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Series GSE117046 Query DataSets for GSE117046
Status Public on Jul 13, 2018
Title Expression of miRNAs in dorsal rat hippocampus: Effect of subchronic and chronic restraint stress
Platform organism synthetic construct
Sample organism Rattus norvegicus
Experiment type Non-coding RNA profiling by array
Summary Studies conducted in rodents subjected to chronic stress and some observations in humans after psychosocial stress, have allowed to establish a link between stress and the susceptibility to many complex diseases, including mood disorders. The studies in rodents have revealed that chronic exposure to stress negatively affects synaptic plasticity by triggering changes in the production of trophic factors, subunit levels of glutamate ionotropic receptors, neuron morphology and neurogenesis in adult hippocampus. These modifications may account for the impairment in learning and memory processes observed in chronically stressed animals. It is plausible then, that stress modifies the interplay between signal transduction cascades and gene expression regulation in the hippocampus, therefore leading to altered neuroplasticity and functioning of neural circuits. Considering that miRNAs play an important role in post-transcriptional-regulation of gene expression and participate in several hippocampus-dependent functions; we evaluated the consequences of chronic stress in the expression of miRNAs in dorsal (anterior) portion of the hippocampus, which participates in memory formation in rodents. Here, we show that male rats exposed to daily restraint stress (2.5 h/day) during 7 and 14 days display a differential profile of miRNA levels in dorsal hippocampus and remarkably, we found that some of these miRNAs belong to the miR-379-410 cluster. We confirmed a rise in miR-92a and miR-485 levels after 14 days of stress by qPCR, an effect that was not mimicked by chronic administration of corticosterone (14 days). Our in silico study identified the top-ten biological functions influenced by miR-92a, nine of which were shared with miR-485: Nervous system development, Tissue development, Behavior, Embryonic development, Organ development, Organismal development, Organismal survival, Tissue morphology, and Organ morphology. Furthermore, our in silico study provided a landscape of potential miRNA-92a and miR-485 targets, along with relevant canonical pathways related to axonal guidance signaling and cAMP signaling, which may influence the functioning of several neuroplastic substrates in dorsal hippocampus. Additionally, the combined effect of miR-92a and miR-485 on transcription factors, along with histone-modifying enzymes, may have a functional relevance by producing changes in gene regulatory networks that modify the neuroplastic capacity of the adult dorsal hippocampus under stress.
 
Overall design Adult male rats were exposed to daily restraint stress (2.5 h/day) during 7 and 14 days. Animals were decapitated 24 h after the last stress exposure and hippocampi were dissected. Then RNA was extracted by using RNeasy minikit. miRNA expression was conducted using Affymetrix GeneChip 3.0 following the hibridization protocol.
 
Contributor(s) Muñoz M, García-Pérez A, Xu X, Tejos M, Vidal E, Moyano T, Gutiérrez R, Aguayo F, García-Rojo G, Pacheco A, Aliaga E, Rojas P, Cidlowski J, Fiedler J
Citation(s) 30127715
Submission date Jul 12, 2018
Last update date Oct 18, 2018
Contact name Wladimir Antonio Corrales
E-mail(s) wcorrales@ug.uchile.cl
Organization name Universidad de Chile
Department Biochemistry and Molecular Biology
Lab Neuroplasticity and Neurogenetics
Street address Olivos 1007
City Independencia
ZIP/Postal code 8380492
Country Chile
 
Platforms (1)
GPL16384 [miRNA-3] Affymetrix Multispecies miRNA-3 Array
Samples (10)
GSM3267721 Dorsal_Hippocampus_Male_Control_Rep 1
GSM3267722 Dorsal_Hippocampus_Male_Control_Rep 2
GSM3267723 Dorsal_Hippocampus_Male_Control_Rep 3
Relations
BioProject PRJNA480901

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Supplementary file Size Download File type/resource
GSE117046_RAW.tar 29.1 Mb (http)(custom) TAR (of CEL)
Processed data included within Sample table

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