Cited by 91Neuroinflammation and Neurodegeneration MechanismsGenomics, phytochemicals, and oxidative stressFlavonoids in Medical Research

Activation of Nrf2 Pathway Contributes to Neuroprotection by the Dietary Flavonoid Tiliroside

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Velagapudi, Ravikanth, El-Bakoush, Abdelmeneim, Olajide, Olumayokun A.·2018·Molecular Neurobiology

Abstract

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.

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Crossref · 10.1007/s12035-018-0975-2

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  • 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].”

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  1. [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
  2. [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

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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
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
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

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