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慢性肾脏病中嘌呤核苷酸代谢紊乱是认知障碍的一个危险因素。

Disturbed purine nucleotide metabolism in chronic kidney disease is a risk factor for cognitive impairment.

机构信息

Cellular & Molecular Neurobiology Laboratory, Department of Life Science and Bioinformatics, Assam University, P.O. Dorgakona, Cachar, Silchar 788011, Assam, India.

Cellular & Molecular Neurobiology Laboratory, Department of Life Science and Bioinformatics, Assam University, P.O. Dorgakona, Cachar, Silchar 788011, Assam, India.

出版信息

Med Hypotheses. 2018 Feb;111:36-39. doi: 10.1016/j.mehy.2017.12.016. Epub 2017 Dec 13.

Abstract

Chronic kidney disease (CKD) is an increasing global health burden. Disturbance in purine metabolism pathway and a higher level of serum uric acid, called hyperuricemia, is a risk factor of CKD, and it has been linked to increased prevalence and progression of the disease. In a recent study, it has been demonstrated that purine nucleotides and uric acid alter the activity of acetylcholinesterase (AChE). Thus, we hypothesize that adenine, hypoxanthine, xanthine, 2,8-dihydroxyadenine and uric acid may potentially interfere with the activity of AChE. The hypothesis has been tested using computational tools. Uric acid has been found to be the most potent inhibitor of AChE, with a binding affinity higher than the known inhibitors of the enzyme. Further, since depleted AChE activity is associated with dementia and cognitive impairment, the present study suggest that disturbed purine nucleotide metabolism in CKD is a risk factor for cognitive impairment.

摘要

慢性肾脏病(CKD)是一个日益严重的全球健康负担。嘌呤代谢途径紊乱和血清尿酸水平升高(称为高尿酸血症)是 CKD 的一个危险因素,并且与疾病的患病率和进展增加有关。在最近的一项研究中,已经证明嘌呤核苷酸和尿酸会改变乙酰胆碱酯酶(AChE)的活性。因此,我们假设腺嘌呤、次黄嘌呤、黄嘌呤、2,8-二羟腺嘌呤和尿酸可能会潜在地干扰 AChE 的活性。这一假设已经使用计算工具进行了测试。已经发现尿酸是 AChE 的最有效抑制剂,其结合亲和力高于该酶的已知抑制剂。此外,由于 AChE 活性的耗竭与痴呆和认知障碍有关,因此本研究表明 CKD 中嘌呤核苷酸代谢紊乱是认知障碍的一个危险因素。

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