Low sodium intake ameliorates hypertension and left ventricular hypertrophy in mice with primary aldosteronism
Title: | Low sodium intake ameliorates hypertension and left ventricular hypertrophy in mice with primary aldosteronism |
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Authors: | Zitian Wang, Xue Zhao, Lifang Bu, Kun Liu, Ziping Li, Huaxing Zhang, Xiaoguang Zhang, Fang Yuan, Sheng Wang, Zan Guo, Luo Shi |
Source: | Frontiers in Physiology, Vol 14 (2023) |
Publisher Information: | Frontiers Media S.A., 2023. |
Publication Year: | 2023 |
Collection: | LCC:Physiology |
Subject Terms: | primary aldosteronism, hypertension, left ventricular hypertrophy, low sodium, myocardial metabolic, Physiology, QP1-981 |
More Details: | The goal of this paper is to elucidate the effects of sodium restriction on hypertension and left ventricular (LV) hypertrophy in a mouse model with primary aldosteronism (PA). Mice with genetic deletion of TWIK-related acid-sensitive K (TASK)-1 and TASK-3 channels (TASK−/−) were used as the animal model of PA. Parameters of the LV were assessed using echocardiography and histomorphology analysis. Untargeted metabolomics analysis was conducted to reveal the mechanisms underlying the hypertrophic changes in the TASK−/− mice. The TASK−/− adult male mice exhibited the hallmarks of PA, including hypertension, hyperaldosteronism, hypernatremia, hypokalemia, and mild acid-base balance disorders. Two weeks of low sodium intake significantly reduced the 24-h average systolic and diastolic BP in TASK−/− but not TASK+/+ mice. In addition, TASK−/− mice showed increasing LV hypertrophy with age, and 2 weeks of the low-sodium diet significantly reversed the increased BP and LV wall thickness in adult TASK−/− mice. Furthermore, a low-sodium diet beginning at 4 weeks of age protected TASK−/− mice from LV hypertrophy at 8–12 weeks of age. Untargeted metabolomics demonstrated that the disturbances in heart metabolism in the TASK−/− mice (e.g., Glutathione metabolism; biosynthesis of unsaturated fatty acids; amino sugar and nucleotide sugar metabolism; pantothenate and CoA biosynthesis; D-glutamine and D-glutamate metabolism), some of which were reversed after sodium restriction, might be involved in the development of LV hypertrophy. In conclusion, adult male TASK−/− mice exhibit spontaneous hypertension and LV hypertrophy, which are ameliorated by a low-sodium intake. |
Document Type: | article |
File Description: | electronic resource |
Language: | English |
ISSN: | 1664-042X |
Relation: | https://www.frontiersin.org/articles/10.3389/fphys.2023.1136574/full; https://doaj.org/toc/1664-042X |
DOI: | 10.3389/fphys.2023.1136574 |
Access URL: | https://doaj.org/article/53c7a200bdd34663925abd2a862eae02 |
Accession Number: | edsdoj.53c7a200bdd34663925abd2a862eae02 |
Database: | Directory of Open Access Journals |
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Items | – Name: Title Label: Title Group: Ti Data: Low sodium intake ameliorates hypertension and left ventricular hypertrophy in mice with primary aldosteronism – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Zitian+Wang%22">Zitian Wang</searchLink><br /><searchLink fieldCode="AR" term="%22Xue+Zhao%22">Xue Zhao</searchLink><br /><searchLink fieldCode="AR" term="%22Lifang+Bu%22">Lifang Bu</searchLink><br /><searchLink fieldCode="AR" term="%22Kun+Liu%22">Kun Liu</searchLink><br /><searchLink fieldCode="AR" term="%22Ziping+Li%22">Ziping Li</searchLink><br /><searchLink fieldCode="AR" term="%22Huaxing+Zhang%22">Huaxing Zhang</searchLink><br /><searchLink fieldCode="AR" term="%22Xiaoguang+Zhang%22">Xiaoguang Zhang</searchLink><br /><searchLink fieldCode="AR" term="%22Fang+Yuan%22">Fang Yuan</searchLink><br /><searchLink fieldCode="AR" term="%22Sheng+Wang%22">Sheng Wang</searchLink><br /><searchLink fieldCode="AR" term="%22Zan+Guo%22">Zan Guo</searchLink><br /><searchLink fieldCode="AR" term="%22Luo+Shi%22">Luo Shi</searchLink> – Name: TitleSource Label: Source Group: Src Data: Frontiers in Physiology, Vol 14 (2023) – Name: Publisher Label: Publisher Information Group: PubInfo Data: Frontiers Media S.A., 2023. – Name: DatePubCY Label: Publication Year Group: Date Data: 2023 – Name: Subset Label: Collection Group: HoldingsInfo Data: LCC:Physiology – Name: Subject Label: Subject Terms Group: Su Data: <searchLink fieldCode="DE" term="%22primary+aldosteronism%22">primary aldosteronism</searchLink><br /><searchLink fieldCode="DE" term="%22hypertension%22">hypertension</searchLink><br /><searchLink fieldCode="DE" term="%22left+ventricular+hypertrophy%22">left ventricular hypertrophy</searchLink><br /><searchLink fieldCode="DE" term="%22low+sodium%22">low sodium</searchLink><br /><searchLink fieldCode="DE" term="%22myocardial+metabolic%22">myocardial metabolic</searchLink><br /><searchLink fieldCode="DE" term="%22Physiology%22">Physiology</searchLink><br /><searchLink fieldCode="DE" term="%22QP1-981%22">QP1-981</searchLink> – Name: Abstract Label: Description Group: Ab Data: The goal of this paper is to elucidate the effects of sodium restriction on hypertension and left ventricular (LV) hypertrophy in a mouse model with primary aldosteronism (PA). Mice with genetic deletion of TWIK-related acid-sensitive K (TASK)-1 and TASK-3 channels (TASK−/−) were used as the animal model of PA. Parameters of the LV were assessed using echocardiography and histomorphology analysis. Untargeted metabolomics analysis was conducted to reveal the mechanisms underlying the hypertrophic changes in the TASK−/− mice. The TASK−/− adult male mice exhibited the hallmarks of PA, including hypertension, hyperaldosteronism, hypernatremia, hypokalemia, and mild acid-base balance disorders. Two weeks of low sodium intake significantly reduced the 24-h average systolic and diastolic BP in TASK−/− but not TASK+/+ mice. In addition, TASK−/− mice showed increasing LV hypertrophy with age, and 2 weeks of the low-sodium diet significantly reversed the increased BP and LV wall thickness in adult TASK−/− mice. Furthermore, a low-sodium diet beginning at 4 weeks of age protected TASK−/− mice from LV hypertrophy at 8–12 weeks of age. Untargeted metabolomics demonstrated that the disturbances in heart metabolism in the TASK−/− mice (e.g., Glutathione metabolism; biosynthesis of unsaturated fatty acids; amino sugar and nucleotide sugar metabolism; pantothenate and CoA biosynthesis; D-glutamine and D-glutamate metabolism), some of which were reversed after sodium restriction, might be involved in the development of LV hypertrophy. In conclusion, adult male TASK−/− mice exhibit spontaneous hypertension and LV hypertrophy, which are ameliorated by a low-sodium intake. – Name: TypeDocument Label: Document Type Group: TypDoc Data: article – Name: Format Label: File Description Group: SrcInfo Data: electronic resource – Name: Language Label: Language Group: Lang Data: English – Name: ISSN Label: ISSN Group: ISSN Data: 1664-042X – Name: NoteTitleSource Label: Relation Group: SrcInfo Data: https://www.frontiersin.org/articles/10.3389/fphys.2023.1136574/full; https://doaj.org/toc/1664-042X – Name: DOI Label: DOI Group: ID Data: 10.3389/fphys.2023.1136574 – Name: URL Label: Access URL Group: URL Data: <link linkTarget="URL" linkTerm="https://doaj.org/article/53c7a200bdd34663925abd2a862eae02" linkWindow="_blank">https://doaj.org/article/53c7a200bdd34663925abd2a862eae02</link> – Name: AN Label: Accession Number Group: ID Data: edsdoj.53c7a200bdd34663925abd2a862eae02 |
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RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.3389/fphys.2023.1136574 Languages: – Text: English Subjects: – SubjectFull: primary aldosteronism Type: general – SubjectFull: hypertension Type: general – SubjectFull: left ventricular hypertrophy Type: general – SubjectFull: low sodium Type: general – SubjectFull: myocardial metabolic Type: general – SubjectFull: Physiology Type: general – SubjectFull: QP1-981 Type: general Titles: – TitleFull: Low sodium intake ameliorates hypertension and left ventricular hypertrophy in mice with primary aldosteronism Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Zitian Wang – PersonEntity: Name: NameFull: Xue Zhao – PersonEntity: Name: NameFull: Lifang Bu – PersonEntity: Name: NameFull: Kun Liu – PersonEntity: Name: NameFull: Ziping Li – PersonEntity: Name: NameFull: Huaxing Zhang – PersonEntity: Name: NameFull: Xiaoguang Zhang – PersonEntity: Name: NameFull: Fang Yuan – PersonEntity: Name: NameFull: Sheng Wang – PersonEntity: Name: NameFull: Zan Guo – PersonEntity: Name: NameFull: Luo Shi IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 02 Type: published Y: 2023 Identifiers: – Type: issn-print Value: 1664042X Numbering: – Type: volume Value: 14 Titles: – TitleFull: Frontiers in Physiology Type: main |
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