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Pregled bibliografske jedinice broj: 259384

Methylglyoxal in food and living organisms


Nemet, Ina; Varga-Defterdarović, Lidija; Turk, Zdenka
Methylglyoxal in food and living organisms // Molecular nutrition & food research, 50 (2006), 12; 1105-1117 doi:10.1002/mnfr.200600065 (međunarodna recenzija, članak, znanstveni)


CROSBI ID: 259384 Za ispravke kontaktirajte CROSBI podršku putem web obrasca

Naslov
Methylglyoxal in food and living organisms

Autori
Nemet, Ina ; Varga-Defterdarović, Lidija ; Turk, Zdenka

Izvornik
Molecular nutrition & food research (1613-4125) 50 (2006), 12; 1105-1117

Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni

Ključne riječi
Advanced glycation end products ; Diabetes ; Food ; Maillard reaction ; Methylglyoxal

Sažetak
Methylglyoxal (MG) is a highly reactive α‐oxoaldehyde formed endogenously in numerous enzymatic and nonenzymatic reactions. It modifies arginine and lysine residues in proteins forming advanced glycation end‐products such as Nδ‐(5‐methyl‐4‐imidazolon‐2‐yl)‐L‐ornithine (MG‐H1), 2‐amino‐5‐(2‐amino‐5‐hydro‐5‐methyl‐4‐imidazolon‐1‐yl)pentanoic acid (MG‐H2), 2‐amino‐5‐(2‐amino‐4‐hydro‐4‐methyl‐5‐imidazolon‐1‐yl)pentanoic acid (MG‐H3), argpyrimidine, Nδ‐(4‐carboxy‐4, 6‐dimethyl‐5, 6‐dihydroxy‐1, 4, 5, 6‐tetrahydropyrimidine‐2‐yl)‐L‐ornithine (THP), Nε‐(1‐carboxyethyl)lysine (CEL), MG‐derived lysine dimer (MOLD), and 2‐ammonio‐6‐({;2–[4‐ammonio‐5‐oxido‐5‐oxopently)amino]‐4‐methyl‐4, 5‐dihydro‐1H‐imidazol‐5‐ylidene};amino)hexanoate (MODIC), which have been identified in vivo and are associated with complications of diabetes and some neurodegenerative diseases. In foodstuffs and beverages, MG is formed during processing, cooking, and prolonged storage. Fasting and metabolic disorders and/or defects in MG detoxification processes cause accumulation of this reactive dicarbonyl in vivo. In addition, the intake of low doses of MG over a prolonged period of time can cause degenerative changes in different tissues, and can also exert anticancer activity. MG in biological samples can be quantified by HPLC or GC methods with preliminary derivatization into more stable chromophores and/or fluorophores, or derivatives suitable for determination by MS by use of diamino derivatives of benzene and naphthalene, 6‐hydroxy‐2, 4, 5‐triaminopyrimidine, cysteamine, and o‐(2, 3, 4, 5, 6‐pentafluorobenzyl) hydroxylamine. The methods include three basic steps: deproteinization, incubation with derivatization agent, and chromatographic analysis with or without preliminary extraction of the formed products.

Izvorni jezik
Engleski

Znanstvena područja
Kemija



POVEZANOST RADA


Projekti:
0098054
0045003

Ustanove:
Klinika za dijabetes, endokrinologiju i bolesti metabolizma Vuk Vrhovac,
Institut "Ruđer Bošković", Zagreb

Profili:

Avatar Url Zdenka Turk (autor)

Avatar Url Lidija Varga-Defterdarović (autor)

Avatar Url Ina Nemet (autor)

Poveznice na cjeloviti tekst rada:

doi onlinelibrary.wiley.com doi.org

Citiraj ovu publikaciju:

Nemet, Ina; Varga-Defterdarović, Lidija; Turk, Zdenka
Methylglyoxal in food and living organisms // Molecular nutrition & food research, 50 (2006), 12; 1105-1117 doi:10.1002/mnfr.200600065 (međunarodna recenzija, članak, znanstveni)
Nemet, I., Varga-Defterdarović, L. & Turk, Z. (2006) Methylglyoxal in food and living organisms. Molecular nutrition & food research, 50 (12), 1105-1117 doi:10.1002/mnfr.200600065.
@article{article, author = {Nemet, Ina and Varga-Defterdarovi\'{c}, Lidija and Turk, Zdenka}, year = {2006}, pages = {1105-1117}, DOI = {10.1002/mnfr.200600065}, keywords = {Advanced glycation end products, Diabetes, Food, Maillard reaction, Methylglyoxal}, journal = {Molecular nutrition and food research}, doi = {10.1002/mnfr.200600065}, volume = {50}, number = {12}, issn = {1613-4125}, title = {Methylglyoxal in food and living organisms}, keyword = {Advanced glycation end products, Diabetes, Food, Maillard reaction, Methylglyoxal} }
@article{article, author = {Nemet, Ina and Varga-Defterdarovi\'{c}, Lidija and Turk, Zdenka}, year = {2006}, pages = {1105-1117}, DOI = {10.1002/mnfr.200600065}, keywords = {Advanced glycation end products, Diabetes, Food, Maillard reaction, Methylglyoxal}, journal = {Molecular nutrition and food research}, doi = {10.1002/mnfr.200600065}, volume = {50}, number = {12}, issn = {1613-4125}, title = {Methylglyoxal in food and living organisms}, keyword = {Advanced glycation end products, Diabetes, Food, Maillard reaction, Methylglyoxal} }

Časopis indeksira:


  • Current Contents Connect (CCC)
  • Web of Science Core Collection (WoSCC)
    • Science Citation Index Expanded (SCI-EXP)
    • SCI-EXP, SSCI i/ili A&HCI
  • Scopus
  • MEDLINE


Uključenost u ostale bibliografske baze podataka::


  • Chemical Abstracts


Citati:





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