Suppr超能文献

通过亲和超滤结合 UPLC-Orbitrap MS 从杜仲茶中鉴定胰脂肪酶抑制剂及体外验证。

Identification of pancreatic lipase inhibitors from Eucommia ulmoides tea by affinity-ultrafiltration combined UPLC-Orbitrap MS and in vitro validation.

机构信息

Key Laboratory of Forest Plant Ecology, Ministry of Education, Northeast Forestry University, Harbin 150040, PR China; Engineering Research Center of Forest Bio-Preparation, Ministry of Education, Northeast Forestry University, Harbin 150040, PR China; College of Chemistry, Chemical Engineering and Resource Utilization, Northeast Forestry University, Harbin 150040, PR China.

The College of Forestry, Beijing Forestry University, Beijing 100083, PR China.

出版信息

Food Chem. 2023 Nov 15;426:136630. doi: 10.1016/j.foodchem.2023.136630. Epub 2023 Jun 14.

Abstract

Pancreatic lipase inhibitors can reduce blood lipids by inactivating the catalytic activity of human pancreatic lipase, a key enzyme involved in triglyceride hydrolysis, which helps control some dyslipidemic diseases. The ability of Eucommia ulmoides tea to improve fat-related diseases is closely related to the natural inhibitory components of pancreatic lipase contained in the tea. In this study, fifteen pancreatic lipase inhibitors were screened and identified from Eucommia ulmoides tea by affinity-ultrafiltration combined UPLC-Q-Exactive Orbitrap/MS. Four representative components of geniposidic acid, quercetin-3-O-sambuboside, isochlorogenic acid A, and quercetin with high binding degrees were further verified by nanoscale differential scanning fluorimetry (nanoDSF) and enzyme inhibitory assays. The results of flow cytometry showed that they could significantly reduce the activity of pancreatic lipase in AR42J cells induced by palmitic acid in a concentration-dependent manner. Our findings suggest that Eucommia ulmoides tea may be a promising resource for pancreatic lipase inhibitors of natural origin.

摘要

胰脂肪酶抑制剂通过使参与甘油三酯水解的关键酶——人胰脂肪酶的催化活性失活,从而降低血脂,有助于控制一些血脂异常疾病。杜仲茶改善脂肪相关疾病的能力与其茶中含有的天然胰脂肪酶抑制成分密切相关。本研究通过亲和超滤结合 UPLC-Q-Exactive Orbitrap/MS 从杜仲茶中筛选并鉴定了 15 种胰脂肪酶抑制剂。通过纳米差示扫描荧光法(nanoDSF)和酶抑制试验进一步验证了具有高结合度的京尼平酸、槲皮素-3-O-桑布双糖苷、异绿原酸 A 和槲皮素这 4 种代表性成分。流式细胞术的结果表明,它们能够显著降低脂肪酸诱导的 AR42J 细胞中胰脂肪酶的活性,且呈浓度依赖性。我们的研究结果表明,杜仲茶可能是天然来源的胰脂肪酶抑制剂的有前途的资源。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验