Cargando…

Metabolites and gene expression in the myocardium of fasting rats in an acute hypoxic environment

With the rising demand for entry to extremely high altitudes (HAs), rapid adaptability to extremely hypoxic environments is a challenge that we need to explore. Fasting was used to evaluate acute hypoxia tolerance at HA and was proven to be an effective method for improving the survival rate at extr...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhao, Ruzhou, Wang, Xiaobo, Zhou, Xiang, Jiang, Shuai, Zhang, Lin, Yu, Zhibin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10173486/
https://www.ncbi.nlm.nih.gov/pubmed/37165337
http://dx.doi.org/10.1186/s12864-023-09309-1
_version_ 1785039828165853184
author Zhao, Ruzhou
Wang, Xiaobo
Zhou, Xiang
Jiang, Shuai
Zhang, Lin
Yu, Zhibin
author_facet Zhao, Ruzhou
Wang, Xiaobo
Zhou, Xiang
Jiang, Shuai
Zhang, Lin
Yu, Zhibin
author_sort Zhao, Ruzhou
collection PubMed
description With the rising demand for entry to extremely high altitudes (HAs), rapid adaptability to extremely hypoxic environments is a challenge that we need to explore. Fasting was used to evaluate acute hypoxia tolerance at HA and was proven to be an effective method for improving the survival rate at extreme HA. Our experiments also showed that fasting pretreatment for 72 h significantly increased the 24 h survival rate of rats at 7620 m from 10 to 85% and protected the myocardium cells of rats. Here, we compared the metabolites and gene expression in the myocardium of SD rats pretreated with fasting and nonfasting at normal altitude and extreme HA. Our findings demonstrated that the dynamic contents of detected differential metabolites (DMs) between different rat groups were consistent with the expression of differentially expressed genes (DEGs), and DM clusters also showed strong correlations with DEG clusters. DM clusters related to amino acids and lipids were significantly lower in the fasting groups, and the correlated DEG clusters were enriched in mitotic pathways, including CDK1, CDC7, NUF2, and MCM6, suggesting that fasting can attenuate mitotic processes in cardiac tissues and reduce the synthesis of amino acids and lipids. L-Glutamine-related metabolites were particularly low at extreme HA without pretreatment but were normal in the fasting groups. The DEGs in the cluster related to L-glutamine-related metabolites were enriched for T-cell receptor V(D)J recombination, the Hippo signaling pathway, the Wnt signaling pathway, the cGMP-PKG signaling pathway, and the mTOR signaling pathway and were significantly downregulated, indicating that the content of L-glutamine decreased at extreme HA, while fasting increased it to adapt to the environment. Moreover, abundant fatty acids were detected when rats were exposed to extreme HA without pretreatment. Our study revealed the fasting and hypoxic environment-related factors in SD rats and provided new insights into the genetic and molecular characteristics in the myocardium, which is critical to developing more potential rapid adaptation methods to extreme HA.
format Online
Article
Text
id pubmed-10173486
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-101734862023-05-12 Metabolites and gene expression in the myocardium of fasting rats in an acute hypoxic environment Zhao, Ruzhou Wang, Xiaobo Zhou, Xiang Jiang, Shuai Zhang, Lin Yu, Zhibin BMC Genomics Research With the rising demand for entry to extremely high altitudes (HAs), rapid adaptability to extremely hypoxic environments is a challenge that we need to explore. Fasting was used to evaluate acute hypoxia tolerance at HA and was proven to be an effective method for improving the survival rate at extreme HA. Our experiments also showed that fasting pretreatment for 72 h significantly increased the 24 h survival rate of rats at 7620 m from 10 to 85% and protected the myocardium cells of rats. Here, we compared the metabolites and gene expression in the myocardium of SD rats pretreated with fasting and nonfasting at normal altitude and extreme HA. Our findings demonstrated that the dynamic contents of detected differential metabolites (DMs) between different rat groups were consistent with the expression of differentially expressed genes (DEGs), and DM clusters also showed strong correlations with DEG clusters. DM clusters related to amino acids and lipids were significantly lower in the fasting groups, and the correlated DEG clusters were enriched in mitotic pathways, including CDK1, CDC7, NUF2, and MCM6, suggesting that fasting can attenuate mitotic processes in cardiac tissues and reduce the synthesis of amino acids and lipids. L-Glutamine-related metabolites were particularly low at extreme HA without pretreatment but were normal in the fasting groups. The DEGs in the cluster related to L-glutamine-related metabolites were enriched for T-cell receptor V(D)J recombination, the Hippo signaling pathway, the Wnt signaling pathway, the cGMP-PKG signaling pathway, and the mTOR signaling pathway and were significantly downregulated, indicating that the content of L-glutamine decreased at extreme HA, while fasting increased it to adapt to the environment. Moreover, abundant fatty acids were detected when rats were exposed to extreme HA without pretreatment. Our study revealed the fasting and hypoxic environment-related factors in SD rats and provided new insights into the genetic and molecular characteristics in the myocardium, which is critical to developing more potential rapid adaptation methods to extreme HA. BioMed Central 2023-05-10 /pmc/articles/PMC10173486/ /pubmed/37165337 http://dx.doi.org/10.1186/s12864-023-09309-1 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Zhao, Ruzhou
Wang, Xiaobo
Zhou, Xiang
Jiang, Shuai
Zhang, Lin
Yu, Zhibin
Metabolites and gene expression in the myocardium of fasting rats in an acute hypoxic environment
title Metabolites and gene expression in the myocardium of fasting rats in an acute hypoxic environment
title_full Metabolites and gene expression in the myocardium of fasting rats in an acute hypoxic environment
title_fullStr Metabolites and gene expression in the myocardium of fasting rats in an acute hypoxic environment
title_full_unstemmed Metabolites and gene expression in the myocardium of fasting rats in an acute hypoxic environment
title_short Metabolites and gene expression in the myocardium of fasting rats in an acute hypoxic environment
title_sort metabolites and gene expression in the myocardium of fasting rats in an acute hypoxic environment
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10173486/
https://www.ncbi.nlm.nih.gov/pubmed/37165337
http://dx.doi.org/10.1186/s12864-023-09309-1
work_keys_str_mv AT zhaoruzhou metabolitesandgeneexpressioninthemyocardiumoffastingratsinanacutehypoxicenvironment
AT wangxiaobo metabolitesandgeneexpressioninthemyocardiumoffastingratsinanacutehypoxicenvironment
AT zhouxiang metabolitesandgeneexpressioninthemyocardiumoffastingratsinanacutehypoxicenvironment
AT jiangshuai metabolitesandgeneexpressioninthemyocardiumoffastingratsinanacutehypoxicenvironment
AT zhanglin metabolitesandgeneexpressioninthemyocardiumoffastingratsinanacutehypoxicenvironment
AT yuzhibin metabolitesandgeneexpressioninthemyocardiumoffastingratsinanacutehypoxicenvironment