脂肪变性
丁酸盐
肠道菌群
果糖
丁酸
脂肪肝
内科学
丁酸钠
化学
内分泌学
生物化学
生物
医学
疾病
发酵
基因
作者
Qu Chen,Lei Wu,Aijia Zhang,Chen Wu,Liuping Cai,Yingping Xiao,Yingdong Ni
标识
DOI:10.26599/fshw.2022.9250082
摘要
Sodium butyrate (NaB) can regulate lipid metabolism and inhibit hepatic steatosis. This study aimed to investigate whether NaB can alleviate fructose-induced hepatic steatosis via remodeling the gut microbiota and evaluate the anti-fatty liver mechanisms. The results showed that NaB and NaB-remodeled gut microbiota significantly alleviated fructose-induced hepatic steatosis and increased plasma uric acid and fructose levels. Furthermore, both NaB and NaB-remodeled gut microbiota increased the abundance of Lactobacillus and altered the levels of plasma amino acids [upregulating gamma-amino butyric acid (GABA) and downregulating L-glutamic acid and L-arginine] in fructose-exposed mice. The correlation analysis showed that GABA levels positively correlated with Lactobacillus abundance, and increased GABA levels might promote the reduction of the hepatic triglyceride content. Further studies confirmed that GABA significantly reduced lipid deposition in mouse hepatocytes induced via fructose pretreatment in vitro. These findings suggested that NaB could ameliorate fructose-induced hepatic steatosis by regulating gut microbiota.
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