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无表面污染、多面体形貌的纳米晶金的纳米催化活性增强了多发性硬化症动物模型中的髓鞘再生。

Nanocatalytic activity of clean-surfaced, faceted nanocrystalline gold enhances remyelination in animal models of multiple sclerosis.

机构信息

Department of Microbiology-Immunology, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.

Clene Nanomedicine, Inc., Salt Lake City, UT, USA.

出版信息

Sci Rep. 2020 Feb 11;10(1):1936. doi: 10.1038/s41598-020-58709-w.


DOI:10.1038/s41598-020-58709-w
PMID:32041968
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7010780/
Abstract

Development of pharmacotherapies that promote remyelination is a high priority for multiple sclerosis (MS), due to their potential for neuroprotection and restoration of function through repair of demyelinated lesions. A novel preparation of clean-surfaced, faceted gold nanocrystals demonstrated robust remyelinating activity in response to demyelinating agents in both chronic cuprizone and acute lysolecithin rodent animal models. Furthermore, oral delivery of gold nanocrystals improved motor functions of cuprizone-treated mice in both open field and kinematic gait studies. Gold nanocrystal treatment of oligodendrocyte precursor cells in culture resulted in oligodendrocyte maturation and expression of myelin differentiation markers. Additional in vitro data demonstrated that these gold nanocrystals act via a novel energy metabolism pathway involving the enhancement of key indicators of aerobic glycolysis. In response to gold nanocrystals, co-cultured central nervous system cells exhibited elevated levels of the redox coenzyme nicotine adenine dinucleotide (NAD+), elevated total intracellular ATP levels, and elevated extracellular lactate levels, along with upregulation of myelin-synthesis related genes, collectively resulting in functional myelin generation. Based on these preclinical studies, clean-surfaced, faceted gold nanocrystals represent a novel remyelinating therapeutic for multiple sclerosis.

摘要

开发促进髓鞘再生的药物疗法是多发性硬化症(MS)的当务之急,因为它们具有通过修复脱髓鞘病变来提供神经保护和恢复功能的潜力。一种新型的表面光滑、有棱角的金纳米晶体制剂在慢性铜缺乏和急性卵磷脂棒状动物模型中对脱髓鞘试剂表现出强大的髓鞘再生活性。此外,金纳米晶体的口服给药在开阔场和运动步态研究中改善了铜缺乏症小鼠的运动功能。金纳米晶体处理培养中的少突胶质前体细胞导致少突胶质细胞成熟和髓鞘分化标志物的表达。额外的体外数据表明,这些金纳米晶体通过涉及增强有氧糖酵解关键指标的新型能量代谢途径起作用。响应金纳米晶体,共培养的中枢神经系统细胞表现出氧化还原辅酶烟酰胺腺嘌呤二核苷酸(NAD+)水平升高、细胞内总 ATP 水平升高和细胞外乳酸水平升高,以及髓鞘合成相关基因的上调,共同导致功能性髓鞘生成。基于这些临床前研究,表面光滑、有棱角的金纳米晶体代表了一种用于多发性硬化症的新型髓鞘修复治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6a6/7010780/7f19ebb67da0/41598_2020_58709_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6a6/7010780/22ae8b932914/41598_2020_58709_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6a6/7010780/a8ce9961e624/41598_2020_58709_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6a6/7010780/daf9e04b7d75/41598_2020_58709_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6a6/7010780/dd35d2afab9c/41598_2020_58709_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6a6/7010780/6a6cb33085a4/41598_2020_58709_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6a6/7010780/210020912a8a/41598_2020_58709_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6a6/7010780/7f19ebb67da0/41598_2020_58709_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6a6/7010780/22ae8b932914/41598_2020_58709_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6a6/7010780/a8ce9961e624/41598_2020_58709_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6a6/7010780/daf9e04b7d75/41598_2020_58709_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6a6/7010780/dd35d2afab9c/41598_2020_58709_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6a6/7010780/6a6cb33085a4/41598_2020_58709_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6a6/7010780/210020912a8a/41598_2020_58709_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6a6/7010780/7f19ebb67da0/41598_2020_58709_Fig7_HTML.jpg

相似文献

[1]
Nanocatalytic activity of clean-surfaced, faceted nanocrystalline gold enhances remyelination in animal models of multiple sclerosis.

Sci Rep. 2020-2-11

[2]
CXCR2 antagonism promotes oligodendrocyte precursor cell differentiation and enhances remyelination in a mouse model of multiple sclerosis.

Neurobiol Dis. 2020-2

[3]
Resveratrol Promotes Remyelination in Cuprizone Model of Multiple Sclerosis: Biochemical and Histological Study.

Mol Neurobiol. 2017-7

[4]
GD1a Overcomes Inhibition of Myelination by Fibronectin via Activation of Protein Kinase A: Implications for Multiple Sclerosis.

J Neurosci. 2017-10-11

[5]
Delayed Demyelination and Impaired Remyelination in Aged Mice in the Cuprizone Model.

Cells. 2020-4-11

[6]
The guanine nucleotide exchange factor Vav3 modulates oligodendrocyte precursor differentiation and supports remyelination in white matter lesions.

Glia. 2018-11-18

[7]
Selective Estrogen Receptor Modulators Enhance CNS Remyelination Independent of Estrogen Receptors.

J Neurosci. 2019-1-29

[8]
Intranasal delivery of SDF-1α-preconditioned bone marrow mesenchymal cells improves remyelination in the cuprizone-induced mouse model of multiple sclerosis.

Cell Biol Int. 2019-11-1

[9]
Donepezil, a drug for Alzheimer's disease, promotes oligodendrocyte generation and remyelination.

Acta Pharmacol Sin. 2019-3-27

[10]
rHIgM22 enhances remyelination in the brain of the cuprizone mouse model of demyelination.

Neurobiol Dis. 2017-5-30

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Int J Mol Sci. 2025-5-29

[2]
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Brain Behav. 2025-5

[3]
Update on novel multiple sclerosis treatments: from dismal defeat to scintillating success.

Curr Opin Neurol. 2025-6-1

[4]
CNM-Au8 in Amyotrophic Lateral Sclerosis: The HEALEY ALS Platform Trial.

JAMA. 2025-2-17

[5]
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Discov Nano. 2024-10-28

[6]
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[7]
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[8]
Knowledge mapping of disease-modifying therapy (DMT) in multiple sclerosis (MS): A bibliometrics analysis.

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[9]
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J Nanobiotechnology. 2024-5-23

[10]
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