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Published on: May 18, 2021
Inhibition Mechanism, Multi-Target Regulation, and Protective Effects of Camel Casein ACE-Inhibitory Peptide on
Fei Zhang1,2, Hao Miao1,2, Chenkun Huo1,2
1College of Smart Agriculture (Research Institute), Xinjiang University, Urumqi 830017, China.
Camel milk peptides show potential for managing hypertension. Researchers identified three ACE-inhibitory peptides from camel casein that protect endothelial cells and may regulate blood pressure through multiple pathways.
Area of Science:
- Biochemistry and Molecular Biology
- Pharmacology
- Nutritional Science
Background:
- Hypertension is a major global health concern, driving research into natural alternatives to synthetic drugs.
- Food-derived peptides, particularly from camel milk casein, are recognized for their potential antihypertensive properties.
- Angiotensin-converting enzyme (ACE) inhibitors are a key therapeutic target for managing blood pressure.
Purpose of the Study:
- To screen and characterize ACE-inhibitory peptides from hydrolyzed camel casein.
- To elucidate the inhibitory mechanisms and endothelial protective effects of these peptides in vitro.
- To explore their potential antihypertensive pathways using network pharmacology.
Main Methods:
- Enzymatic hydrolysis of camel casein and screening of ACE-inhibitory peptides.
- Enzyme kinetics, molecular docking, and molecular dynamics simulations to determine inhibition patterns and binding interactions.
- Network pharmacology analysis to predict antihypertensive pathways and targets.
- In vitro cell experiments using an Ang II-induced HUVEC injury model to assess endothelial protection.
Main Results:
- Three peptides (MVPFLQPK, VPFLQPKVM, QKWKFL) with significant ACE inhibitory activity were identified.
- Kinetic analysis revealed competitive, non-competitive, and mixed inhibition patterns for the peptides.
- Molecular simulations confirmed stable peptide-ACE complexes, highlighting key binding interactions.
- Network pharmacology indicated regulation of the renin-angiotensin system and other pathways.
- Peptides demonstrated no cytotoxicity and offered endothelial protection by promoting NO release and inhibiting ET-1.
Conclusions:
- Camel milk-derived peptides exhibit potent in vitro ACE inhibition and endothelial protective effects.
- These peptides may offer a natural strategy for blood pressure regulation via multiple molecular targets.
- The findings provide a basis for developing functional camel milk products for hypertension management.
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