摘要
背景:胆碱能缺乏的发展被认为是包括阿尔茨海默病在内的许多病理状况的早期征兆。胆碱能功能障碍是与正常衰老和阿尔茨海默病相关的认知衰退的基础。 目的:在这里,我们使用嗅球切除术模型研究了胆碱能神经元功能障碍的可能机制。 方法:雄性小鼠接受嗅球切除术或假手术。三周后,他们在莫里斯水迷宫中接受训练,然后在手术后一个月实施安乐死。使用免疫组织化学、蛋白质印迹和ELISA研究胆碱能指标以及氧化应激指标。使用 RT-qPCR 研究基因表达。 结果:实验治疗之后是水迷宫中标准空间任务的学习受损。这与含有胆碱乙酰转移酶 (ChAT) 的细胞数量减少有关,与内侧隔膜中的神经元总数和海马中较低的 ChAT 酶活性有关。然而,与假手术动物相比,在球根切除小鼠中,ChAT、囊泡 ACh 转运蛋白和乙酰胆碱酯酶的 mRNA 水平保持不变。这些改变之前是蛋白质结合羰基的积累,表明蛋白质的氧化损伤,而核酸的氧化损伤未检测到。 结论:我们假设在嗅球切除模型中,蛋白质的氧化损伤可能导致胆碱能功能障碍,而不是不可逆的神经元损伤。这些数据表明,基底前脑的胆碱能神经元对氧化应激非常敏感,这可能是导致阿尔茨海默病早期认知能力下降的原因
关键词: 嗅球切除术、胆碱能神经元、中隔、氧化应激、羰基、阿尔茨海默病。
Current Alzheimer Research
Title:Oxidative Damage of Proteins Precedes Loss of Cholinergic Phenotype in the Septal Neurons of Olfactory Bulbectomized Mice
Volume: 18 Issue: 14
关键词: 嗅球切除术、胆碱能神经元、中隔、氧化应激、羰基、阿尔茨海默病。
摘要:
Background: The development of cholinergic deficit is considered an early sign of a number of pathological conditions, including Alzheimer’s disease. Cholinergic dysfunction underlies cognitive decline associated with both normal aging and Alzheimer’s disease.
Objective: Here, we studied a possible mechanism of functional impairment of cholinergic neurons using an olfactory bulbectomy model.
Methods: Male mice were subjected to olfactory bulbectomy or sham surgery. Three weeks after that they were trained in Morris water maze and then euthanized one month after surgery. The cholinergic indices as well as the indices of oxidative stress were studied using immunohistochemistry, western blot and ELISA. Gene expression was studied using RT-qPCR.
Results: The experimental treatment was followed by impaired learning of a standard spatial task in a water maze. This was associated with a decrease in the number of cells containing choline acetyltransferase (ChAT), in relation to total number of neurons in the medial septum and lower ChAT enzymatic activity in the hippocampus. However, the levels of mRNAs of ChAT, vesicular ACh transporter and acetylcholine esterase remained unchanged in bulbectomized mice compared to sham-operated animals. These alterations were preceded by the accumulation of protein-bound carbonyls, indicating oxidative damage of proteins, whereas oxidative damage of nucleic acids was not detected.
Conclusion: We assume that in olfactory bulbectomy model, oxidative damage of proteins may cause cholinergic dysfunction rather than irreversible neuronal damage. These data indicate that cholinergic neurons of the basal forebrain are very sensitive to oxidative stress, which may be responsible for the appearance of early cognitive decline in Alzheimer’s disease.
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Cite this article as:
Oxidative Damage of Proteins Precedes Loss of Cholinergic Phenotype in the Septal Neurons of Olfactory Bulbectomized Mice, Current Alzheimer Research 2021; 18 (14) . https://dx.doi.org/10.2174/1567205019666211223094051
DOI https://dx.doi.org/10.2174/1567205019666211223094051 |
Print ISSN 1567-2050 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-5828 |
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