There was no significant difference, however, between Printex® 90- and Aerosil® 150-treated rats. The results of immunohistochemical quantification of OGG1-labeled nuclei in particle-exposed rat lung tissue are shown in Caspase-independent apoptosis Fig. 2D and summarized in Fig. 1. As compared to the negative (saline) control, only the lungs of quartz DQ12-exposed rats demonstrated a significant, 1.7-fold increase in OGG1-positive nuclei per mm2 (p ≤ 0.05, one-way ANOVA, Dunnett’s post hoc test) three months after the first and one month after the last instillation (see Fig. 1). This increase in OGG1-positive nuclei pointed to quartz

DQ12-induced oxidative stress with subsequent oxidative DNA lesions. This is in line with the parallel induction of 8-OH-dG-positive nuclei (see Fig. 2C). In contrast, the frequency of OGG1-positive nuclei in the lungs of Printex® 90- and Aerosil® 150-treated animals was rather decreased compared to the negative www.selleckchem.com/products/PLX-4032.html controls. Interestingly, all particle-treated groups, irrespective of the applied mass doses, demonstrated highly significant increases in the number of cells with OGG1-positive

cytoplasm per mm2 (quartz DQ12 and Printex® 90: p ≤ 0.001; Aerosil® 150: p ≤ 0.01) as compared to the negative controls (saline), but without significant differences among the three treatment groups (Tukey test). The frequency of OGG1-positive cytoplasm amounted to the 3.9-, 2.8-, and 4.1-fold of the negative controls for quartz DQ12, Aerosil® 150, and Printex® 90, respectively. In all cases, alveolar lining cells displayed a granular pattern of OGG1 in the cytoplasm, probably reflecting mitochondrial expression

of the enzyme. In a particle overload situation, inflammation might be a critical determinant of genotoxicity in the rat lung. Correlation of genotoxicity marker expression with the histopathologic inflammation score thus was of special interest. As identical animals of the 3-month study part were used for genotoxicity marker quantification and inflammation scoring, both group mean data and individual animal data could be used for correlation analyses (Fig. 1). Individual animal data displayed a highly significant correlation (p < 0.001) between histopathological inflammation score and occurrence of 8-OH-dG- (r = 0.803) and γ-H2AX-positive nuclei (r = 0.771) diglyceride and OGG1-positive cytoplasm (r = 0.675) in pulmonary alveolar lining cells of particle-treated animals. In addition, appearance of PAR-positive nuclei highly significantly (p < 0.01) correlated with the inflammation score (r = 0.554), whereas OGG1 expression in nuclei displayed no correlation (see Table 3). This is in line with ongoing ROS production and oxidative DNA damage/repair during inflammatory processes. Using the group means for calculation of correlations, the histopathologic inflammation score highly significantly correlated with the number of PAR-positive nuclei (p < 0.01; r = 0.994) and significantly with the number of 8-OH-dG-positive nuclei (p < 0.05; r = 0.978).