Because of their potential to regulate tumoural blood flow and interactions
with nitric oxide the expression of the type 1 and 2 isoforms of heme oxyg
enase (HO-1 and HO-2) were evaluated in implanted C6 striatal gliomas. Immu
nocytochemistry using antibodies specific for HO-1 and HO-2 were used in 20
C6 glioma tumours. The bulk of the tumour parenchyma and endothelium was n
egative for both HO isoforms. Isolated, but weak staining for HO-1 was seen
in most tumours with focally increased expression in perinecrotic regions.
Cells morphologically resembling macrophages stained with both HO-1 and HO
-2, but were not numerous. These findings suggest that carbon monoxide, unl
ike nitric oxide, does not have a major role in regulating tumoural blood f
low in this experimental glioma model. These findings once again demonstrat
e the differences between human malignant glioma and experimental implantat
ion glioma models.