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. 2005 Apr 5;387(Pt 2):473–478. doi: 10.1042/BJ20040828

Figure 7. Intensities of the EPR signals obtained with livers isolated from NOM- or GSNO-treated mice and with NOM or GSNO phosphate buffer solutions.

Figure 7

Columns correspond to the peak-to-peak heights of the two first lines of the EPR signal indicated in arbitrary units (means±S.D. out of at least three experiments). Mice were anaesthetized 7 min after i.p. injections of 0, 2.5 or 5 μmol of NOM, and 5 or 10 μmol of GSNO and then perfused. Livers were homogenized in a fresh (MGD)2–Fe2+ solution. EPR measurements were made at 77 K. The inset shows in vitro experiments performed with mixtures of 10 mM (MGD)2–Fe2+ complex and 1, 2, and 5 μM NOM or GSNO solution, diluted twice in phosphate buffer. Statistical significance (using Student's t test): **P<0.001; *P<0.05; NS, non-significant.

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