Huang Dan, Shen Shuang, Zhuang Qian, Ye Xin, Qian Yueqin, Dong Zhixia, Wan Xinjian
Digestive Endoscopic Center, Shanghai Sixth People's Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, No. 600 Yishan Road, Shanghai, 200233, China.
Chin Med. 2024 Jan 24;19(1):16. doi: 10.1186/s13020-024-00889-y.
Cholesterol gallstone (CG) disease is a worldwide common disease characterized by cholesterol supersaturation in gallbladder bile. Ganoderma lucidum polysaccharide (GLP) has been shown to possess various beneficial effects against metabolic disorders. However, the role and underlying mechanism of GLP in CG formation are still unknown. This study aimed to determine the role of GLP in ameliorating lithogenic diet (LD)-induced CG formation.
Mice were fed either a normal chow diet, a LD, or LD supplemented with GLP. Real-time quantitative polymerase chain reaction (RT-qPCR) and western blotting were used to detect the expression of genes involved in cholesterol and bile acid (BA) metabolism. The BA concentrations in the ileum were quantified by liquid chromatography-tandem mass spectrometry (LC-MS/MS). The microbiota in cecal contents were characterized using 16S ribosomal RNA (16S rRNA) gene sequencing.
GLP effectively alleviated CG formation induced by LD. Specifically, GLP reduced the total cholesterol (TC) levels, increased the total BA levels, and decreased the cholesterol saturation index (CSI) in gallbladder bile. The protective effect of GLP was attributed to the inhibition of farnesoid X receptor (FXR) signaling, increased hepatic BA synthesis and decreased hepatic cholesterol synthesis and secretion. GLP also altered the BA composition in the ileum, reducing FXR-agonistic BAs and increasing FXR-antagonistic BAs, which may contribute to the inhibition of intestinal FXR signaling. Additionally, GLP improved dysbiosis of the intestinal flora and reduced the serum levels of hydrogen sulfide (HS), a bacterial metabolite that can induce hepatic FXR, thereby inhibiting hepatic FXR signaling. Moreover, the protective effect of GLP against CG formation could be reversed by both the global and gut-restricted FXR agonists.
Taken together, GLP ameliorates CG formation by regulating cholesterol and BA metabolism in an FXR-dependent manner. Our study demonstrates that GLP may be a potential strategy for the prevention against CG disease.
胆固醇胆结石(CG)疾病是一种全球常见疾病,其特征是胆囊胆汁中胆固醇过饱和。灵芝多糖(GLP)已被证明对代谢紊乱具有多种有益作用。然而,GLP在CG形成中的作用及潜在机制仍不清楚。本研究旨在确定GLP在改善致石饮食(LD)诱导的CG形成中的作用。
将小鼠分为正常饮食组、LD组或补充GLP的LD组。采用实时定量聚合酶链反应(RT-qPCR)和蛋白质印迹法检测胆固醇和胆汁酸(BA)代谢相关基因的表达。通过液相色谱-串联质谱(LC-MS/MS)定量回肠中的BA浓度。使用16S核糖体RNA(16S rRNA)基因测序对盲肠内容物中的微生物群进行表征。
GLP有效减轻了LD诱导的CG形成。具体而言,GLP降低了总胆固醇(TC)水平,提高了总BA水平,并降低了胆囊胆汁中的胆固醇饱和指数(CSI)。GLP的保护作用归因于对法尼醇X受体(FXR)信号的抑制、肝脏BA合成增加以及肝脏胆固醇合成和分泌减少。GLP还改变了回肠中的BA组成,减少了FXR激动性BA并增加了FXR拮抗性BA,这可能有助于抑制肠道FXR信号。此外,GLP改善了肠道菌群失调并降低了血清硫化氢(HS)水平,HS是一种可诱导肝脏FXR的细菌代谢产物,从而抑制肝脏FXR信号。此外,GLP对CG形成的保护作用可被全身性和肠道限制性FXR激动剂逆转。
综上所述,GLP通过以FXR依赖的方式调节胆固醇和BA代谢来改善CG形成。我们的研究表明,GLP可能是预防CG疾病的一种潜在策略。