Antihypertensive Properties of Lactoferricin B-Derived Peptides

A set of eight lactoferricin B (LfcinB)-derived peptides was examined for inhibitory effects on angiotensin I-converting enzyme (ACE) activity and ACE-dependent vasoconstriction, and their hypotensive effect in spontaneously hypertensive rats (SHR). Peptides were derived from different elongations b...

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Veröffentlicht in:Journal of agricultural and food chemistry 2010-06, Vol.58 (11), p.6721-6727
Hauptverfasser: Ruiz-Giménez, Pedro, Ibáñez, Aida, Salom, Juan B, Marcos, Jose F, López-Díez, Jose Javier, Vallés, Salvador, Torregrosa, Germán, Alborch, Enrique, Manzanares, Paloma
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Sprache:eng
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Zusammenfassung:A set of eight lactoferricin B (LfcinB)-derived peptides was examined for inhibitory effects on angiotensin I-converting enzyme (ACE) activity and ACE-dependent vasoconstriction, and their hypotensive effect in spontaneously hypertensive rats (SHR). Peptides were derived from different elongations both at the C-terminal and N-terminal ends of the representative peptide LfcinB20−25, which is known as the LfcinB antimicrobial core. All of the eight LfcinB-derived peptides showed in vitro inhibitory effects on ACE activity with different IC50 values. Moreover, seven of them showed ex vivo inhibitory effects on ACE-dependent vasoconstriction. No clear correlation between in vitro and ex vivo inhibitory effects was found. Only LfcinB20−25 and one of its fragments, F1, generated after a simulated gastrointestinal digestion, showed significant antihypertensive effects in SHR after oral administration. Remarkably, F1 did not show any effect on ACE-dependent vasoconstriction in contrast to the inhibitory effect showed by LfcinB20−25. In conclusion, two LfcinB-derived peptides lower blood pressure and exhibit potential as orally effective antihypertensive compounds, yet a complete elucidation of the mechanism(s) involved deserves further ongoing research.
ISSN:0021-8561
1520-5118
DOI:10.1021/jf100899u