Fig. 5.
Fig. 5. Effects of heme and HO on leukocyte infiltration. / Light microscopy pictures of liver sections of BALB/c mice stained with hematoxylin and eosin (H&E) (original magnification, × 40 [A,C,E,G], or × 400 [B,D,F,H]). Mice were treated for 24 hours with saline (A, B) or 750 μM heme (C, D). The lower 2 panels represent, respectively, mice pretreated for 24 hours with SnMP, followed by treatment with saline (E,F) or 750 μM heme (G,H) for 24 hours. Heme-treated mice show inflammatory lesions accompanied by leukocyte influx and liver cell injury. Animals in which HO-activity was inhibited by pharmacologic means (SnMP) show more severe inflammatory changes after heme exposure, as exemplified by larger lesions and more aggravated inflammatory cell infiltrates.

Effects of heme and HO on leukocyte infiltration.

Light microscopy pictures of liver sections of BALB/c mice stained with hematoxylin and eosin (H&E) (original magnification, × 40 [A,C,E,G], or × 400 [B,D,F,H]). Mice were treated for 24 hours with saline (A, B) or 750 μM heme (C, D). The lower 2 panels represent, respectively, mice pretreated for 24 hours with SnMP, followed by treatment with saline (E,F) or 750 μM heme (G,H) for 24 hours. Heme-treated mice show inflammatory lesions accompanied by leukocyte influx and liver cell injury. Animals in which HO-activity was inhibited by pharmacologic means (SnMP) show more severe inflammatory changes after heme exposure, as exemplified by larger lesions and more aggravated inflammatory cell infiltrates.

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