The regulation of miRNAs using curcumin and other polyphenols during the prevention and treatment of Alzheimer's disease

被引:3
作者
Wang, Xiyun [1 ]
Zhang, Sale [2 ]
Li, Ying [2 ]
Zhang, Yu [2 ]
机构
[1] Zhejiang Prov Peoples Hosp, Tiantai Peoples Hosp Zhejiang Prov,Tiantai Branch, Hangzhou Med Coll, Dept Neurol, Taizhou, Zhejiang, Peoples R China
[2] Xian Peihua Univ, Med Coll, Xian 710125, Shaanxi, Peoples R China
关键词
miRNAs; curcumin; polyphenols; Alzheimer's disease; TAU HYPERPHOSPHORYLATION; MICRORNA EXPRESSION; A-BETA; RESVERATROL; BRAIN; ACTIVATION; MEMORY; MODEL; DICER; NEURODEGENERATION;
D O I
10.1093/hmg/ddae154
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Alzheimer's disease (AD), a prevalent neurodegenerative disorder, predominantly affects individuals over the age of 65 and poses significant challenges in terms of effective management and treatment. The disease's pathogenesis involves complex molecular pathways including misfolded proteins accumulation, neuroinflammation, and synaptic dysfunction. Recent insights have highlighted the role of microRNAs (miRNAs) as critical regulators within these pathways, where they influence gene expression and contribute to the pathophysiological landscape of AD. Notably, emerging research has demonstrated that polyphenols, including curcumin, might modulate miRNA activity, thus offering a novel approach to mitigate AD symptoms and progression. This review explores the potential mechanisms through which polyphenols regulate miRNA expression and activity, specifically focusing on autophagy enhancement and inflammation reduction in the context of AD. We provide a detailed examination of key studies linking miRNA dysregulation to AD pathogenesis and discuss how polyphenols might correct these aberrations. The findings presented here underscore the therapeutic potential of polyphenols in AD treatment via miRNA modulation, pointing to new directions in disease management strategies and highlighting the need for targeted research into miRNA-based interventions. [GRAPHICS]
引用
收藏
页码:117 / 127
页数:11
相关论文
共 78 条
[11]   Age-dependent neuron loss is associated with impaired adult neurogenesis in forebrain neuron-specific Dicer conditional knockout mice [J].
Cheng, Shanshan ;
Zhang, Chen ;
Xu, Congyu ;
Wang, Long ;
Zou, Xiaoxia ;
Chen, Guiquan .
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 2014, 57 :186-196
[12]   miRNAs as Influencers of Cell-Cell Communication in Tumor Microenvironment [J].
Conti, Ilaria ;
Varano, Gabriele ;
Simioni, Carolina ;
Laface, Ilaria ;
Milani, Daniela ;
Rimondi, Erika ;
Neri, Luca M. .
CELLS, 2020, 9 (01)
[13]   Amyloid Aggregation of hIAPP, Aβ, and Calcitonin Altered by a Curcumin Derivative [J].
Cox, Sarah J. ;
Camargo, Diana C. Rodriguez ;
Lee, Young-Ho ;
Reif, Bernd ;
Ivanova, Magdalena ;
Ramamoorthy, Ayyalusamy .
BIOPHYSICAL JOURNAL, 2018, 114 (03) :226A-226A
[14]   Conditional loss of Dicer disrupts cellular and tissue morphogenesis in the cortex and hippocampus [J].
Davis, Tigwa H. ;
Cuellar, Trinna L. ;
Koch, Selina M. ;
Barker, Allison J. ;
Harfe, Brian D. ;
McManus, Michael T. ;
Ullian, Erik M. .
JOURNAL OF NEUROSCIENCE, 2008, 28 (17) :4322-4330
[15]   Modulation of Amyloid β-Induced Microglia Activation and Neuronal Cell Death by Curcumin and Analogues [J].
De Lorenzi, Ersilia ;
Franceschini, Davide ;
Contardi, Cecilia ;
Di Martino, Rita Maria Concetta ;
Seghetti, Francesca ;
Serra, Massimo ;
Bisceglia, Federica ;
Pagetta, Andrea ;
Zusso, Morena ;
Belluti, Federica .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2022, 23 (08)
[16]   Microglia receptors and their implications in the response to amyloid β for Alzheimer's disease pathogenesis [J].
Doens, Deborah ;
Fernandez, Patricia L. .
JOURNAL OF NEUROINFLAMMATION, 2014, 11
[17]   Effects of quercetin-conjugated with superparamagnetic iron oxide nanoparticles on learning and memory improvement through targeting microRNAs/NF-κB pathway [J].
Ebrahimpour, Shiva ;
Esmaeili, Abolghasem ;
Dehghanian, Fariba ;
Beheshti, Siamak .
SCIENTIFIC REPORTS, 2020, 10 (01)
[18]   MicroRNA-132 provides neuroprotection for tauopathies via multiple signaling pathways [J].
El Fatimy, Rachid ;
Li, Shaomin ;
Chen, Zhicheng ;
Mushannen, Tasnim ;
Gongala, Sree ;
Wei, Zhiyun ;
Balu, Darrick T. ;
Rabinovsky, Rosalia ;
Cantlon, Adam ;
Elkhal, Abdallah ;
Selkoe, Dennis J. ;
Sonntag, Kai C. ;
Walsh, Dominic M. ;
Krichevsky, Anna M. .
ACTA NEUROPATHOLOGICA, 2018, 136 (04) :537-555
[19]   Quercetin disrupts tyrosine-phosphorylated phosphatidylinositol 3-kinase and myeloid differentiation factor-88 association, and inhibits MAPK/AP-1 and IKK/NF-κB-induced inflammatory mediators production in RAW 264.7 cells [J].
Endale, Mehari ;
Park, Seung-Chun ;
Kim, Suk ;
Kim, Seung-Hyung ;
Yang, Yanyan ;
Cho, Jae Youl ;
Rhee, Man Hee .
IMMUNOBIOLOGY, 2013, 218 (12) :1452-1467
[20]   Microglial activation in early Alzheimer trajectory is associated with higher gray matter volume [J].
Femminella, Grazia Daniela ;
Dani, Melanie ;
Wood, Melanie ;
Fan, Zhen ;
Calsolaro, Valeria ;
Atkinson, Rebecca ;
Edginton, Trudi ;
Hinz, Rainer ;
Brooks, David J. ;
Edison, Paul .
NEUROLOGY, 2019, 92 (12) :E1331-E1343