A preliminary study on the formation pathways of glycated phosphatidylethanolamine of food rich in phospholipid during the heat-processing. Issue 21 (21st March 2018)
- Record Type:
- Journal Article
- Title:
- A preliminary study on the formation pathways of glycated phosphatidylethanolamine of food rich in phospholipid during the heat-processing. Issue 21 (21st March 2018)
- Main Title:
- A preliminary study on the formation pathways of glycated phosphatidylethanolamine of food rich in phospholipid during the heat-processing
- Authors:
- Lin, Qingna
Han, Lipeng
Liu, Guoqin
Cheng, Weiwei
Wang, Liqing - Abstract:
- Abstract : The formation of food-derived glycated phosphatidylethanolamine (PE) in thermal process was investigated by designing a 1, 2-dipalmitoyl- sn-glycero -3-phosphoethanolamine (DPPE)-glucose model system heated from 40 to 100 °C for 8 h. Abstract : The formation of food-derived glycated phosphatidylethanolamine (PE) in thermal process was investigated by designing a 1, 2-dipalmitoyl- sn-glycero -3-phosphoethanolamine (DPPE)-glucose model system heated from 40 to 100 °C for 8 h. The main products of glycated PE were determined by high performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS). Results showed that the glycation of DPPE formed three major glycated compounds: amadori-glycated-1, 2-dipalmitoyl- sn-glycero -3-phosphoethanolamine (Amadori-DPPE), carboxymethyl-1, 2-dipalmitoyl- sn-glycero -3-phosphoethanolamine (CM-DPPE), and carboxyethyl-1, 2-dipalmitoyl- sn-glycero -3-phosphoethanolamine (CE-DPPE). Amadori-DPPE was identified to generate CM-DPPE through oxidative cleavage of glycated polar head group under high temperature and extended incubation time. Additionally, during thermal processing, retro-aldol reactions of glucose led to the formation of two reactive dicarbonyl intermediates: glyoxal (GO) and methylglyoxal (MGO), both of them reacted with amino group of DPPE to form CM-DPPE and CE-DPPE, respectively. Thus, the formation pathways of CM-PE might involve the irreversible rearrangements of Amadori-PE following oxidative cleavage, as wellAbstract : The formation of food-derived glycated phosphatidylethanolamine (PE) in thermal process was investigated by designing a 1, 2-dipalmitoyl- sn-glycero -3-phosphoethanolamine (DPPE)-glucose model system heated from 40 to 100 °C for 8 h. Abstract : The formation of food-derived glycated phosphatidylethanolamine (PE) in thermal process was investigated by designing a 1, 2-dipalmitoyl- sn-glycero -3-phosphoethanolamine (DPPE)-glucose model system heated from 40 to 100 °C for 8 h. The main products of glycated PE were determined by high performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS). Results showed that the glycation of DPPE formed three major glycated compounds: amadori-glycated-1, 2-dipalmitoyl- sn-glycero -3-phosphoethanolamine (Amadori-DPPE), carboxymethyl-1, 2-dipalmitoyl- sn-glycero -3-phosphoethanolamine (CM-DPPE), and carboxyethyl-1, 2-dipalmitoyl- sn-glycero -3-phosphoethanolamine (CE-DPPE). Amadori-DPPE was identified to generate CM-DPPE through oxidative cleavage of glycated polar head group under high temperature and extended incubation time. Additionally, during thermal processing, retro-aldol reactions of glucose led to the formation of two reactive dicarbonyl intermediates: glyoxal (GO) and methylglyoxal (MGO), both of them reacted with amino group of DPPE to form CM-DPPE and CE-DPPE, respectively. Thus, the formation pathways of CM-PE might involve the irreversible rearrangements of Amadori-PE following oxidative cleavage, as well as the glycation of amino group of PE with GO. CE-PE could only be formed by reaction of PE with MGO. Moreover, the content of CM-DPPE was higher than that of CE-DPPE in the same incubation conditions, which indicated that CM-PE might be a more useful predictive marker for food-derived glycated amino-phospholipid, rather than Amadori-PE, particularly in thermal processed foodstuffs. … (more)
- Is Part Of:
- RSC advances. Volume 8:Issue 21(2018)
- Journal:
- RSC advances
- Issue:
- Volume 8:Issue 21(2018)
- Issue Display:
- Volume 8, Issue 21 (2018)
- Year:
- 2018
- Volume:
- 8
- Issue:
- 21
- Issue Sort Value:
- 2018-0008-0021-0000
- Page Start:
- 11280
- Page End:
- 11288
- Publication Date:
- 2018-03-21
- Subjects:
- Chemistry -- Periodicals
540.5 - Journal URLs:
- http://pubs.rsc.org/en/Journals/JournalIssues/RA ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c8ra01072b ↗
- Languages:
- English
- ISSNs:
- 2046-2069
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 8036.750300
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 6151.xml