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The differences in brain stem transcriptional profiling in hypertensive ISIAH and normotensive WAG rats

BACKGROUND: The development of essential hypertension is associated with a wide range of mechanisms. The brain stem neurons are essential for the homeostatic regulation of arterial pressure as they control baroreflex and sympathetic nerve activity. The ISIAH (Inherited Stress Induced Arterial Hypert...

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Autores principales: Fedoseeva, Larisa A., Klimov, Leonid O., Ershov, Nikita I., Efimov, Vadim M., Markel, Arcady L., Orlov, Yuriy L., Redina, Olga E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7226933/
https://www.ncbi.nlm.nih.gov/pubmed/32039698
http://dx.doi.org/10.1186/s12864-019-5540-5
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author Fedoseeva, Larisa A.
Klimov, Leonid O.
Ershov, Nikita I.
Efimov, Vadim M.
Markel, Arcady L.
Orlov, Yuriy L.
Redina, Olga E.
author_facet Fedoseeva, Larisa A.
Klimov, Leonid O.
Ershov, Nikita I.
Efimov, Vadim M.
Markel, Arcady L.
Orlov, Yuriy L.
Redina, Olga E.
author_sort Fedoseeva, Larisa A.
collection PubMed
description BACKGROUND: The development of essential hypertension is associated with a wide range of mechanisms. The brain stem neurons are essential for the homeostatic regulation of arterial pressure as they control baroreflex and sympathetic nerve activity. The ISIAH (Inherited Stress Induced Arterial Hypertension) rats reproduce the human stress-sensitive hypertensive disease with predominant activation of the neuroendocrine hypothalamic-pituitary-adrenal and sympathetic adrenal axes. RNA-Seq analysis of the brain stems from the hypertensive ISIAH and normotensive control WAG (Wistar Albino Glaxo) rats was performed to identify the differentially expressed genes (DEGs) and the main central mechanisms (biological processes and metabolic pathways) contributing to the hypertensive state in the ISIAH rats. RESULTS: The study revealed 224 DEGs. Their annotation in databases showed that 22 of them were associated with hypertension and blood pressure (BP) regulation, and 61 DEGs were associated with central nervous system diseases. In accordance with the functional annotation of DEGs, the key role of hormonal metabolic processes and, in particular, the enhanced biosynthesis of aldosterone in the brain stem of ISIAH rats was proposed. Multiple DEGs associated with several Gene Ontology (GO) terms essentially related to modulation of BP were identified. Abundant groups of DEGs were related to GO terms associated with responses to different stimuli including response to organic (hormonal) substance, to external stimulus, and to stress. Several DEGs making the most contribution to the inter-strain differences were detected including the Ephx2, which was earlier defined as a major candidate gene in the studies of transcriptional profiles in different tissues/organs (hypothalamus, adrenal gland and kidney) of ISIAH rats. CONCLUSIONS: The results of the study showed that inter-strain differences in ISIAH and WAG brain stem functioning might be a result of the imbalance in processes leading to the pathology development and those, exerting the compensatory effects. The data obtained in this study are useful for a better understanding of the genetic mechanisms underlying the complexity of the brain stem processes in ISIAH rats, which are a model of stress-sensitive form of hypertension. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12864-019-5540-5) contains supplementary material, which is available to authorized users.
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spelling pubmed-72269332020-05-27 The differences in brain stem transcriptional profiling in hypertensive ISIAH and normotensive WAG rats Fedoseeva, Larisa A. Klimov, Leonid O. Ershov, Nikita I. Efimov, Vadim M. Markel, Arcady L. Orlov, Yuriy L. Redina, Olga E. BMC Genomics Research BACKGROUND: The development of essential hypertension is associated with a wide range of mechanisms. The brain stem neurons are essential for the homeostatic regulation of arterial pressure as they control baroreflex and sympathetic nerve activity. The ISIAH (Inherited Stress Induced Arterial Hypertension) rats reproduce the human stress-sensitive hypertensive disease with predominant activation of the neuroendocrine hypothalamic-pituitary-adrenal and sympathetic adrenal axes. RNA-Seq analysis of the brain stems from the hypertensive ISIAH and normotensive control WAG (Wistar Albino Glaxo) rats was performed to identify the differentially expressed genes (DEGs) and the main central mechanisms (biological processes and metabolic pathways) contributing to the hypertensive state in the ISIAH rats. RESULTS: The study revealed 224 DEGs. Their annotation in databases showed that 22 of them were associated with hypertension and blood pressure (BP) regulation, and 61 DEGs were associated with central nervous system diseases. In accordance with the functional annotation of DEGs, the key role of hormonal metabolic processes and, in particular, the enhanced biosynthesis of aldosterone in the brain stem of ISIAH rats was proposed. Multiple DEGs associated with several Gene Ontology (GO) terms essentially related to modulation of BP were identified. Abundant groups of DEGs were related to GO terms associated with responses to different stimuli including response to organic (hormonal) substance, to external stimulus, and to stress. Several DEGs making the most contribution to the inter-strain differences were detected including the Ephx2, which was earlier defined as a major candidate gene in the studies of transcriptional profiles in different tissues/organs (hypothalamus, adrenal gland and kidney) of ISIAH rats. CONCLUSIONS: The results of the study showed that inter-strain differences in ISIAH and WAG brain stem functioning might be a result of the imbalance in processes leading to the pathology development and those, exerting the compensatory effects. The data obtained in this study are useful for a better understanding of the genetic mechanisms underlying the complexity of the brain stem processes in ISIAH rats, which are a model of stress-sensitive form of hypertension. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12864-019-5540-5) contains supplementary material, which is available to authorized users. BioMed Central 2019-05-08 /pmc/articles/PMC7226933/ /pubmed/32039698 http://dx.doi.org/10.1186/s12864-019-5540-5 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Fedoseeva, Larisa A.
Klimov, Leonid O.
Ershov, Nikita I.
Efimov, Vadim M.
Markel, Arcady L.
Orlov, Yuriy L.
Redina, Olga E.
The differences in brain stem transcriptional profiling in hypertensive ISIAH and normotensive WAG rats
title The differences in brain stem transcriptional profiling in hypertensive ISIAH and normotensive WAG rats
title_full The differences in brain stem transcriptional profiling in hypertensive ISIAH and normotensive WAG rats
title_fullStr The differences in brain stem transcriptional profiling in hypertensive ISIAH and normotensive WAG rats
title_full_unstemmed The differences in brain stem transcriptional profiling in hypertensive ISIAH and normotensive WAG rats
title_short The differences in brain stem transcriptional profiling in hypertensive ISIAH and normotensive WAG rats
title_sort differences in brain stem transcriptional profiling in hypertensive isiah and normotensive wag rats
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7226933/
https://www.ncbi.nlm.nih.gov/pubmed/32039698
http://dx.doi.org/10.1186/s12864-019-5540-5
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