Department of Anatomy and Laboratory of Neuroscience and Tissue Engineering, Basic Medical College, Chongqing Medical University, Chongqing, China; Department of Pharmacology, School of Basic Medical Sciences, And State Key Laboratory of Vascular Homeostasis and Remodeling, Peking University, Beijing, China.
Department of Pharmacology, School of Basic Medical Sciences, And State Key Laboratory of Vascular Homeostasis and Remodeling, Peking University, Beijing, China.
Eur J Pharmacol. 2023 Oct 15;957:175905. doi: 10.1016/j.ejphar.2023.175905. Epub 2023 Aug 26.
Chronic kidney disease (CKD) with anxiety disorder is of a great concern due to its high morbidity and mortality. Urea, as an important toxin in CKD, is not only a pathological factor for complications in patients with CKD, but also is accumulated in the brain of aging and neurodegenerative diseases. However, the pathological role and underlying regulatory mechanism of urea in CKD related mood disorders have not been well established. We previously reported a depression phenotype in mice with abnormal urea metabolism. Since patients with depression are more likely to suffer from anxiety, we speculate that high urea may be an important factor causing anxiety in CKD patients. In adenine-induced CKD mouse model and UT-B mouse model, multiple behavioral studies confirmed that high urea induces anxiety-like behavior. Single-cell transcriptome revealed that down-regulation of Egr1 induced compensatory proliferation of oligodendrocyte progenitor cells (OPC). Myelin-related signaling pathways of oligodendrocytes (OL) were change significant in the urea accumulation amygdala. The study showed that high urea downregulated Egr1 with subsequent upregulation of ERK pathways in OPCs. These data indicate that the pathological role and molecular mechanism of high urea in CKD-related anxiety, and provide objective serological indicator and a potential new drug target for the prevention and treatment of anxiety in CKD patients.
慢性肾脏病(CKD)伴焦虑症发病率和死亡率均较高,值得关注。尿素作为 CKD 患者并发症的重要病理因子,不仅在 CKD 患者中积累,而且在衰老和神经退行性疾病的大脑中积累。然而,尿素在 CKD 相关情绪障碍中的病理作用和潜在调节机制尚未得到很好的建立。我们之前报道了尿素代谢异常的小鼠出现抑郁表型。由于抑郁症患者更容易患焦虑症,我们推测高尿素可能是导致 CKD 患者焦虑的一个重要因素。在腺嘌呤诱导的 CKD 小鼠模型和 UT-B 小鼠模型中,多项行为研究证实高尿素可诱导焦虑样行为。单细胞转录组分析显示,Egr1 的下调可诱导少突胶质前体细胞(OPC)的代偿性增殖。尿素积累的杏仁核中少突胶质细胞(OL)的髓鞘相关信号通路发生显著变化。研究表明,高尿素可下调 OPC 中的 Egr1,随后上调 ERK 通路。这些数据表明,高尿素在 CKD 相关焦虑中的病理作用和分子机制,并为 CKD 患者焦虑的预防和治疗提供了客观的血清学指标和潜在的新药物靶点。