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用一种神经营养化合物抑制老年大鼠和3xTg-AD小鼠的AMD样病理

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

作者信息

Liu Yinghua, Wei Wei, Baazaoui Narjes, Liu Fei, Iqbal Khalid

机构信息

Department of Neurochemistry, Inge Grundke-Iqbal Research Floor, New York State Institute for Basic Research in Developmental Disabilities, Staten Island, NY, United States.

Department of Pharmacology, School of Pharmaceutical Sciences, Guangzhou Medical University, Guangzhou, China.

出版信息

Front Aging Neurosci. 2019 Nov 19;11:309. doi: 10.3389/fnagi.2019.00309. eCollection 2019.

Abstract

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, Aβ/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.

摘要

年龄相关性黄斑变性(AMD)在晚期会导致视力丧失,是老年人中最常见的神经退行性疾病之一。然而,迄今为止,尚无有效的药物疗法可用于预防AMD。在此,我们报告了在老年大鼠和3xTg-AD小鼠中,通过用神经营养肽能化合物P021进行长期治疗,AMD病理的发生情况及其预防作用。我们发现视网膜色素上皮(RPE)以及布鲁赫膜(BM)增厚处出现光感受器退化、脂褐素颗粒、空泡和萎缩;在老年大鼠中,我们甚至发现了玫瑰花结样结构的形成。在不同的视网膜层中观察到了小胶质细胞增生和星形胶质细胞增生。此外,我们还发现总tau蛋白、磷酸化tau蛋白、Aβ/APP和血管内皮生长因子(VEGF)在老年大鼠和3xTg小鼠的视网膜下广泛分布。重要的是,在大鼠中用P021进行3个月的长期治疗以及在3xTg小鼠中进行18个月的长期治疗,改善了上述病理变化。这些发现表明P021在预防和治疗AMD以及与衰老和阿尔茨海默病相关的视网膜变化方面具有治疗潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f833/6877482/a6cb5a2aaf96/fnagi-11-00309-g0001.jpg

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