Abstract |
Estrogen is a vascular protection factor and plays a protective role in the pathogenesis of gender differences in cardiovascular diseases. This study was to address the possible mechanisms that may explain the relationship between estradiol configuration-17β-estradiol (E2) and ventricular remodeling. Here, we show that a total of 1499 LncRNAs and 680 mRNAs significantly differently expressed were identified. This result indicates that estradiol has a global role in regulating heart gene expression profiles in female mice. Go and Pathway functional cluster analysis showed that the antagonism of E2 on cardiac remodeling and AngII-induced pathological changes in female mice may be related to physiological processes such as circadian rhythm disorder and ion channel dysfunction. Graphical Abstract.
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Authors | Jingkang Zhu, Huan Wang, Hui Chen |
Journal | Journal of cardiovascular translational research
(J Cardiovasc Transl Res)
Vol. 14
Issue 4
Pg. 706-727
(08 2021)
ISSN: 1937-5395 [Electronic] United States |
PMID | 32236843
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | © 2020. Springer Science+Business Media, LLC, part of Springer Nature. |
Chemical References |
- RNA, Long Noncoding
- RNA, Messenger
- Angiotensin II
- Estradiol
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Topics |
- Angiotensin II
- Animals
- Blood Pressure
(drug effects, genetics)
- Disease Models, Animal
- Estradiol
(administration & dosage)
- Estrogen Replacement Therapy
- Female
- Gene Expression Profiling
- Hypertension
(chemically induced, genetics, metabolism, physiopathology)
- Mice, Inbred C57BL
- Myocytes, Cardiac
(drug effects, metabolism)
- Ovariectomy
- Oxidative Stress
(drug effects, genetics)
- RNA, Long Noncoding
(genetics, metabolism)
- RNA, Messenger
(genetics, metabolism)
- Transcriptome
- Ventricular Remodeling
(drug effects, genetics)
- Mice
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