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UPLC-Q-TOF/MS-based metabonomics reveals mechanisms for Holothuria leucospilota polysaccharides (HLP)-regulated serum metabolic changes in diabetic rats

文献类型: 外文期刊

作者: Zhang, Xin 1 ; Zhao, Fuqiang 1 ; Ma, Tingting 1 ; Zheng, Yuanping 1 ; Cao, Jun 1 ; Li, Chuan 1 ; Zhu, Kexue 2 ;

作者机构: 1.Hainan Univ, Engn Res Ctr Utilizat Trop Polysaccharide Resource, Hainan Engn Res Ctr Aquat Resources EfficientUtili, Sch Food Sci & Engn,Minist Educ, Haikou 570228, Peoples R China

2.Chinese Acad Trop Agr Sci, Hainan Prov Key Lab Genet Improvement & Qual Regu, Spice & Beverage Res Inst, Wanning 571533, Peoples R China

3.Dalian Polytech Univ, Collaborat Innovat Ctr Prov & Ministerial Coconstr, Dalian 116034, Peoples R China

4.Hainan Univ, Sch Food Sci & Engn, Haikou 570228, Hainan, Peoples R China

5.Chinese Acad Trop Agr Sci, Key Lab Proc Suitabil & Qual Control Special Trop, Wanning 571533, Peoples R China

关键词: Holothuria leucospilota; Polysaccharides; Diabetes mellitus; Metabolomics; Bile acid metabolism

期刊名称:FOOD CHEMISTRY-X ( 影响因子:6.1; 五年影响因子:6.4 )

ISSN: 2590-1575

年卷期: 2023 年 19 卷

页码:

收录情况: SCI

摘要: This study aimed to use metabolomic methods to explore how Holothuria leucospilota polysaccharides (HLP) improved metabolism disorders in the liver of Goto-Kakizaki (GK) rats with spontaneous type 2 diabetes. The results showed that HLP effectively improved the metabolic disorder. Based on KEGG functional analysis, five key biomarkers associated with bile acid metabolism were detected and screened (P < 0.05). The results of serum total bile acid levels and liver damage in diabetic rats further showed the regulatory effects of HLP on bile acid metabolism. The results of bile acid-related gene expression in the liver showed that HLP inhibited liver farnesoid X Receptor - small heterodimer partner (FXR-SHP) signalling and increased the expression of bile acid synthesis genes (P < 0.05). Our results explored the underlying mechanisms by which HLP accelerated cholesterol consumption to anti-hypercholesterolemia and anti-diabetic by inhibiting liver FXR-SHP signaling. HLP's effect on bile acid regulation provides insights into treating T2DM.

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