Biotransformation and metabolism of three mulberry anthocyanin monomers by rat gut microflora. (15th December 2017)
- Record Type:
- Journal Article
- Title:
- Biotransformation and metabolism of three mulberry anthocyanin monomers by rat gut microflora. (15th December 2017)
- Main Title:
- Biotransformation and metabolism of three mulberry anthocyanin monomers by rat gut microflora
- Authors:
- Chen, Yao
Li, Qian
Zhao, Ting
Zhang, Zhen
Mao, Guanghua
Feng, Weiwei
Wu, Xiangyang
Yang, Liuqing - Abstract:
- Highlights: Metabolism of three mulberry anthocyanin monomers by gut microflora was investigated. Characterization of metabolites was performed by HPLC-ESI-MS/MS. In vitro faecal fermentation generated a wide range of phenolic acids. A combination of conversion steps for metabolism of anthocyanins was presented. The differential metabolism of the three ACNs in fresh rat feces was investigated. Abstract: Anthocyanins (ACNs) are naturally occurring components of human diet. Evidence has accumulated regarding the positive association of their intake with chronic disease. Because microbiota has been considered as a metabolic organ, the bacterial-dependent metabolisms of three types of ACNs from mulberry fruits (cyanidin-3-glucoside (C3G), cyanidin-3-rutinoside (C3R), delphinidin-3-rutinoside (D3R)) during a simulation of large intestine conditions were investigated. ACNs and metabolites were analysed and characterized by high performance liquid chromatography-electrospray ionization-mass spectrum (HPLC-ESI-MS/MS). C3G disappeared after 6 h of metabolism, while C3R and D3R were no longer detected after 8 h. The metabolism of C3G and C3R mainly resulted in the formation of protocatechuic, vanillic, and p -coumaric acids, as well as 2, 4, 6-trihydroxybenzaldehyde, while the main metabolites of D3R were gallic acid, syringic acid and 2, 4, 6-trihydroxybenzaldehyde. This research indicated that the intake of ACNs may result in the appearance of specific metabolites that exert aHighlights: Metabolism of three mulberry anthocyanin monomers by gut microflora was investigated. Characterization of metabolites was performed by HPLC-ESI-MS/MS. In vitro faecal fermentation generated a wide range of phenolic acids. A combination of conversion steps for metabolism of anthocyanins was presented. The differential metabolism of the three ACNs in fresh rat feces was investigated. Abstract: Anthocyanins (ACNs) are naturally occurring components of human diet. Evidence has accumulated regarding the positive association of their intake with chronic disease. Because microbiota has been considered as a metabolic organ, the bacterial-dependent metabolisms of three types of ACNs from mulberry fruits (cyanidin-3-glucoside (C3G), cyanidin-3-rutinoside (C3R), delphinidin-3-rutinoside (D3R)) during a simulation of large intestine conditions were investigated. ACNs and metabolites were analysed and characterized by high performance liquid chromatography-electrospray ionization-mass spectrum (HPLC-ESI-MS/MS). C3G disappeared after 6 h of metabolism, while C3R and D3R were no longer detected after 8 h. The metabolism of C3G and C3R mainly resulted in the formation of protocatechuic, vanillic, and p -coumaric acids, as well as 2, 4, 6-trihydroxybenzaldehyde, while the main metabolites of D3R were gallic acid, syringic acid and 2, 4, 6-trihydroxybenzaldehyde. This research indicated that the intake of ACNs may result in the appearance of specific metabolites that exert a protective effect in the host physiology. … (more)
- Is Part Of:
- Food chemistry. Volume 237(2017)
- Journal:
- Food chemistry
- Issue:
- Volume 237(2017)
- Issue Display:
- Volume 237, Issue 2017 (2017)
- Year:
- 2017
- Volume:
- 237
- Issue:
- 2017
- Issue Sort Value:
- 2017-0237-2017-0000
- Page Start:
- 887
- Page End:
- 894
- Publication Date:
- 2017-12-15
- Subjects:
- Anthocyanin monomers -- Metabolism -- Phenolic acid -- HPLC-ESI-MS/MS -- Gut microbiota
Food -- Analysis -- Periodicals
Food -- Composition -- Periodicals
664 - Journal URLs:
- http://www.sciencedirect.com/science/journal/03088146 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.foodchem.2017.06.054 ↗
- Languages:
- English
- ISSNs:
- 0308-8146
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3977.284000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 4624.xml