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Promising Protective Effects of Chrysin in Cardiometabolic Diseases
Marjan Talebi1, Mohsen Talebi2,3, Tahereh Farkhondeh4,5
1Department of Pharmacognosy, School of Pharmacy, Shahid Beheshti University of Medical Sciences, Tehran 1991953381, Iran.
Insights
The natural compound chrysin offers significant protection against cardiometabolic diseases (CMD) by boosting antioxidant defenses and reducing inflammation. Its multifaceted mechanisms combat various CMD risk factors, including diabetes and hypertension.
Area of Science:
- Cardiovascular Pharmacology
- Natural Product Chemistry
- Molecular Medicine
Background:
- Cardiometabolic diseases (CMD) represent a significant global health burden, characterized by interconnected conditions like type II diabetes, hypertension, dyslipidemia, obesity, and atherosclerosis.
- The natural flavonoid chrysin is recognized for its diverse therapeutic properties.
- Understanding chrysin's specific mechanisms against CMD is crucial for developing novel therapeutic strategies.
Purpose of the Study:
- To investigate the novel cardioprotective mechanisms of the natural flavonoid chrysin against cardiometabolic disorders.
- To elucidate how chrysin's properties counteract the complex interplay of factors contributing to CMD.
- To provide an in-depth analysis of chrysin's molecular targets and pathways relevant to cardiovascular health.
Main Methods:
- Literature review and analysis of existing studies on chrysin's effects on cardiovascular health.
- Examination of chrysin's impact on antioxidant defense systems and inflammatory pathways.
- Investigation of chrysin's modulation of key signaling pathways implicated in CMD, including NO, RAS, AGE/RAGE, and PPARs.
Main Results:
- Chrysin enhances the intrinsic antioxidative defense system, mitigating risks associated with atherosclerosis, vascular dysfunction, hypertension, dyslipidemia, and diabetes-induced injuries.
- Chrysin exhibits potent anti-inflammatory effects by inhibiting pro-inflammatory pathways such as NF-κB, MAPK, and PI3k/Akt.
- Chrysin modulates critical pathways including nitric oxide (NO), renin-angiotensin system (RAS), advanced glycation end-products/receptor for advanced glycation end-products (AGE/RAGE), and peroxisome proliferator-activated receptors (PPARs).
Conclusions:
- Chrysin's cardioprotective effects against cardiometabolic disorders extend beyond simple antioxidation and anti-inflammation.
- Chrysin targets multiple interconnected pathways, offering a comprehensive approach to managing CMD.
- The findings highlight chrysin as a promising natural compound for therapeutic interventions in cardiometabolic diseases.
Abstract:
Cardiometabolic diseases (CMD) have caused a great burden in terms of morbidity and mortality worldwide. The vicious cycle of CMD consists of type II diabetes, hypertension, dyslipidemia, obesity, and atherosclerosis. They have interlinked pathways, interacting and interconnecting with each other. The natural flavonoid chrysin has been shown to possess a broad spectrum of therapeutic activities for human health. Herein, we did an in-depth investigation of the novel mechanisms of chrysin's cardioprotection against cardiometabolic disorders. Studies have shown that chrysin protects the cardiovascular system by enhancing the intrinsic antioxidative defense system. This antioxidant property enhanced by chrysin protects against several risk factors of cardiometabolic disorders, including atherosclerosis, vascular inflammation and dysfunction, platelet aggregation, hypertension, dyslipidemia, cardiotoxicity, myocardial infarction, injury, and remodeling, diabetes-induced injuries, and obesity. Chrysin also exhibited anti-inflammatory mechanisms through inhibiting pro-inflammatory pathways, including NF-κB, MAPK, and PI3k/Akt. Furthermore, chrysin modulated NO, RAS, AGE/RAGE, and PPARs pathways which contributed to the risk factors of cardiometabolic disorders. Taken together, the mechanisms in which chrysin protects against cardiometabolic disorder are more than merely antioxidation and anti-inflammation in the cardiovascular system.
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