Inhibition of AMD-Like Pathology With a Neurotrophic Compound in Aged Rats and 3xTg-AD Mice

被引:10
|
作者
Liu, Yinghua [1 ,2 ,3 ]
Wei, Wei [1 ,4 ]
Baazaoui, Narjes [1 ]
Liu, Fei [1 ]
Iqbal, Khalid [1 ]
机构
[1] New York State Inst Basic Res Dev Disabil, Dept Neurochem, Inge Grundke Iqbal Res Floor,1050 Forest Hill Rd, Staten Isl, NY 10314 USA
[2] Guangzhou Med Univ, Sch Pharmaceut Sci, Dept Pharmacol, Guangzhou, Guangdong, Peoples R China
[3] Guangzhou Med Univ, Affiliated Hosp 5, Key Lab Mol Clin Pharmacol, Guangzhou, Guangdong, Peoples R China
[4] Sch Med, Inst Brain Res, Dept Pathophysl, Key Lab State Adm Tradit Chinese Med China, Jinan, Shandong, Peoples R China
来源
关键词
age-related macular degeneration; Alzheimer's disease; retina; neurotrophic peptidergic compound P021; prevention of AMD; aged rats; 3xTg-mice; RETINAL-PIGMENT EPITHELIUM; AMYLOID PRECURSOR PROTEIN; ENDOTHELIAL GROWTH-FACTOR; TRANSGENIC MOUSE MODEL; SUB-RPE DEPOSITS; MACULAR DEGENERATION; ALZHEIMERS-DISEASE; CHOROIDAL NEOVASCULARIZATION; FUNDUS AUTOFLUORESCENCE; SYNAPTIC PLASTICITY;
D O I
10.3389/fnagi.2019.00309
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Age-associated macular degeneration (AMD), which leads to loss of vision at its end stage, is one of the most common neurodegenerative diseases among the elderly. However, to date, no effective drug therapy is available for the prevention of AMD. Here, we report the occurrence of AMD pathology and its prevention by chronic treatment with the neurotrophic peptidergic compound P021, in aged rats and 3xTg-AD mice. We found photoreceptor degeneration, lipofuscin granules, vacuoles, and atrophy in retinal pigment epithelium (RPE) as well as Bruch's membrane (BM) thickening; in aged rats, we even found rosette-like structure formation. Microgliosis and astrogliosis were observed in different retinal layers. In addition, we also found that total tau, phosphorylated tau, A beta/APP, and VEGF were widely distributed in the sub-retina of aged rats and 3xTg mice. Importantly, chronic treatment with P021 for 3 months in rats and for 18 months in 3xTg mice ameliorated the pathological changes above. These findings indicate the therapeutic potential of P021 for prevention and treatment of AMD and retinal changes associated with aging and Alzheimer's disease.
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页数:18
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