Abstract |
Synthetic peptides were microencapsulated into liposomes, cycled with a disulfide bond or modified with d-phenylglycine (d-phg) at the N-terminal, and their antihypertensive effects as orally administered (0.18 mM/kg body weight) to spontaneously hypertensive rats (SHR) were measured. The microencapsulated Leu-Lys-Pro reduced significantly the systolic blood pressures of SHR by 45 mmHg and showed a prolonged duration, revealing the significant protective effect of encapsulation. d-phg- Leu-Arg-Pro showed a duration about 2 h shorter than that of the peptide without modification. In addition, cyclic Leu-Arg-Pro peptide with a disulfide bond between the N- and C-terminal amino acids reduced the systolic blood pressure of SHR by 35 mmHg and displayed a lengthy duration.
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Authors | Tzy-Li Chen, Yung-Chieh Lo, Wei-Tze Hu, Ming-Chang Wu, Shui-Ten Chen, Hung-Min Chang |
Journal | Journal of agricultural and food chemistry
(J Agric Food Chem)
Vol. 51
Issue 6
Pg. 1671-5
(Mar 12 2003)
ISSN: 0021-8561 [Print] United States |
PMID | 12617603
(Publication Type: Journal Article)
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Chemical References |
- Angiotensin-Converting Enzyme Inhibitors
- Antihypertensive Agents
- Dietary Proteins
- Liposomes
- Peptides
- Peptides, Cyclic
- Captopril
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Topics |
- Amino Acid Sequence
- Angiotensin-Converting Enzyme Inhibitors
(administration & dosage)
- Animals
- Antihypertensive Agents
(administration & dosage)
- Blood Pressure
(drug effects)
- Captopril
(pharmacology)
- Dietary Proteins
(analysis)
- Hydrolysis
- Kinetics
- Liposomes
(chemistry)
- Peptides
(administration & dosage, chemistry)
- Peptides, Cyclic
(administration & dosage, chemistry)
- Rats
- Rats, Inbred SHR
- Structure-Activity Relationship
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