Abstract |
Diabetic cardiomyopathy increases the risk of heart failure independent of coronary artery disease and hypertension. Phloretin (PHL) shows anti-inflammatory effects in macrophages. In this study, we explored the protective effects of PHL on high glucose (HG)-induced injury in diabetic cardiomyopathy in vivo and in vitro. Using streptozotocin-induced diabetic mouse model and incubating cardiac cells line under a HG environment, PHL were evaluated of the activities of anti- inflammation and anti- fibrosis. In the study, PHL treatment ameliorated cardiomyocyte inflammation injury, and reduced fibrosis in vivo and in vitro. PHL also improved cardiac biochemical criterions after 8 weeks of induction of diabetes in C57BL/6 mice. Molecular docking results indicated that silent information regulator 2 homolog 1 ( SIRT1) bound to PHL directly and that SIRT1 expression was upregulated in the PHL-treated group in HG-induced H9C2 cells. Protective effect of PHL was been eliminated in silence SIRT1 H9C2 cells. Taken together, these results suggested that PHL suppressed HG-induced cardiomyocyte injury via restoring SIRT1 expression.
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Authors | Yin Ying, Cheng Jiang, Meiling Zhang, Jiye Jin, Shuyu Ge, Xiaodong Wang |
Journal | Aging
(Aging (Albany NY))
Vol. 11
Issue 9
Pg. 2822-2835
(05 10 2019)
ISSN: 1945-4589 [Electronic] United States |
PMID | 31076562
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Sirt1 protein, mouse
- Sirt1 protein, rat
- Sirtuin 1
- Phloretin
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Topics |
- Animals
- Cell Line
- Diabetes Mellitus, Experimental
(chemically induced, complications)
- Diabetic Cardiomyopathies
(prevention & control)
- Fibrosis
(prevention & control)
- Gene Expression Regulation
(drug effects)
- Inflammation
(prevention & control)
- Mice
- Myocytes, Cardiac
(drug effects)
- Phloretin
(pharmacology)
- Rats
- Sirtuin 1
(genetics, metabolism)
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