Deciphering the mechanisms underlying the neuroprotective potential of kaempferol: a comprehensive investigation

被引:1
作者
Chaubey, Satyam [1 ]
Singh, Lovedeep [1 ]
机构
[1] Chandigarh Univ, Univ Inst Pharm Sci, Mohali, Punjab, India
关键词
Kaempferol; Neuroprotection; NRF-2; NADPH oxidase; TLR-4/MAPK; TLR-4/NF-kappa B; NF-KAPPA-B; INDUCED OXIDATIVE STRESS; BLOOD-BRAIN-BARRIER; ORAL KAEMPFEROL; MODEL; NEUROINFLAMMATION; SIRT1; CA1; PHARMACOKINETICS; EXPRESSION;
D O I
10.1007/s00210-024-03515-8
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Neurodegenerative disorders are characterized by neuronal degradation, dysfunction, or death within the CNS. Oxidative and inflammatory stress play crucial roles in the pathogenesis of various neurodegenerative diseases. The interplay between these stressors and dysregulated cellular signaling pathways contributes to neurodegeneration. Downregulation of NRF-2 compromises antioxidant defense, exacerbating neuronal damage, while increased TLR-4/MAPK and TLR-4/NF-kappa B signaling promotes neuroinflammation. Excessive ROS production by NADPH oxidase leads to oxidative damage and neuronal apoptosis. The strategies targeting NRF-2, TLR-4-mediated inflammatory stress, and NADPH oxidase activity promise to mitigate neuronal damage and halt the progression of the disease. Kaempferol is a flavonoid polyphenol antioxidant found abundantly in various fruits and vegetables, including apples, grapes, tomatoes, and broccoli. It is widely found in medicinal plants including Equisetum spp., Sophora japonica, Ginkgo biloba, and Euphorbia pekinensis (Rupr.). A substantial body of in vitro and in vivo evidences have demonstrated the neuroprotective potential of kaempferol against neurodegenerative diseases such as Alzheimer's disease and Parkinson's disease. Kaempferol demonstrates multifaceted potential in mitigating neuroinflammation, apoptosis, and oxidative stress in different neurodegenerative diseases through the modulation of various pathways including NRF-2, NADPH oxidase, TLR-4/MAPK, and TLR-4/NF-kappa B. This review article was developed through a comprehensive analysis and interpretation of research published between 2009 and 2024, sourced from multiple scientific databases, including PubMed, Scopus, ScienceDirect, and Web of Science. This review aims to provide an in-depth overview of the neuroprotective effects of kaempferol, focusing on its underlying molecular mechanisms. A total of 24 research evidence were included to elucidate the molecular pathways by which kaempferol exerts its protective effects against neurodegenerative diseases.
引用
收藏
页码:2275 / 2292
页数:18
相关论文
共 99 条
[1]   The role of neuroinflammation in neurodegenerative diseases: current understanding and future therapeutic targets [J].
Adamu, Alhamdu ;
Li, Shuo ;
Gao, Fankai ;
Xue, Guofang .
FRONTIERS IN AGING NEUROSCIENCE, 2024, 16
[2]   A randomized, placebo-controlled trial evaluating the safety of excessive administration of kaempferol aglycone [J].
Akiyama, Minoru ;
Mizokami, Tsubasa ;
Ito, Hikaru ;
Ikeda, Yasutaka .
FOOD SCIENCE & NUTRITION, 2023, 11 (09) :5427-5437
[3]  
Al-Nour Mosab Yahya, 2019, Curr Pharmacol Rep, V5, P255, DOI [10.1007/s40495-019-00181-w, 10.1007/s40495-019-00181-w]
[4]   Sex-Independent Cognition Improvement in Response to Kaempferol in the Model of Sporadic Alzheimer's Disease [J].
Babaei, Parvin ;
Eyvani, Kimia ;
Kouhestani, Somayeh .
NEUROCHEMICAL RESEARCH, 2021, 46 (06) :1480-1486
[5]   Metabolism, Oral Bioavailability and Pharmacokinetics of Chemopreventive Kaempferol in Rats [J].
Barve, Avantika ;
Chen, Chi ;
Hebbar, Vidya ;
Desiderio, Joseph ;
Saw, Constance Lay-Lay ;
Kong, Ah-Ng .
BIOPHARMACEUTICS & DRUG DISPOSITION, 2009, 30 (07) :356-365
[6]   Protective Effect of Kaempferol on the Transgenic Drosophila Model of Alzheimer's Disease [J].
Beg, Tanveer ;
Jyoti, Smita ;
Naz, Falaq ;
Rahul ;
Ali, Fahad ;
Ali, Syed Kashif ;
Reyad, Ahmed Mohamed ;
Siddique, Yasir Hasan .
CNS & NEUROLOGICAL DISORDERS-DRUG TARGETS, 2018, 17 (06) :421-429
[7]   Dopamine oxidation alters mitochondrial respiration and induces permeability transition in brain mitochondria: Implications for Parkinson's disease [J].
Berman, SB ;
Hastings, TG .
JOURNAL OF NEUROCHEMISTRY, 1999, 73 (03) :1127-1137
[8]   The NLRP3 Inflammasome Pathway: A Review of Mechanisms and Inhibitors for the Treatment of Inflammatory Diseases [J].
Blevins, Hallie M. ;
Xu, Yiming ;
Biby, Savannah ;
Zhang, Shijun .
FRONTIERS IN AGING NEUROSCIENCE, 2022, 14
[9]   Structural mechanism for tyrosine hydroxylase inhibition by dopamine and reactivation by Ser40 phosphorylation [J].
Bueno-Carrasco, Maria Teresa ;
Cuellar, Jorge ;
Flydal, Marte I. ;
Santiago, Cesar ;
Krakenes, Trond-Andre ;
Kleppe, Rune ;
Lopez-Blanco, Jose R. ;
Marcilla, Miguel ;
Teigen, Knut ;
Alvira, Sara ;
Chacon, Pablo ;
Martinez, Aurora ;
Valpuesta, Jose M. .
NATURE COMMUNICATIONS, 2022, 13 (01)
[10]   A Review on the Dietary Flavonoid Kaempferol [J].
Calderon-Montano, J. M. ;
Burgos-Moron, E. ;
Perez-Guerrero, C. ;
Lopez-Lazaro, M. .
MINI-REVIEWS IN MEDICINAL CHEMISTRY, 2011, 11 (04) :298-344