Activation of Nrf2 Pathway Contributes to Neuroprotection by the Dietary Flavonoid Tiliroside
Open accessAbstract
Hyperactivated microglia plays a key role in regulating neuroinflammatory responses which cause damage to neurons. In recent years, substantial attention has been paid in identifying new strategies to abrogate neuroinflammation. Tiliroside, a natural dietary glycosidic flavonoid, is known to inhibit neuroinflammation. This study was aimed at investigating the molecular mechanisms involved in the inhibition of neuroinflammation and neurotoxicity by tiliroside. The effects of tiliroside on Nrf2 and SIRT1 activities in BV2 microglia and HT22 hippocampal neurons were investigated using immunoblotting and DNA binding assays. The roles of Nrf2 and SIRT1 in the anti-inflammatory activity of tiliroside were further investigated using RNA interference experiments. HT22 neuronal viability was determined by XTT, calcium influx, DNA fragmentation assays. The effect of tiliroside on MAP2 protein expression in HT22 neurons was investigated using western blotting and immunofluorescence. We also studied the impact of tiliroside on DNA fragmentation and ROS generation in APPSwe-transfected 3D neuronal stem cells. Results show that tiliroside increased protein levels of Nrf2, HO-1 and NQO1, indicating an activation of the Nrf2 protective mechanisms in the microglia. Furthermore, transfection of BV2 cells with Nrf2 siRNA resulted in the loss of anti-inflammatory activity by tiliroside. Tiliroside reduced protein levels of acetylated-NF-κB-p65, and increased SIRT1 in LPS/IFNγ-activated BV2 microglia. RNAi experiments revealed that inhibition of neuroinflammation by tiliroside was not affected by silencing SIRT1 gene. Results of neurotoxicity experiments revealed that neuroinflammation-induced toxicity, DNA fragmentation, ROS generation and calcium accumulation in HT22 neurons were significantly reduced by tiliroside treatment. In addition, the compound also protected differentiated human neural progenitor cells by blocking ROS generation and DNA fragmentation. Overall, this study has established that tiliroside protected BV2 microglia from LPS/IFNγ-induced neuroinflammation and HT22 neuronal toxicity by targeting Nrf2 antioxidant mechanisms. The compound also produced inhibition of NF-κB acetylation through activation of SIRT1, as well as increasing SIRT1 activity in mouse hippocampal neurons. Results from this study have further established the mechanisms involved in the anti-neuroinflammatory and neuroprotective activities of tiliroside.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
A plethora of plant-derived, quinone-related compounds have been demonstrated to limit microglial inflammation by activation of the Nrf2 pathway and subsequent upregulation of ARE-containing genes.
“A plethora of plant-derived, quinone-related compounds have been demonstrated to limit microglial inflammation by activation of the Nrf2 pathway and subsequent upregulation of ARE-containing genes, including tiliroside, petatewalide B, emodin and β-lapachone, to name a few [176,177,178,179].”
From ROS Generation in Microglia: Understanding Oxidative Stress and Inflammation in Neurodegenerative Disease (2020) · cites this paper as [176]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
Glutamate neurotoxicity and diseases of the nervous system
Choi, D. W. (1988) · Neuron · doi:10.1016/0896-6273(88)90162-6 · Cited by 8,152 · see citing works
Microglia-mediated neurotoxicity: uncovering the molecular mechanisms
Block, M. L., Zecca, L., & Hong, J.-S. (2007) · Nature Reviews Neuroscience · doi:10.1038/nrn2038 · Cited by 4,110 · see citing works
Targeting the KEAP1-NRF2 system to prevent kidney disease progression
Nezu, M., Suzuki, N., & Yamamoto, M. (2017) · American Journal of Nephrology · doi:10.1159/000475890 · Cited by 3,447 · see citing works
Modulation of NF‐κB‐dependent transcription and cell survival by the SIRT1 deacetylase
Yeung, F., Hoberg, J. E., Ramsey, C. S., Keller, M. D., Jones, D. R., Frye, R. A., & Mayo, M. W. (2004) · The EMBO Journal · doi:10.1038/sj.emboj.7600244 · Cited by 2,750 · see citing works
Differential Roles of M1 and M2 Microglia in Neurodegenerative Diseases
Tang, Y., & Le, W. (2016) · Molecular Neurobiology · doi:10.1007/s12035-014-9070-5 · Cited by 2,190 · see citing works
Price, N. L., Gomes, A. P., Ling, A. J. Y., Duarte, F. V., Martin-Montalvo, A., North, B. J., Agarwal, B., Ye, L., Ramadori, G., Teodoro, J. S., et al. (2012) · Cell Metabolism · doi:10.1016/j.cmet.2012.04.003 · Cited by 1,602 · see citing works
Kim, D., Nguyen, M. D., Dobbin, M. M., Fischer, A., Sananbenesi, F., Rodgers, J. T., Delalle, I., Baur, J. A., Sui, G., Armour, S. M., et al. (2007) · The EMBO Journal · doi:10.1038/sj.emboj.7601758 · Cited by 1,074 · see citing works
Nrf2 is a critical regulator of the innate immune response and survival during experimental sepsis
Thimmulappa, R. K. (2006) · Journal of Clinical Investigation · doi:10.1172/jci25790 · Cited by 1,028 · see citing works
DNA damage responses to oxidative stress
Barzilai, A., & Yamamoto, K.-I. (2004) · DNA Repair · doi:10.1016/j.dnarep.2004.03.002 · Cited by 796 · see citing works
Takeuchi, H., Jin, S., Wang, J., Zhang, G., Kawanokuchi, J., Kuno, R., Sonobe, Y., Mizuno, T., & Suzumura, A. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m600504200 · Cited by 749 · see citing works
SIRT1 Protects against Microglia-dependent Amyloid-β Toxicity through Inhibiting NF-κB Signaling
Chen, J., Zhou, Y., Mueller-Steiner, S., Chen, L.-F., Kwon, H., Yi, S., Mucke, L., & Gan, L. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m509329200 · Cited by 740 · see citing works
Activation of Nrf2-antioxidant signaling attenuates NFκB-inflammatory response and elicits apoptosis
Li, W., Khor, T. O., Xu, C., Shen, G., Jeong, W.-S., Yu, S., & Kong, A.-N. (2008) · Biochemical Pharmacology · doi:10.1016/j.bcp.2008.07.017 · Cited by 738 · see citing works
When NRF2 Talks, Who's Listening?
Wakabayashi, N., Slocum, S. L., Skoko, J. J., Shin, S., & Kensler, T. W. (2010) · Antioxidants & Redox Signaling · doi:10.1089/ars.2010.3216 · Cited by 595 · see citing works
Crosstalk between Oxidative Stress and SIRT1: Impact on the Aging Process
Salminen, A., Kaarniranta, K., & Kauppinen, A. (2013) · International Journal of Molecular Sciences · doi:10.3390/ijms14023834 · Cited by 457 · see citing works
NRF2-regulation in brain health and disease: Implication of cerebral inflammation
Sandberg, M., Patil, J., D’Angelo, B., Weber, S. G., & Mallard, C. E. (2013) · Neuropharmacology · doi:10.1016/j.neuropharm.2013.11.004 · Cited by 389 · see citing works
Nrf2 regulates microglial dynamics and neuroinflammation in experimental Parkinson's disease
Rojo, A. I., Innamorato, N. G., Martín-Moreno, A. M., CEBALLOS, M. L. D., Yamamoto, M. P., & Cuadrado, A. (2009) · Glia · doi:10.1002/glia.20947 · Cited by 381 · see citing works
Nioi, P., & Hayes, J. D. (2004) · Mutation research. Fundamental and molecular mechanisms of mutagenesis · doi:10.1016/j.mrfmmm.2004.05.023 · Cited by 359 · see citing works
Nakahira, K., Kim, H. P., Geng, X. H., Nakao, A., Wang, X., Murase, N., Drain, P. F., Wang, X., Sasidhar, M., Nabel, E. G., et al. (2006) · The Journal of Experimental Medicine · doi:10.1084/jem.20060845 · Cited by 356 · see citing works
Jaźwa, A., Rojo, A. I., Innamorato, N. G., Hesse, M., Fernández‐Ruíz, J., & Cuadrado, A. (2011) · Antioxidants and Redox Signaling · doi:10.1089/ars.2010.3731 · Cited by 329 · see citing works
Nuclear factor p65 interacts with Keap1 to repress the Nrf2-ARE pathway
Yu, M., Li, H., Liu, Q., Liu, F., Tang, L., Li, C., Yuan, Y., Zhan, Y., Xu, W., Li, W., et al. (2011) · Cellular Signalling · doi:10.1016/j.cellsig.2011.01.014 · Cited by 319 · see citing works
Redox Control of Microglial Function: Molecular Mechanisms and Functional Significance
Rojo, A. I., McBean, G. J., Cindrić, M., Egea, J., López, M. G., Rada, P., Žarković, N., & Cuadrado, A. (2014) · Antioxidants and Redox Signaling · doi:10.1089/ars.2013.5745 · Cited by 313 · see citing works
Oxidative damage and the Nrf2-ARE pathway in neurodegenerative diseases
Gan, L., & Johnson, J. A. (2014) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2013.12.011 · Cited by 288 · see citing works
Cho, S.-H., Chen, J. A., Sayed, F., Ward, M. E., Gao, F., Nguyen, T. A., Krabbe, G., Sohn, P. D., Lo, I., Minami, S., et al. (2015) · The Journal of Neuroscience · doi:10.1523/jneurosci.2939-14.2015 · Cited by 275 · see citing works
Na, H., Kim, E., Jung, J., Lee, H., Hyun, J. W., & Surh, Y. (2008) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2008.04.003 · Cited by 268 · see citing works
Activation of Sirt1 by Resveratrol Inhibits TNF-α Induced Inflammation in Fibroblasts
Zhu, X., Liu, Q., Wang, M., Liang, M., Yang, X., Xu, X., Zou, H., & Qiu, J. (2011) · PLoS ONE · doi:10.1371/journal.pone.0027081 · Cited by 256 · see citing works
Ledeboer, A., Brev�, J. J. P., Poole, S., Tilders, F. J. H., & van Dam, A. (2000) · Glia · doi:10.1002/(sici)1098-1136(200004)30:2 · Cited by 225 · see citing works
Surh, Y., & Na, H. (2007) · Genes & Nutrition · doi:10.1007/s12263-007-0063-0 · Cited by 224 · see citing works
Lee, I., Lim, J., Gal, J., Kang, J. C., Kim, H. J., Kang, B. Y., & Choi, H. J. (2010) · Neurochemistry International · doi:10.1016/j.neuint.2010.11.008 · Cited by 198 · see citing works
Huang, C., Lii, C., Lin, A., Yeh, Y.-W., Yao, H., Li, C., Wang, T., & Chen, H. (2012) · Archives of Toxicology · doi:10.1007/s00204-012-0913-4 · Cited by 184 · see citing works
Pan, H., Wang, H., Wang, X., Zhu, L., & Mao, L. (2012) · Mediators of Inflammation · doi:10.1155/2012/217580 · Cited by 179 · see citing works
Thornton, P., Pinteaux, E., Gibson, R. M., Allan, S. M., & Rothwell, N. J. (2006) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2006.03872.x · Cited by 165 · see citing works
TGFβ signalling plays an important role in IL4-induced alternative activation of microglia
Zhou, X., Spittau, B., & Krieglstein, K. (2012) · Journal of Neuroinflammation · doi:10.1186/1742-2094-9-210 · Cited by 159 · see citing works
Turpaev, K. T. (2013) · Biochemistry (Moscow) · doi:10.1134/s0006297913020016 · Cited by 135 · see citing works
The role of COX-2 and Nrf2/ARE in anti-inflammation and antioxidative stress: Aging and anti-aging
Luo, C., Urgard, E., Vooder, T., & Metspalu, A. (2011) · Medical Hypotheses · doi:10.1016/j.mehy.2011.04.002 · Cited by 119 · see citing works
Okorji, U. P., Velagapudi, R., El‐Bakoush, A., Fiebich, B. L., & Olajide, O. A. (2015) · Molecular Neurobiology · doi:10.1007/s12035-015-9543-1 · Cited by 112 · see citing works
Self-citationLinalool Inhibits LPS-Induced Inflammation in BV2 Microglia Cells by Activating Nrf2
Li, Y., Lv, O., Zhou, F., Li, Q., Wu, Z., & Zheng, Y. (2015) · Neurochemical Research · doi:10.1007/s11064-015-1629-7 · Cited by 106 · see citing works
Velagapudi, R., El‐Bakoush, A., Lepiarz‐Raba, I., Ogunrinade, F., & Olajide, O. A. (2017) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-017-3064-3 · Cited by 99 · see citing works
Self-citationPunicalagin inhibits neuroinflammation in LPS‐activated rat primary microglia
Olajide, O. A., Kumar, A., Velagapudi, R., Okorji, U. P., & Fiebich, B. L. (2014) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.201400163 · Cited by 94 · see citing works
Self-citationInhibition of neuroinflammation by thymoquinone requires activation of Nrf2/ARE signalling
Velagapudi, R., Kumar, A., Bhatia, H. S., El‐Bakoush, A., Lepiarz‐Raba, I., Fiebich, B. L., & Olajide, O. A. (2017) · International Immunopharmacology · doi:10.1016/j.intimp.2017.04.018 · Cited by 94 · see citing works
Self-citationVelagapudi, R., Aderogba, M. A., & Olajide, O. A. (2014) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2014.08.008 · Cited by 93 · see citing works
Self-citationYe, J.-M., Liu, Z., Wei, J.-P., Lu, L., Huang, Y., Luo, L., & Xie, H. (2013) · Neuroscience Letters · doi:10.1016/j.neulet.2013.08.020 · Cited by 93 · see citing works
Lee, E.-J., Ko, H.-M., Jeong, Y.-H., Park, E.-M., & Kim, H.-S. (2015) · Journal of Neuroinflammation · doi:10.1186/s12974-015-0355-z · Cited by 91 · see citing works
Onasanwo, S. A., Velagapudi, R., El‐Bakoush, A., & Olajide, O. A. (2016) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-016-2655-8 · Cited by 80 · see citing works
Self-citationNeuroprotective role of microglia expressing interleukin‐4
Park, K. W., Lee, D. Y., Joe, E.-H., Kim, S. U., & Jin, B. K. (2005) · Journal of Neuroscience Research · doi:10.1002/jnr.20483 · Cited by 76 · see citing works
Xi, Y., Yu, H., Ding, J., Ma, W., Yuan, L., Feng, J., Xiao, Y., & Xiao, R. (2012) · Current Neurovascular Research · doi:10.2174/156720212799297092 · Cited by 67 · see citing works
Heme oxygenase-1 deficiency accompanies neuropathogenesis of HIV-associated neurocognitive disorders
Gill, A. J., Kovacsics, C. E., Cross, S. A., Vance, P. J., Kolson, L. L., Jordan‐Sciutto, K. L., Gelman, B. B., & Kolson, D. L. (2014) · Journal of Clinical Investigation · doi:10.1172/jci72279 · Cited by 67 · see citing works
Cao, Q., Li, P., Lü, J., Dheen, S. T., Kaur, C., & Ling, E. A. (2010) · Journal of Neuroscience Research · doi:10.1002/jnr.22429 · Cited by 62 · see citing works
SIRT1 Regulates CD40 Expression Induced by TNF-a via NF-?B Pathway in Endothelial Cells
Yang, L., Zhang, J., Yan, C., Zhou, J., Lin, R., Lin, Q., Wang, W., Zhang, K., Yang, G., Bian, X., et al. (2012) · Cellular Physiology and Biochemistry · doi:10.1159/000343318 · Cited by 56 · see citing works
Pomegranate inhibits neuroinflammation and amyloidogenesis in IL-1β-stimulated SK-N-SH cells
Velagapudi, R., Baco, G., Khela, S., Okorji, U. P., & Olajide, O. A. (2015) · European Journal of Nutrition · doi:10.1007/s00394-015-0984-0 · Cited by 41 · see citing works
Self-citationAssessing acetylation of NF-κB
Chen, L., & Greene, W. C. (2005) · Methods · doi:10.1016/j.ymeth.2005.03.011 · Cited by 31 · see citing works
Forestier, A., Douki, T., Sauvaigo, S., Rosa, V. D., Demeilliers, C., & Rachidi, W. (2012) · International Journal of Molecular Sciences · doi:10.3390/ijms131114766 · Cited by 24 · see citing works
Kang, C., Kim, M. J., Seo, M. J., Choi, Y. H., Jo, W. S., Lee, K., Jeong, Y. K., & Kim, G. (2013) · Food and Chemical Toxicology · doi:10.1016/j.fct.2013.03.019 · Cited by 19 · see citing works
Protective effects of curcumin in APPswe transfected SH-SY5Y cells.
Yin, W., Zhang, X., & Yu, L. (2012) · PubMed · doi:10.3969/j.issn.1673-5374.2012.06.001 · Cited by 18 · see citing works
Xue, M., Zhu, L., Zhang, J., Qiu, J., Du, G., Qiao, Z., Jin, G., Gao, F., & Zhang, Q. (2015) · PLoS ONE · doi:10.1371/journal.pone.0120267 · Cited by 14 · see citing works
Sirtuins in Aging and Age-Related Diseases
Haigis, M. C., & Sinclair, D. A. (2010) · Elsevier eBooks · doi:10.1016/b978-0-12-378638-8.00011-7 · Cited by 13 · see citing works
Tang, Y., & Le, W. (2014) · Springer eBooks · doi:10.1007/978-3-319-08046-8_4 · Cited by 9 · see citing works
Flagged first, then by citations
Research works printed but not linked: 2
- [18]Ye J Liu Z Wei J Lu L Huang Y Luo L Xie H Protective effect of SIRT1 on toxicity of microglial-derived factors induced by LPS to PC12 cells via the p53-caspase-3-dependent apoptotic pathway Neurosci Lett 2013 553 72 77 10.1016/j.neulet.2013.08.020 23973301 · DOI
- [56]Huang B-R SIRT1 deficiency in microglia contributes to cognitive decline in aging and neurodegeneration via epigenetic regulation of IL-1β J Neurosci 2015 35 2 807 818 10.1523/JNEUROSCI.2939-14.2015 25589773 PMC4293425 · DOI · Paper page
Cited by
Sorted by citations
Simpson, D. S. A., & Oliver, P. L. (2020) · Antioxidants · doi:10.3390/antiox9080743 · Cited by 1,044 · see citing works
- Authors
- Velagapudi, R., El-Bakoush, A., & Olajide, O. A.
- Affiliations
- National Institutes of Health (US)
- University of Huddersfield (GB)
- Corresponding author
- Velagapudi, Ravikanth
- Olajide, Olumayokun A.
- Venue
- Molecular Neurobiology
- Published
- 2018-03-05
- Volume
- 55
- Issue
- 10
- Pages
- 8103-8123
- ISSN
- 0893-7648 (ISSN-L)
- 1559-1182
- PMC
- PMC6132780
- OpenAlex
- W2793124150
- Cited by
- 91
- References
- 56
- Citations by year
- 2026: 5 · 2025: 6 · 2024: 11 · 2023: 24 · 2022: 7 · 2021: 15 · 2020: 10 · 2019: 12 · 2018: 1
- FWCI
- 4.26
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Molecular Neurobiology (publishedVersion, cc-by)
- Europe PMC (PubMed Central) (publishedVersion, other-oa)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Huddersfield Research Portal (University of Huddersfield) (submittedVersion, cc-by)
- Funders
- University of Huddersfield
- Topics
- Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics, phytochemicals, and oxidative stress
- Health Sciences › Medicine › Pharmacology › Flavonoids in Medical Research
- Keywords
- tiliroside, Nrf2 signaling, SIRT1, neuroinflammation, neuroprotection, microglia, NF-κB acetylation, reactive oxygen species, DNA fragmentation, hippocampal neurons, neurotoxicity, flavonoids, NQO1, heme oxygenase-1, neural progenitor cells, calcium influx
- MeSH terms
- Neuroprotection, Acetylation, Animals, Antioxidants, Cell Differentiation, Cell Line, Diet, Flavonoids, Humans, Inflammation, Interferon-gamma, Lipopolysaccharides, Neurons, Neurotoxins, Signal Transduction, Up-Regulation, Cytokines, NF-kappa B, Amyloid beta-Protein Precursor, NAD(P)H Dehydrogenase (Quinone), Microglia, Mice, Knockout, Neuroprotective Agents, NF-E2-Related Factor 2, Heme Oxygenase-1, Sirtuin 1, Neural Stem Cells, Antioxidant Response Elements
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review