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Research Article

Evaluation of respiratory parameters in rats and rabbits exposed to methyl iodide

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Pages 505-511 | Received 15 Oct 2008, Accepted 04 Nov 2008, Published online: 01 May 2009
 

Abstract

Laboratory animals exposed to methyl iodide (MeI) have previously demonstrated lesions of the olfactory epithelium that were associated with local metabolism in the nasal tissues. Interactions of MeI in the nasal passage may, therefore, alter systemic toxicokinetics. The current study used unrestrained plethysmographs to determine the MeI effect on the breathing frequency and minute volume (MV) in rats and rabbits. Groups of 4 rats each were exposed to 0, 25, or 100 ppm and groups of 4 rabbits each were exposed to 0 and 20 ppm MeI for 6 h. Breathing frequency and MV were measured and recorded during the exposure. Blood samples were collected for inorganic serum iodide and the globin adduct S-methylcysteine (SMC) as biomarkers of systemic kinetics immediately following exposure. No significant reductions in breathing frequency were observed for either rats or rabbits. Significant changes in minute volume were demonstrated by both rats and rabbits; however, the changes observed in rats were not concentration dependent. The MeI-induced changes in MV resulted in significant differences in the total volume of test substance atmosphere inhaled over the 6-h period. Rats demonstrated a concentration-dependent increase in both inorganic serum iodide and SMC. Rabbits exposed to 20 ppm MeI demonstrated a significant increase of inorganic serum iodide; SMC was also increased but was not statistically significant. The results of this study are consistent with previous kinetic studies with MeI, and the data presented here can be integrated into a computational fluid dynamics physiologically based pharmacokinetic model for both rats and rabbits.

Acknowledgements

This work was performed under contract for Arysta LifeScience Corporation, Cary NC (formerly named Arvesta Corporation). The technical assistance from members of the Haskell Clinical Pathology (D. Hoban, E. Wilkinson), Necropsy (J. Holt, J. Joyce, L. Lewis, C. Lloyd, S. Records), Investigative Toxicology (R. Manning, R. Mingoia, S. Mazumdar, B. Shertz, S. Snajdr), Results Communication (M. Wilford), and Quality Assurance (R. Rhea) groups is greatly appreciated.

Declaration of interest: The authors report no conflicts of interest. The authors alone are responsible for the content and writing of the paper.

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