Mechanistic Insights and Therapeutic Potential of Quercetin in Neuroprotection: A Comprehensive Review of Pathways and Clinical Perspectives

Ishita Debnath , Suman Ghosh , Sajal Kumar Jha , Sobhanjan Bhunia , Aditi Nayak , Souvik Basak , Sumit Nandi , Soumik Bhattacharjee

BIO Integration ›› 2025, Vol. 6 ›› Issue (1) : 22

PDF (5633KB)
BIO Integration ›› 2025, Vol. 6 ›› Issue (1) :22 DOI: 10.15212/bioi-2025-0073
Review
research-article
Mechanistic Insights and Therapeutic Potential of Quercetin in Neuroprotection: A Comprehensive Review of Pathways and Clinical Perspectives
Author information +
History +
PDF (5633KB)

Abstract

Quercetin, a bioactive flavonoid abundant in diverse plant species, has been extensively investigated for its neuroprotective properties against neurodegenerative diseases (NDDs), such as Alzheimer’s, Parkinson’s, and Huntington’s diseases. This review systematically explored the multifaceted therapeutic potential of quercetin, emphasizing the mechanisms of action, pharmacologic efficacy, and translational significance in modern neurotherapeutics. Quercetin demonstrated potent antioxidant effects by scavenging reactive oxygen species and modulating the Nrf2-ARE pathway, thereby mitigating oxidative stress, a hallmark of NDDs associated with mitochondrial dysfunction, protein aggregation, and neuronal apoptosis. Furthermore, the ability of quercetin to regulate the PI3K/Akt pathway promoted mitochondrial biogenesis and preserved neuronal integrity by stabilizing membrane potential. Anti-inflammatory effects were evident vis-a-vis inhibition of the NF-κB and MAPK pathways, suppression of microglial activation, and cytokine release. In addition, quercetin disrupted tau hyperphosphorylation via GSK3β inhibition and attenuated amyloid-beta toxicity, offering cognitive protection. Preclinical studies highlighted the ability of quercetin to modulate excitotoxicity and enhance neuroplasticity, while emerging evidence support synergy of quercetin with existing pharmacologic agents. Genetic variations influencing key pathways, including Nrf2 and PI3K, underscore the necessity for personalized therapeutic approaches. Advances in drug delivery systems, scaffold modelling, and CRISPR-mediated interventions revealed the potential for optimizing the bioavailability and specificity of quercetin. This review bridges critical knowledge gaps by integrating mechanistic insights with clinical perspectives, advocating for translating quercetin-based therapies into precision medicine. By addressing challenges in bioavailability and exploring innovative strategies, this article underscores the promise of quercetin as a cornerstone for neuroprotective interventions in NDDs.

Keywords

Inflammatory pathways / neurodegenerative diseases / neuroprotection / oxidative stress / quercetin / therapeutic potential

Cite this article

Download citation ▾
Ishita Debnath, Suman Ghosh, Sajal Kumar Jha, Sobhanjan Bhunia, Aditi Nayak, Souvik Basak, Sumit Nandi, Soumik Bhattacharjee. Mechanistic Insights and Therapeutic Potential of Quercetin in Neuroprotection: A Comprehensive Review of Pathways and Clinical Perspectives. BIO Integration, 2025, 6 (1) : 22 DOI:10.15212/bioi-2025-0073

登录浏览全文

4963

注册一个新账户 忘记密码

References

[1]

Amanzadeh E, Esmaeili A, Rahgozar S, Nourbakhshnia M. Application of quercetin in neurological disorders: from nutrition to nanomedicine. Rev Neurosci 2019; 30(5): 555-72. [PMID: 30753166 DOI: 10.1515/revneuro-2018-0080]

[2]

Islam MS, Quispe C, Hossain R, Islam MT, Al-Harrasi A, et al. Neuropharmacological effects of quercetin: a literature-based review. Front Pharmacol 2021; 12: 665031. [PMID: 34220504 DOI: 10.3389/fphar.2021.665031]

[3]

Grewal AK, Singh TG, Sharma D, Sharma V, Singh M, et al. Mechanistic insights and perspectives involved in neuroprotective action of quercetin. Biomed Pharmacother 2021; 140: 111729. [PMID: 34044274 DOI: 10.1016/j.biopha.2021.111729]

[4]

Zhang L, Xu L-Y, Tang F, Liu D, Zhao X-L, et al. New perspectives on the therapeutic potential of quercetin in non-communicable diseases: targeting Nrf2 to counteract oxidative stress and inflammation. J Pharm Anal 2024; 14(6): 100930. [PMID: 39005843 DOI: 10.1016/j.jpha.2023.12.020]

[5]

Singh S, Nagalakshmi D, Sharma KK, Ravichandiran V. Natural antioxidants for neuroinflammatory disorders and possible involvement of Nrf2 pathway: a review. Heliyon 2021; 7(2): e06216. [PMID: 33659743 DOI: 10.1016/j.heliyon.2021.e06216]

[6]

Khan H, Ullah H, Aschner M, Cheang WS, Akkol EK. Neuroprotective effects of quercetin in Alzheimer’s disease. Biomolecules 2019; 10(1): 59. [PMID: 31905923 DOI: 10.3390/biom10010059]

[7]

Jomova K, Raptova R, Alomar SY, Alwasel SH, Nepovimova E, et al. Reactive oxygen species, toxicity, oxidative stress, and antioxidants: chronic diseases and aging. Arch Toxicol 2023; 97(10): 2499-574. [PMID: 37597078 DOI: 10.1007/s00204-023-03562-9]

[8]

Ho C-L, Kao N-J, Lin C-I, Cross T-WL, Lin S-H. Quercetin increases mitochondrial biogenesis and reduces free radicals in neuronal SH-SY5Y cells. Nutrients 2022; 14(16): 3310. [PMID: 36014814 DOI: 10.3390/nu14163310]

[9]

Wang J, Zhang J, Yu Z-L, Chung SK, Xu B. The roles of dietary polyphenols at crosstalk between type 2 diabetes and Alzheimer’s disease in ameliorating oxidative stress and mitochondrial dysfunction via PI3K/Akt signaling pathways. Ageing Res Rev 2024; 99: 102416. [PMID: 39002644 DOI: 10.1016/j.arr.2024.102416]

[10]

Jazvinšćak Jembrek M, Oršolić N, Mandić L, Sadžak A, Šegota S. Anti-oxidative, anti-inflammatory and anti-apoptotic effects of flavonols: targeting Nrf2, NF-κB and p53 pathways in neurodegeneration. Antioxidants (Basel) 2021; 10(10): 1628. [PMID: 34679762 DOI: 10.3390/antiox10101628]

[11]

Costa LG, Garrick JM, Roquè PJ, Pellacani C. Mechanisms of neuroprotection by quercetin: counteracting oxidative stress and more. Oxid Med Cell Longev 2016; 2016: 2986796. [PMID: 26904161 DOI: 10.1155/2016/2986796]

[12]

Jakaria M, Park S-Y, Haque ME, Karthivashan G, Kim I-S, et al. Neurotoxic agent-induced injury in neurodegenerative disease model: focus on involvement of glutamate receptors. Front Mol Neurosci 2018; 11: 307. [PMID: 30210294 DOI: 10.3389/fnmol.2018.00307]

[13]

Almatroodi SA, Alsahli MA, Almatroudi A, Verma AK, Aloliqi A, et al. Potential therapeutic targets of quercetin, a plant flavonol, and its role in the therapy of various types of cancer through the modulation of various cell signaling pathways. Molecules 2021; 26(5): 1315. [PMID: 33804548 DOI: 10.3390/molecules26051315]

[14]

Orhan IE. Cholinesterase inhibitory potential of quercetin towards Alzheimer’s disease - a promising natural molecule or fashion of the day? A narrowed review. Curr Neuropharmacol 2021; 19(12): 2205-13. [PMID: 33213346 DOI: 10.2174/1570159X18666201119153807]

[15]

Cui Z, Zhao X, Amevor FK, Du X, Wang Y, et al. Therapeutic application of quercetin in aging-related diseases: SIRT1 as a potential mechanism. Front Immunol 2022; 13: 943321. [PMID: 35935939 DOI: 10.3389/fimmu.2022.943321]

[16]

McKay TB, Emmitte KA, German C, Karamichos D. Quercetin and related analogs as therapeutics to promote tissue repair. Bioengineering (Basel) 2023; 10(10): 1127. [PMID: 37892857 DOI: 10.3390/bioengineering10101127]

[17]

Pereira L, Cotas J. Therapeutic potential of polyphenols and other micronutrients of marine origin. Mar Drugs 2023; 21(6): 323. [PMID: 37367648 DOI: 10.3390/md21060323]

[18]

Qi W, Qi W, Xiong D, Long M. Quercetin: its antioxidant mechanism, antibacterial properties and potential application in prevention and control of toxipathy. Molecules 2022; 27(19): 6545. [PMID: 36235082 DOI: 10.3390/molecules27196545]

[19]

Patel K, Kumar V, Rahman M, Verma A, Patel DK. New insights into the medicinal importance, physiological functions and bioanalytical aspects of an important bioactive compound of foods ‘Hyperin’: health benefits of the past, the present, the future. Beni Suef Univ J Basic Appl Sci 2018; 7(1): 31-42. [DOI: 10.1016/j.bjbas.2017.05.009]

[20]

Rana A, Samtiya M, Dhewa T, Mishra V, Aluko RE. Health benefits of polyphenols: a concise review. J Food Biochem 2022; 46(10): e14264. [PMID: 35694805 DOI: 10.1111/jfbc.14264]

[21]

Montané X, Kowalczyk O, Reig-Vano B, Bajek A, Roszkowski K, et al. Current perspectives of the applications of polyphenols and flavonoids in cancer therapy. Molecules 2020; 25(15): 3342. [PMID: 32717865 DOI: 10.3390/molecules25153342]

[22]

Sabiu S, Madende M, Ajao AA, Aladodo RA, Nurain IO, et al. The genus Allium (Amaryllidaceae: Alloideae): features, phytoconstituents, and mechanisms of antidiabetic potential of Allium cepa and Allium sativum . In: Watson RR, Preedy VR, editors. Bioactive food as dietary interventions for diabetes. Elsevier; 2019. pp. 137-54. [DOI: 10.1016/B978-0-12-813822-9.00009-6]

[23]

Chan EWC, Wong SK, Tangah J, Inoue T, Chan HT. Phenolic constituents and anticancer properties of Morus alba (white mulberry) leaves. J Integr Med 2020; 18(3): 189-95. [PMID: 32115383 DOI: 10.1016/j.joim.2020.02.006]

[24]

Al-Zughbi I, Krayem M . Quince fruit Cydonia oblonga Mill nutritional composition, antioxidative properties, health benefits and consumers preferences towards some industrial quince products: a review. Food Chem 2022; 393: 133362. [PMID: 35661598 DOI: 10.1016/j.foodchem.2022.133362]

[25]

Patocka J, Bhardwaj K, Klimova B, Nepovimova E, Wu Q, et al. Malus domestica: a review on nutritional features, chemical composition, traditional and medicinal value. Plants (Basel) 2020; 9(11): 1408. [PMID: 33105724 DOI: 10.3390/plants9111408]

[26]

Nunes AR, Gonçalves AC, Falcão A, Alves G, Silva LR. Prunus avium L. (Sweet Cherry) by-products: a source of phenolic compounds with antioxidant and anti-hyperglycemic properties-a review. Appl Sci 2021; 11(18): 8516. [DOI: 10.3390/app11188516]

[27]

Navarro M, Moreira I, Arnaez E, Quesada S, Azofeifa G, et al. Polyphenolic characterization and antioxidant activity of malus domestica and prunus domestica cultivars from Costa Rica. Foods 2018; 7(2): 15. [PMID: 29385709 DOI: 10.3390/foods7020015]

[28]

Klimek-Szczykutowicz M, Gaweł-Bęben K, Rutka A, Blicharska E, Tatarczak-Michalewska M, et al. Moringa oleifera (drumstick tree)-nutraceutical, cosmetological and medicinal importance: a review. Front Pharmacol 2024; 15: 1288382. [PMID: 38370483 DOI: 10.3389/fphar.2024.1288382]

[29]

Ranjha MMAN, Shafique B, Wang L, Irfan S, Safdar MN, et al. A comprehensive review on phytochemistry, bioactivity and medicinal value of bioactive compounds of pomegranate (Punica granatum) . Adv Tradit Med 2023; 23(1): 37-57. [DOI: 10.1007/s13596-021-00566-7]

[30]

Hudz N, Kobylinska L, Pokajewicz K, Horčinová Sedláčková V, Fedin R, et al. Mentha piperita: essential oil and extracts, their biological activities, and perspectives on the development of new medicinal and cosmetic products. Molecules 2023; 28(21): 7444. [PMID: 37959863 DOI: 10.3390/molecules28217444]

[31]

Mahendran G, Verma SK, Rahman L-U. The traditional uses, phytochemistry and pharmacology of spearmint (Mentha spicata L.): a review. J Ethnopharmacol 2021; 278: 114266. [PMID: 34087400 DOI: 10.1016/j.jep.2021.114266]

[32]

Nekkaa A, Benaissa A, Mutelet F, Canabady-Rochelle L. Rhamnusalaternus plant: extraction of bioactive fractions and evaluation of their pharmacological and phytochemical properties. Antioxidants (Basel) 2021; 10(2): 300. [PMID: 33669348 DOI: 10.3390/antiox10020300]

[33]

Applequist WL, Moerman DE. Yarrow (Achillea millefolium L.): a neglected panacea? A review of ethnobotany, bioactivity, and biomedical research. Econ Bot 2011; 65(2): 209-25 [DOI: 10.1007/s12231-011-9154-3]

[34]

Assefa AD, Choi S, Lee J-E, Sung J-S, Hur O-S, et al. Identification and quantification of selected metabolites in differently pigmented leaves of lettuce (Lactuca sativa L.) cultivars harvested at mature and bolting stages. BMC Chem 2019; 13(1): 56. [PMID: 31384804 DOI: 10.1186/s13065-019-0570-2]

[35]

Guo J, Wang Y, Li J, Zhang J, Wu Y, et al. Overview and recent progress on the biosynthesis and regulation of flavonoids in Ginkgo biloba L. Int J Mol Sci 2023; 24(19): 14604. [PMID: 37834050 DOI: 10.3390/ijms241914604]

[36]

Kumar M, Saurabh V, Tomar M, Hasan M, Changan S, et al. Mango (Mangifera indica L.) leaves: nutritional composition, phytochemical profile, and health-promoting bioactivities. Antioxidants (Basel) 2021; 10(2): 299. [PMID: 33669341 DOI: 10.3390/antiox10020299]

[37]

Perović J, Tumbas Šaponjac V, Kojić J, Krulj J, Moreno DA, et al. Chicory (Cichorium intybus L.) as a food ingredient - nutritional composition, bioactivity, safety, and health claims: a review. Food Chem 2021; 336: 127676. [PMID: 32768902 DOI: 10.1016/j.foodchem.2020.127676]

[38]

Vrhovsek U, Masuero D, Palmieri L, Mattivi F. Identification and quantification of flavonol glycosides in cultivated blueberry cultivars. J Food Compos Anal 2012; 25(1): 9-16. [DOI: 10.1016/j.jfca.2011.04.015]

[39]

Tundis R, Tenuta MC, Loizzo MR, Bonesi M, Finetti F, et al. Vaccinium species (Ericaceae): from chemical composition to bio-functional activities. Appl Sci 2021; 11(12): 5655. [DOI: 10.3390/app11125655]

[40]

Kingori SM, Ochanda SO, Koech RK. Variation in levels of flavonols myricetin, quercetin and kaempferol-in Kenyan tea (Camellia sinensis L.) with processed tea types and geographic location. Open J Appl Sci 2021; 11(6): 736-49. [DOI: 10.4236/ojapps.2021.116054]

[41]

Gudiño I, Martín A, Casquete R, Prieto MH, Ayuso MC, et al. Evaluation of broccoli (Brassica oleracea var. italica) crop by-products as sources of bioactive compounds. Sci Hortic 2022; 304: 111284. [DOI: 10.1016/j.scienta.2022.111284]

[42]

Zietz M, Weckmüller A, Schmidt S, Rohn S, Schreiner M, et al. Genotypic and climatic influence on the antioxidant activity of flavonoids in Kale (Brassica oleracea var. sabellica) . J Agric Food Chem 2010; 58(4): 2123-30. [PMID: 20095605 DOI: 10.1021/jf9033909]

[43]

Kyriakou S, Michailidou K, Amery T, Stewart K, Winyard PG, et al. Polyphenolics, glucosinolates and isothiocyanates profiling of aerial parts of Nasturtium officinale (Watercress) . Front Plant Sci 2022; 13: 998755. [PMID: 36457522 DOI: 10.3389/fpls.2022.998755]

[44]

Galeotti N. Hypericum perforatum (St John’s wort) beyond depression: a therapeutic perspective for pain conditions. J Ethnopharmacol 2017; 200: 136-46. [PMID: 28216196 DOI: 10.1016/j.jep.2017.02.016]

[45]

Rusalepp L, Raal A, Püssa T, Mäeorg U. Comparison of chemical composition of Hypericum perforatum and H. maculatum in Estonia. Biochem Syst Ecol 2017; 73: 41-6. [DOI: 10.1016/j.bse.2017.06.004]

[46]

Mohammad Azmin SNH, Mat Nor MS . Chemical fingerprint of Centella Asiatica’s bioactive compounds in the ethanolic and aqueous extracts. Adv Biomark Sci Technol 2020; 2: 35-44. [DOI: 10.1016/j.abst.2020.10.001]

[47]

Minaiyan M, Ghanadian S-M, Hossaini M. Protective effect of Apium graveolens L. (Celery) seeds extracts and luteolin on acetic acid-induced colitis in rats. Int J Prev Med 2021; 12: 100. [PMID: 34729134 DOI: 10.4103/ijpvm.IJPVM_651_20]

[48]

Saygi KO. Quantification of phenolics from Coriandrum sativum vulgare and Coriandrum sativum microcarpum by HPLC-DAD. Iran J Sci Technol Trans A Sci 2021; 45(4): 1319-26. [DOI: 10.1007/s40995-021-01132-1]

[49]

Udaya Rajesh R, Dhanaraj S . A critical review on quercetin bioflavonoid and its derivatives: scope, synthesis, and biological applications with future prospects. Arab J Chem 2023; 16(8): 104881. [DOI: 10.1016/j.arabjc.2023.104881]

[50]

Sarkar S, Singh RP, Bhattacharya G. Exploring the role of Azadirachta indica (neem) and its active compounds in the regulation of biological pathways: an update on molecular approach. 3 Biotech 2021; 11(4): 178. [PMID: 33927969 DOI: 10.1007/s13205-021-02745-4]

[51]

Adurosakin OE, Iweala EJ, Otike JO, Dike ED, Uche ME, et al. Ethnomedicinal uses, phytochemistry, pharmacological activities and toxicological effects of Mimosa pudica- a review. Pharmacol Res Mod Chin Med 2023; 7: 100241. [DOI: 10.1016/j.prmcm.2023.100241]

[52]

Thissera B, Visvanathan R, Khanfar MA, Qader MM, Hassan MHA, et al. Sesbania grandiflora L. Poir leaves: a dietary supplement to alleviate type 2 diabetes through metabolic enzymes inhibition. S Afr J Bot 2020; 130: 282-99. [DOI: 10.1016/j.sajb.2020.01.011]

[53]

Azab SS, Abdel-Daim M, Eldahshan OA. Phytochemical, cytotoxic, hepatoprotective and antioxidant properties of Delonix regia leaves extract. Med Chem Re 2013; 22(9): 4269-77. [DOI: 10.1007/s00044-012-0420-4]

[54]

Izzo L, Castaldo L, Narváez A, Graziani G, Gaspari A, et al. Analysis of phenolic compounds in commercial Cannabis sativa L. inflorescences using UHPLC-Q-Orbitrap HRMS. Molecules 2020; 25(3): 631. [PMID: 32024009 DOI: 10.3390/molecules25030631]

[55]

Okhuarobo A, Falodun JE, Erharuyi O, Imieje V, Falodun A, et al. Harnessing the medicinal properties of Andrographis paniculata for diseases and beyond: a review of its phytochemistry and pharmacology. Asian Pac J Trop Dis 2014; 4(3): 213-22. [DOI: 10.1016/S2222-1808(14)60509-0]

[56]

Basit A, Shutian T, Khan A, Khan SM, Shahzad R, et al. Anti-inflammatory and analgesic potential of leaf extract of Justicia adhatoda L. (Acanthaceae) in Carrageenan and Formalin-induced models by targeting oxidative stress. Biomed Pharmacother 2022; 153: 113322. [PMID: 35763968 DOI: 10.1016/j.biopha.2022.113322]

[57]

Jain S, Mehata MS. Medicinal plant leaf extract and pure flavonoid mediated green synthesis of silver nanoparticles and their enhanced antibacterial property. Sci Rep 2017; 7(1): 15867. [PMID: 29158537 DOI: 10.1038/s41598-017-15724-8]

[58]

Dong C, Hu H, Hu Y, Xie J. Metabolism of flavonoids in novel banana germplasm during fruit development. Front Plant Sci 2016; 7: 1291. [PMID: 27625665 DOI: 10.3389/fpls.2016.01291]

[59]

Aghofack-Nguemezi J, Schwab W . Differential accumulation of flavonoids by tomato (Solanum lycopersicum) fruits tissues during maturation and ripening. J Appl Biosci 2015; 84(1): 7682. [DOI: 10.4314/jab.v84i1.2]

[60]

Alhaithloul HAS, Galal FH, Seufi AM. Effect of extreme temperature changes on phenolic, flavonoid contents and antioxidant activity of tomato seedlings (Solanum lycopersicum L.) . PeerJ 2021; 9: e11193. [PMID: 34026345 DOI: 10.7717/peerj.11193]

[61]

Jing Z, Wang Z, Li X, Li X, Cao T, et al. Protective effect of quercetin on posttraumatic cardiac injury. Sci Rep 2016; 6: 30812. [PMID: 27470932 DOI: 10.1038/srep30812]

[62]

Xiong F, Zhang Y, Li T, Tang Y, Song S-Y, et al. A detailed overview of quercetin: implications for cell death and liver fibrosis mechanisms. Front Pharmacol 2024; 15: 1389179. [PMID: 38855739 DOI: 10.3389/fphar.2024.1389179]

[63]

Kandemir K, Tomas M, McClements DJ, Capanoglu E. Recent advances on the improvement of quercetin bioavailability. Trends Food Sci Technol 2022; 119: 192-200. [DOI: 10.1016/j.tifs.2021.11.032]

[64]

Wang W, Sun C, Mao L, Ma P, Liu F, et al. The biological activities, chemical stability, metabolism and delivery systems of quercetin: a review. Trends Food Sci Technol 2016; 56: 21-38. [DOI: 10.1016/j.tifs.2016.07.004]

[65]

Scalbert A, Williamson G. Dietary intake and bioavailability of polyphenols. J Nutr 2000; 130(8S Suppl): 2073S-85S. [PMID: 10917926 DOI: 10.1093/jn/130.8.2073S]

[66]

Tomou E-M, Papakyriakopoulou P, Saitani E-M, Valsami G, Pippa N, et al. Recent advances in nanoformulations for quercetin delivery. Pharmaceutics 2023; 15(6): 1656. [PMID: 37376104 DOI: 10.3390/pharmaceutics15061656]

[67]

Koo J, Lim C, Oh KT. Recent advances in intranasal administration for brain-targeting delivery: a comprehensive review of lipid-based nanoparticles and stimuli-responsive gel formulations. Int J Nanomedicine 2024; 19: 1767-807. [PMID: 38414526 DOI: 10.2147/IJN.S439181]

[68]

Michala A-S, Pritsa A . Quercetin: a molecule of great biochemical and clinical value and its beneficial effect on diabetes and cancer. Diseases 2022; 10(3): 37. [PMID: 35892731 DOI: 10.3390/diseases10030037]

[69]

De Marchi U, Biasutto L, Garbisa S, Toninello A, Zoratti M. Quercetin can act either as an inhibitor or an inducer of the mitochondrial permeability transition pore: a demonstration of the ambivalent redox character of polyphenols. Biochim Biophys Acta 2009; 1787(12): 1425-32. [PMID: 19523917 DOI: 10.1016/j.bbabio.2009.06.002]

[70]

Kim G-N, Jang H-D. Protective mechanism of quercetin and rutin using glutathione metabolism on HO-induced oxidative stress in HepG2 cells. Ann N Y Acad Sci 2009; 1171: 530-7. [PMID: 19723100 DOI: 10.1111/j.1749-6632.2009.04690.x]

[71]

Someya Y, Saito S, Takeda S, Adachi N, Kurosawa A. Quercetin exhibits cytotoxicity in cancer cells by inducing two-ended DNA double-strand breaks. Biochem Biophys Res Commun 2024; 739: 150977. [PMID: 39549336 DOI: 10.1016/j.bbrc.2024.150977]

[72]

Fakhri KU, Sharma D, Fatma H, Yasin D, Alam M, et al. The dual role of dietary phytochemicals in oxidative stress: implications for oncogenesis, cancer chemoprevention, and ncRNA regulation. Antioxidants (Basel) 2025; 14(6): 620. [PMID: 40563255 DOI: 10.3390/antiox14060620]

[73]

Bardestani A, Ebrahimpour S, Esmaeili A, Esmaeili A. Quercetin attenuates neurotoxicity induced by iron oxide nanoparticles. J Nanobiotechnology 2021; 19(1): 327. [PMID: 34663344 DOI: 10.1186/s12951-021-01059-0]

[74]

Vollmannová A, Bojňanská T, Musilová J, Lidiková J, Cifrová M. Quercetin as one of the most abundant represented biological valuable plant components with remarkable chemoprotective effects - a review. Heliyon 2024; 10(12): e33342. [PMID: 39021910 DOI: 10.1016/j.heliyon.2024.e33342]

[75]

Aghababaei F, Hadidi M. Recent advances in potential health benefits of quercetin. Pharmaceuticals (Basel) 2023; 16(7): 1020. [PMID: 37513932 DOI: 10.3390/ph16071020]

[76]

Nam J-S, Sharma AR, Nguyen LT, Chakraborty C, Sharma G, et al. Application of bioactive quercetin in oncotherapy: from nutrition to nanomedicine. Molecules 2016; 21(1): E108. [PMID: 26797598 DOI: 10.3390/molecules21010108]

[77]

Kawabata K, Mukai R, Ishisaka A. Quercetin and related polyphenols: new insights and implications for their bioactivity and bioavailability. Food Funct 2015; 6(5): 1399-417. [PMID: 25761771 DOI: 10.1039/c4fo01178c]

[78]

Hai Y, Zhang Y, Liang Y, Ma X, Qi X, et al. Advance on the absorption, metabolism, and efficacy exertion of quercetin and its important derivatives. Food Front 2020; 1(4): 420-34. [DOI: 10.1002/fft2.50]

[79]

Chen X, Yin OQP, Zuo Z, Chow MSS. Pharmacokinetics and modeling of quercetin and metabolites. Pharm Res 2005; 22(6): 892-901. [PMID: 15948033 DOI: 10.1007/s11095-005-4584-1]

[80]

Kyriakoudi A, Spanidi E, Mourtzinos I, Gardikis K. Innovative delivery systems loaded with plant bioactive ingredients: formulation approaches and applications. Plants (Basel) 2021; 10(6): 1238. [PMID: 34207139 DOI: 10.3390/plants10061238]

[81]

Sun J, Jing H, Liu T, Dong S, Obadi M, et al. Evaluation of antioxidant modification on the functional and structural properties of EWP conjugates. RSC Adv 2020; 10(18): 10666-72. [PMID: 35492916 DOI: 10.1039/d0ra00023j]

[82]

Veiko AG, Lapshina EA, Zavodnik IB. Comparative analysis of molecular properties and reactions with oxidants for quercetin, catechin, and naringenin. Mol Cell Biochem 2021; 476(12): 4287-99. [PMID: 34406575 DOI: 10.1007/s11010-021-04243-w]

[83]

Chiorcea-Paquim A-M. Electrochemistry of flavonoids: a comprehensive review. Int J Mol Sci 2023; 24(21): 15667. [PMID: 37958651 DOI: 10.3390/ijms242115667]

[84]

Evans JA, Mendonca P, Soliman KFA. Neuroprotective effects and therapeutic potential of the citrus flavonoid hesperetin in neurodegenerative diseases. Nutrients 2022; 14(11): 2228. [PMID: 35684025 DOI: 10.3390/nu14112228]

[85]

Xu D, Hu M-J, Wang Y-Q, Cui Y-L. Antioxidant activities of quercetin and its complexes for medicinal application. Molecules 2019; 24(6): 1123. [PMID: 30901869 DOI: 10.3390/molecules24061123]

[86]

Nam G, Hong M, Lee J, Lee HJ, Ji Y, et al. Multiple reactivities of flavonoids towards pathological elements in Alzheimer’s disease: structure-activity relationship. Chem Sci 2020; 11(37): 10243-54. [PMID: 34094290 DOI: 10.1039/d0sc02046j]

[87]

Jeon H, Kim H, Choi D, Kim D, Park S-Y, et al. Quercetin activates an angiogenic pathway, hypoxia inducible factor (HIF)-1-vascular endothelial growth factor, by inhibiting HIF-prolyl hydroxylase: a structural analysis of quercetin for inhibiting HIF-prolyl hydroxylase. Mol Pharmacol 2007; 71(6): 1676-84. [PMID: 17377063 DOI: 10.1124/mol.107.034041]

[88]

Cheignon C, Tomas M, Bonnefont-Rousselot D, Faller P, Hureau C, et al. Oxidative stress and the amyloid beta peptide in Alzheimer’s disease. Redox Biol 2018; 14: 450-64. [PMID: 29080524 DOI: 10.1016/j.redox.2017.10.014]

[89]

Dini I, Grumetto L. Recent advances in natural polyphenol research. Molecules 2022; 27(24): 8777. [PMID: 36557912 DOI: 10.3390/molecules27248777]

[90]

Yang K, Lv Z, Zhao W, Lai G, Zheng C, et al. The potential of natural products to inhibit abnormal aggregation of α-Synuclein in the treatment of Parkinson’s disease. Front Pharmacol 2024; 15: 1468850. [PMID: 39508052 DOI: 10.3389/fphar.2024.1468850]

[91]

Ribeiro D, Freitas M, Lima JLFC, Fernandes E. Proinflammatory pathways: the modulation by flavonoids. Med Res Rev 2015; 35(5): 877-936. [PMID: 25926332 DOI: 10.1002/med.21347]

[92]

Aleebrahim-Dehkordi E, Soveyzi F, Arian AS, Hamedanchi NF, Hasanpour-Dehkordi A, et al. Quercetin and its role in reducing the expression of pro-inflammatory cytokines in osteoarthritis. Antiinflamm Antiallergy Agents Med Chem 2023; 21(3): 153-65. [PMID: 36518039 DOI: 10.2174/1871523022666221213155905]

[93]

Spagnuolo C, Moccia S, Russo GL. Anti-inflammatory effects of flavonoids in neurodegenerative disorders. Eur J Med Chem 2018; 153: 105-15. [PMID: 28923363 DOI: 10.1016/j.ejmech.2017.09.001]

[94]

Dorta DJ, Pigoso AA, Mingatto FE, Rodrigues T, Prado IMR, et al. The interaction of flavonoids with mitochondria: effects on energetic processes. Chem Biol Interact 2005; 152(2-3): 67-78. [PMID: 15840381 DOI: 10.1016/j.cbi.2005.02.004]

[95]

Koklesova L, Liskova A, Samec M, Zhai K, Al-Ishaq RK, et al. Protective effects of flavonoids against mitochondriopathies and associated pathologies: focus on the predictive approach and personalized prevention. Int J Mol Sci 2021; 22(16): 8649. [PMID: 34445360 DOI: 10.3390/ijms22168649]

[96]

Chiang M-C, Tsai T-Y, Wang C-J. The potential benefits of quercetin for brain health: a review of anti-inflammatory and neuroprotective mechanisms. Int J Mol Sci 2023; 24(7): 6328. [PMID: 37047299 DOI: 10.3390/ijms24076328]

[97]

Massi A, Bortolini O, Ragno D, Bernardi T, Sacchetti G, et al. Research progress in the modification of quercetin leading to anticancer agents. Molecules 2017; 22(8): 1270. [PMID: 28758919 DOI: 10.3390/molecules22081270]

[98]

Duan N, Hu X, Zhou R, Li Y, Wu W, et al. A review on dietary flavonoids as modulators of the tumor microenvironment. Mol Nutr Food Res 2023; 67(7): e2200435. [PMID: 36698331 DOI: 10.1002/mnfr.202200435]

[99]

Eisvand F, Tajbakhsh A, Seidel V, Zirak MR, Tabeshpour J, et al. Quercetin and its role in modulating endoplasmic reticulum stress: a review. Phytother Res 2022; 36(1): 73-84. [PMID: 34528309 DOI: 10.1002/ptr.7283]

[100]

Jakaria M, Azam S, Jo S-H, Kim I-S, Dash R, et al. Potential therapeutic targets of quercetin and its derivatives: its role in the therapy of cognitive impairment. J Clin Med 2019; 8(11): 1789. [PMID: 31717708 DOI: 10.3390/jcm8111789]

[101]

Jabir NR, Khan FR, Tabrez S. Cholinesterase targeting by polyphenols: a therapeutic approach for the treatment of Alzheimer’s disease. CNS Neurosci Ther 2018; 24(9): 753-62. [PMID: 29770579 DOI: 10.1111/cns.12971]

[102]

Breijyeh Z, Karaman R. Comprehensive review on Alzheimer’s disease: causes and treatment. Molecules 2020; 25(24): 5789. [PMID: 33302541 DOI: 10.3390/molecules25245789]

[103]

Walczak-Nowicka ŁJ, Herbet M. Acetylcholinesterase inhibitors in the treatment of neurodegenerative diseases and the role of acetylcholinesterase in their pathogenesis. Int J Mol Sci 2021; 22(17): 9290. [PMID: 34502198 DOI: 10.3390/ijms22179290]

[104]

Andrés CMC, Pérez de la Lastra JM, Bustamante Munguira E, Juan CA, Plou FJ, et al. Electrophilic compounds in the human diet and their role in the induction of the transcription factor NRF2. Int J Mol Sci 2024; 25(6): 3521. [PMID: 38542492 DOI: 10.3390/ijms25063521]

[105]

Moosavi F, Hosseini R, Saso L, Firuzi O. Modulation of neurotrophic signaling pathways by polyphenols. Drug Des Devel Ther 2015; 10: 23-42. [PMID: 26730179 DOI: 10.2147/DDDT.S96936]

[106]

Naoi M, Inaba-Hasegawa K, Shamoto-Nagai M, Maruyama W. Neurotrophic function of phytochemicals for neuroprotection in aging and neurodegenerative disorders: modulation of intracellular signaling and gene expression. J Neural Transm (Vienna) 2017; 124(12): 1515-27. [PMID: 29030688 DOI: 10.1007/s00702-017-1797-5]

[107]

Gómez-Ganau S, de Julián-Ortiz JV, Gozalbes R. Recent advances in computational approaches for designing potential anti-Alzheimer’s agents. In: Roy K, editor. Computational modeling of drugs against Alzheimer’s disease. New York, NY: Humana Press; 2018. pp. 25-59. [DOI: 10.1007/978-1-4939-7404-7_2]

[108]

Fakhri S, Gravandi MM, Abdian S, Moradi SZ, Echeverría J. Quercetin derivatives in combating spinal cord injury: a mechanistic and systematic review. Life (Basel) 2022; 12(12): 1960. [PMID: 36556325 DOI: 10.3390/life12121960]

[109]

Liu Y, Guo M. Studies on transition metal-quercetin complexes using electrospray ionization tandem mass spectrometry. Molecules 2015; 20(5): 8583-94. [PMID: 25985359 DOI: 10.3390/molecules20058583]

[110]

Lamptey RNL, Chaulagain B, Trivedi R, Gothwal A, Layek B, et al. A review of the common neurodegenerative disorders: current therapeutic approaches and the potential role of nanotherapeutics. Int J Mol Sci 2022; 23(3): 1851. [PMID: 35163773 DOI: 10.3390/ijms23031851]

[111]

Toader C, Tataru CP, Munteanu O, Serban M, Covache-Busuioc R-A, et al. Decoding neurodegeneration: a review of molecular mechanisms and therapeutic advances in Alzheimer’s, Parkinson’s, and ALS. Int J Mol Sci 2024; 25(23): 12613. [PMID: 39684324 DOI: 10.3390/ijms252312613]

[112]

Sehar U, Rawat P, Reddy AP, Kopel J, Reddy PH. Amyloid beta in aging and Alzheimer’s disease. Int J Mol Sci 2022; 23(21): 12924. [PMID: 36361714 DOI: 10.3390/ijms232112924]

[113]

Zhang ZJ, Cheang LCV, Wang MW, Lee SM-Y. Quercetin exerts a neuroprotective effect through inhibition of the iNOS/NO system and pro-inflammation gene expression in PC12 cells and in zebrafish. Int J Mol Med 2011; 27(2): 195-203. [PMID: 21132259 DOI: 10.3892/ijmm.2010.571]

[114]

Vaz M, Silva V, Monteiro C, Silvestre S. Role of aducanumab in the treatment of Alzheimer’s disease: challenges and opportunities. Clin Interv Aging 2022; 17: 797-810. [PMID: 35611326 DOI: 10.2147/CIA.S325026]

[115]

Das B, Yan R. A close look at BACE1 inhibitors for Alzheimer’s disease treatment. CNS Drugs 2019; 33(3): 251-63. [PMID: 30830576 DOI: 10.1007/s40263-019-00613-7]

[116]

Reddy PH. Abnormal tau, mitochondrial dysfunction, impaired axonal transport of mitochondria, and synaptic deprivation in Alzheimer’s disease. Brain Res 2011; 1415: 136-48. [PMID: 21872849 DOI: 10.1016/j.brainres.2011.07.052]

[117]

Reyes ST, Deacon RMJ, Guo SG, Altimiras FJ, Castillo JB, et al. Effects of the sigma-1 receptor agonist blarcamesine in a murine model of fragile X syndrome: neurobehavioral phenotypes and receptor occupancy. Sci Rep 2021; 11(1): 17150. [PMID: 34433831 DOI: 10.1038/s41598-021-94079-7]

[118]

Huang L-K, Chao S-P, Hu C-J. Clinical trials of new drugs for Alzheimer disease. J Biomed Sci 2020; 27(1): 18. [PMID: 31906949 DOI: 10.1186/s12929-019-0609-7]

[119]

Miao J, Ma H, Yang Y, Liao Y, Lin C, et al. Microglia in Alzheimer’s disease: pathogenesis, mechanisms, and therapeutic potentials. Front Aging Neurosci 2023; 15: 1201982. [PMID: 37396657 DOI: 10.3389/fnagi.2023.1201982]

[120]

Jung YJ, Tweedie D, Scerba MT, Kim DS, Palmas MF, et al. Repurposing immunomodulatory imide drugs (IMiDs) in neuropsychiatric and neurodegenerative disorders. Front Neurosci 2021; 15: 656921. [PMID: 33854417 DOI: 10.3389/fnins.2021.656921]

[121]

Hampel H, Mesulam M-M, Cuello AC, Farlow MR, Giacobini E, et al. The cholinergic system in the pathophysiology and treatment of Alzheimer’s disease. Brain 2018; 141(7): 1917-33. [PMID: 29850777 DOI: 10.1093/brain/awy132]

[122]

Marucci G, Buccioni M, Ben DD, Lambertucci C, Volpini R, et al. Efficacy of acetylcholinesterase inhibitors in Alzheimer’s disease. Neuropharmacology 2021; 190: 108352. [PMID: 33035532 DOI: 10.1016/j.neuropharm.2020.108352]

[123]

Negi S, Khurana N, Duggal N. The misfolding mystery: α-synuclein and the pathogenesis of Parkinson’s disease. Neurochem Int 2024; 177: 105760. [PMID: 38723900 DOI: 10.1016/j.neuint.2024.105760]

[124]

Savitt D, Jankovic J. Targeting α-synuclein in Parkinson’s disease: progress towards the development of disease-modifying therapeutics. Drugs 2019; 79(8): 797-810. [PMID: 30982161 DOI: 10.1007/s40265-019-01104-1]

[125]

Gouda NA, Elkamhawy A, Cho J. Emerging therapeutic strategies for Parkinson’s disease and future prospects: a 2021 update. Biomedicines 2022; 10(2): 371. [PMID: 35203580 DOI: 10.3390/biomedicines10020371]

[126]

Masato A, Plotegher N, Boassa D, Bubacco L . Impaired dopamine metabolism in Parkinson’s disease pathogenesis. Mol Neurodegener 2019; 14(1): 35. [PMID: 31488222 DOI: 10.1186/s13024-019-0332-6]

[127]

Kwon DK, Kwatra M, Wang J, Ko HS. Levodopa-induced dyskinesia in Parkinson’s disease: pathogenesis and emerging treatment strategies. Cells 2022; 11(23): 3736. [PMID: 36496996 DOI: 10.3390/cells11233736]

[128]

Ferraiolo M, Hermans E. The complex molecular pharmacology of the dopamine D2 receptor: implications for pramipexole, ropinirole, and rotigotine. Pharmacol Ther 2023; 245: 108392. [PMID: 36958527 DOI: 10.1016/j.pharmthera.2023.108392]

[129]

Mazzio EA, Close F, Soliman KFA. The biochemical and cellular basis for nutraceutical strategies to attenuate neurodegeneration in Parkinson’s disease. Int J Mol Sci 2011; 12(1): 506-69. [PMID: 21340000 DOI: 10.3390/ijms12010506]

[130]

Yang N, Guan Q-W, Chen F-H, Xia Q-X, Yin X-X, et al. Antioxidants targeting mitochondrial oxidative stress: promising neuroprotectants for epilepsy. Oxid Med Cell Longev 2020; 2020: 6687185. [PMID: 33299529 DOI: 10.1155/2020/6687185]

[131]

Kobayashi K, Imagama S, Ohgomori T, Hirano K, Uchimura K, et al. Minocycline selectively inhibits M1 polarization of microglia. Cell Death Dis 2013; 4(3): e525. [PMID: 23470532 DOI: 10.1038/cddis.2013.54]

[132]

Wixey JA, Sukumar KR, Pretorius R, Lee KM, Colditz PB, et al. Ibuprofen treatment reduces the neuroinflammatory response and associated neuronal and white matter impairment in the growth restricted newborn. Front Physiol 2019; 10: 541. [PMID: 31133875 DOI: 10.3389/fphys.2019.00541]

[133]

Bhat AA, Moglad E, Afzal M, Thapa R, Almalki WH, et al. Therapeutic approaches targeting aging and cellular senescence in Huntington’s disease. CNS Neurosci Ther 2024; 30(10): e70053. [PMID: 39428700 DOI: 10.1111/cns.70053]

[134]

Tong H, Yang T, Xu S, Li X, Liu L, et al. Huntington’s disease: complex pathogenesis and therapeutic strategies. Int J Mol Sci 2024; 25(7): 3845. [PMID: 38612657 DOI: 10.3390/ijms25073845]

[135]

Sampaio C. Huntington disease - update on ongoing therapeutic developments and a look toward the future. Parkinsonism Relat Disord 2024; 122: 106049. [PMID: 38418319 DOI: 10.1016/j.parkreldis.2024.106049]

[136]

Tabrizi SJ, Leavitt BR, Landwehrmeyer GB, Wild EJ, Saft C, et al. Targeting huntingtin expression in patients with Huntington’s disease. N Engl J Med 2019; 380(24): 2307-16. [PMID: 31059641 DOI: 10.1056/NEJMoa1900907]

[137]

Imbimbo BP, Triaca V, Imbimbo C, Nisticò R. Investigational treatments for neurodegenerative diseases caused by inheritance of gene mutations: lessons from recent clinical trials. Neural Regen Res 2023; 18(8): 1679-83. [PMID: 36751779 DOI: 10.4103/1673-5374.363185]

[138]

Kwon D. Failure of genetic therapies for Huntington’s devastates community. Nature 2021; 593(7858): 180. [PMID: 33963316 DOI: 10.1038/d41586-021-01177-7]

[139]

Jodeiri Farshbaf M, Ghaedi K. Huntington’s disease and mitochondria. Neurotox Res 2017; 32(3): 518-29. [PMID: 28639241 DOI: 10.1007/s12640-017-9766-1]

[140]

Beal MF. Neuroprotective effects of creatine. Amino Acids 2011; 40(5): 1305-13. [PMID: 21448659 DOI: 10.1007/s00726-011-0851-0]

[141]

Orsucci D, Mancuso M, Ienco EC, LoGerfo A, Siciliano G. Targeting mitochondrial dysfunction and neurodegeneration by means of coenzyme Q10 and its analogues. Curr Med Chem 2011; 18(26): 4053-64. [PMID: 21824087 DOI: 10.2174/092986711796957257]

[142]

Anitha M, Nandhu MS, Anju TR, Jes P, Paulose CS. Targeting glutamate mediated excitotoxicity in Huntington’s disease: neural progenitors and partial glutamate antagonist——memantine. Med Hypotheses 2011; 76(1): 138-40. [PMID: 20943326 DOI: 10.1016/j.mehy.2010.09.003]

[143]

Singh K, Jain D, Sethi P, Gupta JK, Tripathi AK, et al. Emerging pharmacological approaches for Huntington’s disease. Eur J Pharmacol 2024; 980: 176873. [PMID: 39117264 DOI: 10.1016/j.ejphar.2024.176873]

[144]

Choi Y, Kim H-S, Shin KY, Kim E-M, Kim M, et al. Minocycline attenuates neuronal cell death and improves cognitive impairment in Alzheimer’s disease models. Neuropsychopharmacology 2007; 32(11): 2393-404. [PMID: 17406652 DOI: 10.1038/sj.npp.1301377]

[145]

Talebi M, Talebi M, Kakouri E, Farkhondeh T, Pourbagher-Shahri AM, et al. Tantalizing role of p53 molecular pathways and its coherent medications in neurodegenerative diseases. Int J Biol Macromol 2021; 172: 93-103. [PMID: 33440210 DOI: 10.1016/j.ijbiomac.2021.01.042]

[146]

Ayyalasomayajula N, Suresh C. Mechanistic comparison of current pharmacological treatments and novel phytochemicals to target amyloid peptides in Alzheimer’s and neurodegenerative diseases. Nutr Neurosci 2018; 21(10): 682-94. [PMID: 28683598 DOI: 10.1080/1028415X.2017.1345425]

[147]

Cheng M, Yuan C, Ju Y, Liu Y, Shi B, et al. Quercetin attenuates oxidative stress and apoptosis in brain tissue of APP/PS1 double transgenic AD mice by regulating Keap1/Nrf2/HO-1 pathway to improve cognitive impairment. Behav Neurol 2024; 2024: 5698119. [PMID: 39233848 DOI: 10.1155/2024/5698119]

[148]

Cheng S-C, Huang W-C, Pang J-HS, Wu Y-H, Cheng C-Y. Quercetin inhibits the production of IL-1β-induced inflammatory cytokines and chemokines in ARPE-19 cells via the MAPK and NF-κB signaling pathways. Int J Mol Sci 2019; 20(12): 2957. [PMID: 31212975 DOI: 10.3390/ijms20122957]

[149]

Ebrahimpour S, Zakeri M, Esmaeili A. Crosstalk between obesity, diabetes, and Alzheimer’s disease: introducing quercetin as an effective triple herbal medicine. Ageing Res Rev 2020; 62: 101095. [PMID: 32535272 DOI: 10.1016/j.arr.2020.101095]

[150]

Chakraborty S, Vishwas S, Harish V, Gupta G, Paudel KR, et al. Exploring nanoparticular platform in delivery of repurposed drug for Alzheimer’s disease: current approaches and future perspectives. Expert Opin Drug Deliv 2024; 21(12): 1771-92. [PMID: 39397403 DOI: 10.1080/17425247.2024.2414768]

[151]

Sabogal-Guáqueta AM, Muñoz-Manco JI, Ramírez-Pineda JR, Lamprea-Rodriguez M, Osorio E, et al. The flavonoid quercetin ameliorates Alzheimer’s disease pathology and protects cognitive and emotional function in aged triple transgenic Alzheimer’s disease model mice. Neuropharmacology 2015; 93: 134-45. [PMID: 25666032 DOI: 10.1016/j.neuropharm.2015.01.027]

[152]

Jiang W, Luo T, Li S, Zhou Y, Shen X-Y, et al. Quercetin protects against okadaic acid-induced injury via MAPK and PI3K/Akt/GSK3β signaling pathways in HT22 hippocampal neurons. PLoS One 2016; 11(4): e0152371. [PMID: 27050422 DOI: 10.1371/journal.pone.0152371]

[153]

Saeedi-Boroujeni A, Mahmoudian-Sani M-R. Anti-inflammatory potential of Quercetin in COVID-19 treatment. J Inflamm (Lond) 2021; 18(1): 3. [PMID: 33509217 DOI: 10.1186/s12950-021-00268-6]

[154]

Zu G, Sun K, Li L, Zu X, Han T, et al. Mechanism of quercetin therapeutic targets for Alzheimer disease and type 2 diabetes mellitus. Sci Rep 2021; 11(1): 22959. [PMID: 34824300 DOI: 10.1038/s41598-021-02248-5]

[155]

Rao AV, Balachandran B. Role of oxidative stress and antioxidants in neurodegenerative diseases. Nutr Neurosci 2002; 5(5): 291-309. [PMID: 12385592 DOI: 10.1080/1028415021000033767]

[156]

Vila M. Neuromelanin, aging, and neuronal vulnerability in Parkinson’s disease. Mov Disord 2019; 34(10): 1440-51. [PMID: 31251435 DOI: 10.1002/mds.27776]

[157]

Saha S, Buttari B, Profumo E, Tucci P, Saso L. A perspective on Nrf2 signaling pathway for neuroinflammation: a potential therapeutic target in Alzheimer’s and Parkinson’s diseases. Front Cell Neurosci 2022; 15: 787258. [PMID: 35126058 DOI: 10.3389/fncel.2021.787258]

[158]

Subramaniam SR, Chesselet M-F. Mitochondrial dysfunction and oxidative stress in Parkinson’s disease. Prog Neurobiol 2013; 106-107: 17-32. [PMID: 23643800 DOI: 10.1016/j.pneurobio.2013.04.004]

[159]

Wang W-W, Han R, He H-J, Li J, Chen S-Y, et al. Administration of quercetin improves mitochondria quality control and protects the neurons in 6-OHDA-lesioned Parkinson’s disease models. Aging (Albany NY) 2021; 13(8): 11738-51. [PMID: 33878030 DOI: 10.18632/aging.202868]

[160]

Sriraksa N, Wattanathorn J, Muchimapura S, Tiamkao S, Brown K, et al. Cognitive-enhancing effect of quercetin in a rat model of Parkinson’s disease induced by 6-hydroxydopamine. Evid Based Complement Alternat Med 2012; 2012: 823206. [PMID: 21792372 DOI: 10.1155/2012/823206]

[161]

Khan MM, Raza SS, Javed H, Ahmad A, Khan A, et al. Rutin protects dopaminergic neurons from oxidative stress in an animal model of Parkinson’s disease. Neurotox Res 2012; 22(1): 1-15. [PMID: 22194158 DOI: 10.1007/s12640-011-9295-2]

[162]

Acıkara OB, Karatoprak , Yücel Ç, Akkol EK, Sobarzo-Sánchez E, et al. A critical analysis of quercetin as the attractive target for the treatment of Parkinson’s disease. CNS Neurol Disord Drug Targets 2022; 21(9): 795-817. [PMID: 34872486 DOI: 10.2174/1871527320666211206122407]

[163]

Iova O-M, Marin G-E, Lazar I, Stanescu I, Dogaru G, et al. Nitric oxide/nitric oxide synthase system in the pathogenesis of neurodegenerative disorders-an overview. Antioxidants (Basel) 2023; 12(3): 753. [PMID: 36979000 DOI: 10.3390/antiox12030753]

[164]

Josiah SS, Famusiwa CD, Crown OO, Lawal AO, Olaleye MT, et al. Neuroprotective effects of catechin and quercetin in experimental Parkinsonism through modulation of dopamine metabolism and expression of IL-1β, TNF-α, NF-κB, IκKB, and p53 genes in male Wistar rats. Neurotoxicology 2022; 90: 158-71. [PMID: 35337893 DOI: 10.1016/j.neuro.2022.03.004]

[165]

Henríquez G, Gomez A, Guerrero E, Narayan M. Potential role of natural polyphenols against protein aggregation toxicity: in vitro, in vivo, and clinical studies. ACS Chem Neurosci 2020; 11(19): 2915-34. [PMID: 32822152 DOI: 10.1021/acschemneuro.0c00381]

[166]

Tan S, Caparros-Martin JA, Matthews VB, Koch H, O’Gara F, et al. Isoquercetin and inulin synergistically modulate the gut microbiome to prevent development of the metabolic syndrome in mice fed a high fat diet. Sci Rep 2018; 8(1): 10100. [PMID: 29973701 DOI: 10.1038/s41598-018-28521-8]

[167]

Lum PT, Sekar M, Gan SH, Bonam SR, Shaikh MF. Protective effect of natural products against Huntington’s disease: an overview of scientific evidence and understanding their mechanism of action. ACS Chem Neurosci 2021; 12(3): 391-418. [PMID: 33475334 DOI: 10.1021/acschemneuro.0c00824]

[168]

Riche K, Lenard NR. Quercetin’s effects on glutamate cytotoxicity. Molecules 2022; 27(21): 7620. [PMID: 36364448 DOI: 10.3390/molecules27217620]

[169]

Silvestro S, Bramanti P, Mazzon E. Role of quercetin in depressive-like behaviors: findings from animal models. Appl Sci 2021; 11(15): 7116. [DOI: 10.3390/app11157116]

[170]

Vishwas S, Kumar R, Khursheed R, Ramanunny AK, Kumar R, et al. Expanding arsenal against neurodegenerative diseases using quercetin based nanoformulations: breakthroughs and bottlenecks. Curr Neuropharmacol 2023; 21(7): 1558-74. [PMID: 35950245 DOI: 10.2174/1570159X20666220810105421]

[171]

Ryu H, Rosas HD, Hersch SM, Ferrante RJ. The therapeutic role of creatine in Huntington’s disease. Pharmacol Ther 2005; 108(2): 193-207. [PMID: 16055197 DOI: 10.1016/j.pharmthera.2005.04.008]

[172]

Kuhad A, Singla S, Arora V, Chopra K. Neuroprotective effect of sesamol and quercetin against QA induced neurotoxicity: an experimental paradigm of Huntington’s disease. J Neurol Sci 2013; 333: e149-50. [DOI: 10.1016/j.jns.2013.07.498]

[173]

Tayab MA, Islam MN, Chowdhury KAA, Tasnim FM. Targeting neuroinflammation by polyphenols: a promising therapeutic approach against inflammation-associated depression. Biomed Pharmacother 2022; 147: 112668. [PMID: 35104696 DOI: 10.1016/j.biopha.2022.112668]

[174]

Sandhir R, Mehrotra A. Quercetin supplementation is effective in improving mitochondrial dysfunctions induced by 3-nitropropionic acid: implications in Huntington’s disease. Biochim Biophys Acta 2013; 1832(3): 421-30. [PMID: 23220257 DOI: 10.1016/j.bbadis.2012.11.018]

[175]

Kumar A, Ratan RR. Oxidative stress and Huntington’s disease: the good, the bad, and the ugly. J Huntingtons Dis 2016; 5(3): 217-37. [PMID: 27662334 DOI: 10.3233/JHD-160205]

[176]

Khan H, Ullah H, Tundis R, Belwal T, Devkota HR, et al. Dietary flavonoids in the management of Huntington’s disease: mechanism and clinical perspective eFood 2020; 1(1): 38-52. [DOI: 10.2991/efood.k.200203.001]

[177]

Gao C, Jiang J, Tan Y, Chen S. Microglia in neurodegenerative diseases: mechanism and potential therapeutic targets. Signal Transduct Target Ther 2023; 8(1): 359. [PMID: 37735487 DOI: 10.1038/s41392-023-01588-0]

[178]

Kalonia H, Mishra J, Kumar A. Targeting neuro-inflammatory cytokines and oxidative stress by minocycline attenuates quinolinic-acid-induced Huntington’s disease-like symptoms in rats. Neurotox Res 2012; 22(4): 310-20. [PMID: 22392362 DOI: 10.1007/s12640-012-9315-x]

[179]

Moré MI. Taxifolin from dahurian larch - application for the approval as novel food. Amur District, Russia; 2010.

[180]

Yu X, Ji C, Shao A. Neurovascular unit dysfunction and neurodegenerative disorders. Front Neurosci 2020; 14: 334. [PMID: 32410936 DOI: 10.3389/fnins.2020.00334]

[181]

Liu R, Zhang TT, Zhou D, Bai XY, Zhou WL, et al. Quercetin protects against the Aβ(25-35)-induced amnesic injury: involvement of inactivation of rage-mediated pathway and conservation of the NVU. Neuropharmacology 2013; 67: 419-31. [PMID: 23231807 DOI: 10.1016/j.neuropharm.2012.11.018]

[182]

Sun P, Yang Y, Yang L, Qian Y, Liang M, et al. Quercetin protects blood-brain barrier integrity via the PI3K/Akt/Erk signaling pathway in a mouse model of meningitis induced by Glaesserella parasuis . Biomolecules 2024; 14(6): 696. [PMID: 38927100 DOI: 10.3390/biom14060696]

[183]

Dagher O, Mury P, Thorin-Trescases N, Noly PE, Thorin E, et al. Therapeutic potential of quercetin to alleviate endothelial dysfunction in age-related cardiovascular diseases. Front Cardiovasc Med 2021; 8: 658400. [PMID: 33860002 DOI: 10.3389/fcvm.2021.658400]

[184]

Li L, Jiang W, Yu B, Liang H, Mao S, et al. Quercetin improves cerebral ischemia/reperfusion injury by promoting microglia/macrophages M2 polarization via regulating PI3K/Akt/NF-κB signaling pathway. Biomed Pharmacother 2023; 168: 115653. [PMID: 37812891 DOI: 10.1016/j.biopha.2023.115653]

[185]

Kobuchi H, Roy S, Sen CK, Nguyen HG, Packer L. Quercetin inhibits inducible ICAM-1 expression in human endothelial cells through the JNK pathway. Am J Physiol 1999; 277(3): C403-11. [PMID: 10484327 DOI: 10.1152/ajpcell.1999.277.3.C403]

[186]

Chen T, Zhang X, Zhu G, Liu H, Chen J, et al. Quercetin inhibits TNF-α induced HUVECs apoptosis and inflammation via downregulating NF-kB and AP-1 signaling pathway in vitro. Medicine (Baltimore) 2020; 99(38): e22241. [PMID: 32957369 DOI: 10.1097/MD.0000000000022241]

[187]

Zhang Y, Fu K, Wang C, Ma C, Gong L, et al. Protective effects of dietary quercetin on cerebral ischemic injury: pharmacology, pharmacokinetics and bioavailability-enhancing nanoformulations. Food Funct 2023; 14(10): 4470-89. [PMID: 37067239 DOI: 10.1039/d2fo03122a]

[188]

Silva Dos Santos J, Gonçalves Cirino JP, de Oliveira Carvalho P, Ortega MM . The pharmacological action of kaempferol in central nervous system diseases: a review. Front Pharmacol 2021; 11: 565700. [PMID: 33519431 DOI: 10.3389/fphar.2020.565700]

[189]

Alexander C, Parsaee A, Vasefi M . Polyherbal and multimodal treatments: kaempferol- and quercetin-rich herbs alleviate symptoms of Alzheimer’s disease. Biology (Basel) 2023; 12(11): 1453. [PMID: 37998052 DOI: 10.3390/biology12111453]

[190]

Zhang J-X, Xing J-G, Wang L-L, Jiang H-L, Guo S-L, et al. Luteolin inhibits fibrillary β-amyloid1-40-induced inflammation in a human blood-brain barrier model by suppressing the p38 MAPK-mediated NF-κB signaling pathways. Molecules 2017; 22(3): 334. [PMID: 28245546 DOI: 10.3390/molecules22030334]

[191]

Gonçalves PB, Sodero ACR, Cordeiro Y. Green tea epigallocatechin-3-gallate (EGCG) targeting protein misfolding in drug discovery for neurodegenerative diseases. Biomolecules 2021; 11(5): 767. [PMID: 34065606 DOI: 10.3390/biom11050767]

[192]

Nargeh H, Aliabadi F, Ajami M, Pazoki-Toroudi H. Role of polyphenols on gut microbiota and the ubiquitin-proteasome system in neurodegenerative diseases. J Agric Food Chem 2021; 69(22): 6119-44. [PMID: 34038102 DOI: 10.1021/acs.jafc.1c00923]

[193]

Maan G, Sikdar B, Kumar A, Shukla R, Mishra A. Role of flavonoids in neurodegenerative diseases: limitations and future perspectives. Curr Top Med Chem 2020; 20(13): 1169-94. [PMID: 32297582 DOI: 10.2174/1568026620666200416085330]

[194]

Liang H, Ma Z, Zhong W, Liu J, Sugimoto K, et al. Regulation of mitophagy and mitochondrial function: natural compounds as potential therapeutic strategies for Parkinson’s disease. Phytother Res 2024; 38(4): 1838-62. [PMID: 38356178 DOI: 10.1002/ptr.8156]

[195]

Li Y, Zhao J, Hölscher C. Therapeutic potential of baicalein in Alzheimer’s disease and Parkinson’s disease. CNS Drugs 2017; 31(8): 639-52. [PMID: 28634902 DOI: 10.1007/s40263-017-0451-y]

[196]

Kunachowicz D, Ściskalska M, Kepinska M. Modulatory effect of lifestyle-related, environmental and genetic factors on paraoxonase-1 activity: a review. Int J Environ Res Public Health 2023; 20(4): 2813. [PMID: 36833509 DOI: 10.3390/ijerph20042813]

[197]

Sreekumar PG, Su F, Spee C, Hong E, Komirisetty R, et al. Paraoxonase 2 deficiency causes mitochondrial dysfunction in retinal pigment epithelial cells and retinal degeneration in mice. Antioxidants (Basel) 2023; 12(10): 1820. [PMID: 37891899 DOI: 10.3390/antiox12101820]

[198]

Altenhöfer S, Witte I, Teiber JF, Wilgenbus P, Pautz A, et al. One enzyme, two functions: PON2 prevents mitochondrial superoxide formation and apoptosis independent from its lactonase activity. J Biol Chem 2010; 285(32): 24398-403. [PMID: 20530481 DOI: 10.1074/jbc.M110.118604]

[199]

Devarajan A, Su F, Grijalva V, Yalamanchi M, Yalamanchi A, et al. Paraoxonase 2 overexpression inhibits tumor development in a mouse model of ovarian cancer. Cell Death Dis 2018; 9(3): 392. [PMID: 29531225 DOI: 10.1038/s41419-018-0395-2]

[200]

Garrick JM, Dao K, Costa LG, Marsillach J, Furlong CE. Examining the role of paraoxonase 2 in the dopaminergic system of the mouse brain. BMC Neurosci 2022; 23(1): 52. [PMID: 36056313 DOI: 10.1186/s12868-022-00738-4]

[201]

Giordano G, Cole TB, Furlong CE, Costa LG. Paraoxonase 2 (PON2) in the mouse central nervous system: a neuroprotective role? Toxicol Appl Pharmacol 2011; 256(3): 369-78. [PMID: 21354197 DOI: 10.1016/j.taap.2011.02.014]

[202]

Costa LG, de Laat R, Dao K, Pellacani C, Cole TB, et al. Paraoxonase-2 (PON2) in brain and its potential role in neuroprotection. Neurotoxicology 2014; 43: 3-9. [PMID: 24012887 DOI: 10.1016/j.neuro.2013.08.011]

[203]

Farid AS, Horii Y. Modulation of paraoxonases during infectious diseases and its potential impact on atherosclerosis. Lipids Health Dis 2012; 11: 92. [PMID: 22824324 DOI: 10.1186/1476-511X-11-92]

[204]

Parween F, Gupta RD. Insights into the role of paraoxonase 2 in human pathophysiology. J Biosci 2022; 47(1): 4. [PMID: 35092416 DOI: 10.1007/s12038-021-00234-7]

[205]

Romero M, Jiménez R, Sánchez M, López-Sepúlveda R, Zarzuelo MJ, et al. Quercetin inhibits vascular superoxide production induced by endothelin-1: role of NADPH oxidase, uncoupled eNOS and PKC. Atherosclerosis 2009; 202(1): 58-67. [PMID: 18436224 DOI: 10.1016/j.atherosclerosis.2008.03.007]

[206]

Oakley RH, Cidlowski JA. The biology of the glucocorticoid receptor: new signaling mechanisms in health and disease. J Allergy Clin Immunol 2013; 132(5): 1033-44. [PMID: 24084075 DOI: 10.1016/j.jaci.2013.09.007]

[207]

Loboda A, Damulewicz M, Pyza E, Jozkowicz A, Dulak J. Role of Nrf2/HO-1 system in development, oxidative stress response and diseases: an evolutionarily conserved mechanism. Cell Mol Life Sci 2016; 73(17): 3221-47. [PMID: 27100828 DOI: 10.1007/s00018-016-2223-0]

[208]

Rai SR, Bhattacharyya C, Sarkar A, Chakraborty S, Sircar E, et al. Glutathione: role in oxidative/nitrosative stress, antioxidant defense, and treatments. ChemistrySelect 2021; 6(18): 4566-90. [DOI: 10.1002/slct.202100773]

[209]

Kanninen K, Malm TM, Jyrkkänen H-K, Goldsteins G, Keksa-Goldsteine V, et al. Nuclear factor erythroid 2-related factor 2 protects against beta amyloid. Mol Cell Neurosci 2008; 39(3): 302-13. [PMID: 18706502 DOI: 10.1016/j.mcn.2008.07.010]

[210]

Liang L, Gao C, Luo M, Wang W, Zhao C, et al. Dihydroquercetin (DHQ) induced HO-1 and NQO1 expression against oxidative stress through the Nrf2-dependent antioxidant pathway. J Agric Food Chem 2013; 61(11): 2755-61. [PMID: 23419114 DOI: 10.1021/jf304768p]

[211]

Saw CLL, Guo Y, Yang AY, Paredes-Gonzalez X, Ramirez C, et al. The berry constituents quercetin, kaempferol, and pterostilbene synergistically attenuate reactive oxygen species: involvement of the Nrf2-ARE signaling pathway. Food Chem Toxicol 2014; 72: 303-11. [PMID: 25111660 DOI: 10.1016/j.fct.2014.07.038]

[212]

Dalle S, Abderrahmani A. Receptors and signaling pathways controlling beta-cell function and survival as targets for anti-diabetic therapeutic strategies. Cells 2024; 13(15): 1244. [PMID: 39120275 DOI: 10.3390/cells13151244]

[213]

Danielsen SA, Eide PW, Nesbakken A, Guren T, Leithe E, et al. Portrait of the PI3K/AKT pathway in colorectal cancer. Biochim Biophys Acta 2015; 1855(1): 104-21. [PMID: 25450577 DOI: 10.1016/j.bbcan.2014.09.008]

[214]

Penna E, Pizzella A, Cimmino F, Trinchese G, Cavaliere G, et al. Neurodevelopmental disorders: effect of high-fat diet on synaptic plasticity and mitochondrial functions. Brain Sci 2020; 10(11): 805. [PMID: 33142719 DOI: 10.3390/brainsci10110805]

[215]

Dong YS, Wang JL, Feng DY, Qin HZ, Wen H, et al. Protective effect of quercetin against oxidative stress and brain edema in an experimental rat model of subarachnoid hemorrhage. Int J Med Sci 2014; 11(3): 282-90. [PMID: 24516353 DOI: 10.7150/ijms.7634]

[216]

da Silva MF, Lins AA, Gomes MC, Marinho WPJ, de Araújo RSA, et al. Anticancer drug discovery from natural compounds targeting PI3K/AKT/mTOR signaling pathway. Curr Med Chem 2024. [PMID: 39390838 DOI: 10.2174/0109298673325229240928040758]

[217]

Yan H, He L, Lv D, Yang J, Yuan Z. The role of the dysregulated JNK signaling pathway in the pathogenesis of human diseases and its potential therapeutic strategies: a comprehensive review. Biomolecules 2024; 14(2): 243. [PMID: 38397480 DOI: 10.3390/biom14020243]

[218]

Garg R, Kumariya S, Katekar R, Verma S, Goand UK, et al. JNK signaling pathway in metabolic disorders: an emerging therapeutic target. Eur J Pharmacol 2021; 901: 174079. [PMID: 33812885 DOI: 10.1016/j.ejphar.2021.174079]

[219]

Ha J, Kang E, Seo J, Cho S. Phosphorylation dynamics of JNK signaling: effects of dual-specificity phosphatases (DUSPs) on the JNK pathway. Int J Mol Sci 2019; 20(24): 6157. [PMID: 31817617 DOI: 10.3390/ijms20246157]

[220]

Zaplatic E, Bule M, Shah SZA, Uddin MS, Niaz K. Molecular mechanisms underlying protective role of quercetin in attenuating Alzheimer’s disease. Life Sci 2019; 224: 109-19. [PMID: 30914316 DOI: 10.1016/j.lfs.2019.03.055]

[221]

Dhanasekaran DN, Reddy EP. JNK signaling in apoptosis. Oncogene 2008; 27(48): 6245-51. [PMID: 18931691 DOI: 10.1038/onc.2008.301]

[222]

Uchida K, Shiraishi M, Naito Y, Torii Y, Nakamura Y, et al. Activation of stress signaling pathways by the end product of lipid peroxidation. 4-hydroxy-2-nonenal is a potential inducer of intracellular peroxide production. J Biol Chem 1999; 274(4): 2234-42. [PMID: 9890986 DOI: 10.1074/jbc.274.4.2234]

[223]

Merecz-Sadowska A, Sitarek P, Śliwiński T, Zajdel R. Anti-inflammatory activity of extracts and pure compounds derived from plants via modulation of signaling pathways, especially PI3K/AKT in macrophages. Int J Mol Sci 2020; 21(24): 9605. [PMID: 33339446 DOI: 10.3390/ijms21249605]

[224]

Megha KB, Joseph X, Akhil V, Mohanan PV. Cascade of immune mechanism and consequences of inflammatory disorders. Phytomedicine 2021; 91: 153712. [PMID: 34511264 DOI: 10.1016/j.phymed.2021.153712]

[225]

Abidar S, Hritcu L, Nhiri M. The natural neuroprotective compounds used in the 6-hydroxydopamine- induced Parkinson’s disease in zebrafish: the current applications and perspectives. CNS Neurol Disord Drug Targets 2023; 22(10): 1472-83. [PMID: 36306449 DOI: 10.2174/1871527322666221028152600]

[226]

Suganthy N, Devi KP, Nabavi SF, Braidy N, Nabavi SM. Bioactive effects of quercetin in the central nervous system: focusing on the mechanisms of actions. Biomed Pharmacother 2016; 84: 892-908. [PMID: 27756054 DOI: 10.1016/j.biopha.2016.10.011]

[227]

Isik S, Yeman Kiyak B, Akbayir R, Seyhali R, Arpaci T. Microglia mediated neuroinflammation in Parkinson’s disease. Cells 2023; 12(7): 1012. [PMID: 37048085 DOI: 10.3390/cells12071012]

[228]

Zamin LL, Filippi-Chiela EC, Dillenburg-Pilla P, Horn F, Salbego C, et al. Resveratrol and quercetin cooperate to induce senescence-like growth arrest in C6 rat glioma cells. Cancer Sci 2009; 100(9): 1655-62. [PMID: 19496785 DOI: 10.1111/j.1349-7006.2009.01215.x]

[229]

Benameur T, Soleti R, Porro C. The potential neuroprotective role of free and encapsulated quercetin mediated by miRNA against neurological diseases. Nutrients 2021; 13(4): 1318. [PMID: 33923599 DOI: 10.3390/nu13041318]

[230]

Qian L, Zhu Y, Deng C, Liang Z, Chen J, et al. Peroxisome proliferator-activated receptor gamma coactivator-1 (PGC-1) family in physiological and pathophysiological process and diseases. Signal Transduct Target Ther 2024; 9(1): 50. [PMID: 38424050 DOI: 10.1038/s41392-024-01756-w]

[231]

Song J, Du G, Wu H, Gao X, Yang Z, et al. Protective effects of quercetin on traumatic brain injury induced inflammation and oxidative stress in cortex through activating Nrf2/HO-1 pathway. Restor Neurol Neurosci 2021; 39(1): 73-84. [PMID: 33612499 DOI: 10.3233/RNN-201119]

[232]

Dong W, Quo W, Wang F, Li C, Xie Y, et al. Electroacupuncture upregulates SIRT1-dependent PGC-1α expression in SAMP8 mice. Med Sci Monit 2015; 21: 3356-62. [PMID: 26530101 DOI: 10.12659/msm.894864]

[233]

Wang R, Li JJ, Diao S, Kwak Y-D, Liu L, et al. Metabolic stress modulates Alzheimer’s β-secretase gene transcription via SIRT1-PPARγ-PGC-1 in neurons. Cell Metab 2013; 17(5): 685-94. [PMID: 23663737 DOI: 10.1016/j.cmet.2013.03.016]

[234]

Kratz EM, Sołkiewicz K, Kubis-Kubiak A, Piwowar A. Sirtuins as important factors in pathological states and the role of their molecular activity modulators. Int J Mol Sci 2021; 22(2): 630. [PMID: 33435263 DOI: 10.3390/ijms22020630]

[235]

Nakagawa T, Ohta K. Quercetin regulates the integrated stress response to improve memory. Int J Mol Sci 2019; 20(11): 2761. [PMID: 31195662 DOI: 10.3390/ijms20112761]

[236]

Yue J, López JM. Understanding MAPK signaling pathways in apoptosis. Int J Mol Sci 2020; 21(7): 2346. [PMID: 32231094 DOI: 10.3390/ijms21072346]

[237]

Moratilla-Rivera I, Sánchez M, Valdés-González JA, Gómez-Serranillos MP. Natural products as modulators of Nrf2 signaling pathway in neuroprotection. Int J Mol Sci 2023; 24(4): 3748. [PMID: 36835155 DOI: 10.3390/ijms24043748]

[238]

Islam MA, Medha MM, Nahar AU, Al Fahad MA, Siraj MA, et al. Cancer protective role of selected dietary polyphenols via modulating Keap1/Nrf2/ARE and interconnected signaling pathways. Nutr Cancer 2023; 75(4): 1065-102. [PMID: 37078744 DOI: 10.1080/01635581.2023.2183546]

[239]

Gravandi MM, Fakhri S, Zarneshan SN, Yarmohammadi A, Khan H. Flavonoids modulate AMPK/PGC-1α and interconnected pathways toward potential neuroprotective activities. Metab Brain Dis 2021; 36(7): 1501-21. [PMID: 33988807 DOI: 10.1007/s11011-021-00750-3]

[240]

Rullah K, Shamsudin NF, Koeberle A, Tham CL, Fasihi Mohd Aluwi MF, et al. Flavonoid diversity and roles in the lipopolysaccharide-mediated inflammatory response of monocytes and macrophages. Future Med Chem 2024; 16(1): 75-99. [PMID: 38205612 DOI: 10.4155/fmc-2023-0174]

[241]

Habtemariam S. Anti-inflammatory therapeutic mechanisms of natural products: insight from rosemary diterpenes, carnosic acid and carnosol. Biomedicines 2023; 11(2): 545. [PMID: 36831081 DOI: 10.3390/biomedicines11020545]

[242]

Islam MR, Al-Imran MIK, Zehravi M, Sweilam SH, Mortuza MR, et al. Targeting signaling pathways in neurodegenerative diseases: quercetin’s cellular and molecular mechanisms for neuroprotection. Animal Model Exp Med 2025; 8(5): 798-818. [PMID: 39843406 DOI: 10.1002/ame2.12551]

[243]

Zarneshan SN, Fakhri S, Khan H. Targeting Akt/CREB/BDNF signaling pathway by ginsenosides in neurodegenerative diseases: a mechanistic approach. Pharmacol Res 2022; 177: 106099. [PMID: 35092819 DOI: 10.1016/j.phrs.2022.106099]

[244]

Wolf D, Muralidharan A, Mohan S. Role of prolyl hydroxylase domain proteins in bone metabolism. Osteoporos Sarcopenia 2022; 8(1): 1-10. [PMID: 35415275 DOI: 10.1016/j.afos.2022.03.001]

[245]

Cai H, Yang J, Wang J-N, Gong Y, Dai H-Z, Chen G-J, et al. Quercetin alleviates cerebral ischemia/reperfusion injury by regulating Tnf-1a/Hif-1α activation of Vegfa/Vegfr/Akt/Pi3k pathway. 2024. [DOI: 10.2139/ssrn.4997549]

[246]

Zhang L, Ma J, Yang F, Li S, Ma W, et al. Neuroprotective effects of quercetin on ischemic stroke: a literature review. Front Pharmacol 2022; 13: 854249. [PMID: 35662707 DOI: 10.3389/fphar.2022.854249]

[247]

Su K, Li Z, Yu Y, Zhang X. The prolyl hydroxylase inhibitor roxadustat: paradigm in drug discovery and prospects for clinical application beyond anemia. Drug Discov Today 2020; 25(7): 1262-9. [PMID: 32380083 DOI: 10.1016/j.drudis.2020.04.017]

[248]

Miao M, Wu M, Li Y, Zhang L, Jin Q, et al. Clinical potential of hypoxia inducible factors prolyl hydroxylase inhibitors in treating nonanemic diseases. Front Pharmacol 2022; 13: 837249. [PMID: 35281917 DOI: 10.3389/fphar.2022.837249]

[249]

Patil N, Bhatt LK. Targeting Acyl-CoA synthetase long-chain family member 4: a potential approach for the treatment of cerebral ischemia/reperfusion injury. Metab Brain Dis 2025; 40(5): 212. [PMID: 40418418 DOI: 10.1007/s11011-025-01638-2]

[250]

Alqahtani F, Mohamed Ali YS, Almutairi MM, Alotaibi AF, Imran I, et al. Therapeutic benefits of quercetin in traumatic brain injury model exposed to cigarette smoke. Saudi Pharm J 2024; 32(1): 101895. [PMID: 38226352 DOI: 10.1016/j.jsps.2023.101895]

[251]

Gao Y, Zhang J, Tang T, Liu Z. Hypoxia pathways in Parkinson’s disease: from pathogenesis to therapeutic targets. Int J Mol Sci 2024; 25(19): 10484. [PMID: 39408813 DOI: 10.3390/ijms251910484]

[252]

Jha NK, Jha SK, Sharma R, Kumar D, Ambasta RK, et al. Hypoxia-induced signaling activation in neurodegenerative diseases: targets for new therapeutic strategies. J Alzheimers Dis 2018; 62(1): 15-38. [PMID: 29439330 DOI: 10.3233/JAD-170589]

[253]

Ossola B, Kääriäinen TM, Männistö PT. The multiple faces of quercetin in neuroprotection. Expert Opin Drug Saf 2009; 8(4): 397-409. [PMID: 19538101 DOI: 10.1517/14740330903026944]

[254]

Hashemzaei M, Delarami Far A, Yari A, Heravi RE, Tabrizian K, et al. Anticancer and apoptosis-inducing effects of quercetin in vitro and in vivo. Oncol Rep 2017; 38(2): 819-28. [PMID: 28677813 DOI: 10.3892/or.2017.5766]

[255]

Zhao P, Mao J-M, Zhang S-Y, Zhou Z-Q, Tan Y, et al. Quercetin induces HepG2 cell apoptosis by inhibiting fatty acid biosynthesis. Oncol Lett 2014; 8(2): 765-9. [PMID: 25009654 DOI: 10.3892/ol.2014.2159]

[256]

Sonmez E, Cacciatore I, Bakan F, Turkez H, Mohtar YI, et al. Toxicity assessment of hydroxyapatite nanoparticles in rat liver cell model in vitro. Hum Exp Toxicol 2016; 35(10): 1073-83. [PMID: 26655636 DOI: 10.1177/0960327115619770]

[257]

Zhang X-Y, Li Y-Q, Yin Z-H, Bao Q-N, Xia M-Z, et al. Supplements for cognitive ability in patients with mild cognitive impairment or Alzheimer’s disease: a protocol for systematic review and network meta-analysis of randomised controlled trials. BMJ Open 2024; 14(4): e077623. [PMID: 38569691 DOI: 10.1136/bmjopen-2023-077623]

[258]

Bayazid AB, Lim BO. Quercetin is an active agent in berries against neurodegenerative diseases progression through modulation of Nrf2/HO1. Nutrients 2022; 14(23): 5132. [PMID: 36501161 DOI: 10.3390/nu14235132]

[259]

Lama A, Pirozzi C, Avagliano C, Annunziata C, Mollica MP, et al. Nutraceuticals: an integrative approach to starve Parkinson’s disease. Brain Behav Immun Health 2020; 2: 100037. [PMID: 34589828 DOI: 10.1016/j.bbih.2020.100037]

PDF (5633KB)

0

Accesses

0

Citation

Detail

Sections
Recommended

/