Effect of Tin Protoporphyrin on the Excretion Rate of Carbon Monoxide in Newborn Rats After Hematoma Formation

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Abstract
This study evaluated the efficacy of tin protoporphyrin (TP), a competitive inhibitor of heme oxygenase, in suppressing the total body excretion rate of carbon monoxide (CO), an index of total bilirubin formation, in neonatal rats with artificially created hematomas. Wistar rat litters less than 12 h old were each divided into three groups of similar weight and treated as follows: (a) saline control (S); (b) hematoma, 80 μl blood (H); (c) TP, 65 (μmol/kg, and hematoma (TP H). CO excretion of the H group increased rapidly after hematoma formation, reaching a maximum value of 79 ± 4 SE μl/kg/h 25 h later. Treatment with TP did not affect the pattern of CO excretion or its magnitude (78 ± 2 SE μl/kg/h, 25 h posthematoma). The S group showed no increase in CO excretion at this time (40 ± 2 SE μl/kg/h). At the conclusion of the experiment (45 h posthematoma), the plasma total bilirubin levels were slightly lower in the TP H rats (1.0 ± 0.1 SE mg/dl) than in H rats (1.2 ± 0.1 SE mg/dl). The S rats had a plasma total bilirubin concentration of 0.8 ± 0.1 SE mg/ dl. The hepatic and splenic heme oxygenase activities were decreased by 61% (p < 0.001) and 48% (p < 0.05), respectively, in the TP H rats as compared to the H rats. The S and H rats had similar enzyme activities. The results of this study suggest that though single dose TP decreased tissue heme oxygenase activity, it did not significantly affect total bilirubin formation.