过氧化物酶体增殖物激活受体
阿尔法(金融)
内分泌学
内科学
调制(音乐)
化学
生物
受体
医学
物理
声学
结构效度
护理部
患者满意度
作者
Isabela Macedo Lopes Vasques-Monteiro,Aline Fernandes‐da‐Silva,Carolline Santos Miranda,Flávia Maria Silva-Veiga,Julio Beltrame Daleprane,Vanessa Souza‐Mello
标识
DOI:10.1016/j.mce.2024.112177
摘要
To evaluate the effects of PPARα and PPARγ activation (alone or in combination) on the gut-liver axis, emphasizing the integrity of the intestinal barrier and hepatic steatosis in mice fed a high saturated fat diet. Male C57BL/6J were fed a control diet (C) or a high-fat diet (HF) for ten weeks. Then, a four-week treatment started: HF-α (WY14643), HF-γ (low-dose pioglitazone), and HF-αγ (combination). The HF caused overweight, insulin resistance, impaired gut-liver axis, and marked hepatic steatosis. Treatments reduced body mass, improved glucose homeostasis, and restored the gut microbiota diversity and intestinal barrier gene expression. Treatments also lowered the plasma lipopolysaccharide concentrations and favored beta-oxidation genes, reducing macrophage infiltration and steatosis in the liver. Treatment with PPAR agonists modulated the gut microbiota and rescued the integrity of the intestinal barrier, alleviating hepatic steatosis. These results show that these agonists can contribute to metabolic-associated fatty liver disease treatment.
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