Elsevier

Phytomedicine

Volume 2, Issue 4, March 1996, Pages 319-325
Phytomedicine

Isolation of an angiotensin converting enzyme (ACE) inhibitor from Olea europaea and Olea lancea

https://doi.org/10.1016/S0944-7113(96)80076-6Get rights and content

Summary

The aqueous extract of the leaves of Olea europaea and Olea lancea both inhibited Angiotensin Converting Enzyme (ACE) in vitro. A bioassay-directed fractionation resulted in the isolation of a strong ACE-inhibitor namely the secoiridoid 2-(3,4-dihydroxyphenyl)ethyl 4-formyl-3-(2-oxoethyl)-4 E-hexenoate (oleacein) (IC50 = 26 μM). Five secoiridoid glycosides (oleuropein, ligstroside, excelcioside, oleoside 11-methyl ester, oleoside) isolated from Oleaceous plants showed no significant ACE-inhibition whereas, after enzymatic hydrolysis, the ACE-inhibition at 0.33 mg/ml was between 64% to 95%. Secoiridoids have not been described previously in the literature as inhibitors of ACE. Oleacein showed a low toxicity in the brine shrimp (Artemia satina) lethality test (LC50 (24 h) = 969 ppm).

References (29)

  • G. Eibl et al.

    A New Method for the in vitro Screening of Inhibitors of Angiotensin-converting Enzyme (ACE), Using the Chromophore- and Fluorophore-Labellede Substrate, Dansyltriglycine

    Planta Med.

    (1991)
  • I. Esdorn

    Folia Oleae, eine neue blutdrucksenkende Droge

    Planta Med.

    (1954)
  • G.A. Fakim

    Medicinal Plants of Mauritius

    Int. J. Crude Drug Res.

    (1990)
  • J. Ipsen et al.
  • Cited by (0)

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    Address K. Hansen, Department of Pharmacognosy, The Royal Danish School of Pharmacy, Universitetsparken 2, DK-2100 Copenhagen Ø, Denmark.

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