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Antioxidant Activity of NADH and Its Analogue - An In Vitro Study

  • Olek, Robert Antoni (Department of Bioenergetics, Jedrzej Sniadecki Academy, School of Physical Education and Sport) ;
  • Ziolkowski, Wieslaw (Department of Bioenergetics, Jedrzej Sniadecki Academy, School of Physical Education and Sport) ;
  • Kaczor, Jan Jacek (Department of Bioenergetics, Jedrzej Sniadecki Academy, School of Physical Education and Sport) ;
  • Greci, Lucedio (Dipartimento di Scienze dei Materiali e della Terra, via Brecce Bianche, University of Ancona) ;
  • Popinigis, Jerzy (Department of Bioenergetics, Jedrzej Sniadecki Academy, School of Physical Education and Sport) ;
  • Antosiewicz, Jedrzej (Department of Bioenergetics, Jedrzej Sniadecki Academy, School of Physical Education and Sport)
  • Published : 2004.07.31

Abstract

The antioxidant activities of NADH and of its analogue, 1,4-dihydro-2,6-dimethyl-3,5-dicarbethoxy-pyridine ($PyH_2$), were evaluated in vitro. NADH was found to be oxidized by the peroxyl radical derived from 2,2-azobis-(2-amidinopropane) dihydrochloride (AAPH) decomposition, in a pH-dependent manner. Both NADH and $PyH_2$ inhibited the peroxidation of egg yolk lecithin (EYL) liposomes, although $PyH_2$ was more effective than NADH when 2,2'-azobis-4-methoxy-2,4-dimethyl-valeronitrile (methoxy-AMVN) was employed to induce EYL liposome peroxidation. The antioxidant activities of NADH and $PyH_2$ were also evaluated by measuring their influences on 1,3-diphenylisobenzofuran (DPBF) fluorescence decay in the presence of peroxyl radicals. NADH and $PyH_2$ were much more effective at inhibiting DPBF quenching in Triton X-100 micelles than in liposomes. These results indicate that NADH can inhibit lipid peroxidation despite being hydrophilic. Nevertheless, membrane penetration is an important factor and limits its antioxidant activity.

Keywords

References

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