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CSF 氨基酸谱在雄性 Wistar 大鼠脑室内注射链脲佐菌素诱导的散发性阿尔茨海默病中的变化:代谢组学和系统生物学视角。

CSF amino acid profiles in ICV-streptozotocin-induced sporadic Alzheimer's disease in male Wistar rat: a metabolomics and systems biology perspective.

机构信息

Electrophysiology Research Center, Neuroscience Institute, Tehran University of Medical Sciences, Iran.

Department of Human Anatomy and Cell Science, College of Medicine, University of Manitoba, Winnipeg, Canada.

出版信息

FEBS Open Bio. 2024 Jul;14(7):1116-1132. doi: 10.1002/2211-5463.13814. Epub 2024 May 20.

Abstract

Alzheimer's disease (AD) is an increasingly important public health concern due to the increasing proportion of older individuals within the general population. The impairment of processes responsible for adequate brain energy supply primarily determines the early features of the aging process. Restricting brain energy supply results in brain hypometabolism prior to clinical symptoms and is anatomically and functionally associated with cognitive impairment. The present study investigated changes in metabolic profiles induced by intracerebroventricular-streptozotocin (ICV-STZ) in an AD-like animal model. To this end, male Wistar rats received a single injection of STZ (3 mg·kg) by ICV (2.5 μL into each ventricle for 5 min on each side). In the second week after receiving ICV-STZ, rats were tested for cognitive performance using the Morris Water Maze test and subsequently prepared for positron emission tomography (PET) to confirm AD-like symptoms. Tandem Mass Spectrometry (MS/MS) analysis was used to detect amino acid changes in cerebrospinal fluid (CFS) samples. Our metabolomics study revealed a reduction in the concentrations of various amino acids (alanine, arginine, aspartic acid, glutamic acid, glycine, isoleucine, methionine, phenylalanine, proline, serine, threonine, tryptophane, tyrosine, and valine) in CSF of ICV-STZ-treated animals as compared to controls rats. The results of the current study indicate amino acid levels could potentially be considered targets of nutritional and/or pharmacological interventions to interfere with AD progression.

摘要

阿尔茨海默病(AD)是一个日益重要的公共卫生问题,因为在总人口中老年人的比例不断增加。负责大脑能量供应的过程受损是导致衰老过程早期特征的主要原因。限制大脑能量供应会导致大脑在出现临床症状之前出现低代谢,并与认知障碍在解剖和功能上相关。本研究调查了脑室注射链脲佐菌素(ICV-STZ)在 AD 样动物模型中引起的代谢谱变化。为此,雄性 Wistar 大鼠通过 ICV 接受单次 STZ 注射(3mg·kg)(每侧脑室 2.5μL,持续 5min)。在接受 ICV-STZ 后的第二周,大鼠接受 Morris 水迷宫测试以测试认知表现,随后进行正电子发射断层扫描(PET)以确认 AD 样症状。串联质谱(MS/MS)分析用于检测脑脊液(CSF)样本中的氨基酸变化。我们的代谢组学研究表明,与对照组大鼠相比,脑室注射 STZ 处理的动物脑脊液中各种氨基酸(丙氨酸、精氨酸、天冬氨酸、谷氨酸、甘氨酸、异亮氨酸、蛋氨酸、苯丙氨酸、脯氨酸、丝氨酸、苏氨酸、色氨酸、酪氨酸和缬氨酸)的浓度降低。目前的研究结果表明,氨基酸水平可能被认为是营养和/或药物干预的靶点,以干扰 AD 的进展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/131f/11216934/ff34a96d7926/FEB4-14-1116-g005.jpg

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