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Updated: May 31, 2026

Extraction and Purification of Polyphenols from Freeze-dried Berry Powder for the Treatment of Vascular Smooth Muscle Cells In Vitro
Published on: July 5, 2017
Preclinical Evaluation of Berry Extracts as a Nutritional Intervention to Alleviate Myocardial Ischemia-Reperfusion
Lydia Symeonidi1, Panagiota-Efstathia Nikolaou1,2, Panagiotis Stathopoulos3
1Laboratory of Pharmacology, Department of Pharmacy, National and Kapodistrian University of Athens, Athens, Greece.
Abstract:
Cardiovascular disease (CVD) remains the leading cause of morbidity and mortality worldwide. While studies suggest that berry fruits offer beneficial effects in CVD prevention, the bioactive compounds within different berries vary, and the specific mechanisms behind their protective effects are not yet fully elucidated. Our study aimed to evaluate and compare the cardioprotective and anti-atherosclerotic effects of Morus alba (white mulberries, WMex) and Vaccinium myrtillus L. fruit extracts (blueberries, BBex), focusing on acute myocardial infarction (AMI), CVD risk factors, atherosclerosis development, and the underlying mechanisms. WMex and BBex were produced and their qualitative compositions were characterized. We evaluated the infarct size (IS) limiting potential of 8-weeks supplementation with both WMex and BBex at nutritional doses in mice with western diet (WD)-induced metabolic syndrome (MS). We further evaluated atherosclerosis development mitigation after 4-weeks supplementation with the extracts in both male and female WD-fed ApoE-/- mice as well as the putative cardioprotective and atheroprotective mechanisms. The total flavonoids in WMex and BBex were 49.50 and 98.92 mg rutin/g extract, respectively, while the total phenolic content was 50.74 and 110.00 mg gallic acid/g extract, respectively. Both extracts limited IS compared to Control by suppressing apoptosis. WMex upregulated endothelial nitric oxide synthase (eNOS) phosphorylation and pathway along with circulating nitrite levels. WMex suppressed the extent of atheromatic area in both male and female ApoE-/- mice, while BBex was effective in females without any of the extracts affecting estrogen levels. WMex downregulated NF-kB-ICAM-1 axis in the atherosclerotic area and reduced circulating triglyceride levels. None of the extracts caused signs of toxicity, supporting a safety profile. In conclusion, WMex exerts potent cardioprotective and anti-atherosclerotic properties in vivo and could be further exploited for CVD prevention.
Insights
White mulberry extract (WMex) and blueberry extract (BBex) show cardioprotective effects against cardiovascular disease (CVD). WMex demonstrated potent anti-atherosclerotic properties in vivo, suggesting its potential for CVD prevention.
Area of Science:
- Nutritional Science
- Cardiovascular Research
- Pharmacology
Background:
- Cardiovascular disease (CVD) is a leading global cause of death.
- Berry fruits show promise for CVD prevention, but mechanisms are unclear.
- Bioactive compounds differ among berries, necessitating comparative studies.
Purpose of the Study:
- To compare cardioprotective and anti-atherosclerotic effects of Morus alba (white mulberry, WMex) and Vaccinium myrtillus L. (blueberry, BBex) extracts.
- To investigate underlying mechanisms in models of acute myocardial infarction (AMI) and atherosclerosis.
- To evaluate effects on CVD risk factors and safety.
Main Methods:
- Characterization of WMex and BBex bioactive compounds (flavonoids, phenolics).
- Evaluation of infarct size (IS) limitation in mice with metabolic syndrome (MS).
- Assessment of atherosclerosis development in ApoE-/- mice and mechanistic studies (e.g., eNOS, NF-kB pathways).
Main Results:
- Both WMex and BBex limited IS by suppressing apoptosis.
- WMex upregulated endothelial nitric oxide synthase (eNOS) and improved nitrite levels.
- WMex reduced atherosclerotic area and triglyceride levels; BBex was effective in females.
Conclusions:
- Morus alba extract (WMex) exhibits significant cardioprotective and anti-atherosclerotic effects in vivo.
- WMex's benefits may involve eNOS pathway activation and NF-kB inhibition.
- WMex shows potential for further development in cardiovascular disease prevention strategies.
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