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Published on: December 2, 2016
Role of puerarin in pathological cardiac remodeling: A review
Jiayu Lv1, Shuqing Shi1, Bingxuan Zhang1
1Department of General Internal Medicine, Guang'anmen Hospital, China Academy of Chinese Medical Sciences, Beijing, China.
Insights
Puerarin, a natural compound, effectively prevents pathological cardiac remodeling by inhibiting detrimental changes like cell death and inflammation. This offers a promising therapeutic strategy for heart failure.
Area of Science:
- Cardiology
- Pharmacology
- Biochemistry
Background:
- Pathological cardiac remodeling, a process involving structural and functional heart changes, is a key driver of heart failure.
- Cardiac remodeling is a significant therapeutic target for various heart failure etiologies.
- Puerarin, a natural isoflavone from Pueraria lobata, is clinically used for cardiovascular diseases in East Asia.
Purpose of the Study:
- To review the roles and molecular mechanisms of puerarin in attenuating pathological cardiac remodeling.
- To explore puerarin's potential as a therapeutic agent for preventing or reversing cardiac remodeling.
Main Methods:
- Literature review of studies investigating puerarin's effects on cardiac remodeling.
- Analysis of molecular mechanisms underlying puerarin's cardioprotective actions.
Main Results:
- Puerarin inhibits myocardial hypertrophy, myocyte death, and fetal gene expression.
- It improves cardiac energy metabolism and promotes angiogenesis.
- Puerarin suppresses inflammation and oxidative stress, mitigating cardiac remodeling.
Conclusions:
- Puerarin demonstrates significant cardioprotective effects against diverse stimuli causing cardiac remodeling.
- Its multifaceted mechanisms suggest potential for novel therapeutic strategies in heart failure management.
Abstract:
Pathological cardiac remodeling normally involves changes in structure, function, and energy metabolism of the heart induced by cardiac injury or load, terminally leading to heart failure. Cardiac remodeling plays an essential role in the progression of cardiovascular disease, thus increasingly identified as an important therapeutic target for heart failure of all pathogenesis. Puerarin, as a natural isoflavone mainly from Pueraria lobata (Willd.)Ohwi, has been developed as injections, eye drops, microemulsions, etc., and is widely used in the clinical treatment of cardiovascular diseases in eastern Asia countries. In recent years, a growing number of studies have shown that puerarin significantly inhibits myocardial hypertrophic growth, myocyte death, fetal gene expression, fibroblast proliferation and activation, improves energy metabolism, promotes post-infarction angiogenesis, and suppresses inflammation and oxidative stress, consequently attenuating or preventing cardiac remodeling in response to multiple stimuli ( e.g., pressure overload, MIRI, MI, Iso, and Ang II stimulation). This review summarized the roles and underlying molecular mechanisms of puerarin in cardiac remodeling induced by diverse etiologies, aiming to help develop novel therapeutic strategies to prevent or reverse pathological ventricular remodeling.
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