Mental Depression
|
0.400 |
Biomarker
|
disease |
BEFREE |
Monoamine oxidase-A (MAO-A) is considered an important therapeutic target in depression.
|
30712820 |
2019 |
Mental Depression
|
0.400 |
Biomarker
|
disease |
BEFREE |
In men, there was only a weak effect of MAOA-uVNTR on depression.
|
30943524 |
2019 |
Mental Depression
|
0.400 |
GeneticVariation
|
disease |
BEFREE |
The functional polymorphism of MAOA gene and genes in serotonin signal pathway are associated with depression.
|
28293733 |
2018 |
Mental Depression
|
0.400 |
Biomarker
|
disease |
BEFREE |
MAO-A and MAO-B may be considered as targets for inhibitors to treat neurodegenerative diseases and depression and for managing symptoms associated with Parkinson's and Alzheimer's diseases.
|
29496172 |
2018 |
Mental Depression
|
0.400 |
GeneticVariation
|
disease |
BEFREE |
This review article aims to discuss the current status of the treatment for depression with MAO-A inhibitors and the regulatory factors of MAO-A.
|
30271325 |
2018 |
Mental Depression
|
0.400 |
PosttranslationalModification
|
disease |
BEFREE |
Hypermethylation of MAOA first exon mediated the association of SA with current depression, and both methylation levels and SA independently predicted lifetime depression.
|
29600412 |
2018 |
Mental Depression
|
0.400 |
AlteredExpression
|
disease |
BEFREE |
Our results show a significant upregulation of MAOA and TAC1 in the medial area frontopolaris which is a node in the limbic-cortical network and known to be susceptible for gray matter loss and behavioral dysfunction in patients with depression.
|
29478144 |
2018 |
Mental Depression
|
0.400 |
AlteredExpression
|
disease |
BEFREE |
Thus 5,7-dimethoxycoumarin prevented the chronic mild stress induced depression in rats through an increase in the expression of heat shock protein-70 and inhibition of monoamine oxidase-A levels.
|
29472774 |
2018 |
Mental Depression
|
0.400 |
Biomarker
|
disease |
BEFREE |
Nowadays, therapeutic attention on MAOIs engrosses two imperative categories; MAO-A inhibitors, in certain mental disorders such as depression and anxiety, and MAO-B inhibitors, in neurodegenerative disorders like Alzheimer's disease (AD) and Parkinson's disease (PD).
|
29335210 |
2018 |
Mental Depression
|
0.400 |
Biomarker
|
disease |
BEFREE |
Significant binding affinity of ursolic acid was seen with MAO-A, which indicated its potential role in other neurological disorders, for example, Alzheimer's disease and Parkinson disease besides depression.
|
28034283 |
2017 |
Mental Depression
|
0.400 |
Biomarker
|
disease |
BEFREE |
The second part summarizes the novel regulatory pathways of MAO-A, which have high potential as novel therapeutic targets for depression.
|
29163009 |
2017 |
Mental Depression
|
0.400 |
Biomarker
|
disease |
BEFREE |
In addition, AME could be a useful lead compound for developing reversible MAO-A inhibitors to treat depression, Parkinson's disease, and Alzheimer's disease.
|
27840401 |
2017 |
Mental Depression
|
0.400 |
Biomarker
|
disease |
BEFREE |
However, the precise relationship between sleep and depression and the role of MAOA in this process remains unknown.
|
28365314 |
2017 |
Mental Depression
|
0.400 |
Biomarker
|
disease |
BEFREE |
The findings suggest compounds 4 and 11 be considered as new potent and reversible MAO-A inhibitors or useful lead compounds for the developments of MAO inhibitors for the treatment of disorders like depression, Parkinson's disease and Alzheimer disease.
|
28109809 |
2017 |
Mental Depression
|
0.400 |
Biomarker
|
disease |
BEFREE |
We tested depression and anxiety like behaviors of burn C57 mice with the sucrose preference test, forced swimming test (FST), open field test and elevated plus maze test and then detected the MAOA content and MAOA gene transcriptional levels in the hippocampus with western blot analysis and real-time quantitative PCR analysis.
|
28413107 |
2017 |
Mental Depression
|
0.400 |
Biomarker
|
disease |
BEFREE |
The docking experiments revealed that the synthesized derivatives were potential inhibitors of MAO-A protein, which plays a central role in managing depression and anxiety disorders.
|
28694764 |
2017 |
Mental Depression
|
0.400 |
GeneticVariation
|
disease |
BEFREE |
Our study substantiates the involvement of the MAOA and MTHFR polymorphisms in climacteric depression and offers evidence that the COMT and ESR1 genes may also play a role in the susceptibility to depressive mood in postmenopausal women.
|
26620113 |
2016 |
Mental Depression
|
0.400 |
Biomarker
|
disease |
BEFREE |
This study supports a potential therapeutic use for MAO-A inhibitors in the treatment of depression and anxiety in patients with HD.
|
26825854 |
2016 |
Mental Depression
|
0.400 |
GeneticVariation
|
disease |
BEFREE |
Pharmacoepigenetics of depression: no major influence of MAO-A DNA methylation on treatment response.
|
24809685 |
2015 |
Mental Depression
|
0.400 |
PosttranslationalModification
|
disease |
BEFREE |
Here we report on a small-scale (n=44) replication study of MAOA methylation which (a) confirms that female subjects with a history of depression are hypomethylated compared to controls and (b) shows that females are hypermethylated in the same region compared to males.
|
25623016 |
2015 |
Mental Depression
|
0.400 |
Biomarker
|
disease |
PSYGENET |
Hypomethylation of MAOA's first exon region in depression: a replication study.
|
25623016 |
2015 |
Mental Depression
|
0.400 |
Biomarker
|
disease |
BEFREE |
However, it has been reported that monoamine oxidase A (MAO A, a major neurotransmitter-degrading enzyme) is significantly increased in the brains of human subjects affected with MDD and rats exposed to chronic social defeat (CSD) stress, which is used to model depression.
|
25502632 |
2015 |
Mental Depression
|
0.400 |
Biomarker
|
disease |
PSYGENET |
The frontal abnormality of patients with depression had certain 5-HT genetic basis, and 5-HT2A receptor CC allele and MAOA-H genotype had synergistic effect on the activity abnormality when recognizing negative emotion in right frontal middle gyrus of patients with depression.
|
24314147 |
2014 |
Mental Depression
|
0.400 |
GeneticVariation
|
disease |
BEFREE |
The frontal abnormality of patients with depression had certain 5-HT genetic basis, and 5-HT2A receptor CC allele and MAOA-H genotype had synergistic effect on the activity abnormality when recognizing negative emotion in right frontal middle gyrus of patients with depression.
|
24314147 |
2014 |
Mental Depression
|
0.400 |
Biomarker
|
disease |
BEFREE |
MAOA-uVNTR did not associate with either AD or DE.
|
24443391 |
2014 |