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. 1999 Sep 28;96(20):11507–11512. doi: 10.1073/pnas.96.20.11507

Figure 2.

Figure 2

Effect of ischemic PC on iNOS expression and activity in WT and iNOS−/− mice. Tissue samples were obtained as described in the legend to Fig. 1. (A) Myocardial content of iNOS (cytosolic fraction). In WT mice, the iNOS protein content in the ischemic-reperfused region was increased by 47 ± 12% 24 h after ischemic PC. In iNOS−/− mice, immunoreactive iNOS protein was undetectable, either after sham surgery or after ischemic PC. (B) Calcium-independent NOS (iNOS) activity in the cytosolic fraction. In WT mice, iNOS activity in the ischemic-reperfused region increased by 227% 24 h after ischemic PC. In iNOS−/− mice, low levels of calcium-independent NOS activity were noted in iNOS−/− mice, either after sham operation or after ischemic PC. These levels probably represent cNOS activity (20, 21). (C) Total myocardial content of nitrite and nitrate (NOx). In WT mice, NOx levels in the ischemic-reperfused region increased significantly 24 h after ischemic PC. In iNOS−/− mice, ischemic PC did not bring about any increase in NOx levels; furthermore, NOx levels were significantly lower in iNOS−/− mice compared with WT mice. Data are means ± SEM.