Literature DB >> 28720960

Levels and formation of α-dicarbonyl compounds in beverages and the preventive effects of flavonoids.

Chen Wang1, Yongling Lu1, Qiju Huang1, Tiesong Zheng1, Shengmin Sang2, Lishuang Lv1.   

Abstract

ABSTRACT: Methylglyoxal (MGO) and glyoxal (GO), α-dicarbonyl compounds found in the Maillard reaction, progressively and irreversibly modify proteins. Beverages are an exogenous source of α-dicarbonyl compounds and may potentially increase MGO and GO levels in vivo. Using GC-FID method, we detected the MGO and GO contents of 86 beverages in Chinese supermarkets. The highest MGO and GO 587.5 µg/100 mL and 716.7 µg/100 mL respectively found in soyamilk and coffee. Herbal beverages, which contained bioactive components, had lower average levels of MGO (48.1 µg/100 mL) and GO (25.9 µg/100 mL). A box-and-whisker plot was used to display variation of the same group drinks, and comparing distributions between six different groups. It was further discovered that fat, protein and flavonoids, in addition to sweeteners, had notable effects on the formation of MGO and GO in soybean milk. The result of LC/MS indicated that quercetin could prevent the formation of MGO by trapping MGO to form the mono-MGO and di-MGO adducts during soybean milk manufacturing.

Entities:  

Keywords:  Beverages; Glyoxal; Methylglyoxal; Soy milk; α-Dicarbonyl compounds

Year:  2017        PMID: 28720960      PMCID: PMC5495730          DOI: 10.1007/s13197-017-2639-z

Source DB:  PubMed          Journal:  J Food Sci Technol        ISSN: 0022-1155            Impact factor:   2.701


  27 in total

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Review 4.  Advanced glycoxidation and lipoxidation end products (AGEs and ALEs): an overview of their mechanisms of formation.

Authors:  G Vistoli; D De Maddis; A Cipak; N Zarkovic; M Carini; G Aldini
Journal:  Free Radic Res       Date:  2013-08

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Journal:  J Food Sci       Date:  2011-03-16       Impact factor: 3.167

6.  Classification and characterization of manuka honeys based on phenolic compounds and methylglyoxal.

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7.  Tea polyphenol (-)-epigallocatechin-3-gallate: a new trapping agent of reactive dicarbonyl species.

Authors:  Shengmin Sang; Xi Shao; Naisheng Bai; Chih-Yu Lo; Chung S Yang; Chi-Tang Ho
Journal:  Chem Res Toxicol       Date:  2007-11-15       Impact factor: 3.739

8.  Binding and modification of proteins by methylglyoxal under physiological conditions. A kinetic and mechanistic study with N alpha-acetylarginine, N alpha-acetylcysteine, and N alpha-acetyllysine, and bovine serum albumin.

Authors:  T W Lo; M E Westwood; A C McLellan; T Selwood; P J Thornalley
Journal:  J Biol Chem       Date:  1994-12-23       Impact factor: 5.157

9.  Role of the Maillard reaction in aging of tissue proteins. Advanced glycation end product-dependent increase in imidazolium cross-links in human lens proteins.

Authors:  E B Frye; T P Degenhardt; S R Thorpe; J W Baynes
Journal:  J Biol Chem       Date:  1998-07-24       Impact factor: 5.157

10.  Glyoxal formation and its role in endogenous oxalate synthesis.

Authors:  Jessica N Lange; Kyle D Wood; John Knight; Dean G Assimos; Ross P Holmes
Journal:  Adv Urol       Date:  2012-04-08
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  2 in total

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2.  Determination of 14 Isoflavone Isomers in Natto by UPLC-ESI-MS/MS and Antioxidation and Antiglycation Profiles.

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  2 in total

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