Protective and anti-oxidative effects of curcumin and resveratrol on Aβ-oligomer-induced damage in the SH-SY5Y cell line
Abstract
Alzheimer's disease (AD) is a degenerative disorder characterized by the loss of synapses and neurons in the brain, and results in the accumulation of amyloid-based neurotic plaques. Amyloid-β oligomers (AβO) are widely accepted as the main neurotoxin that induces oxidative stress and neuronal loss in AD. In this study, an oxidative stress model of the neuroblastoma SH-SY5Y cell line exposed to AβO was established to simulate an AD cell model. Exposure to AβO significantly reduced the viability of cultured SH-SY5Y cells (p < 0.05) and significantly increased intracellular reactive oxygen species (ROS) (p < 0.01). AβO exposure also induced oxidative stress in SH-SY5Y cells. Furthermore, AβO significantly increased the level of hyperphosphorylation of tau at sites T181 and T205 in SH-SY5Y cells (p < 0.01). Using edaravone, a free radical scavenger with neuroprotective properties, as the control, the possible protective and anti-oxidative effects of curcumin (40 μM) and resveratrol (20 μM) were evaluated. The results suggest that curcumin and resveratrol decreased ROS generation, attenuated oxidative stress, inhibited tau hyperphosphorylation, and protected SH-SY5Y cells from AβO damage. Both curcumin and resveratrol are promising supplements or medicine as therapeutic agents for the treatment of AD.
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Oxidative stress and tau hyperphosphorylation levels were raised after exposure to amyloid beta oligomers.
“In addition, oxidative stress and tau hyperphosphorylation levels were also raised.”
From Unlocking the Therapeutic Potential of Medicinal Plants for Alzheimer’s Disease: Preclinical to Clinical Trial Insights (2023) · cites this paper as [85]
Curcumin is a promising therapeutic agent for managing Alzheimer's disease.
“Conclusively, curcumin was considered a promising therapeutic agent for managing AD [85].”
From Unlocking the Therapeutic Potential of Medicinal Plants for Alzheimer’s Disease: Preclinical to Clinical Trial Insights (2023) · cites this paper as [85]
The viability of cultured SH-SY5Y cells was considerably decreased after exposure to amyloid beta oligomers.
“Moreover, the viability of cultured SH-SY5Y cells was considerably decreased after exposure to AβO.”
From Unlocking the Therapeutic Potential of Medicinal Plants for Alzheimer’s Disease: Preclinical to Clinical Trial Insights (2023) · cites this paper as [85]
Curcumin reduced reactive oxygen species production, alleviated oxidative stress, prevented tau hyperphosphorylation, and protected SH-SY5Y cells from amyloid beta oligomer damage.
“Furthermore, according to the findings, curcumin reduced ROS production, alleviated oxidative stress, prevented tau hyperphosphorylation, and protected SH-SY5Y cells from AβO damage.”
From Unlocking the Therapeutic Potential of Medicinal Plants for Alzheimer’s Disease: Preclinical to Clinical Trial Insights (2023) · cites this paper as [85]
Cites
Mitochondrial Dysfunction and Oxidative Stress in Neurodegenerative Diseases
Lin, M. T., & Beal, M. F. (2006) · Nature · doi:10.1038/nature05292 · Cited by 6,455 · see citing works
Lambert, M. P., Barlow, A. K., Chromy, B. A., Edwards, C., Freed, R., Liosatos, M., Morgan, T. E., Rozovsky, I., Trommer, B., Viola, K. L., et al. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.11.6448 · Cited by 3,506 · see citing works
Oxidative Stress, Synaptic Dysfunction, and Alzheimer’s Disease
Tönnies, E., & Trushina, E. (2017) · Journal of Alzheimer s Disease · doi:10.3233/jad-161088 · Cited by 1,750 · see citing works
Lim, G. P., Chu, T., Yang, F., Beech, W., Frautschy, S. A., & Cole, G. M. (2001) · The Journal of Neuroscience · doi:10.1523/jneurosci.21-21-08370.2001 · Cited by 1,530 · see citing works
Curcumin has potent anti‐amyloidogenic effects for Alzheimer's β‐amyloid fibrils in vitro
Ono, K., Hasegawa, K., Naiki, H., & Yamada, M. (2004) · Journal of Neuroscience Research · doi:10.1002/jnr.20025 · Cited by 1,254 · see citing works
Alzheimer’s disease: Clinical trials and drug development
Mangialasche, F., Solomon, A., Winblad, B., Mecocci, P., & Kivipelto, M. (2010) · The Lancet Neurology · doi:10.1016/s1474-4422(10)70119-8 · Cited by 1,217 · see citing works
Considerations for the use of SH-SY5Y neuroblastoma cells in neurobiology
Kovalevich, J., & Langford, D. (2013) · Methods in molecular biology · doi:10.1007/978-1-62703-640-5_2 · Cited by 1,005 · see citing works
Neurotoxicity of Amyloid -Protein: Synaptic and Network Dysfunction
Mucke, L., & Selkoe, D. J. (2012) · Cold Spring Harbor Perspectives in Medicine · doi:10.1101/cshperspect.a006338 · Cited by 1,000 · see citing works
Amalraj, A., Pius, A., Gopi, S., & Gopi, S. (2016) · Journal of Traditional and Complementary Medicine · doi:10.1016/j.jtcme.2016.05.005 · Cited by 976 · see citing works
Curcumin: Biological, Pharmaceutical, Nutraceutical, and Analytical Aspects
Kotha, R. R., & Luthria, D. L. (2019) · Molecules · doi:10.3390/molecules24162930 · Cited by 900 · see citing works
The case for rejecting the amyloid cascade hypothesis
Herrup, K. (2015) · Nature Neuroscience · doi:10.1038/nn.4017 · Cited by 768 · see citing works
Resveratrol Promotes Clearance of Alzheimer's Disease Amyloid-β Peptides
Marambaud, P., Zhao, H., & Davies, P. J. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m508246200 · Cited by 750 · see citing works
The Alzheimer’s Disease Mitochondrial Cascade Hypothesis
Swerdlow, R. H., Burns, J. M., & Khan, S. M. (2010) · Journal of Alzheimer s Disease · doi:10.3233/jad-2010-100339 · Cited by 562 · see citing works
Aβ toxicity in Alzheimer’s disease: globular oligomers (ADDLs) as new vaccine and drug targets
Klein, W. L. (2002) · Neurochemistry International · doi:10.1016/s0197-0186(02)00050-5 · Cited by 541 · see citing works
Deshpande, A. M., Mina, E. W., Glabe, C. G., & Busciglio, J. A. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.1189-06.2006 · Cited by 490 · see citing works
Baum, L., & Ng, A. (2004) · Journal of Alzheimer s Disease · doi:10.3233/jad-2004-6403 · Cited by 483 · see citing works
Neuroprotective action of resveratrol
Bastianetto, S., Ménard, C., & Quirion, R. (2014) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2014.09.011 · Cited by 411 · see citing works
Protective effect of resveratrol on β-amyloid-induced oxidative PC12 cell death
Jang, J.-H. (2003) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(03)00062-5 · Cited by 391 · see citing works
Naturally occurring phytochemicals for the prevention of Alzheimer’s disease
Kim, J., Lee, H. J., & Lee, K. W. (2009) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2009.06562.x · Cited by 354 · see citing works
Cao, Z., & Li, Y. (2004) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2004.02.031 · Cited by 229 · see citing works
Candelario-Jalil, E., de Oliveira, A. C. P., Gräf, S., Bhatia, H. S., Hüll, M., Muñoz, E., & Fiebich, B. L. (2007) · Journal of Neuroinflammation · doi:10.1186/1742-2094-4-25 · Cited by 223 · see citing works
Edaravone: A new drug approved for ALS
Rothstein, J. D. (2017) · Cell · doi:10.1016/j.cell.2017.10.011 · Cited by 219 · see citing works
Martínez, M., Rodríguez, J.-L., López-Torres, B., Martínez, M., Martínez‐Larrañaga, M., Maximiliano, J.-E., Anadón, A., & Arés, I. (2019) · Environment International · doi:10.1016/j.envint.2019.105414 · Cited by 209 · see citing works
Potential Mechanism by Which Resveratrol, a Red Wine Constituent, Protects Neurons
Zhuang, H., Kim, Y., Koehler, R. C., & Doré, S. (2003) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2003.tb07534.x · Cited by 186 · see citing works
Edaravone alleviates Alzheimer’s disease-type pathologies and cognitive deficits
Jiao, S., Yao, X., Liu, Y.-H., Wang, Q., Zeng, F., Lu, J., Liu, J., Zhu, C., Shen, L., Liu, C., et al. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1422998112 · Cited by 173 · see citing works
Wei, Q., Chen, W., Zhou, B., Li, Y., & Liu, Z. (2005) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2005.09.008 · Cited by 172 · see citing works
Nishinaka, T., Ichijo, Y., Ito, M., Kimura, S., Katsuyama, M., Iwata, K., Miura, T., Terada, T., & Yabe‐Nishimura, C. (2007) · Toxicology Letters · doi:10.1016/j.toxlet.2007.03.011 · Cited by 153 · see citing works
Resveratrol as a Therapeutic Agent for Alzheimer’s Disease
Ma, T., Tan, M., Yu, J., & Tan, L. (2014) · BioMed Research International · doi:10.1155/2014/350516 · Cited by 144 · see citing works
The Efficacy of Edaravone (Radicut), a Free Radical Scavenger, for Cardiovascular Disease
Kikuchi, K., Tancharoen, S., Takeshige, N., Yoshitomi, M., Morioka, M., Murai, Y., & Tanaka, E. (2013) · International Journal of Molecular Sciences · doi:10.3390/ijms140713909 · Cited by 133 · see citing works
Richard, T., Poupard, P., Nassra, M., Papastamoulis, Y., Iglésias, M., Krisa, S., Waffo‐Téguo, P., Mérillon, J., & Monti, J. (2011) · Bioorganic & Medicinal Chemistry · doi:10.1016/j.bmc.2011.04.001 · Cited by 88 · see citing works
Aβ oligomers trigger and accelerate Aβ seeding
Katzmarski, N., Ziegler‐Waldkirch, S., Scheffler, N., Witt, C. C., Abou‐Ajram, C., Nuscher, B., Prinz, M., Haass, C., & Meyer‐Luehmann, M. (2019) · Brain Pathology · doi:10.1111/bpa.12734 · Cited by 85 · see citing works
Agnihotri, N. P., & Mishra, P. (2011) · The Journal of Physical Chemistry A · doi:10.1021/jp209318f · Cited by 66 · see citing works
Curcumin Alters the Salt Bridge-containing Turn Region in Amyloid β(1–42) Aggregates
Mithu, V. S., Sarkar, B., Bhowmik, D., Das, A. K., Chandrakesan, M., Maiti, S., & Madhu, P. K. (2014) · Journal of Biological Chemistry · doi:10.1074/jbc.m113.519447 · Cited by 66 · see citing works
Sahu, P. K. (2016) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2016.05.037 · Cited by 57 · see citing works
Pre and post treatment with curcumin and resveratrol protects astrocytes after oxidative stress
Daverey, A., & Agrawal, S. K. (2018) · Brain Research · doi:10.1016/j.brainres.2018.05.001 · Cited by 54 · see citing works
Sarkar, S., Jun, S., & Simpkins, J. W. (2015) · Brain Research · doi:10.1016/j.brainres.2015.04.059 · Cited by 47 · see citing works
Effect of Curcumin on the metal ion induced fibrillization of Amyloid-β peptide
Banerjee, R. (2013) · Spectrochimica Acta Part A Molecular and Biomolecular Spectroscopy · doi:10.1016/j.saa.2013.09.064 · Cited by 42 · see citing works
Biological and Computational Evaluation of Resveratrol Inhibitors against Alzheimer's Disease
Koukoulitsa, C., Villalonga-Barber, C., Csonka, R., Alexi, X., Leonis, G., Dellis, D., Hamelink, E., Belda, O., Steele, B. R., Micha-Screttas, M., et al. (2016) · Journal of Enzyme Inhibition and Medicinal Chemistry · doi:10.3109/14756366.2014.1003928 · Cited by 37 · see citing works
Zhang, L., Guo, Y., Wang, H., Zhao, L., Ma, Z., Li, T., Liu, J., Sun, M., Jian, Y., Li, Y., et al. (2019) · Life Sciences · doi:10.1016/j.lfs.2019.02.025 · Cited by 36 · see citing works
A synthetic cell permeable antioxidant protects neurons against acute oxidative stress
Drummond, N. J., Davies, N. O., Lovett, J. E., Miller, M. R., Cook, G., Becker, T., Becker, C. G., McPhail, D. B., & Kunath, T. (2017) · Scientific Reports · doi:10.1038/s41598-017-12072-5 · Cited by 30 · see citing works
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Grabska-Kobyłecka, I., Szpakowski, P., Król, A., Książek-Winiarek, D., Kobyłecki, A., Głąbiński, A., & Nowak, D. (2023) · Nutrients · doi:10.3390/nu15153454 · Cited by 273 · see citing works
Shoaib, S., Ansari, M. A., Fatease, A. M. A., Safhi, A. Y., Hani, U., Jahan, R., Alomary, M. N., Ansari, M. N., Ahmed, N., Wahab, S., et al. (2023) · Pharmaceutics · doi:10.3390/pharmaceutics15030749 · Cited by 129 · see citing works
Rodríguez-Giraldo, M., González-Reyes, R. E., Ramírez-Guerrero, S., Bonilla-Trilleras, C. E., Guardo-Maya, S., & Nava-Mesa, M. O. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms232113630 · Cited by 118 · see citing works
Cavaliere, G., Cimmino, F., Trinchese, G., Catapano, A., Petrella, L., D’Angelo, M., Lucchin, L., & Mollica, M. P. (2023) · Antioxidants · doi:10.3390/antiox12061172 · Cited by 97 · see citing works
Nagori, K., Nakhate, K. T., Yadav, K., Ajazuddin, & Pradhan, M. (2023) · Future Pharmacology · doi:10.3390/futurepharmacol3040053 · Cited by 61 · see citing works
Li, N., Yan, X., Huang, W., Chu, M., Yang, D., Song, H., Peng, Y., Shi, J., & Liu, Q. (2023) · Biochemical Pharmacology · doi:10.1016/j.bcp.2023.115575 · Cited by 41 · see citing works
Grosso, C., Santos, M., & Barroso, M. F. (2023) · Antioxidants · doi:10.3390/antiox12081603 · Cited by 30 · see citing works
Zhang, Y., Lu, L., Li, Y., Liu, H., Zhou, W., & Zhang, L. (2024) · Foods · doi:10.3390/foods13203328 · Cited by 26 · see citing works
Natural products targeting amyloid-β oligomer neurotoxicity in Alzheimer's disease
Gonçalves, P. B., Sodero, A. C. R., & Cordeiro, Y. (2024) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2024.116684 · Cited by 26 · see citing works
Lai, G., Wu, H., Yang, K., Hu, K., Zhao, W., Chen, X., Li, J., Haifeng, W., Lv, Z., Xie, G., et al. (2025) · International Journal of Nanomedicine · doi:10.2147/ijn.s525960 · Cited by 17 · see citing works
Probing differences among Aβ oligomers with two triangular trimers derived from Aβ
Kreutzer, A. G., Guaglianone, G., Yoo, S., Parrocha, C. M. T., Ruttenberg, S. M., Malonis, R. J., Tong, K., Lin, Y.-F., Nguyen, J. T., Howitz, W. J., et al. (2023) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2219216120 · Cited by 17 · see citing works
Li, S., Wei, Y., Liang, Z., Guo, L., Hao, X., & Zhang, Y. (2023) · Food Science and Human Wellness · doi:10.26599/fshw.2022.9250150 · Cited by 16 · see citing works
Enhanced brain delivery and antiproliferative activity of resveratrol using milk-derived exosomes
Ávila‐Gálvez, M. Á., Garay-Mayol, B., Giménez‐Bastida, J. A., Hazas, M. L. D. L., Mazarío‐Gárgoles, C., Brito, M. A., Dávalos, A., Espı́n, J. C., & González‐Sarrías, A. (2024) · Journal of Agriculture and Food Research · doi:10.1016/j.jafr.2024.101370 · Cited by 15 · see citing works
Zhu, Y., Tian, M., Lu, S., Qin, Y., Zhao, T. S., Shi, H., Li, Z., & Qin, D. (2025) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2025.111253 · Cited by 13 · see citing works
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Wang, P., Yin, Y., Zhang, Y., & Shao, J. (2025) · Frontiers in Nutrition · doi:10.3389/fnut.2025.1641620 · Cited by 5 · see citing works
Ding, Z., Hou, Q. L., Shao, N., Gao, W., Cai, B., & Hu, S. (2025) · Molecular Neurobiology · doi:10.1007/s12035-025-05470-8 · Cited by 5 · see citing works
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Kiruthiga, N., Chandrasekaran, R., Rajamanikandan, S., Joseph, J., & Aasaithambi, K. (2024) · Neurochemical Research · doi:10.1007/s11064-024-04312-8 · Cited by 5 · see citing works
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Sun, S., Ma, Q., Sheng, Q., Huang, S., Wu, C., Liu, J., & Xu, J. (2024) · Sensors · doi:10.3390/s24041211 · Cited by 4 · see citing works
Santoro, D., Nadeau, P. E., & Archer, L. L. (2024) · Research in Veterinary Science · doi:10.1016/j.rvsc.2024.105441 · Cited by 4 · see citing works
You, Y.-L., Byun, H.-J., Kang, N., Lee, M. S., Lee, J.-I., Park, I., & Choi, H. (2026) · Molecules · doi:10.3390/molecules31020336 · Cited by 2 · see citing works
Xu, M., Li, T., Liu, X., Islam, B., Xiang, Y., Zou, X., & Wang, J. (2024) · Neurochemical Research · doi:10.1007/s11064-024-04311-9 · Cited by 2 · see citing works
Guleria, M., Malhan, A., Teli, G., Bisht, N., & Jain, S. K. (2025) · Molecular Diversity · doi:10.1007/s11030-025-11278-4 · Cited by 1 · see citing works
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Dar, N. J., Gull, B., Hamid, A., Ahmed, Z., & Ahmad, M. (2025) · Steroids · doi:10.1016/j.steroids.2025.109662 · Cited by 1 · see citing works
Zhao, J., Chen, J., Lu, J., Shi, Q., Wang, Q., Gao, Z., Zeng, L., & Liu, Q. (2025) · Journal of Neurochemistry · doi:10.1111/jnc.70218 · Cited by 1 · see citing works
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Du, Y., Zheng, X., Yue, X., Fu, P., Diao, J., Zhang, A., Cheng, H., Yang, H., Bi, J., Zhou, Q., et al. (2025) · International Immunopharmacology · doi:10.1016/j.intimp.2025.116039
Yang, J., Cao, Y., Shu, S., Yue, C., Shen, Z., Zhang, Y., & Zhao, Z. (2026) · Results in Chemistry · doi:10.1016/j.rechem.2026.103162
Zhang, H.-X., & Li, H.-Y. (2026) · Medicine · doi:10.1097/md.0000000000048105
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- Authors
- Yu, H., Yamashita, T., Hu, X., Bian, Z., Hu, X., Feng, T., Tadokoro, K., Morihara, R., & Abe, K.
- Affiliations
- Okayama University (JP)
- Corresponding author
- Abe, Koji
- Venue
- Journal of the Neurological Sciences
- Publisher
- Elsevier BV
- Published
- 2022-10
- Volume
- 441
- Pages
- 120356
- ISSN
- 0022-510X (ISSN-L)
- OpenAlex
- W4289339159
- Cited by
- 37
- References
- 40
- Citations by year
- 2026: 6 · 2025: 14 · 2024: 8 · 2023: 8 · 2022: 1
- FWCI
- 4.82
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- Locations
- Journal of the Neurological Sciences (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Japan Agency for Medical Research and Development (7211700121, 7211800049, 7211800130)
- Japan Society for the Promotion of Science (17H0975609, 20 K09370)
- Topics
- Health Sciences › Medicine › Physiology › Alzheimer's disease research and treatments
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Medicine › Curcumin's Biomedical Applications
- Health Sciences › Medicine › Complementary and alternative medicine › Medicinal Plants and Neuroprotection
- Keywords
- curcumin, resveratrol, amyloid-beta oligomers, Alzheimer's disease, oxidative stress, reactive oxygen species, tau hyperphosphorylation, neuroprotection, SH-SY5Y cells, edaravone, neurotoxicity
- MeSH terms
- Resveratrol, Edaravone, Alzheimer Disease, Curcumin, Humans, Neuroblastoma, Neurotoxins, Free Radical Scavengers, Amyloid beta-Peptides, Reactive Oxygen Species, Oxidative Stress, Neuroprotective Agents, Cell Line, Tumor
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