Chronic renal function impairment‐induced cognitive changes and related pathology in mice after unilateral ureteral obstruction (UUO) surgery

突触素 医学 突触蛋白I 海马体 内科学 泌尿科 结扎 认知 肾切除术 病理 内分泌学 外科 免疫组织化学 生物 精神科 小泡 突触小泡 遗传学
作者
YS Ho,Chi‐Fai Lau,Wing‐Yan Tang,Jia‐Yan Tian,Joyce Lee,Susan Yung,Raymond Chuen‐Chung Chang
出处
期刊:Alzheimers & Dementia [Wiley]
卷期号:16 (S3)
标识
DOI:10.1002/alz.047507
摘要

Abstract Background Chronic kidney disease is associated with cognitive impairment. While the pathophysiology remains unclear, it has been suggested that it shares some similarity to those in Alzheimer’s disease. Currently, most studies in this area used the 5/6 nephrectomy and high adenine diet to induce renal impairment in rat or mice. Our group had successfully used the unilateral ureteral obstruction (UUO) mice as an animal model to study the cognitive changes and related pathology. Method Eight‐week‐old male C57BL/6N mice received the UUO operation with double ligation of their left ureter under general anesthesia. Sham operated mice received the same experimental procedure without ureteral obstruction. Cognitive and behavioral tests were performed to examine potential changes in cognition and other behavior 2, 4 or 12 weeks after the surgery. The serum, kidneys and brains were harvested for the detection of systematic inflammation markers and neurodegenerative changes. Result Progressive renal impairment were observed after the UUO surgery. Systematic inflammation was evident by detecting an increase in C‐reactive protein and TNF‐a levels in the UUO mice. These mice also showed a significantly worse performance in the novel object recognition test, Y‐maze test, and puzzle box test when compared to the sham control, indicated cognitive impairment. Reduction in synaptic proteins such as synapsin‐1, synaptophysin, synaptotagmin, PSD95, NMDAR2B and AMPAR, elevation of Nrf2 and 8‐Hydroxyguanosine and hyperphosphorylation of tau were found in their hippocampus. Conclusion We have characterized the cognitive and neuropathological changes in the UUO mice. This mouse model can be used for studying chronic kidney disease‐induced cognitive impairment and may have an implication for understanding the pathogenesis of Alzheimer’s disease.

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