Challenges for Alzheimer's Disease Therapy: Insights from Novel Mechanisms Beyond Memory Defects

被引:139
作者
Frozza, Rudimar L. [1 ]
Lourenco, Mychael V. [2 ,3 ]
De Felice, Fernanda G. [2 ,4 ]
机构
[1] Fundacao Oswaldo Cruz FIOCRUZ, Inst Oswaldo Cruz, Rio De Janeiro, Brazil
[2] Inst Med Biochem Leopoldo Meis, Rio De Janeiro, Brazil
[3] Univ Fed Rio de Janeiro, Inst Biophys Carlos Chagas Filho, Rio De Janeiro, Brazil
[4] Queens Univ, Dept Biomed & Mol Sci, Ctr Neurosci Studies, Kingston, ON, Canada
关键词
Alzheimer'sdisease; inflammation; metabolic derangements; memory defects; preclinical; therapy; AMYLOID-BETA-PROTEIN; ENDOPLASMIC-RETICULUM STRESS; RECEPTOR-DEPENDENT MECHANISM; IMPAIR SYNAPTIC PLASTICITY; GROWTH-FACTOR EXPRESSION; DEPRESSIVE-LIKE BEHAVIOR; CENTRAL-NERVOUS-SYSTEM; A-BETA; INSULIN-RESISTANCE; MOUSE MODEL;
D O I
10.3389/fnins.2018.00037
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Alzheimer's disease (AD), the most common form of dementia in late life, will become even more prevalent by midcentury, constituting a major global health concern with huge implications for individuals and society. Despite scientific breakthroughs during the past decades that have expanded our knowledge on the cellular and molecular bases of AD, therapies that effectively halt disease progression are still lacking, and focused efforts are needed to address this public health challenge. Because AD is classically recognized as a disease of memory, studies have mainly focused on investigating memory-associated brain defects. However, compelling evidence has indicated that additional brain regions, not classically linked to memory, are also affected in the course of disease. In this review, we outline the current understanding of key pathophysiological mechanisms in AD and their clinical manifestation. We also highlight how considering the complex nature of AD pathogenesis, and exploring repurposed drug approaches can pave the road toward the development of novel therapeutics for AD.
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页数:13
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共 201 条
[1]   Relationship Between β-Secretase, Inflammation and Core Cerebrospinal Fluid Biomarkers for Alzheimer's Disease [J].
Alcolea, Daniel ;
Carmona-Iragui, Maria ;
Suarez-Calvet, Marc ;
Belen Sanchez-Saudinos, M. ;
Sala, Isabel ;
Anton-Aguirre, Sofia ;
Blesa, Rafael ;
Clarimon, Jordi ;
Fortea, Juan ;
Lleo, Alberto .
JOURNAL OF ALZHEIMERS DISEASE, 2014, 42 (01) :157-167
[2]  
Alzheimers Association, 2017, Alzheimers Dementia, V13, P325, DOI 10.1016/j.jalz.2017.02.001
[3]   Detection and Identification of Bioanalytes with High Resolution LSPR Spectroscopy and MALDI Mass Spectrometry [J].
Anker, Jeffrey N. ;
Hall, W. Paige ;
Lambert, Mary P. ;
Velasco, Pauline T. ;
Mrksich, Milan ;
Klein, William L. ;
Van Duyne, Richard P. .
JOURNAL OF PHYSICAL CHEMISTRY C, 2009, 113 (15) :5891-5894
[4]   Discovering New Treatments for Alzheimer's Disease by Repurposing Approved Medications [J].
Appleby, Brian S. ;
Cummings, Jeffrey L. .
CURRENT TOPICS IN MEDICINAL CHEMISTRY, 2013, 13 (18) :2306-2327
[5]   Low-Grade Hypothalamic Inflammation Leads to Defective Thermogenesis, Insulin Resistance, and Impaired Insulin Secretion [J].
Arruda, Ana Paula ;
Milanski, Marciane ;
Coope, Andressa ;
Torsoni, Adriana S. ;
Ropelle, Eduardo ;
Carvalho, Denise P. ;
Carvalheira, Jose B. ;
Velloso, Licio A. .
ENDOCRINOLOGY, 2011, 152 (04) :1314-1326
[6]   Axonally Synthesized ATF4 Transmits a Neurodegenerative Signal across Brain Regions [J].
Baleriola, Jimena ;
Walker, Chandler A. ;
Jean, Ying Y. ;
Crary, John F. ;
Troy, Carol M. ;
Nagy, Peter L. ;
Hengst, Ulrich .
CELL, 2014, 158 (05) :1159-1172
[7]   The Hypothalamus in Alzheimer's Disease: A Golgi and Electron Microscope Study [J].
Baloyannis, Stavros J. ;
Mavroudis, Ioannis ;
Mitilineos, Demetrios ;
Baloyannis, Ioannis S. ;
Costa, Vassiliki G. .
AMERICAN JOURNAL OF ALZHEIMERS DISEASE AND OTHER DEMENTIAS, 2015, 30 (05) :478-487
[8]   PD-1 immune checkpoint blockade reduces pathology and improves memory in mouse models of Alzheimer's disease [J].
Baruch, Kuti ;
Deczkowska, Aleksandra ;
Rosenzweig, Neta ;
Tsitsou-Kampeli, Afroditi ;
Sharif, Alaa Mohammad ;
Matcovitch-Natan, Orit ;
Kertser, Alexander ;
David, Eyal ;
Amit, Ido ;
Schwartz, Michal .
NATURE MEDICINE, 2016, 22 (02) :135-137
[9]   Breaking immune tolerance by targeting Foxp3+ regulatory T cells mitigates Alzheimer's disease pathology [J].
Baruch, Kuti ;
Rosenzweig, Neta ;
Kertser, Alexander ;
Deczkowska, Aleksandra ;
Sharif, Alaa Mohammad ;
Spinrad, Amit ;
Tsitsou-Kampeli, Afroditi ;
Sarel, Ayelet ;
Cahalon, Liora ;
Schwartz, Michal .
NATURE COMMUNICATIONS, 2015, 6
[10]   Clinical and Biomarker Changes in Dominantly Inherited Alzheimer's Disease [J].
Bateman, Randall J. ;
Xiong, Chengjie ;
Benzinger, Tammie L. S. ;
Fagan, Anne M. ;
Goate, Alison ;
Fox, Nick C. ;
Marcus, Daniel S. ;
Cairns, Nigel J. ;
Xie, Xianyun ;
Blazey, Tyler M. ;
Holtzman, David M. ;
Santacruz, Anna ;
Buckles, Virginia ;
Oliver, Angela ;
Moulder, Krista ;
Aisen, Paul S. ;
Ghetti, Bernardino ;
Klunk, William E. ;
McDade, Eric ;
Martins, Ralph N. ;
Masters, Colin L. ;
Mayeux, Richard ;
Ringman, John M. ;
Rossor, Martin N. ;
Schofield, Peter R. ;
Sperling, Reisa A. ;
Salloway, Stephen ;
Morris, John C. .
NEW ENGLAND JOURNAL OF MEDICINE, 2012, 367 (09) :795-804