Pharmacokinetics of sodium nitrite-induced methemoglobinemia in the rat
Abstract
A biologically based mathematical model was created to characterize time and dose-dependent relationships between exposure to nitrite and induction of methemoglobinemia. The model includes mass action equations for processes known to occur: oral absorption of nitrite, elimination from the plasma, partitioning between plasma and erythrocytes, binding of nitrite to hemoglobin and methemoglobin, and the free radical chain reaction for hemoglobin oxidation. The model also includes Michaelis-Menten kinetics for methemoglobin reductase-catalyzed regeneration of hemoglobin. Body weight-scaled rate constants for absorption (k(a)) and elimination (k(e)), the effective erythrocyte/plasma partition coefficient (P), and the apparent K(m) for methemoglobin reductase were the only parameters estimated by formal optimization to reproduce the observed time course data. Time courses of plasma nitrite concentrations and blood levels of hemoglobin and methemoglobin in male and female rats that had received single intravenous or oral doses of sodium nitrite were measured. Peak plasma levels of nitrite were achieved in both sexes approximately 30 min after oral exposure, and peak methemoglobin levels were achieved after 100 min. The model predicts that 10% of the hemoglobin is oxidized to the ferric form after oral doses of 15.9 mg/kg in male rats and 11.0 mg/kg in female rats and after intravenous doses of 8.9 and 7.1 mg/kg in male and female rats, respectively. The t(1/2) for recovery from methemoglobinemia was 60 to 120 min depending on dose and route of administration. A sensitivity analysis of the model was performed to identify to which parameters the predictions of the model were most sensitive and guide attempts to simplify the model. Replacement of the V(max) of methemoglobin reductase with a value representative of humans predicted a 10% methemoglobinemia following an intravenous dose of 5.8 mg/kg, in close agreement with an observed value of 5.7 mg/kg for humans.
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- Authors
- Kohn, M. C., Melnick, R. L., Ye, F., & Portier, C. J.
- Affiliations
- National Institutes of Health (US)
- Venue
- Drug Metabolism and Disposition
- Publisher
- Elsevier BV
- Published
- 2002-06
- Volume
- 30
- Issue
- 6
- Pages
- 676-683
- ISSN
- 0090-9556 (ISSN-L)
- OpenAlex
- W2118746293
- Cited by
- 98
- References
- 24
- Citations by year
- 2026: 1 · 2025: 3 · 2024: 2 · 2023: 1 · 2022: 5 · 2021: 5 · 2020: 8 · 2019: 3 · 2018: 7 · 2017: 2 · 2016: 6 · 2015: 9 · 2014: 7 · 2013: 4 · 2012: 7
- FWCI
- 2.46
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Drug Metabolism and Disposition (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Methemoglobinemia and Tumor Lysis Syndrome
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Hemoglobin structure and function
- Health Sciences › Medicine › Emergency Medicine › Poisoning and overdose treatments
- Keywords
- sodium nitrite, methemoglobinemia, pharmacokinetics, mathematical model, hemoglobin oxidation, methemoglobin reductase, Michaelis-Menten kinetics, free radical chain reaction, oral absorption, dose-response relationship, sex differences, recovery time, rats
- MeSH terms
- Animals, Female, Hemoglobins, Male, Methemoglobin, Methemoglobinemia, Models, Biological, Rats, Inbred F344, Sodium Nitrite, Rats
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