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脑内甲基乙二醛:从糖酵解代谢物到信号分子。

Methylglyoxal in the Brain: From Glycolytic Metabolite to Signalling Molecule.

机构信息

Department of Anesthesiology, International Peace Maternity and Child Health Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai Key Laboratory of Embryo Original Disease, Shanghai Municipal Key Clinical Specialty, Huashan Rd. 1961, Shanghai 200030, China.

Department of Anesthesiology, Women and Children's Hospital of Jiaxing University, No. 2468 Zhonghuan East Road, Jiaxing 314000, China.

出版信息

Molecules. 2022 Nov 15;27(22):7905. doi: 10.3390/molecules27227905.


DOI:10.3390/molecules27227905
PMID:36432007
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9696358/
Abstract

Advances in molecular biology technology have piqued tremendous interest in glycometabolism and bioenergetics in homeostasis and neural development linked to ageing and age-related diseases. Methylglyoxal (MGO) is a by-product of glycolysis, and it can covalently modify proteins, nucleic acids, and lipids, leading to cell growth inhibition and, eventually, cell death. MGO can alter intracellular calcium homeostasis, which is a major cell-permeant precursor to advanced glycation end-products (AGEs). As side-products or signalling molecules, MGO is involved in several pathologies, including neurodevelopmental disorders, ageing, and neurodegenerative diseases. In this review, we demonstrate that MGO (the metabolic side-product of glycolysis), the GLO system, and their analogous relationship with behavioural phenotypes, epigenetics, ageing, pain, and CNS degeneration. Furthermore, we summarise several therapeutic approaches that target MGO and the glyoxalase (GLO) system in neurodegenerative diseases.

摘要

分子生物学技术的进步极大地激发了人们对糖代谢和生物能量学的兴趣,这些与衰老和与年龄相关的疾病有关的领域包括内稳定和神经发育。甲基乙二醛 (MGO) 是糖酵解的副产物,它可以共价修饰蛋白质、核酸和脂质,导致细胞生长抑制,最终导致细胞死亡。MGO 可以改变细胞内钙稳态,这是晚期糖基化终产物 (AGEs) 的主要细胞通透性前体。作为副产物或信号分子,MGO 参与了多种病理学,包括神经发育障碍、衰老和神经退行性疾病。在这篇综述中,我们证明了 MGO(糖酵解的代谢副产物)、GLO 系统及其与行为表型、表观遗传学、衰老、疼痛和中枢神经系统退化的类似关系。此外,我们总结了几种针对神经退行性疾病中 MGO 和 glyoxalase (GLO) 系统的治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4401/9696358/93ed61cf80a1/molecules-27-07905-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4401/9696358/1b22cefdf043/molecules-27-07905-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4401/9696358/baec106446f0/molecules-27-07905-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4401/9696358/93ed61cf80a1/molecules-27-07905-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4401/9696358/1b22cefdf043/molecules-27-07905-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4401/9696358/baec106446f0/molecules-27-07905-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4401/9696358/93ed61cf80a1/molecules-27-07905-g003.jpg

相似文献

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Methylglyoxal in the Brain: From Glycolytic Metabolite to Signalling Molecule.

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[2]
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[3]
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[7]
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[8]
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Oral Prodrug of a Novel Glutathione Surrogate Reverses Metabolic Dysregulation and Attenuates Neurodegenerative Process in Transgenic Alzheimer's Mice.

ACS Pharmacol Transl Sci. 2025-7-18

[2]
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Int J Mol Sci. 2025-5-26

[3]
Depletion of MGO or Its Derivatives Ameliorate CUMS-Induced Neuroinflammation.

Cells. 2025-3-8

[4]
Oral prodrug of a novel glutathione surrogate reverses metabolic dysregulation and attenuates neurodegenerative process in APP/PS1 mice.

bioRxiv. 2025-1-17

[5]
Metabolic Dysfunction in Parkinson's Disease: Unraveling the Glucose-Lipid Connection.

Biomedicines. 2024-12-13

[6]
African walnut () oil promotes glucose uptake while improving energy metabolism and steroidogenesis and maintaining surface architecture in rat testes.

Front Nutr. 2024-11-19

[7]
3D human stem-cell-derived neuronal spheroids for neurotoxicity testing of methylglyoxal, highly reactive glycolysis byproduct and potent glycating agent.

Curr Res Toxicol. 2024-6-9

[8]
Glyoxalase System in Breast and Ovarian Cancers: Role of MEK/ERK/SMAD1 Pathway.

Biomolecules. 2024-5-15

[9]
Molecular Assessment of Methylglyoxal-Induced Toxicity and Therapeutic Approaches in Various Diseases: Exploring the Interplay with the Glyoxalase System.

Life (Basel). 2024-2-17

[10]
Glucose Fluctuation Inhibits Nrf2 Signaling Pathway in Hippocampal Tissues and Exacerbates Cognitive Impairment in Streptozotocin-Induced Diabetic Rats.

J Diabetes Res. 2024

本文引用的文献

[1]
A metabolite-derived protein modification integrates glycolysis with KEAP1-NRF2 signalling.

Nature. 2018-10-15

[2]
The Role of Advanced Glycation End Products in Aging and Metabolic Diseases: Bridging Association and Causality.

Cell Metab. 2018-9-4

[3]
Methylglyoxal-derived posttranslational arginine modifications are abundant histone marks.

Proc Natl Acad Sci U S A. 2018-8-27

[4]
Diabetes Mellitus as a Risk Factor for Parkinson's Disease: a Molecular Point of View.

Mol Neurobiol. 2018-3-28

[5]
Neuroprotective effect of phosphocreatine on oxidative stress and mitochondrial dysfunction induced apoptosis in vitro and in vivo: Involvement of dual PI3K/Akt and Nrf2/HO-1 pathways.

Free Radic Biol Med. 2018-3-17

[6]
Conflicting Effects of Methylglyoxal and Potential Significance of miRNAs for Seizure Treatment.

Front Mol Neurosci. 2018-3-5

[7]
Glyoxalase 1 (GLO1) Inhibition or Genetic Overexpression Does Not Alter Ethanol's Locomotor Effects: Implications for GLO1 as a Therapeutic Target in Alcohol Use Disorders.

Alcohol Clin Exp Res. 2018-4-18

[8]
KRIT1 loss-of-function induces a chronic Nrf2-mediated adaptive homeostasis that sensitizes cells to oxidative stress: Implication for Cerebral Cavernous Malformation disease.

Free Radic Biol Med. 2017-11-21

[9]
N-acetylcysteine attenuates systemic platelet activation and cerebral vessel thrombosis in diabetes.

Redox Biol. 2017-9-20

[10]
Comparative Examination of Temporal Glyoxalase 1 Variations Following Perforant Pathway Transection, Excitotoxicity, and Controlled Cortical Impact Injury.

Neurotox Res. 2017-9-12

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