Are Retinoids a Promise for Alzheimer's Disease Management?

被引:0
|
作者
Carratu, M. R.
Marasco, C.
Signorile, A. [1 ]
Scuderi, C. [2 ]
Steardo, L. [2 ]
机构
[1] Univ Bari Aldo Moro, Dept Basic Med Sci, Sect Med Biochem, I-70124 Bari, Italy
[2] Univ Roma La Sapienza, Dept Physiol & Pharmacol V Erspamer, I-00185 Rome, Italy
关键词
Alzheimer's disease; retinoid; cognitive decline; oxidative stress; amyloid cascade; secretases; mitochondrial dysfunction; neuroinflammation; cerebral microvessels; neuroprotection; therapeutic strategy; AMYLOID PRECURSOR PROTEIN; ENDOPLASMIC-RETICULUM STRESS; IL-1-INDUCED IL-6 PRODUCTION; RELATIONAL MEMORY DEFICIT; VITAMIN-A; ADULT-RAT; GENE-EXPRESSION; MITOCHONDRIAL ABNORMALITIES; SUBVENTRICULAR ZONE; OXIDATIVE STRESS;
D O I
暂无
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
Retinoids regulate several physiological and pathological processes through the interaction with nuclear receptors. Retinoid-associated signaling which plays an essential role in neurodevelopment appears to remain active in the adult central nervous system (CNS), thus assuming a high significance in the context of neurodegeneration, and indeed retinoid analogs are thought to be promising therapeutic agents for the treatment of neurodegenerative disorders. The ability of retinoids to exert antioxidant effects, inhibit amyloid-beta(A beta) deposits and likely A beta-induced mitochondrial dysfunction, tau hyperphosphorylation, A beta-induced IL6 production and neuroinflammation, increase survival in hippocampal neurons, and reverse cognitive deficits in animal models of Alzheimer's disease (AD) is discussed. Although retinoids with their multi-target activity are revealing to be promising for management of AD which is a multifaceted biochemical phenomenon, timing as well as appropriate dosage and safety remain, however, a challenge. The end-stage lesions, namely senile plaques and neurofibrillary tangles, are, at present, considered an adaptive response to oxidative stress underlying AD, thus paradoxically late administration of retinoids could even suppress a protective mechanism by inhibiting A beta deposits.
引用
收藏
页码:6119 / 6125
页数:7
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