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短链脂肪酸丙酸盐对血清代谢组的调节:对其降胆固醇作用的潜在影响。

Modulation of the Serum Metabolome by the Short-Chain Fatty Acid Propionate: Potential Implications for Its Cholesterol-Lowering Effect.

机构信息

Department of Cardiology, University Hospital St Josef-Hospital Bochum, Ruhr University Bochum, 44791 Bochum, Germany.

Department of Cardiology, Angiology and Intensive Care, Deutsches Herzzentrum der Charité, Campus Benjamin Franklin, 12203 Berlin, Germany.

出版信息

Nutrients. 2024 Jul 22;16(14):2368. doi: 10.3390/nu16142368.

Abstract

(1) Background: Dyslipidemia represents a major risk factor for atherosclerosis-driven cardiovascular disease. Emerging evidence suggests a close relationship between cholesterol metabolism and gut microbiota. Recently, we demonstrated that the short-chain fatty acid (SCFA) propionate (PA) reduces serum cholesterol levels through an immunomodulatory mechanism. Here, we investigated the effects of oral PA supplementation on the human serum metabolome and analyzed changes in the serum metabolome in relation to the cholesterol-lowering properties of PA. (2) Methods: The serum metabolome of patients supplemented with either placebo or propionate orally for 8 weeks was assessed using a combination of flow injection analysis-tandem (FIA-MS/MS) as well as liquid chromatography (LC-MS/MS) and mass spectrometry using a targeted metabolomics kit (MxPQuant 500 kit: BIOCRATES Life Sciences AG, Innsbruck, Austria). A total of 431 metabolites were employed for further investigation in this study. (3) Results: We observed a significant increase in distinct bile acids (GCDCA: fold change = 1.41, DCA: fold change = 1.39, GUDCA: fold change = 1.51) following PA supplementation over the study period, with the secondary bile acid DCA displaying a significant negative correlation with the serum cholesterol levels. (4) Conclusions: Oral supplementation with PA modulates the serum metabolome with a particular impact on the circulatory bile acid profile. Since cholesterol and bile acid metabolism are interconnected, the elevation of the secondary bile acid DCA may contribute to the cholesterol-lowering effect of PA.

摘要

(1)背景:血脂异常是动脉粥样硬化性心血管疾病的主要危险因素。新出现的证据表明胆固醇代谢与肠道微生物群之间存在密切关系。最近,我们证明短链脂肪酸(SCFA)丙酸盐(PA)通过免疫调节机制降低血清胆固醇水平。在这里,我们研究了口服 PA 补充对人体血清代谢组的影响,并分析了血清代谢组的变化与 PA 降低胆固醇特性之间的关系。(2)方法:使用组合流注射分析-串联(FIA-MS/MS)以及液相色谱(LC-MS/MS)和使用靶向代谢组学试剂盒(MxPQuant 500 试剂盒:BIOCRATES Life Sciences AG,因斯布鲁克,奥地利)评估了接受安慰剂或丙酸盐口服补充 8 周的患者的血清代谢组。共对 431 种代谢物进行了进一步研究。(3)结果:我们观察到在 PA 补充期间,特定胆汁酸(GCDCA:倍数变化= 1.41,DCA:倍数变化= 1.39,GUDCA:倍数变化= 1.51)的明显增加,次级胆汁酸 DCA 与血清胆固醇水平呈显著负相关。(4)结论:口服补充 PA 可调节血清代谢组,特别是对循环胆汁酸谱的影响。由于胆固醇和胆汁酸代谢是相互关联的,次级胆汁酸 DCA 的升高可能有助于 PA 的降胆固醇作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ee7/11280296/c16a6d8120d1/nutrients-16-02368-g001.jpg

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