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胆汁酸与植物化合物相互作用的机制研究进展。

Mechanisms of Interactions between Bile Acids and Plant Compounds-A Review.

机构信息

ZIEL-Institute for Food & Health, TUM School of Life Sciences Weihenstephan, Technical University of Munich, 85354 Freising, Germany.

Fraunhofer Institute for Process Engineering and Packaging (IVV), 85354 Freising, Germany.

出版信息

Int J Mol Sci. 2020 Sep 5;21(18):6495. doi: 10.3390/ijms21186495.

Abstract

Plant compounds are described to interact with bile acids during small intestinal digestion. This review will summarise mechanisms of interaction between bile acids and plant compounds, challenges in in vivo and in vitro analyses, and possible consequences on health. The main mechanisms of interaction assume that increased viscosity during digestion results in reduced micellar mobility of bile acids, or that bile acids and plant compounds are associated or complexed at the molecular level. Increasing viscosity during digestion due to specific dietary fibres is considered a central reason for bile acid retention. Furthermore, hydrophobic interactions are proposed to contribute to bile acid retention in the small intestine. Although frequently hypothesised, no mechanism of permanent binding of bile acids by dietary fibres or indigestible protein fractions has yet been demonstrated. Otherwise, various polyphenolic structures were recently associated with reduced micellar solubility and modification of steroid and bile acid excretion but underlying molecular mechanisms of interaction are not yet fully understood. Therefore, future research activities need to consider the complex composition and cell-wall structures as influenced by processing when investigating bile acid interactions. Furthermore, influences of bile acid interactions on gut microbiota need to be addressed to clarify their role in bile acid metabolism.

摘要

植物化合物被描述为在小肠消化过程中与胆汁酸相互作用。这篇综述将总结胆汁酸和植物化合物之间相互作用的机制、体内和体外分析的挑战,以及对健康可能产生的影响。相互作用的主要机制假设,在消化过程中增加的粘度会导致胆汁酸胶束的流动性降低,或者胆汁酸和植物化合物在分子水平上发生关联或复合。由于特定的膳食纤维在消化过程中增加了粘度,被认为是胆汁酸保留的主要原因。此外,疏水相互作用被认为有助于胆汁酸在小肠中的保留。尽管经常假设,但膳食纤维或不可消化的蛋白质部分与胆汁酸永久结合的机制尚未得到证实。另一方面,最近有研究表明,各种多酚结构与胶束溶解度降低和甾体及胆汁酸排泄改变有关,但相互作用的潜在分子机制尚不完全清楚。因此,在研究胆汁酸相互作用时,未来的研究活动需要考虑到加工过程中复杂的组成和细胞壁结构。此外,需要解决胆汁酸相互作用对肠道微生物群的影响,以阐明它们在胆汁酸代谢中的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5db7/7555273/9400bbd6b99f/ijms-21-06495-g001.jpg

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