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Published on: May 4, 2018
Antihypertensive effect of the bovine casein-derived peptide Met-Lys-Pro
Akio Yamada1, Takuma Sakurai1, Daisuke Ochi1
1Morinaga Milk Industry Co., Ltd, Functional Food Research Department, Food Science & Technology Institute, 1-83, 5-Chome, Higashihara, Zama-City, Kanagawa-Pref. 252-8583, Japan.
Abstract:
The antihypertensive effect of the bovine casein-derived peptide Met-Lys-Pro (MKP) was examined in vitro and in vivo. MKP showed angiotensin I-converting enzyme (ACE)-inhibitory activity in vitro (IC50 = 0.43 μM). An in vivo kinetics study using radiolabeled Met-[1-(14)C]Lys-Pro ((14)C-MKP) showed that orally administered (14)C-MKP to spontaneously hypertensive rats (SHRs) was absorbed and moved into the plasma. In vitro vasoconstriction of thoracic aorta preparations, which was induced by adding angiotensin I, was reduced by prior exposure of MKP. A single oral dose of MKP lowered systolic blood pressure (SBP) of SHRs, and repeated oral administration of MKP for 28 days significantly lowered SBP of SHRs. The results obtained in the present study suggest that orally administrated MKP can be absorbed into the plasma and its ACE-inhibitory activity may contribute to induce the antihypertensive effect in vivo.
Insights
Bovine casein peptide Met-Lys-Pro (MKP) effectively inhibits angiotensin I-converting enzyme (ACE). Oral administration of MKP lowers blood pressure in spontaneously hypertensive rats, suggesting its potential as an antihypertensive agent.
Area of Science:
- Biochemistry
- Pharmacology
- Physiology
Background:
- Hypertension remains a significant global health concern.
- Dietary peptides are increasingly recognized for their potential health benefits.
- Angiotensin I-converting enzyme (ACE) plays a crucial role in blood pressure regulation.
Purpose of the Study:
- To investigate the antihypertensive effects of the bovine casein-derived peptide Met-Lys-Pro (MKP).
- To evaluate the in vitro and in vivo efficacy of MKP as an ACE inhibitor.
Main Methods:
- In vitro assessment of ACE-inhibitory activity.
- In vivo pharmacokinetic study using radiolabeled MKP in spontaneously hypertensive rats (SHRs).
- Measurement of thoracic aorta vasoconstriction.
- Evaluation of systolic blood pressure (SBP) following single and repeated oral MKP administration in SHRs.
Main Results:
- MKP demonstrated significant in vitro ACE-inhibitory activity (IC50 = 0.43 μM).
- Orally administered MKP was absorbed into the plasma of SHRs.
- MKP reduced angiotensin I-induced vasoconstriction in vitro.
- Both single and repeated oral doses of MKP lowered SBP in SHRs.
Conclusions:
- Orally administered MKP is absorbed and circulates in the plasma.
- The ACE-inhibitory activity of MKP likely contributes to its observed antihypertensive effect.
- MKP shows promise as a potential therapeutic agent for managing hypertension.
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