Identification and quantification of inhibitors for angiotensin-converting enzyme in hypoallergenic infant milk formulas
Publikation: Beitrag in Fachzeitschrift › Forschungsartikel › Beigetragen › Begutachtung
Beitragende
Abstract
The potential of hypoallergenic (HA) infant milk formulas containing hydrolyzed milk proteins as main constituents to inhibit angiotensin-converting enzyme (ACE) in vitro was investigated. Seven commercially available HA products designed for babies up to 4 months showed a potent inhibition of ACE in vitro, with IC50 values ranging between 3.2 and 68.5 mg of nitrogen/L. For six samples of conventional milk-based infant formulas and three breast milk samples, no inhibition was observed. Inhibitory potential did not correlate with the degree of hydrolysis. Using reversed-phase high-pressure liquid chromatography (RP-HPLC) coupled to electrospray ionization-time of flight-mass spectrometry (ESI-TOF-MS), 15 peptides known to inhibit ACE were identified. Among them, the highly potent ACE inhibitor Ile-Trp (IC50 = 0.7 mu M) was detected and quantified for the first time in the HA samples, representing the most effective ACE-inhibiting peptide that has ever been detected in food items. The overall inhibitory potential of the HA infant milk formulas could partly be explained by Ile-Trp.
Details
Originalsprache | Englisch |
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Seiten (von - bis) | 6333-6338 |
Seitenumfang | 6 |
Fachzeitschrift | Journal of agricultural and food chemistry |
Jahrgang | 56 |
Ausgabenummer | 15 |
Publikationsstatus | Veröffentlicht - 13 Aug. 2008 |
Peer-Review-Status | Ja |
Externe IDs
Scopus | 50449107794 |
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Schlagworte
Schlagwörter
- angiotensin-converting enzyme, blood pressure, bioactive peptides, HPLC-MS, infant nutrition, BLOOD-PRESSURE, SOUR MILK, PEPTIDES