• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

金属毒性及其与阿尔茨海默病中基因表达的关系。

Metals toxicity and its correlation with the gene expression in Alzheimer's disease.

机构信息

Forensic Medicine & Toxicology Department, King George's Medical University, Lucknow, Uttar Pradesh, 226003, India.

Biochemistry Department, KGMU, Lucknow, India.

出版信息

Mol Biol Rep. 2021 Apr;48(4):3245-3252. doi: 10.1007/s11033-021-06386-x. Epub 2021 May 10.

DOI:10.1007/s11033-021-06386-x
PMID:33970397
Abstract

Alzheimer's disease is a common neurodegenerative disease in the elderly population and a leading cause of dementia. Genetics and environmental risk factors were considered to play a major role in the onset of the disease. This study aimed to examine the correlation between different metals levels and the gene expression in Alzheimer's patients with age-matched control subjects. Non- essential metals were measured in the whole blood due to its higher concentration in red blood corpuscles (RBCs) and essential biometals in the serum samples of Alzheimer's disease (AD) by using Inductively coupled plasma optical emission spectroscopy (ICP-OES) that allows the analysis and detection of the different elements at low levels. Gene expression level was performed by quantitative real-time PCR (qRT-PCR). In this study, the levels of Lead and Arsenic metals were not detected in the AD patient samples. Cadmium, Mercury, and Aluminum were found higher in cases as compared to controls with 0.009240 ± 0.0007707 (P =  < 0.0001), 0.02332 ± 0.001041 (P =  < 0.0001), and 0.09222 ± 0.02804 (P = 0.0087) respectively. Essential biometal like copper was higher 0.1274 ± 0.02453 (P = 0.0254) in cases, while iron 0.1117 ± 0.009599 (P = 0.0304) and zinc 0.03800 ± 0.003462 mg/L were found significantly lower as compared to controls. All targeted genes such as APP, PSEN1, PSEN2, and APOE4 were found up-regulated in AD patients. We concluded that there was no significant correlation between metals dyshomeostasis and gene expressions in this study.

摘要

阿尔茨海默病是老年人中常见的神经退行性疾病,也是痴呆症的主要原因。遗传和环境风险因素被认为在疾病的发生中起主要作用。本研究旨在检查不同金属水平与年龄匹配的对照组阿尔茨海默病患者基因表达之间的相关性。由于全血中红细胞(RBC)中浓度较高,因此用电感耦合等离子体发射光谱法(ICP-OES)测量非必需金属,而血清样本中的必需生物金属通过电感耦合等离子体发射光谱法(ICP-OES)测量。可以分析和检测低水平的不同元素。通过定量实时 PCR(qRT-PCR)进行基因表达水平的测定。在本研究中,在 AD 患者样本中未检测到铅和砷金属的水平。与对照组相比,病例中发现镉、汞和铝的水平更高,分别为 0.009240±0.0007707(P<0.0001)、0.02332±0.001041(P<0.0001)和 0.09222±0.02804(P=0.0087)。像铜这样的必需生物金属在病例中更高,为 0.1274±0.02453(P=0.0254),而铁 0.1117±0.009599(P=0.0304)和锌 0.03800±0.003462 mg/L 则明显低于对照组。所有靶向基因,如 APP、PSEN1、PSEN2 和 APOE4,在 AD 患者中均发现上调。我们得出的结论是,在这项研究中,金属动态平衡与基因表达之间没有显著相关性。

相似文献

1
Metals toxicity and its correlation with the gene expression in Alzheimer's disease.金属毒性及其与阿尔茨海默病中基因表达的关系。
Mol Biol Rep. 2021 Apr;48(4):3245-3252. doi: 10.1007/s11033-021-06386-x. Epub 2021 May 10.
2
Plasma metals as potential biomarkers in dementia: a case-control study in patients with sporadic Alzheimer's disease.血浆金属作为痴呆症的潜在生物标志物:散发性阿尔茨海默病患者的病例对照研究。
Biometals. 2018 Apr;31(2):267-276. doi: 10.1007/s10534-018-0089-3. Epub 2018 Mar 7.
3
PSEN1 and PSEN2 gene expression in Alzheimer's disease brain: a new approach.早发性阿尔茨海默病大脑中PSEN1和PSEN2基因的表达:一种新方法。
J Alzheimers Dis. 2014;42(3):757-60. doi: 10.3233/JAD-140033.
4
Gene Expression of Quaking in Sporadic Alzheimer's Disease Patients is Both Upregulated and Related to Expression Levels of Genes Involved in Amyloid Plaque and Neurofibrillary Tangle Formation.散发性阿尔茨海默病患者中震颤蛋白的基因表达上调,且与淀粉样斑块和神经原纤维缠结形成相关基因的表达水平有关。
J Alzheimers Dis. 2016 May 6;53(1):209-19. doi: 10.3233/JAD-160160.
5
Genetics of Alzheimer's disease.阿尔茨海默病的遗传学。
Arch Med Res. 2012 Nov;43(8):622-31. doi: 10.1016/j.arcmed.2012.10.017. Epub 2012 Nov 8.
6
Molecular Genetics of Early- and Late-Onset Alzheimer's Disease.早发性和晚发性阿尔茨海默病的分子遗传学。
Curr Gene Ther. 2021;21(1):43-52. doi: 10.2174/1566523220666201123112822.
7
Metal Toxicity Links to Alzheimer's Disease and Neuroinflammation.金属毒性与阿尔茨海默病和神经炎症有关。
J Mol Biol. 2019 Apr 19;431(9):1843-1868. doi: 10.1016/j.jmb.2019.01.018. Epub 2019 Jan 18.
8
Interactome mapping suggests new mechanistic details underlying Alzheimer's disease.相互作用组图谱提示阿尔茨海默病的新机制细节。
Genome Res. 2011 Mar;21(3):364-76. doi: 10.1101/gr.114280.110. Epub 2010 Dec 16.
9
Circulatory Levels of Toxic Metals (Aluminum, Cadmium, Mercury, Lead) in Patients with Alzheimer's Disease: A Quantitative Meta-Analysis and Systematic Review.患有阿尔茨海默病患者体内的循环毒性金属(铝、镉、汞、铅)水平:定量荟萃分析和系统评价。
J Alzheimers Dis. 2018;62(1):361-372. doi: 10.3233/JAD-170811.
10
Mutational analysis in early-onset familial Alzheimer's disease in Mainland China.中国大陆早发性家族性阿尔茨海默病的突变分析
Neurobiol Aging. 2014 Aug;35(8):1957.e1-6. doi: 10.1016/j.neurobiolaging.2014.02.014. Epub 2014 Feb 20.

引用本文的文献

1
Epidemiological Evidence on the Associations of Metal Exposure with Alzheimer's Disease and Related Dementias Among Elderly Women.老年女性中金属暴露与阿尔茨海默病及相关痴呆症关联的流行病学证据
J Clin Med. 2025 May 28;14(11):3776. doi: 10.3390/jcm14113776.
2
Longitudinal Evaluation of the Detection Potential of Serum Oligoelements Cu, Se and Zn for the Diagnosis of Alzheimer's Disease in the 3xTg-AD Animal Model.血清微量元素铜、硒和锌对3xTg-AD动物模型中阿尔茨海默病诊断的检测潜力的纵向评估
Int J Mol Sci. 2025 Apr 12;26(8):3657. doi: 10.3390/ijms26083657.
3
Protective potential of BM-MSC extracted Exosomes in a rat model of Alzheimer's disease.

本文引用的文献

1
Understanding Aspects of Aluminum Exposure in Alzheimer's Disease Development.了解阿尔茨海默病发展过程中铝暴露的相关方面。
Brain Pathol. 2016 Mar;26(2):139-54. doi: 10.1111/bpa.12333. Epub 2015 Dec 8.
2
Serum Iron, Zinc, and Copper Levels in Patients with Alzheimer's Disease: A Replication Study and Meta-Analyses.阿尔茨海默病患者的血清铁、锌和铜水平:一项重复研究与荟萃分析
J Alzheimers Dis. 2015;47(3):565-81. doi: 10.3233/JAD-143108.
3
PSEN1 and PSEN2 gene expression in Alzheimer's disease brain: a new approach.早发性阿尔茨海默病大脑中PSEN1和PSEN2基因的表达:一种新方法。
骨髓间充质干细胞提取的外泌体在阿尔茨海默病大鼠模型中的保护潜力。
PLoS One. 2025 May 6;20(5):e0320883. doi: 10.1371/journal.pone.0320883. eCollection 2025.
4
The Role of Copper in Alzheimer's Disease Etiopathogenesis: An Updated Systematic Review.铜在阿尔茨海默病病因发病机制中的作用:一项最新的系统评价
Toxics. 2024 Oct 17;12(10):755. doi: 10.3390/toxics12100755.
5
Metal Toxicity and Dementia Including Frontotemporal Dementia: Current State of Knowledge.金属毒性与痴呆症,包括额颞叶痴呆症:当前的知识状况
Antioxidants (Basel). 2024 Aug 1;13(8):938. doi: 10.3390/antiox13080938.
6
Mammalian copper homeostasis: physiological roles and molecular mechanisms.哺乳动物的铜稳态:生理作用和分子机制。
Physiol Rev. 2025 Jan 1;105(1):441-491. doi: 10.1152/physrev.00011.2024. Epub 2024 Aug 22.
7
Alzheimer's Disease and Circulatory Imbalance of Toxic Heavy Metals: A Systematic Review and Meta-analysis of Clinical Studies.阿尔茨海默病与有毒重金属的循环失衡:临床研究的系统评价与荟萃分析
Biol Trace Elem Res. 2025 Apr;203(4):1871-1885. doi: 10.1007/s12011-024-04326-x. Epub 2024 Jul 30.
8
Epigenetic Mechanisms of Aluminum-Induced Neurotoxicity and Alzheimer's Disease: A Focus on Non-Coding RNAs.铝诱导神经毒性和阿尔茨海默病的表观遗传机制:聚焦于非编码 RNA。
Neurochem Res. 2024 Nov;49(11):2988-3005. doi: 10.1007/s11064-024-04214-9. Epub 2024 Jul 27.
9
Environmental risk factors provoke new thinking for prevention and treatment of dementia with Lewy bodies.环境风险因素引发了对路易体痴呆症预防和治疗的新思考。
Heliyon. 2024 Apr 26;10(9):e30175. doi: 10.1016/j.heliyon.2024.e30175. eCollection 2024 May 15.
10
Are high copper levels related to Alzheimer's and Parkinson's diseases? A systematic review and meta-analysis of articles published between 2011 and 2022.高铜水平与阿尔茨海默病和帕金森病有关吗?对 2011 年至 2022 年发表的文章进行的系统评价和荟萃分析。
Biometals. 2024 Feb;37(1):3-22. doi: 10.1007/s10534-023-00530-9. Epub 2023 Aug 18.
J Alzheimers Dis. 2014;42(3):757-60. doi: 10.3233/JAD-140033.
4
Characterization of biometal profiles in neurological disorders.神经紊乱相关生物金属谱的特征。
Metallomics. 2014 May;6(5):960-77. doi: 10.1039/c4mt00008k.
5
Epigenetic changes in the progression of Alzheimer's disease.阿尔茨海默病进展中的表观遗传改变。
Mech Ageing Dev. 2013 Oct;134(10):486-95. doi: 10.1016/j.mad.2013.08.005. Epub 2013 Sep 3.
6
Cadmium-induced apoptosis in primary rat cerebral cortical neurons culture is mediated by a calcium signaling pathway.镉诱导原代大鼠皮质神经元培养细胞凋亡是通过钙信号通路介导的。
PLoS One. 2013 May 31;8(5):e64330. doi: 10.1371/journal.pone.0064330. Print 2013.
7
Early-onset familial Alzheimer's disease (EOFAD).早发性家族性阿尔茨海默病(EOFAD)。
Can J Neurol Sci. 2012 Jul;39(4):436-45. doi: 10.1017/s0317167100013949.
8
Alzheimer's disease-linked mutations in presenilin-1 result in a drastic loss of activity in purified γ-secretase complexes.早老素-1 相关突变导致纯化 γ-分泌酶复合物活性急剧丧失。
PLoS One. 2012;7(4):e35133. doi: 10.1371/journal.pone.0035133. Epub 2012 Apr 18.
9
Alzheimer's disease and environmental exposure to lead: the epidemiologic evidence and potential role of epigenetics.阿尔茨海默病与环境铅暴露:流行病学证据及表观遗传学的潜在作用。
Curr Alzheimer Res. 2012 Jun;9(5):563-73. doi: 10.2174/156720512800617991.
10
Increased expression of PS1 is sufficient to elevate the level and activity of γ-secretase in vivo.PS1 表达水平升高足以使体内 γ-分泌酶的水平和活性升高。
PLoS One. 2011;6(11):e28179. doi: 10.1371/journal.pone.0028179. Epub 2011 Nov 29.