Literature DB >> 20334883

Decreased level of 5-methyltetrahydrofolate: a potential biomarker for pre-symptomatic amyotrophic lateral sclerosis.

X Zhang1, S Chen, L Li, Q Wang, W Le.   

Abstract

BACKGROUND: Several studies have reported that homocysteine (Hcy) is associated with amyotrophic lateral sclerosis (ALS), a neurodegenerative disease without special biomarkers for early diagnosis. Here, we examined the levels of Hcy, folic acid and its metabolic molecule 5-methyltetrahydrofolate (5-MTHF) in SOD1(G93A) transgenic mouse model of ALS in an attempt to determine whether the change in those molecules can be used as potential biomarkers for the disease.
METHODS: According to the disease progression, SOD1(G93A) transgenic mice were divided into early stage group (30d); pre-symptom group (60d); symptom group (90d) and terminal stage group (120d). LC-MS/MS was used to measure the level of Hcy, folic acid and 5-MTHF in the plasma, spinal cord and cortex of the ALS transgenic SOD1(G93A) mice at different disease stages. Nissl staining was used to detect the motor neurons survival in the anterior horn of the spinal cord of the SOD1(G93A) mice.
RESULTS: In this study, we demonstrated that the level of 5-MTHF is significantly decreased in the plasma, spinal cord and cortex at the early stages of pre-symptomatic ALS transgenic SOD1(G93A) mice while folic acid is decreased at the middle to late stages of the disease. Furthermore, we found that the level of Hcy is markedly elevated after the motor symptoms appeared in the ALS mice.
CONCLUSION: Our study suggests that decreased 5-MTHF level may be a potential biomarker for the early stage of the disease in the ALS mice, which may warrant further validating study of 5-MTHF level in ALS patients. Copyright 2010 Elsevier B.V. All rights reserved.

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Year:  2010        PMID: 20334883     DOI: 10.1016/j.jns.2010.02.024

Source DB:  PubMed          Journal:  J Neurol Sci        ISSN: 0022-510X            Impact factor:   3.181


  7 in total

1.  Repurposing carbamazepine for the treatment of amyotrophic lateral sclerosis in SOD1-G93A mouse model.

Authors:  Jing-Jing Zhang; Qin-Ming Zhou; Sheng Chen; Wei-Dong Le
Journal:  CNS Neurosci Ther       Date:  2018-04-14       Impact factor: 5.243

Review 2.  Amyotrophic lateral sclerosis: a focus on disease progression.

Authors:  Ana C Calvo; Raquel Manzano; Deise M F Mendonça; María J Muñoz; Pilar Zaragoza; Rosario Osta
Journal:  Biomed Res Int       Date:  2014-08-03       Impact factor: 3.411

Review 3.  Nutrient Effects on Motor Neurons and the Risk of Amyotrophic Lateral Sclerosis.

Authors:  Polina S Goncharova; Tatiana K Davydova; Tatiana E Popova; Maxim A Novitsky; Marina M Petrova; Oksana A Gavrilyuk; Mustafa Al-Zamil; Natalia G Zhukova; Regina F Nasyrova; Natalia A Shnayder
Journal:  Nutrients       Date:  2021-10-26       Impact factor: 5.717

4.  Transcriptome Profiling Following Neuronal and Glial Expression of ALS-Linked SOD1 in Drosophila.

Authors:  Emily L Kumimoto; Taylor R Fore; Bing Zhang
Journal:  G3 (Bethesda)       Date:  2013-04-09       Impact factor: 3.154

5.  Resveratrol ameliorates motor neuron degeneration and improves survival in SOD1(G93A) mouse model of amyotrophic lateral sclerosis.

Authors:  Lin Song; Liang Chen; Xiaojie Zhang; Jia Li; Weidong Le
Journal:  Biomed Res Int       Date:  2014-06-26       Impact factor: 3.411

6.  Scolopendra subspinipes mutilans attenuates neuroinflammation in symptomatic hSOD1(G93A) mice.

Authors:  MuDan Cai; Sun-Mi Choi; Bong Keun Song; Ilhong Son; Sungchul Kim; Eun Jin Yang
Journal:  J Neuroinflammation       Date:  2013-10-29       Impact factor: 8.322

7.  Dynamic changes of CX3CL1/CX3CR1 axis during microglial activation and motor neuron loss in the spinal cord of ALS mouse model.

Authors:  Jingjing Zhang; Yufei Liu; Xinyao Liu; Song Li; Cheng Cheng; Sheng Chen; Weidong Le
Journal:  Transl Neurodegener       Date:  2018-12-21       Impact factor: 8.014

  7 in total

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