Yu Yeon Hee, Kim Seong-Wook, Park Dae-Kyoon, Song Ho-Yeon, Kim Duk-Soo, Gil Hyo-Wook
Department of Anatomy, College of Medicine, Soonchunhyang University, Cheonan-si 31151, Korea.
Graduate School of New Drug Discovery & Development, Chungnam National University, Daejeon 34134, Korea.
Brain Sci. 2021 Jun 30;11(7):882. doi: 10.3390/brainsci11070882.
Increased prevalence of chronic kidney disease (CKD) and neurological disorders including cerebrovascular disease, cognitive impairment, peripheral neuropathy, and dysfunction of central nervous system have been reported during the natural history of CKD. Psychological distress and depression are serious concerns in patients with CKD. However, the relevance of CKD due to decline in renal function and the pathophysiology of emotional deterioration is not clear. Male Sprague Dawley rats were divided into three groups: sham control, 5/6 nephrectomy at 4 weeks, and 5/6 nephrectomy at 10 weeks. Behavior tests, local field potentials, and histology and laboratory tests were conducted and investigated. We provided direct evidence showing that CKD rat models exhibited anxiogenic behaviors and depression-like phenotypes, along with altered hippocampal neural oscillations at 1-12 Hz. We generated CKD rat models by performing 5/6 nephrectomy, and identified higher level of serum creatinine and blood urea nitrogen (BUN) in CKD rats than in wild-type, depending on time. In addition, the level of α-smooth muscle actin (α-SMA) and collagen I for renal tissue was markedly elevated, with worsening fibrosis due to renal failures. The level of anxiety and depression-like behaviors increased in the 10-week CKD rat models compared with the 4-week rat models. In the recording of local field potentials, the power of delta (1-4 Hz), theta (4-7 Hz), and alpha rhythm (7-12 Hz) was significantly increased in the hippocampus of CKD rats compared with wild-type rats. Together, our findings indicated that anxiogenic behaviors and depression can be induced by CKD, and these abnormal symptoms can be worsened as the onset of CKD was prolonged. In conclusion, our results show that the hippocampus is vulnerable to uremia.
慢性肾脏病(CKD)自然病程中,慢性肾脏病及包括脑血管疾病、认知障碍、周围神经病变和中枢神经系统功能障碍在内的神经疾病患病率均有所上升。心理困扰和抑郁是慢性肾脏病患者的严重问题。然而,肾功能下降所致慢性肾脏病与情绪恶化的病理生理学之间的相关性尚不清楚。将雄性斯普拉格-道利大鼠分为三组:假手术对照组、4周龄时进行5/6肾切除术组和10周龄时进行5/6肾切除术组。进行并研究了行为测试、局部场电位、组织学和实验室检查。我们提供了直接证据表明,慢性肾脏病大鼠模型表现出焦虑行为和抑郁样表型,同时伴有1-12赫兹的海马神经振荡改变。我们通过实施5/6肾切除术建立了慢性肾脏病大鼠模型,并确定慢性肾脏病大鼠血清肌酐和血尿素氮(BUN)水平高于野生型大鼠,且与时间有关。此外,肾组织的α平滑肌肌动蛋白(α-SMA)和I型胶原水平显著升高,肾衰竭导致纤维化加重。与4周龄大鼠模型相比,10周龄慢性肾脏病大鼠模型的焦虑和抑郁样行为水平有所增加。在局部场电位记录中,与野生型大鼠相比,慢性肾脏病大鼠海马区的δ波(1-4赫兹)、θ波(4-7赫兹)和α节律(7-12赫兹)功率显著增加。总之,我们的研究结果表明,慢性肾脏病可诱发焦虑行为和抑郁,且随着慢性肾脏病发病时间延长,这些异常症状会加重。总之,我们的结果表明海马对尿毒症敏感。