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Relationship: 867
Title
Inhibition, UROD leads to Oxidation, Uroporphyrinogen
Upstream event
Downstream event
AOPs Referencing Relationship
Taxonomic Applicability
Sex Applicability
Life Stage Applicability
Through the normal heme biosynthesis pathway, uroporphyrinogen is converted to coproporphyrinogen by uroporphyrinogen decarboxylase (UROD)[1]. In the event that UROD activity is reduced (due to genetic disorders or chemical inhibition) uroporphyrinogen, and other porphyrinogen substrates of UROD, are oxidized to highly stable porphyrins, which accumulation and lead to a heme disorder known as porphyria[2].
| ID | Experimental Design | Species | Upstream Observation | Downstream Observation | Citation (first author, year) | Notes |
|---|
| Title | First Author | Biological Plausibility |
Dose Concordance |
Temporal Concordance |
Incidence Concordance |
|---|
Biological Plausibility
Dose Concordance Evidence
Temporal Concordance Evidence
Incidence Concordance Evidence
Uncertainties and Inconsistencies
Uroporphyrin accumulation in avian models is less consistently accompanied by decreased UROD activity, and when it does occur, it is less marked than in mammals[6][7]. Although numerous studies show both a decrease in UROD activity and porphyrin accumulation in avian species, Lambrecht et al.[7] reported the accumulation of porphyrins in chicken embryo hepatocytes and japanese quail liver without a decrease in UROD activity. They also note that the modest reduction in UROD activity (often less than 50%) is not enough to explain the extent of porphyrin accumulation observed and suggests there may be another mechanism at play.
Is it known how much change in the first event is needed to impact the second? Are there known modulators of the response-response relationships? Are there models or extrapolation approaches that help describe those relationships?
A reduction in UROD activity of at least 70% is required to achieve a makeable increase in hepatic porphyrins, and therefore UROX, in mammals.[8][9][10]