Secretory Peptide Hormones Are Biochemical Antioxidants: Structure-Activity Relationship

  1. Bernd Moosmann1,2 and
  2. Christian Behl1
  1. 1Max Planck Institute of Psychiatry, Munich, Germany (B.M., C.B.); and 2Institute for Biochemistry, Free University of Berlin, Germany (B.M.)
  1. Christian Behl, Ph.D., Neurodegeneration Group, Max Planck Institute of Psychiatry, Kraepelinstrasse 2–10, 80804 Munich, Germany. E-mail:chris{at}mpipsykl.mpg.de

Abstract

The secretory peptides luteinizing hormone-releasing hormone, enkephalin, angiotensin, and oxytocin are biochemical antioxidants in aqueous medium. These hormones scavenge free peroxyl radicals, prevent the oxidation of low-density lipoprotein, and inhibit lipid peroxidation in brain membranes. Their capacity to directly suppress free radical-mediated reactions is demonstrated by electron-spin resonance spectroscopy. Electrospray ionization-mass spectrometry analysis of the free radical-quenching reaction reveals distinct oxidation products, including peptide dimers. Moreover, secretory peptide hormones can scavenge reactive nitrogen species derived from nitric oxide and peroxynitrite. An analysis of the structure-activity relationship indicates that their antioxidant activity is derived from the occurrence of solvent-exposed tyrosine and tryptophan residues, which is consistent with the mass spectrometry results. Significant effects in vitro can be observed at nanomolar concentrations, which makes these peptides comparable in potency with classic antioxidants having low molecular mass. Secretory peptide hormones may constitute an important part of the antioxidant defense system, and the sequences of the described antioxidant peptides may be unique lead structures for the rational design of novel antioxidant drugs having an improved pharmacological profile.

Footnotes

  • This work was supported in part by a grant from the Peter und Beate Heller Stiftung.

  • Abbreviations:
    LHRH
    luteinizing hormone-releasing hormone
    PBN
    N-tert-butyl-α-phenylnitrone
    luminol
    5-amino-2,3-dihydro-1,4-phthalazinedione
    AIBN
    2,2′-azo-bis-(2-methylpropionamidine)
    ACCH
    1,1′-azo-bis-(1-cyanocyclohexane)
    SIN-1
    3-morpholinosydnonimine
    LDL
    low-density lipoprotein
    ESR
    electron-spin resonance
    UV/VIS
    UV/visible
    FSHRF
    follicle-stimulating hormone-releasing factor
    amu
    atomic mass units
    Hb
    hemoglobin
    RNS
    reactive nitrogen species
    • Received May 7, 2001.
    • Accepted November 1, 2001.
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