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Chemistry and biochemistry of 4-hydroxynonenal, malonaldehyde and related aldehydes
Abstract
Lipid peroxidation often occurs in response to oxidative stress, and a great diversity of aldehydes are formed when lipid hydroperoxides break down in biological systems. Some of these aldehydes are highly reactive and may be considered as second toxic messengers which disseminate and augment initial free radical events. The aldehydes most intensively studied so far are 4-hydroxynonenal, 4-hydroxyhexenal, and malonaldehyde. The purpose of this review is to provide a comprehensive summary on the chemical properties of these aldehydes, the mechanisms of their formation and their occurrence in biological systems and methods for their determination. We will also review the reactions of 4-hydroxyalkenals and malonaldehyde with biomolecules (amino acids, proteins, nucleic acid bases), their metabolism in isolated cells and excretion in whole animals, as well as the many types of biological activities described so far, including cytotoxicity, genotoxicity, chemotactic activity, and effects on cell proliferation and gene expression. Structurally related compounds, such as acrolein, crotonaldehyde, and other 2-alkenals are also briefly discussed, since they have some properties in common with 4-hydroxyalkenals.
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“These effects include the up-or down-regulation of the synthesis of resistin (138) , leptin, adiponectin (139) , lipocalin 2 (140) , osteopontin (141) , and of insulin itself.”
From Dietary factors and low-grade inflammation in relation to overweight and obesity (2011) · cites this paper as [139]
In the citing paper
“The direct assessment of MDA and 4-HNE is not very sensitive, since the major portion of these reactive aldehydes is attached to proteins or other biomolecules and therefore before analysis, should be released, otherwise, they remain undetected (Esterbauer et al. 1991).”
From Reactive Oxygen Species, Toxicity, Oxidative Stress, and Antioxidants: Chronic Diseases and Aging (2023) · cites this paper as Esterbauer et al. 1991
In the citing paper
“Reactive aldehydes from lipid peroxidation have biological active functions [59].”
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Cites
Epstein, F. H., Steinberg, D. I., Parthasarathy, S., Carew, T. E., Khoo, J. C., & Witztum, J. L. (1989) · New England Journal of Medicine · doi:10.1056/nejm198904063201407 · Cited by 6,425
[43] Malondialdehyde determination as index of lipid Peroxidation
Draper, H. H., & Hadley, M. (1990) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/0076-6879(90)86135-i · Cited by 4,291
[42] Determination of aldehydic lipid peroxidation products: Malonaldehyde and 4-hydroxynonenal
Esterbauer, H., & Cheeseman, K. H. (1990) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/0076-6879(90)86134-h · Cited by 3,360
Self-citationProoxidant States and Tumor Promotion
Cerutti, P. (1985) · Science · doi:10.1126/science.2981433 · Cited by 2,513
A simple fluorometric assay for lipoperoxide in blood plasma
Yagi, K. (1976) · Biochemical Medicine · doi:10.1016/0006-2944(76)90049-1 · Cited by 2,116
Serum lipid peroxide in cerebrovascular disorders determined by a new colorimetric method
Kei, S. (1978) · Clinica Chimica Acta · doi:10.1016/0009-8981(78)90081-5 · Cited by 1,730
Serum lipid peroxide in cerebrovascular disorders determined by a new colorimetric method
佐藤, 敬. (1979) · Medical Entomology and Zoology · Cited by 1,520
Low density lipoprotein undergoes oxidative modification in vivo.
Palinski, W., Rosenfeld, M. E., Ylä‐Herttuala, S., Gurtner, G. C., Socher, S. S., Butler, S. W., Parthasarathy, S., Carew, T. E., Steinberg, D. H., & Witztum, J. L. (1989) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.86.4.1372 · Cited by 1,514
DAOUD, G. (1965) · Archives of Pediatrics and Adolescent Medicine · doi:10.1001/archpedi.1965.02090030355030 · Cited by 1,170
Benedetti, A., Comporti, M., & Esterbauer, H. (1980) · Biochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism · doi:10.1016/0005-2760(80)90209-x · Cited by 1,085
Self-citation
Research works printed but not linked: 25
- Esterbauer, 1988, Hydroxyalkenals: cytotoxic products of lipid peroxidation, ISI Atlas of Science, 1, 311
- Ramenghi, 1985, Increased production of carbonyls other than malonaldehyde in red blood cells from homocygous thalassemic subjects exposed to oxidative stress, IRCS Med. Sci., 13, 273
- Curzio, 1986, Detection of carbonyl products of lipid peroxidation in rat pleural exudate, IRCS Med. Sci., 14, 984
- Sodum, 1987, Formation of 1,N2-ethenodeoxyguanosine and propano-deoxyguanosine adducts with trans-4-hydroxy-2-nonenal, Carcinogenesis, 28, 98
- Eckl, 1989, Genotoxic effects of 4-hydroxynonenals, Adv. Biosci., 76, 141
- Cajelli, 1984, Mutagenicity of 4-hydroxynonenal in V79 Chinese hamster lung cells, Mutation Res., 44, 169
- Curzio, 1990, Influence of the lipid peroxidation product 4-hydroxynonenal on human neutrophil migration, Int. J. Tissue React., 6, 13
- Hofer, 1983, Some effects of 4-hydroxypentenal on the synchronous mitotic cycle of Physarum polycephalum, IRCS Med. Science, 11, 356
- Zollner, 1973, Effects of 4-hydroxypentenal on succinate respiration and succinate dehydrogenase in liver and tumor cells, Z. Krebsforsch., 79, 108
- Koster, 1986, Comparison of the inactivation of microsomal glucose-6-phosphatase by in situ lipid peroxidation-derived 4-hydroxynonenal and exogenous 4-hydroxynonenal, Free Radic. Res. Commun., 1, 273, 10.3109/10715768609051637 · DOI
- Claisen, 1903, On the knowledge about propagylaldehyde and phenyl propagylaldehyde, Berichte, 36, 3664
- Hüttel, 1941, On malonaldehyde, Berichte, 74, 1825
- Scherz, 1978, Über die bildung von malondialdehyd bei der bestrahlung von lebensmitteln, Chem. Mikrobiol. Technol. Lebensm., 1, 103
- Napetschnig, 1988, Formation of a pyridinium derivative by reaction of 4-hydroxypentenal with glycine, Chem. Biol. Interact., 68, 165, 10.1016/0009-2797(88)90014-2 · DOI
- Loeper, 1983, Study of fatty acids and lipid peroxidation during the course of human atherosclerosis, Sem. Hop. Paris, 59, 1657
- Janero, 1986, Isolation by HPLC of free malondialdehyde as a product of the xanthine-oxidase dependent, iron-promoted peroxidation of cardiac membrane phospholipid, J. Am. Oil Chem. Soc., 63, 476
- Jeny, 1986, Study of lipidperoxidation in human and experimental atheroma by measurement of plasma malonaldehyde, Presse Medicale, 15, 1131
- Mahanty, 1986, Aspirin stimulates malonaldehyde production in mouse-liver microsomes, Pediatric Res., 20, 651
- Skornyakov, 1988, Lipid peroxidation products in the cerebrospinal fluid of patients with craniocerebral injuries, Lab. Delo., 14
- Kergonou, 1988, Immunogenicity of proteins reacted with malonic dialdehyde (MDA), Adv. Biosci., 71, 121
- Esterbauer, H.; Schaur, R. J.; Zollner, H. Biological activities of 4-hydroxyalkenals. In: Sies, H., ed. Oxidative stress. New York: Academic Press; in press.
- Fisher, 1954, Depolymerization of desoxyribonucleic acid preparations by oxidized methyl linoleate, J. Eli. Mitchell Soc., 70, 124
- Akasaka, 1985, Mutation induction in Escherichia coli incubated in the reaction mixture of NADPH-dependent lipid peroxidation of rat-liver microsomes, Mutation Res., 149, 321, 10.1016/0027-5107(85)90147-2 · DOI
- Spalding, 1989, Toxicology and carinogenesis studies of malondialdehyde sodium salt (3-hydroxy-2-propenal, sodium salt) in F344/N rats and B6C3F1 mice, Natl. Toxicol. Program Ser., 331, 5
- Stone, 1990, Investigation of the adducts formed by reaction of malondialdehyde with adenosine, Chem. Res. Toxicol., 3, 33, 10.1021/tx00013a006 · DOI
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Subramaniam, R., Roediger, F., Jordan, B., Mattson, M. P., Keller, J. N., Waeg, G., & Butterfield, D. A. (1997) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.1997.69031161.x · Cited by 270
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Yokota, T., Igarashi, K., Uchihara, T., Jishage, K.-I., Tomita, H., Inaba, A., Li, Y., Arita, M., Suzuki, H., Mizusawa, H., et al. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.261456098 · Cited by 261
Reed, T., Perluigi, M., Sultana, R., Pierce, W. M., Klein, J. B., Turner, D. M., Coccia, R., Markesbery, W. R., & Butterfield, D. A. (2008) · Neurobiology of Disease · doi:10.1016/j.nbd.2007.12.007 · Cited by 257
Lamprecht, M., Bogner, S., Schippinger, G., Steinbauer, K., Fankhauser, F., Hallstroem, S., Schuetz, B., & Greilberger, J. F. (2012) · Journal of the International Society of Sports Nutrition · doi:10.1186/1550-2783-9-45 · Cited by 257
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Metadata
- Authors
- Esterbauer, H., Schaur, R. J., & Zollner, H.
- Affiliations
- University of Graz (AT)
- Corresponding author
- Esterbauer, Hermann
- Venue
- Free Radical Biology and Medicine
- Publisher
- Elsevier BV
- Published
- 1991
- Volume
- 11
- Issue
- 1
- Pages
- 81-128
- ISSN
- 0891-5849 (ISSN-L)
- OpenAlex
- W2057522312
- Cited by
- 6,672
- References
- 370
- Citations by year
- 2026: 109 · 2025: 116 · 2024: 119 · 2023: 159 · 2022: 156 · 2021: 217 · 2020: 221 · 2019: 210 · 2018: 192 · 2017: 198 · 2016: 224 · 2015: 243 · 2014: 257 · 2013: 261 · 2012: 290
- FWCI
- 6.17
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Free Radical Biology and Medicine (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Biochemistry (medical) › Antioxidant Activity and Oxidative Stress
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Redox biology and oxidative stress
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Cancer and biochemical research
- Keywords
- 4-hydroxynonenal, malondialdehyde, lipid peroxidation, lipid hydroperoxides, 4-hydroxyhexenal, 2-alkenals, acrolein, crotonaldehyde, oxidative stress, aldehyde determination, aldehyde metabolism, cytotoxicity, genotoxicity, chemotactic activity, cell proliferation, gene expression
- MeSH terms
- Aldehydes, Animals, Free Radicals, Humans, Malondialdehyde
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