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[微生物群对维生素代谢与消化道阳性微生物群存活之间关系的系统分析]

[System analysis of the relationship between the metabolism of vitamins by micro-biota and the survival of the positive microflora of the digestive tract].

作者信息

Gromova O A, Torshin I Iu, Garas'ko E V, Limanova O A, Grishina T R, Rudakov K V

出版信息

Eksp Klin Gastroenterol. 2013(2):28-36.

PMID:23947161
Abstract

A perspective direction of the treatment of dysbacteriosis is the use of so-called metabolic prebiotics--products of metabolism of positive flora (for example, water substrate of the products of metabolism of E. coli, S. faecalis, L. acidophilus, L. helveticus (strains of DSM), out of which, as known, drug Hylak Forte is made. Our earlier systematic analysis of metabolomics, representatives of positive microflora, pointed to the fact that the latter contain specific biochemical mechanisms for biosynthesis and processing of a number of vitamins. In the present paper the results of a systematic analysis of the effects of vitamins B2, B6 and K on the survival of the representatives of the positive microflora on the basis of the substrate of metabolic products of positive flora have been presented. The results of the analysis allow us clarify the molecular mechanisms of the therapeutic effects of this drug with a very complex structure and confirm the available clinical data and are an important foundation for subsequent microbiological research. Metabolites in the preparation composition contribute to the normalization of metabolism of pyridoxalphosphate (vitamin B6), flavin adenin dinucleotide (FAD, a derivative of vitamin B2) and nicotinamide dinucleotide (NAD, a derivative of vitamin B3)--cofactors of enzymes that have a significant impact on the survival of microbiota. The proposed molecular mechanisms also indicate on a possible synergies between certain vitamins and micro elements, on the one hand, and molecular components of the preparations on the basis of waste products of microbiota on the other.

摘要

治疗菌群失调症的一个前瞻性方向是使用所谓的代谢益生元——有益菌群的代谢产物(例如大肠杆菌、粪肠球菌、嗜酸乳杆菌、瑞士乳杆菌(DSM菌株)代谢产物的水性底物,众所周知,药物海乐福胶囊就是由这些制成的。我们早期对代谢组学、有益微生物群代表的系统分析表明,后者含有多种维生素生物合成和加工的特定生化机制。在本文中,展示了基于有益菌群代谢产物底物,对维生素B2、B6和K对有益微生物群代表存活率影响的系统分析结果。分析结果使我们能够阐明这种结构非常复杂的药物治疗作用的分子机制,证实现有的临床数据,并且是后续微生物学研究的重要基础。制剂成分中的代谢产物有助于磷酸吡哆醛(维生素B6)、黄素腺嘌呤二核苷酸(FAD,维生素B2的衍生物)和烟酰胺二核苷酸(NAD,维生素B3的衍生物)——对微生物群存活率有重大影响的酶的辅助因子——的代谢正常化。所提出的分子机制还表明,一方面某些维生素和微量元素之间可能存在协同作用,另一方面基于微生物群废物产物的制剂分子成分之间也可能存在协同作用。

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