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Increased levels of 4-hydroxynonenal and acrolein in the brain in preclinical Alzheimer disease
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Previous studies demonstrate increased levels of 4-hydroxynonenal (HNE) and acrolein in vulnerable brain regions of subjects with mild cognitive impairment and late-stage Alzheimer disease (LAD). Recently preclinical AD (PCAD) subjects, who demonstrate normal antemortem neuropsychological test scores but abundant AD pathology at autopsy, have become the focus of increased study. Levels of extractable HNE and acrolein were quantified by gas chromatography-mass spectrometry with negative chemical ionization, and protein-bound HNE and acrolein were quantified by dot-blot immunohistochemistry in the hippocampus/parahippocampal gyrus (HPG), superior and middle temporal gyri (SMTG), and cerebellum (CER) of 10 PCAD and 10 age-matched normal control (NC) subjects. Results of the analyses show a significant (P<0.05) increase in levels of extractable acrolein in the HPG of PCAD subjects compared to age-matched NC subjects and a significant decrease in extractable acrolein in PCAD CER. Significant increases in protein-bound HNE in HPG and a significant decrease in CER of PCAD subjects compared to NC subjects were observed. No significant alterations were observed in either extractable or protein-bound HNE or acrolein in the SMTG of PCAD subjects. Additionally, no significant differences in levels of protein carbonyls were observed in the HPG, SMTG, or CER of PCAD subjects compared to NC subjects.
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Citations
Cites
Neuropathological stageing of Alzheimer-related changes.
Braak, H., & Braak, E. (1991) · Acta Neuropathologica · doi:10.1007/bf00308809 · Cited by 16,123
Chemistry and biochemistry of 4-hydroxynonenal, malonaldehyde and related aldehydes
Esterbauer, H., Schaur, R. J., & Zollner, H. (1991) · Free Radical Biology and Medicine · doi:10.1016/0891-5849(91)90192-6 · Cited by 6,672
Oxidative Damage Is the Earliest Event in Alzheimer Disease
Nunomura, A., Perry, G., Aliev, G., Hirai, K., Takeda, A., Balraj, E. K., Jones, P. K., Ghanbari, H., Wataya, T., Shimohama, S., et al. (2001) · Journal of Neuropathology & Experimental Neurology · doi:10.1093/jnen/60.8.759 · Cited by 1,885
Saiki, R. K., Bugawan, T. L., Horn, G. T., Mullis, K. B., & Erlich, H. A. (1986) · Nature · doi:10.1038/324163a0 · Cited by 1,816
4-Hydroxy-2-nonenal: a product and mediator of oxidative stress
Uchida, K. (2003) · Progress in Lipid Research · doi:10.1016/s0163-7827(03)00014-6 · Cited by 1,164
Oxidative damage to mitochondrial DNA is increased in Alzheimer’s disease
Mecocci, P., MacGarvey, U., & Beal, M. F. (1994) · Annals of Neurology · doi:10.1002/ana.410360510 · Cited by 1,037
RNA Oxidation Is a Prominent Feature of Vulnerable Neurons in Alzheimer’s Disease
Nunomura, A., Perry, G., Pappolla, M., Wade, R., Hirai, K., Chiba, S., & Smith, M. A. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-06-01959.1999 · Cited by 768
Catalá, A. (2009) · Chemistry and Physics of Lipids · doi:10.1016/j.chemphyslip.2008.09.004 · Cited by 745
Markesbery, W. R., & Lovell, M. A. (1998) · Neurobiology of Aging · doi:10.1016/s0197-4580(98)00009-8 · Cited by 680
Self-citationFatty acid composition of brain phospholipids in aging and in Alzheimer’s disease
Söderberg, M., Edlund, C., Kristensson, K., & Dallner, G. (1991) · Lipids · doi:10.1007/bf02536067 · Cited by 667
Research works printed but not linked: 3
- Shao, 2008, Altered 8-oxoguanine glycosylase in mild cognitive impairment and late-stage Alzheimer's disease brain, Free Radic. Biol. Med., 45, 813, 10.1016/j.freeradbiomed.2008.06.003 · DOI · Paper page
- Calingansan, 1999, Protein-bound acrolein: a novel marker of oxidative stress in Alzheimer's disease, J. Neurochem., 72, 751, 10.1046/j.1471-4159.1999.0720751.x · DOI
- Lovell, 1999, Increased DNA oxidation and decreased levels of repair products in Alzheimer's disease ventricular CSF, J. Neurochem., 72, 771, 10.1046/j.1471-4159.1999.0720771.x · DOI
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Oxidative stress, protein modification and Alzheimer disease
Tramutola, A., Lanzillotta, C., Perluigi, M., & Butterfield, D. A. (2017) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2016.06.005 · Cited by 303
Alzheimer’s disease: pathological mechanisms and the beneficial role of melatonin
Rosales‐Corral, S., Acuña-Castroviejo, D., Coto‐Montes, A. M., Boga, J. A., Manchester, L. C., Fuentes‐Broto, L., Korkmaz, A., Ma, S., Tan, D. X., & Reiter, R. J. (2011) · Journal of Pineal Research · doi:10.1111/j.1600-079x.2011.00937.x · Cited by 299
4-Hydroxy-2-nonenal: a critical target in oxidative stress?
Breitzig, M., Bhimineni, C., Lockey, R. F., & Kolliputi, N. (2016) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00101.2016 · Cited by 284
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Menzel, A., Samouda, H., Dohet, F., Loap, S., Ellulu, M. S., & Bohn, T. (2021) · Antioxidants · doi:10.3390/antiox10030414 · Cited by 255
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Swomley, A. M., & Butterfield, D. A. (2015) · Archives of Toxicology · doi:10.1007/s00204-015-1556-z · Cited by 173
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Ayton, S., Portbury, S. D., Kalinowski, P., Agarwal, P., Diouf, I., Schneider, J. A., Morris, M. C., & Bush, A. I. (2021) · Alzheimer s & Dementia · doi:10.1002/alz.12282 · Cited by 168
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Singh, M., Nam, D. T., Arseneault, M., & Ramassamy, C. (2010) · Journal of Alzheimer s Disease · doi:10.3233/jad-2010-100405 · Cited by 162
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Gianazza, E., Brioschi, M., Fernandez, A. M., & Banfi, C. (2019) · Redox Biology · doi:10.1016/j.redox.2019.101119 · Cited by 152
Zhang, J., Wu, J., Liu, F., Tong, L., Chen, Z., Chen, J., He, H., Xu, R., Ma, Y., & Huang, C. (2019) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2019.172500 · Cited by 147
Connecting the “Dots”: From Free Radical Lipid Autoxidation to Cell Pathology and Disease
Foret, M. K., Lincoln, R., Carmo, S. D., Cuello, A. C., & Cosa, G. (2020) · Chemical Reviews · doi:10.1021/acs.chemrev.0c00761 · Cited by 150
Lipid Peroxidation and Its Toxicological Implications
Nam, T. G. (2011) · Toxicological Research · doi:10.5487/tr.2011.27.1.001 · Cited by 144
DNA polymerase β deficiency leads to neurodegeneration and exacerbates Alzheimer disease phenotypes
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Calabrese, V., Cornelius, C., Stella, A. M. G., & Calabrese, E. J. (2010) · Neurochemical Research · doi:10.1007/s11064-010-0307-z · Cited by 134
Amyloid-β Toxicity and Tau Hyperphosphorylation are Linked Via RCAN1 in Alzheimer's Disease
Lloret, A., Badía, M.-C., Giraldo, E., Ermak, G., Alonso, M.-D., Pallardó, F. V., Davies, K. J. A., & Viña, J. (2011) · Journal of Alzheimer s Disease · doi:10.3233/jad-2011-110890 · Cited by 133
Ates, G., Goldberg, J., Currais, A. J. M., & Maher, P. A. (2020) · Redox Biology · doi:10.1016/j.redox.2020.101648 · Cited by 131
Nunomura, A., Tamaoki, T., Motohashi, N., Nakamura, M., McKeel, D. W., Tabaton, M., Lee, H., Smith, M. A., Perry, G. L., & Zhu, X. (2012) · Journal of Neuropathology & Experimental Neurology · doi:10.1097/nen.0b013e318248e614 · Cited by 134
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George, R. C., Lew, J., & Graves, D. J. (2013) · Journal of Alzheimer s Disease · doi:10.3233/jad-122113 · Cited by 114
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Self-citationUddin, M. S., Mamun, A. A., Hossain, M. S., Akter, F., Iqbal, M. A., & Asaduzzaman, M. (2016) · Annals of Neurosciences · doi:10.1159/000449482 · Cited by 109
Chen, W.-Y., Wang, M., Zhang, J., Barve, S. S., McClain, C. J., & Joshi‐Barve, S. (2017) · American Journal Of Pathology · doi:10.1016/j.ajpath.2017.08.015 · Cited by 109
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Aluise, C. D., Robinson, R. A. S., Cai, J., Pierce, W. M., Markesbery, W. R., & Butterfield, D. A. (2011) · Journal of Alzheimer's Disease · doi:10.3233/jad-2010-101083 · Cited by 94
Self-citationRaefsky, S. M., Furman, R., Milne, G., Pollock, E., Axelsen, P., Mattson, M. P., & Shchepinov, M. S. (2018) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2018.02.024 · Cited by 90
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Huang, Y., Jin, M., Pi, R., Zhang, J., Chen, M., Ouyang, Y., Liu, A., Chao, X., Liu, P., Liu, J., et al. (2013) · Neuroscience Letters · doi:10.1016/j.neulet.2012.12.051 · Cited by 87
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Shen, L., Chen, C., Yang, A., Chen, Y., Liu, Q., & Ni, J. (2015) · Journal of Proteomics · doi:10.1016/j.jprot.2015.04.005 · Cited by 73
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Cervellati, C., Cremonini, E., Bosi, C., Magon, S., Zurlo, A., Bergamini, C. M., & Zuliani, G. (2013) · Current Alzheimer Research · doi:10.2174/1567205011310040003 · Cited by 70
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Son, S., Lee, J., Kim, H.-G., Kim, D. W., Ahn, Y., & Son, C. (2015) · Journal of Neurochemistry · doi:10.1111/jnc.13371 · Cited by 59
Dixit, S., Fessel, J. P., & Harrison, F. E. (2017) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2017.08.021 · Cited by 57
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Waragai, M., Yoshida, M., Mizoi, M., Saiki, R., Kashiwagi, K., Takagi, K., Arai, H., Tashiro, J., Hashimoto, M., Iwai, N., et al. (2012) · Journal of Alzheimer s Disease · doi:10.3233/jad-2012-120253 · Cited by 56
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Yin, R., Liu, S., Zhao, C., Lü, M., Tang, M., & Wang, H. (2013) · Analytical Chemistry · doi:10.1021/ac3034695 · Cited by 55
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Ferroptosis mechanism and Alzheimer's disease
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Corsinovi, L., Biasi, F., Poli, G., Leonarduzzi, G., & Isaia, G. (2011) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.201100208 · Cited by 54
Doggui, S., Belkacemi, A., Paka, G. D., Perrotte, M., Pi, R., & Ramassamy, C. (2013) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.201300130 · Cited by 51
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Lull, M. E., Levesque, S., Surace, M. J., & Block, M. L. (2011) · PLoS ONE · doi:10.1371/journal.pone.0020153 · Cited by 53
Liu, J., Wang, T.-W., Lin, Y., Ho, W.-C., Tsai, H., Chen, S., Lin, A. M.-Y., Liu, T., & Wang, H. (2019) · Experimental Neurology · doi:10.1016/j.expneurol.2019.113066 · Cited by 50
Bromfield, E. G., Aitken, R. J., McLaughlin, E. A., & Nixon, B. (2016) · Molecular Human Reproduction · doi:10.1093/molehr/gaw074 · Cited by 47
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Tsai, S., Hsu, L., Tsai, H., Yeh, Y., Lu, C., Chen, P., Wang, J., Chiu, Y., Lin, C., & Hsu, Y. (2020) · The FASEB Journal · doi:10.1096/fj.201902550rrr · Cited by 47
Wang, H., Dharmalingam, P., Vasquez, V., Mitra, J., Boldogh, I. R., Rao, K. S. J., Kent, T. A., MITRA, S. P., & Hegde, M. L. (2016) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2016.09.005 · Cited by 46
Shen, Y., Zhang, G., Wei, C., Zhao, P., Wang, Y., Li, M., & Sun, L. (2024) · Neural Regeneration Research · doi:10.4103/nrr.nrr-d-23-01343 · Cited by 44
Wang, Y.-T., Lin, H., Zhao, W.-Z., Huang, H.-J., Lo, Y., Wang, H., & Lin, A. M. (2017) · Scientific Reports · doi:10.1038/srep45741 · Cited by 42
Ko, K., Suzuki, T., Ishikawa, R., Hattori, N., Ito, R., Umehara, K., Furihata, T., Dohmae, N., Linhardt, R. J., Igarashi, K., et al. (2020) · Journal of Biological Chemistry · doi:10.1074/jbc.ra120.015105 · Cited by 42
Oxidative damage and amyloid‐β metabolism in brain regions of the longest‐lived rodents
Edrey, Y. H., Oddo, S., Cornelius, C., Caccamo, A., Calabrese, V., & Buffenstein, R. (2013) · Journal of Neuroscience Research · doi:10.1002/jnr.23320 · Cited by 41
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Metadata
- Authors
- Bradley, M. A., Markesbery, W. R., & Lovell, M. A.
- Affiliations
- University of Kentucky (US)
- Corresponding author
- Lovell, M.A.
- ORCID
- Lovell, M.A.
- Venue
- Free Radical Biology and Medicine
- Publisher
- Elsevier BV
- Published
- 2010-06
- Volume
- 48
- Issue
- 12
- Pages
- 1570-1576
- ISSN
- 0891-5849 (ISSN-L)
- PMC
- PMC2881698
- OpenAlex
- W2056044698
- Cited by
- 193
- References
- 41
- Citations by year
- 2026: 7 · 2025: 8 · 2024: 4 · 2023: 12 · 2022: 12 · 2021: 16 · 2020: 13 · 2019: 17 · 2018: 3 · 2017: 7 · 2016: 13 · 2015: 14 · 2014: 10 · 2013: 17 · 2012: 14
- FWCI
- 12.34
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Free Radical Biology and Medicine (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institutes of Health
- National Institute on Aging (5P01-AG05119, P30AG028383, P01AG005119)
- National Cancer Institute
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Alzheimer's disease research and treatments
- Health Sciences › Medicine › Psychiatry and Mental health › Dementia and Cognitive Impairment Research
- Health Sciences › Medicine › Biochemistry (medical) › Antioxidant Activity and Oxidative Stress
- Keywords
- preclinical Alzheimer's disease, 4-hydroxynonenal, acrolein, lipid peroxidation, protein carbonyls, hippocampus, parahippocampal gyrus, cerebellum, temporal lobe, oxidative stress, brain biomarkers
- MeSH terms
- Acrolein, Aged, 80 and over, Aldehydes, Alzheimer Disease, Brain, Brain Chemistry, Female, Humans, Immunohistochemistry, Male, Gas Chromatography-Mass Spectrometry, Immunoblotting
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