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Integrating transcriptomics and metabolomics to analyze the mechanism of hypertension-induced hippocampal injury
OBJECTIVE: Hypertension is a public health challenge worldwide due to its high prevalence and multiple complications. Hypertension-induced damage to the hippocampus leads to behavioral changes and various brain diseases. Despite the multifaceted effects of hypertension on the hippocampus, the mechan...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10115962/ https://www.ncbi.nlm.nih.gov/pubmed/37089694 http://dx.doi.org/10.3389/fnmol.2023.1146525 |
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author | Li, Yanan Chu, Xue Xie, Xin Guo, Jinxiu Meng, Junjun Si, Qingying Jiang, Pei |
author_facet | Li, Yanan Chu, Xue Xie, Xin Guo, Jinxiu Meng, Junjun Si, Qingying Jiang, Pei |
author_sort | Li, Yanan |
collection | PubMed |
description | OBJECTIVE: Hypertension is a public health challenge worldwide due to its high prevalence and multiple complications. Hypertension-induced damage to the hippocampus leads to behavioral changes and various brain diseases. Despite the multifaceted effects of hypertension on the hippocampus, the mechanisms underlying hippocampal lesions are still unclear. METHODS: The 32-week-old spontaneously hypertensive rats (SHR) and Wistar-Kyoto (WKY) rats were selected as the study subjects. Behavioral experiments such as an open field test (OFT), an elevated plus maze (EPM) test, and the Morris water maze (MWM) test were performed to show the behavioral characteristics of the rats. A comprehensive transcriptomic and metabolomic analysis was performed to understand the changes in the hippocampus at the metabolic and genetic levels. RESULTS: Behavioral tests showed that, compared to WKY rats, SHR showed not only reduced memory capacity but more hyperactive and impulsive behavior. In addition, transcriptomic analysis screened for 103 differentially expressed genes. Metabolomic analysis screened 56 metabolites with significant differences, including various amino acids and their related metabolites. CONCLUSION: Comprehensive analysis showed that hypertension-induced hippocampal lesions are closely associated with differential metabolites and differential genes detected in this study. The results provide a basis for analyzing the mechanisms of hypertension-induced hippocampal damage. |
format | Online Article Text |
id | pubmed-10115962 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-101159622023-04-21 Integrating transcriptomics and metabolomics to analyze the mechanism of hypertension-induced hippocampal injury Li, Yanan Chu, Xue Xie, Xin Guo, Jinxiu Meng, Junjun Si, Qingying Jiang, Pei Front Mol Neurosci Molecular Neuroscience OBJECTIVE: Hypertension is a public health challenge worldwide due to its high prevalence and multiple complications. Hypertension-induced damage to the hippocampus leads to behavioral changes and various brain diseases. Despite the multifaceted effects of hypertension on the hippocampus, the mechanisms underlying hippocampal lesions are still unclear. METHODS: The 32-week-old spontaneously hypertensive rats (SHR) and Wistar-Kyoto (WKY) rats were selected as the study subjects. Behavioral experiments such as an open field test (OFT), an elevated plus maze (EPM) test, and the Morris water maze (MWM) test were performed to show the behavioral characteristics of the rats. A comprehensive transcriptomic and metabolomic analysis was performed to understand the changes in the hippocampus at the metabolic and genetic levels. RESULTS: Behavioral tests showed that, compared to WKY rats, SHR showed not only reduced memory capacity but more hyperactive and impulsive behavior. In addition, transcriptomic analysis screened for 103 differentially expressed genes. Metabolomic analysis screened 56 metabolites with significant differences, including various amino acids and their related metabolites. CONCLUSION: Comprehensive analysis showed that hypertension-induced hippocampal lesions are closely associated with differential metabolites and differential genes detected in this study. The results provide a basis for analyzing the mechanisms of hypertension-induced hippocampal damage. Frontiers Media S.A. 2023-04-06 /pmc/articles/PMC10115962/ /pubmed/37089694 http://dx.doi.org/10.3389/fnmol.2023.1146525 Text en Copyright © 2023 Li, Chu, Xie, Guo, Meng, Si and Jiang. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Molecular Neuroscience Li, Yanan Chu, Xue Xie, Xin Guo, Jinxiu Meng, Junjun Si, Qingying Jiang, Pei Integrating transcriptomics and metabolomics to analyze the mechanism of hypertension-induced hippocampal injury |
title | Integrating transcriptomics and metabolomics to analyze the mechanism of hypertension-induced hippocampal injury |
title_full | Integrating transcriptomics and metabolomics to analyze the mechanism of hypertension-induced hippocampal injury |
title_fullStr | Integrating transcriptomics and metabolomics to analyze the mechanism of hypertension-induced hippocampal injury |
title_full_unstemmed | Integrating transcriptomics and metabolomics to analyze the mechanism of hypertension-induced hippocampal injury |
title_short | Integrating transcriptomics and metabolomics to analyze the mechanism of hypertension-induced hippocampal injury |
title_sort | integrating transcriptomics and metabolomics to analyze the mechanism of hypertension-induced hippocampal injury |
topic | Molecular Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10115962/ https://www.ncbi.nlm.nih.gov/pubmed/37089694 http://dx.doi.org/10.3389/fnmol.2023.1146525 |
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