Glucose-stimulated acrolein production from unsaturated fatty acids

Human and Experimental Toxicology

Volumn 23, Issue 2, 2004, Pages 101-105

  Medina Navarro, R ^a,c   Duran Reyes, G ^a   Diaz Flores, M ^a   Hicks, J J ^b   Kumate, R J ^a  

^a INSTITUTO MEXICANO DEL SEGURO SOCIAL   (Mexico)

^b HOSPITAL JUÁREZ DE MÉXICO   (Mexico)

^c NONE   (Mexico)

Author keywords

Acrolein; Capillary electrophoresis; Diabetes; Free fatty acids; Glucose; Oxidative stress

Indexed keywords

ACROLEIN; ALDEHYDE; ARACHIDONIC ACID; FATTY ACID; FREE RADICAL; GLUCOSE; HYDROPEROXIDE; LINOLEIC ACID; ORGANIC SOLVENT; REACTIVE OXYGEN METABOLITE; UNSATURATED FATTY ACID;

ARTICLE; AUTOOXIDATION; CAPILLARY ELECTROPHORESIS; CONCENTRATION RESPONSE; CONTROLLED STUDY; CORRELATION ANALYSIS; ENZYME ACTIVATION; HYPERGLYCEMIA; IN VITRO STUDY; IN VIVO STUDY; INCUBATION TIME; LIPID PEROXIDATION; MASS SPECTROMETRY; PRIORITY JOURNAL; TISSUE INJURY;

ACROLEIN; FATTY ACIDS, UNSATURATED; GLUCOSE; LIPID PEROXIDATION;

EID: 1642301677     PISSN: 09603271     EISSN: None     Source Type: Journal    
DOI: 10.1191/0960327104ht416oa     Document Type: Article

References (23)

1. Uchida K, Kanematsu M, Morimitsu Y, Osawa T, Noguchi N, Niki E. Acrolein is a product of lipid peroxidation reaction. Formation of free acroleín and its conjugate with lysine residues in oxidized low density lipoproteins. J Biol Chem 1998; 273: 16058-66.
2. Medina-Navarro R, Mercado-Pichardo E, Hernández-Pérez O, Hicks JJ. Identification of acrolein from the ozone oxidation of unsaturated fatty acids. Hum Exp Toxicol 1999; 18: 677-82.
3. Uchida K, Kanematsu M, Sakai K, Matsuda T, Hattori N, Mizuno Y, Suzuki D, Miyata T, Noguchi N, Niki E, Osawa T. Protein-bound acrolein: Potential markers for oxidative stress. Proc Natl Acad Sci USA 1998; 95: 4882-87.
4. Friguet B, Szweda LI. Inhibition of the multicatalytic proteinase (proteosome) by 4-hydroxy-2-nonenal cross-linked protein. FEBS Letts 1997; 405: 21-25.
5. Hyun DH, Lee MH, Halliwell B, Jenner P. Proteosomal dysfunction induced by 4-hydroxy-2,3-trans-nonenal, an end-product of lipid peroxidation: A mechanism contributing to neurodegeneration? J Neurochem 2002; 83: 360-70.
6. Kern JC, Kehrer JP. Acrolein-induced cell death: A caspase-influenced decision between apoptosis and oncosis/necrosis. Chem Biol Interact 2002; 139: 79-95.
7. Horton ND, Mamiya BM, Kehrer JP. Relationship between cell density, glutathione and proliferation of A549 human lung adenocarcinoma cells treated with acrolein. Toxicology 1997; 122: 111-22.
8. Ferrali M, Ciccoli L, Signorini C, Comporti M. Iron release and erythrocyte damage in allyl alcohol intoxication in mice. Biochem Pharmacol 1990; 40: 1485-90.
9. Yamagami K, Yamamoto Y, Toyokuni S, Hata K, Yamaoka Y. Heat shock preconditioned reduces the formation of 8-hydroxy-2′-deoxyguanosine and 4-hydroxy-2-nonenal modified proteins in ischemia-reperfused liver of rats. Free Radic Res 2002; 36: 169-76.
10. Kurtz AJ, Lloyd RS. 1, N2-deoxyguanosine adducts of acrolein, crotonaldehyde, and trans-4-hydroxynonenal cross-link to peptides via Schiff Base Linkage. J Biol Chem 2003; 278: 5970-76.
11. Allevi P, Anastasia M, Cajone F, Ciuffreda P, Sanvito AM. Structural requierements of aldehydes produced in LPO for the activation of the heat-shock genes in HeLa cells. Free Radic Biol Med 1995; 18: 107-16.
12. Slater TF. Overview of methods used for detecting lipid peroxidation. Method Enzymol 1984; 105: 283-376.
13. Cighetti G, Debiasi S, Ciuffreda P, Allevi P. Beta-ethoxyacrolein contamination increases malondialdehyde inhibition of milk xanthine oxidase activity. Free Radic Biol Med 1998; 25: 818-25.
14. Hicks M, Delbridge L, Yue DK, Reeve TS. Catalysis of lipid peroxidation by glucose and glycosylated collagen. Biochem Biophys Res Commun 1988; 151: 649-55.
15. Kawamura M, Heinecke JW, Chait A. Pathophysiological concentrations of glucose promote oxidative modification of low-density lipoprotein by a superoxide-dependent pathway. J Clin Invest 1994; 94: 771-78.
16. Halliwell B, Gutteridge MC. Free radicals, other reactive species and disease. In Halliwell B, Guteridge MC eds, Free radicals in biology and medicine. New York: Oxford University Press, 1999: 642-43.
17. Hunt JV. Ascorbic acid and diabetes mellitus. In Harris RJ ed., SubcBlular biochemistry, volume 25: Ascorbic acid: biochemistry and biomedical cell biology. New York: Plenum Press, 1995: 369.
18. Gutteridge JM, Stocks J, Dormandy TL. Thiobarbituric acid-reacting substances derived from autoxidizing linoleic and linolenic acids. Anal Chim Acta 1970; 70: 107-109.
19. Uchida K, Szweda KI, Chae HZ, Stadtman ER. Immunochemical detection of 4-hydroxynonenal protein adducts in oxidized hepatocytes. Proc Natl Acad Sci USA 1993; 9: 8742-46.
20. Esterbauer H, Jörg Schaur R, Zollner H. Chemistry and biochemistry of 4-hydroxynonenal, malondialdehyde and related aldehydes. Free Radic Biol Med 1991; 11: 81-128.
21. Oberley LW. Free radicals and diabetes. Free Radic Biol Med 1988; 5: 113-24.
22. Nishikawa T, Edelstein D, Du XL, Yamagishi S, Matsumura T, Kaneda Y, Yorek MA, Beebe D, Oates PJ, Hammes HP, Giardino I, Brownlee M. Normalizing mitochondrial superoxide production blocks three pathways of hyperglycaemic damage. Nature 2000; 404: 787-90.
23. Thorpe SR, Baynes JW. Role of the Maillard reaction in diabetes mellitus and diseases of aging. Drugs Aging 1996; 9: 69-73.