2017
DOI: 10.1134/s0026893317020133
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Serotonergic genes in the development of anxiety/depression-like state and pathology of aggressive behavior in male mice: RNA-seq data

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Cited by 34 publications
(34 citation statements)
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“…These pathways mostly down-regulate MAOA, MAOB, EGFR, and CYP2E1, while simultaneously up-regulating CALM1. This matches with the hub genes from PPI network, in which EGFR has been proved to be a significant depression-related gene [28], MAOA and MAOB are crucial target genes of various mental diseases, and MAOA is particularly important in depression and anxiety [25,26]. Moreover, CYP2E1, a member of the cytochrome P450 enzymes family, is referred to as toxicant metabolic enzyme in the liver cell [29].…”
Section: Discussionsupporting
confidence: 75%
See 1 more Smart Citation
“…These pathways mostly down-regulate MAOA, MAOB, EGFR, and CYP2E1, while simultaneously up-regulating CALM1. This matches with the hub genes from PPI network, in which EGFR has been proved to be a significant depression-related gene [28], MAOA and MAOB are crucial target genes of various mental diseases, and MAOA is particularly important in depression and anxiety [25,26]. Moreover, CYP2E1, a member of the cytochrome P450 enzymes family, is referred to as toxicant metabolic enzyme in the liver cell [29].…”
Section: Discussionsupporting
confidence: 75%
“…The results show that HR can down-regulate MAOA, MAOB, and simultaneously up-regulate CALM1 (Figure 11). MAOA and MAOB are crucial target genes of various mental diseases, and MAOA is particularly important in depression and anxiety [25,26]. MAOA is a major degrading enzyme-is encoded by the MAOA gene in humans-in the metabolic pathways of monoamine neurotransmitters such as norepinephrine, dopamine, and serotonin.…”
Section: Pathway Analysis To Explore the Therapeutic Mechanisms Of Hrmentioning
confidence: 99%
“…The midbrain raphe nuclei contain the bodies of serotonergic neurons which are involved in the regulation of many physiological, behavioral, and emotional processes. Repeated experience of aggression and defeats is accompanied by the decrease of serotonergic activity [Kudryavtseva 2006;Avgustinovich et al 2004], which is accompanied by decreased expression of serotonergic genes -Tph2, Maoa, Slc6a4, Htr's Smagin et al 2013;Kudryavtseva et al 2017] in this brain region.…”
Section: Resultsmentioning
confidence: 99%
“…Changes in DNA methylation, histone acetylation and chromatin remodeling often accompany these changes [Hollis et al 2010;Kenworthy et al 2014], as well as decreases in hippocampal neurogenesis rates [Ferragud et al 2010;Lagace et al 2010;Van Bokhoven et al 2011] in defeated mice. We found changes in activity of monoaminergic gene expression in brain regions, activation of cell proliferations in the hippocampus, as well as growth of new neurons under repeated experience of aggression in male mice [Kudryavtseva et al 2004;Filipenko et al 2001;Smagin et al 2013;Smagin et al 2015;Kudryavtseva et al 2017]. Using the transcriptome analysis on RNA-seq data this report is aimed to study the changes of the collagen family gene expression in the 5 brain regions of the male mice with alternative social experience in daily agonistic interactions over a 20-day period.…”
Section: Introductionmentioning
confidence: 99%
“…Animals were placed in pairs in experimental cells separated by a septum which prevents physical contact but has openings that provide sensory contact. Every day the partition was removed for 10 minutes which overwhelmingly led to agonistic collisions (confrontations) [2]. Groups of animals with alternative types of behavior were formed: aggressive type -in case of repeated victories experience (winner, aggressor) and submissive type -in case of defeats (victim).…”
Section: A T E R I a L A N D M E T H O D Smentioning
confidence: 99%