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全脑缺血再灌注损伤后诱导的高同型半胱氨酸血症与大鼠皮质神经元阿尔茨海默病样神经退行性变的关系。

Association of Induced Hyperhomocysteinemia with Alzheimer's Disease-Like Neurodegeneration in Rat Cortical Neurons After Global Ischemia-Reperfusion Injury.

机构信息

Jessenius Faculty of Medicine in Martin, Institute of Histology and Embryology, Comenius University in Bratislava, Martin, Slovakia.

BioMed, Division of Oncology, Jessenius Faculty of Medicine in Martin, Comenius University in Bratislava, Martin, Slovakia.

出版信息

Neurochem Res. 2018 Sep;43(9):1766-1778. doi: 10.1007/s11064-018-2592-x. Epub 2018 Jul 12.

Abstract

Alzheimer's disease (AD) is a progressive and irreversible neurodegenerative disorder that results in massive hippocampal and neocortical neuronal loss leading to dementia and eventual death. The exact cause of Alzheimer's disease is not fully explored, although a number of risk factors have been recognized, including high plasma concentration of homocysteine (Hcy). Hyperhomocysteinemia (hHcy) is considered a strong, independent risk factor for stroke and dementia. However, the molecular background underlying these mechanisms linked with hHcy and ischemic stroke is not fully understood. Paper describes rat model of global forebrain ischemia combined with the experimentally induced hHcy. Global ischemia-reperfusion injury (IRI) was developed by 4-vessels occlusion lasting for 15 min followed by reperfusion period of 72 h. hHcy was induced by subcutaneous injection of 0.45 µmol/g of Hcy in duration of 14 days. The results showed remarkable neural cell death induced by hHcy in the brain cortex and neurodegeneration is further aggravated by global IRI. We demonstrated degeneration of cortical neurons, alterations in number and morphology of tissue astrocytes and dysregulation of oxidative balance with increased membrane protein oxidation. Complementary to, an immunohistochemical analysis of tau protein and β-amyloid peptide showed that combination of hHcy with the IRI might lead to the progression of AD-like pathological features. Conclusively, these findings suggest that combination of risk factor hHcy with IRI aggravates neurodegeneration processes and leads to development of AD-like pathology in cerebral cortex.

摘要

阿尔茨海默病(AD)是一种进行性和不可逆的神经退行性疾病,导致大量海马和新皮质神经元丢失,导致痴呆和最终死亡。尽管已经认识到许多危险因素,包括同型半胱氨酸(Hcy)的血浆浓度高,但阿尔茨海默病的确切原因尚未完全探索。高同型半胱氨酸血症(hHcy)被认为是中风和痴呆的强烈独立危险因素。然而,与 hHcy 和缺血性中风相关的这些机制的分子背景尚不完全清楚。本文描述了结合实验诱导的 hHcy 的大鼠全脑缺血模型。通过持续 15 分钟的 4 血管闭塞来建立全脑缺血再灌注损伤(IRI),然后进行 72 小时的再灌注期。通过皮下注射 0.45µmol/g 的 Hcy 持续 14 天来诱导 hHcy。结果显示,hHcy 可引起大脑皮质明显的神经细胞死亡,全脑 IRI 进一步加重神经退行性变。我们证明了皮质神经元的退化,组织星形胶质细胞数量和形态的改变以及氧化平衡失调,膜蛋白氧化增加。作为补充,tau 蛋白和 β-淀粉样肽的免疫组织化学分析表明,hHcy 与 IRI 的结合可能导致 AD 样病理特征的进展。总之,这些发现表明,危险因素 hHcy 与 IRI 的结合加重了神经退行性过程,并导致大脑皮质出现 AD 样病理学。

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