Dapagliflozin attenuates LPS-induced myocardial injury by reducing ferroptosis.
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| Title: | Dapagliflozin attenuates LPS-induced myocardial injury by reducing ferroptosis. |
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| Authors: | Hu, Ke1 (AUTHOR), Jiang, Pin2 (AUTHOR), Hu, Jiaxin3 (AUTHOR), Song, Bing4 (AUTHOR), Hou, Ya5 (AUTHOR), Zhao, Jinxuan5 (AUTHOR) njuzhaojinxuan@163.com, Chen, Haiting4 (AUTHOR) cht141230004@163.com, Xie, Jun1,4 (AUTHOR) xiejun@ahmu.edu.cn |
| Source: | Journal of Bioenergetics & Biomembranes. Aug2024, Vol. 56 Issue 4, p361-371. 11p. |
| Subjects: | Myocardial injury, Dapagliflozin, Sodium-glucose cotransporter 2 inhibitors, Treatment effectiveness, Iron metabolism |
| Abstract: | Septic cardiomyopathy is a severe cardiovascular disease with a poor prognosis. Previous studies have reported the involvement of ferroptosis in the pathogenesis of septic cardiomyopathy. SGLT2 inhibitors such as dapagliflozin have been demonstrated to improve ischemia–reperfusion injury by alleviating ferroptosis in cardiomyocyte. However, the role of dapagliflozin in sepsis remains unclear. Therefore, our study aims to investigate the therapeutic effects of dapagliflozin on LPS-induced septic cardiomyopathy. Our results indicate that dapagliflozin improved cardiac function in septic cardiomyopathy experimental mice. Mechanistically, dapagliflozin works by inhibiting the translation of key proteins involved in ferroptosis, such as GPX4, FTH1, and SLC7A11. It also reduces the transcription of lipid peroxidation-related mRNAs, including PTGS2 and ACSL4, as well as iron metabolism genes TFRC and HMOX1. [ABSTRACT FROM AUTHOR] |
| Copyright of Journal of Bioenergetics & Biomembranes is the property of Springer Nature and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.) | |
| Database: | Engineering Source |
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| Header | DbId: egs DbLabel: Engineering Source An: 178209685 AccessLevel: 6 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Dapagliflozin attenuates LPS-induced myocardial injury by reducing ferroptosis. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Hu%2C+Ke%22">Hu, Ke</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Jiang%2C+Pin%22">Jiang, Pin</searchLink><relatesTo>2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Hu%2C+Jiaxin%22">Hu, Jiaxin</searchLink><relatesTo>3</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Song%2C+Bing%22">Song, Bing</searchLink><relatesTo>4</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Hou%2C+Ya%22">Hou, Ya</searchLink><relatesTo>5</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Zhao%2C+Jinxuan%22">Zhao, Jinxuan</searchLink><relatesTo>5</relatesTo> (AUTHOR)<i> njuzhaojinxuan@163.com</i><br /><searchLink fieldCode="AR" term="%22Chen%2C+Haiting%22">Chen, Haiting</searchLink><relatesTo>4</relatesTo> (AUTHOR)<i> cht141230004@163.com</i><br /><searchLink fieldCode="AR" term="%22Xie%2C+Jun%22">Xie, Jun</searchLink><relatesTo>1,4</relatesTo> (AUTHOR)<i> xiejun@ahmu.edu.cn</i> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22Journal+of+Bioenergetics+%26+Biomembranes%22">Journal of Bioenergetics & Biomembranes</searchLink>. Aug2024, Vol. 56 Issue 4, p361-371. 11p. – Name: Subject Label: Subjects Group: Su Data: <searchLink fieldCode="DE" term="%22Myocardial+injury%22">Myocardial injury</searchLink><br /><searchLink fieldCode="DE" term="%22Dapagliflozin%22">Dapagliflozin</searchLink><br /><searchLink fieldCode="DE" term="%22Sodium-glucose+cotransporter+2+inhibitors%22">Sodium-glucose cotransporter 2 inhibitors</searchLink><br /><searchLink fieldCode="DE" term="%22Treatment+effectiveness%22">Treatment effectiveness</searchLink><br /><searchLink fieldCode="DE" term="%22Iron+metabolism%22">Iron metabolism</searchLink> – Name: Abstract Label: Abstract Group: Ab Data: Septic cardiomyopathy is a severe cardiovascular disease with a poor prognosis. Previous studies have reported the involvement of ferroptosis in the pathogenesis of septic cardiomyopathy. SGLT2 inhibitors such as dapagliflozin have been demonstrated to improve ischemia–reperfusion injury by alleviating ferroptosis in cardiomyocyte. However, the role of dapagliflozin in sepsis remains unclear. Therefore, our study aims to investigate the therapeutic effects of dapagliflozin on LPS-induced septic cardiomyopathy. Our results indicate that dapagliflozin improved cardiac function in septic cardiomyopathy experimental mice. Mechanistically, dapagliflozin works by inhibiting the translation of key proteins involved in ferroptosis, such as GPX4, FTH1, and SLC7A11. It also reduces the transcription of lipid peroxidation-related mRNAs, including PTGS2 and ACSL4, as well as iron metabolism genes TFRC and HMOX1. [ABSTRACT FROM AUTHOR] – Name: AbstractSuppliedCopyright Label: Group: Ab Data: <i>Copyright of Journal of Bioenergetics & Biomembranes is the property of Springer Nature and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract.</i> (Copyright applies to all Abstracts.) |
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| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1007/s10863-024-10020-3 Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 11 StartPage: 361 Subjects: – SubjectFull: Myocardial injury Type: general – SubjectFull: Dapagliflozin Type: general – SubjectFull: Sodium-glucose cotransporter 2 inhibitors Type: general – SubjectFull: Treatment effectiveness Type: general – SubjectFull: Iron metabolism Type: general Titles: – TitleFull: Dapagliflozin attenuates LPS-induced myocardial injury by reducing ferroptosis. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Hu, Ke – PersonEntity: Name: NameFull: Jiang, Pin – PersonEntity: Name: NameFull: Hu, Jiaxin – PersonEntity: Name: NameFull: Song, Bing – PersonEntity: Name: NameFull: Hou, Ya – PersonEntity: Name: NameFull: Zhao, Jinxuan – PersonEntity: Name: NameFull: Chen, Haiting – PersonEntity: Name: NameFull: Xie, Jun IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 08 Text: Aug2024 Type: published Y: 2024 Identifiers: – Type: issn-print Value: 0145479X Numbering: – Type: volume Value: 56 – Type: issue Value: 4 Titles: – TitleFull: Journal of Bioenergetics & Biomembranes Type: main |
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