis of gut microbiota, increased the relative abundance of Bacteroidetes phylum and Barnesiella genus, and decreased the relative abundance of Firmicutes phylum and Ruminococcus_torques_group and Romboutsia genus (p < 0.05). Moreover, GABA supplementation promoted the production of propionic acid and butyric acid in cecal contents. Correlation analysis further suggested the ratio of Firmicutes/Bacteroidetes negatively correlated with hepatic TG content, and positively correlated with cecal short chain fatty acids content (r > 0.6, p < 0.01). Together, these data suggest that GABA supplementation can inhibit hepatic TG deposition and steatosis via regulating gut microbiota in broilers.
引用
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页数:16
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