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本文引用的文献

1
Manganese Uptake and Accumulation in the Human Brain.锰在人脑中的摄取与蓄积
AJNR Am J Neuroradiol. 2020 Jan;41(1):E3. doi: 10.3174/ajnr.A6347. Epub 2020 Jan 2.
2
Manganese Acts upon Insulin/IGF Receptors to Phosphorylate AKT and Increase Glucose Uptake in Huntington's Disease Cells.锰通过作用于胰岛素/IGF 受体来磷酸化 AKT 并增加亨廷顿病细胞的葡萄糖摄取。
Mol Neurobiol. 2020 Mar;57(3):1570-1593. doi: 10.1007/s12035-019-01824-1. Epub 2019 Dec 4.
3
Manganese transporter Slc30a10 controls physiological manganese excretion and toxicity.锰转运蛋白 Slc30a10 控制生理锰排泄和毒性。
J Clin Invest. 2019 Dec 2;129(12):5442-5461. doi: 10.1172/JCI129710.
4
Genetic Disorders of Manganese Metabolism.锰代谢遗传障碍。
Curr Neurol Neurosci Rep. 2019 May 14;19(6):33. doi: 10.1007/s11910-019-0942-y.
5
The intestinal metal transporter ZIP14 maintains systemic manganese homeostasis.肠道金属转运蛋白 ZIP14 维持全身锰稳态。
J Biol Chem. 2019 Jun 7;294(23):9147-9160. doi: 10.1074/jbc.RA119.008762. Epub 2019 Apr 26.
6
A systematic literature review of epidemiologic studies of developmental manganese exposure and neurodevelopmental outcomes.发育性锰暴露与神经发育结局的流行病学研究系统综述。
Toxicology. 2019 May 15;420:46-65. doi: 10.1016/j.tox.2019.03.004. Epub 2019 Mar 27.
7
The role of astrocytic glutamate transporters GLT-1 and GLAST in neurological disorders: Potential targets for neurotherapeutics.星形胶质细胞谷氨酸转运体 GLT-1 和 GLAST 在神经紊乱中的作用:神经治疗学的潜在靶点。
Neuropharmacology. 2019 Dec 15;161:107559. doi: 10.1016/j.neuropharm.2019.03.002. Epub 2019 Mar 6.
8
Polymorphisms in Manganese Transporters 0 and Are Associated With Children's Neurodevelopment by Influencing Manganese Homeostasis.锰转运蛋白0和[此处原文缺失信息]中的多态性通过影响锰稳态与儿童神经发育相关。
Front Genet. 2018 Dec 20;9:664. doi: 10.3389/fgene.2018.00664. eCollection 2018.
9
Effects of Preweaning Manganese in Combination with Adult Striatal Dopamine Lesions on Monoamines, BDNF, TrkB, and Cognitive Function in Sprague-Dawley Rats.新生期锰暴露联合成年纹状体多巴胺损伤对 Sprague-Dawley 大鼠单胺类递质、BDNF、TrkB 及认知功能的影响。
Neurotox Res. 2019 Apr;35(3):606-620. doi: 10.1007/s12640-018-9992-1. Epub 2019 Jan 5.
10
SLC30A10 transporter in the digestive system regulates brain manganese under basal conditions while brain SLC30A10 protects against neurotoxicity.消化系统中的 SLC30A10 转运蛋白在基础条件下调节大脑中的锰,而大脑中的 SLC30A10 则可防止神经毒性。
J Biol Chem. 2019 Feb 8;294(6):1860-1876. doi: 10.1074/jbc.RA118.005628. Epub 2018 Dec 17.

脑锰与必需角色和神经毒性之间的平衡。

Brain manganese and the balance between essential roles and neurotoxicity.

机构信息

School of Health Sciences, Purdue University, West Lafayette, Indiana 47907.

Division of Pharmacology and Toxicology, College of Pharmacy, Institute for Cellular and Molecular Biology, and Institute for Neuroscience, University of Texas, Austin, Texas 78712.

出版信息

J Biol Chem. 2020 May 8;295(19):6312-6329. doi: 10.1074/jbc.REV119.009453. Epub 2020 Mar 18.

DOI:10.1074/jbc.REV119.009453
PMID:32188696
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7212623/
Abstract

Manganese (Mn) is an essential micronutrient required for the normal development of many organs, including the brain. Although its roles as a cofactor in several enzymes and in maintaining optimal physiology are well-known, the overall biological functions of Mn are rather poorly understood. Alterations in body Mn status are associated with altered neuronal physiology and cognition in humans, and either overexposure or (more rarely) insufficiency can cause neurological dysfunction. The resultant balancing act can be viewed as a hormetic U-shaped relationship for biological Mn status and optimal brain health, with changes in the brain leading to physiological effects throughout the body and vice versa. This review discusses Mn homeostasis, biomarkers, molecular mechanisms of cellular transport, and neuropathological changes associated with disruptions of Mn homeostasis, especially in its excess, and identifies gaps in our understanding of the molecular and biochemical mechanisms underlying Mn homeostasis and neurotoxicity.

摘要

锰(Mn)是许多器官(包括大脑)正常发育所必需的一种必需微量元素。尽管其作为几种酶的辅助因子和维持最佳生理机能的作用是众所周知的,但 Mn 的整体生物学功能仍知之甚少。体内 Mn 状态的改变与人类神经元生理和认知的改变有关,过度暴露或(更罕见)不足都会导致神经功能障碍。由此产生的平衡作用可以被视为生物 Mn 状态和最佳大脑健康的应激 U 型关系,大脑的变化会导致全身的生理效应,反之亦然。本综述讨论了 Mn 的动态平衡、生物标志物、细胞转运的分子机制,以及与 Mn 动态平衡破坏相关的神经病理学变化,特别是在 Mn 过量的情况下,并确定了我们对 Mn 动态平衡和神经毒性的分子和生化机制的理解存在差距。