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Published on: December 5, 2017
Ameliorative effect of mussel-derived ACE inhibitory peptides on spontaneous hypertension rats
Qiaoni You1, Xiaopeng Sun1, Jinli Chen2
1College of Life Sciences, Qingdao University, 308 Ningxia Road, Qingdao, 266071, China.
Purpose:
The purpose of this study was to prepare the novel mussel-derived ACE inhibitory peptides (MEPs) by enzymatic hydrolysis of Mytilus edulis and investigate their antihypertensive effects in vivo.
Methods:
After assessing the stability of MEPs in vitro, we investigated the effect of MEPs on hypertension using spontaneously hypertensive rats (SHRs). Subsequently, MEPs were purified and identified by ultrafiltration, gel filtration chromatography and liquid chromatography-tandem mass spectrometry (LC-MS/MS).
Results:
Our study demonstrated that MEPs could keep stable ACE inhibitory activity after treatment with heat, acid, alkali, metal ions and simulated gastrointestinal digestive fluid. Additionally, the animal experiments showed that both short-term and long-term treatment with MEPs resulted in a significant reduction in systolic and diastolic blood pressure in SHRs. Mechanistically, the results suggested that MEPs could reduce vascular remodeling, regulate renin-angiotensin system (RAS), and inhibit kidney and myocardial fibrosis. Finally, we isolated and identified five peptides from MEPs, with the peptide Ile-Leu-Thr-Glu-Arg showed the highest ACE inhibition rate.
Conclusion:
Our findings demonstrate the potential use of MEPs as active components in functional foods designed to lower blood pressure.
Insights
Novel mussel-derived peptides (MEPs) show stable angiotensin-converting enzyme (ACE) inhibitory activity and effectively lower blood pressure in hypertensive rats. These findings suggest MEPs
Area of Science:
- Biotechnology
- Food Science
- Pharmacology
Background:
- Hypertension is a major global health concern.
- Angiotensin-converting enzyme (ACE) plays a key role in blood pressure regulation.
- Natural sources are being explored for antihypertensive compounds.
Purpose of the Study:
- To prepare novel mussel-derived ACE inhibitory peptides (MEPs).
- To investigate the in vivo antihypertensive effects of MEPs.
- To assess the stability and identify active peptide components.
Main Methods:
- Enzymatic hydrolysis of Mytilus edulis to obtain MEPs.
- In vitro stability assessment (heat, pH, ions, digestion).
- In vivo antihypertensive study in spontaneously hypertensive rats (SHRs).
- Purification and identification using chromatography and LC-MS/MS.
Main Results:
- MEPs exhibited stability under various conditions.
- MEPs significantly reduced systolic and diastolic blood pressure in SHRs.
- MEPs modulated vascular remodeling, renin-angiotensin system (RAS), and fibrosis.
- Five peptides were identified, with Ile-Leu-Thr-Glu-Arg showing highest ACE inhibition.
Conclusions:
- MEPs possess significant antihypertensive properties.
- MEPs demonstrate potential as functional food ingredients for blood pressure management.
- Further research into MEPs' therapeutic applications is warranted.
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