Watanabe Kimio, Sato Emiko, Mishima Eikan, Watanabe Mayu, Abe Takaaki, Takahashi Nobuyuki, Nakayama Masaaki
Department of Nephrology, Hypertension, Diabetology, Endocrinology and Metabolism, Fukushima Medical University School of Medicine, Fukushima, 960-1295, Japan.
Department of Blood Purification, Tohoku University Graduate School of Medicine, Sendai, 980-8575, Japan.
Heliyon. 2021 Feb 10;7(2):e06221. doi: 10.1016/j.heliyon.2021.e06221. eCollection 2021 Feb.
One third of the patients with chronic kidney disease (CKD) develop cognitive impairment, which is also an independent risk factor for mortality. However, the concise mechanism of cerebro-renal interaction has not been clarified. The present study examines the effects of uremic toxins on neuronal cells and analyzes the pathological condition of the brain using mouse hippocampal neuronal HT-22 cells and adenine-induced CKD model rats. Among the uremic toxins analyzed, indoxyl sulfate, indole, 3-indoleacetate, and methylglyoxal significantly decreased viability and glutathione level in HT-22 cells. The mixture of these uremic toxins also decreased viability and glutathione level at a lower dose. Adenine-induced CKD rat showed marked renal damage, increased urinary oxidative stress markers, and increased numbers of pyknotic neuronal cells in hippocampus. CKD rats with damaged hippocampus demonstrated poor learning process when tested using the Morris water maze test. Our results suggest that uremic toxins have a toxic effect on hippocampal neuronal cells and uremic CKD rats shows pyknosis in hippocampus.
三分之一的慢性肾脏病(CKD)患者会出现认知障碍,这也是死亡率的一个独立危险因素。然而,脑-肾相互作用的确切机制尚未阐明。本研究使用小鼠海马神经元HT-22细胞和腺嘌呤诱导的CKD模型大鼠,研究了尿毒症毒素对神经元细胞的影响,并分析了大脑的病理状况。在所分析的尿毒症毒素中,硫酸吲哚酚、吲哚、3-吲哚乙酸和甲基乙二醛显著降低了HT-22细胞的活力和谷胱甘肽水平。这些尿毒症毒素的混合物在较低剂量时也降低了活力和谷胱甘肽水平。腺嘌呤诱导的CKD大鼠表现出明显的肾损伤、尿氧化应激标志物增加以及海马中固缩神经元细胞数量增加。使用莫里斯水迷宫试验测试时,海马受损的CKD大鼠表现出较差的学习过程。我们的结果表明,尿毒症毒素对海马神经元细胞有毒性作用,尿毒症CKD大鼠海马出现固缩。