Abstract
Conclusions
A clonal strain (MH1C1) of rat hepatoma cells synthesized labeled bilirubin with either glycine-2-14C or δ-ami-nolevulinic acid-3,5-3H as precursor. In contrast to the findings in living rats, labeled bilirubin production is only slightly enhanced in MH1C1 cells that have been preincubated with phenobarbital. These studies indicate that hepatic parenchymal cells are capable of producing at least part of the nonerythroid fraction of bile pigment. Moreover, they provide a unique experimental model for the further study of hepatic heme and bilirubin metabolism.
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