Mode-of-action-based dosimeters for interspecies extrapolation of vinyl acetate inhalation risk.

Vinyl acetate is used in the manufacture of many polymers. The Clean Air Act Amendments of 1990 require that an inhalation risk assessment be conducted to assess risks to human health from ambient exposures. Vinyl acetate is a nasal carcinogen in rats and induces olfactory degeneration in rats and mice. Because of the many unique aspects of the rodent nasal cavity compared to that of humans, conventional means for extrapolating dosimetry between species are not appropriate. Physiologically based pharmacokinetic (PBPK) and pharmacodynamic (PD) modeling can address many of these unique aspects. A PBPK/PD model has been developed for vinyl acetate, but the choice of appropriate dosimeter(s) to use for interspecies extrapolation depends on a hypothesis regarding mode of action. This article summarizes the key studies that formulate a mode of action hypothesis for vinyl acetate. Dose-response relationships for vinyl acetate-induced nonneoplastic and neoplastic responses are highly nonlinear, suggesting complex kinetic processes. Carboxylesterase-dependent metabolism of vinyl acetate forms acetic acid, a potent cytotoxicant, and acetaldehyde, a weak clastogen. Cell death, proposed to be the result of intracellular acidification, results in restorative cell proliferation. In conjunction with sufficient genetic damage, induced by spontaneous mutation and acetaldehyde-induced DNA-protein cross-links (DPX), olfactory degeneration progresses to a state of elevated proliferation and eventually, at high vinyl acetate concentrations, to neoplastic transformation. Thus, reduction in intracellular pH (pHi) is proposed as the dosimeter most closely linked to the earliest stages of vinyl acetate toxicity. Consequently, risk assessments that are based on protection of nasal epithelium from intracellular acidification will be protective of all subsequent pathological responses related to vinyl acetate exposure. Proposing a reasonable mode of action is an important step in any risk assessment and is critical to the choice of dosimeter(s) to be used for interspecies dosimetry extrapolation.

[1]  V. Feron,et al.  Chronic Toxicity and Oncogenicity Inhalation Study with Vinyl Acetate in the Rat and Mouse , 1994 .

[2]  R. M. David,et al.  Oxidation of formaldehyde and acetaldehyde by NAD+-dependent dehydrogenases in rat nasal mucosal homogenates. , 1984, Biochemical pharmacology.

[3]  L. Ellwein,et al.  Genetic errors, cell proliferation, and carcinogenesis. , 1991, Cancer research.

[4]  M. Bogdanffy,et al.  Kinetics of nasal carboxylesterase-mediated metabolism of vinyl acetate. , 1993, Drug metabolism and disposition: the biological fate of chemicals.

[5]  S. Frame,et al.  FOUR-WEEK INHALATION CELL PROLIFERATION STUDY OF THE EFFECTS OF VINYL ACETATE ON RAT NASAL EPITHELIUM , 1997 .

[6]  M. Feldman,et al.  Reactions of nucleic acids and nucleoproteins with formaldehyde. , 1973, Progress in nucleic acid research and molecular biology.

[7]  J. Kuykendall,et al.  Reaction kinetics of DNA-histone crosslinking by vinyl acetate and acetaldehyde. , 1992, Carcinogenesis.

[8]  H. Järventaus,et al.  Chromosome damage induced by vinyl acetate through in vitro formation of acetaldehyde in human lymphocytes and Chinese hamster ovary cells. , 1985, Cancer research.

[9]  V. Dellarco A mutagenicity assessment of acetaldehyde. , 1988, Mutation research.

[10]  J. Kuykendall,et al.  Efficiency of DNA-histone crosslinking induced by saturated and unsaturated aldehydes in vitro. , 1992, Mutation research.

[11]  T. Morita,et al.  Low pH leads to sister-chromatid exchanges and chromosomal aberrations, and its clastogenicity is S-dependent. , 1995, Mutation research.

[12]  S H Moolgavkar,et al.  Two-event model for carcinogenesis: biological, mathematical, and statistical considerations. , 1990, Risk analysis : an official publication of the Society for Risk Analysis.

[13]  Y. Morimitsu,et al.  Reaction of formaldehyde with calf-thymus nucleohistone. , 1979, European journal of biochemistry.

[14]  D. Batlle,et al.  Regulation of Intracellular pH and the Na+/H+ Antiporter in Vascular Smooth Muscle , 1996 .

[15]  G. Obe,et al.  Acetaldehyde, but not ethanol, induces sister chromatid exchanges in chinese hamster cells in vitro , 1977 .

[16]  R. Miller,et al.  Inhalation toxicity of acrylic acid. , 1981, Fundamental and applied toxicology : official journal of the Society of Toxicology.

[17]  J. Kuykendall,et al.  Formation and stability of acetaldehyde-induced crosslinks between poly-lysine and poly-deoxyguanosine. , 1994, Mutation research.

[18]  B. Lambert,et al.  Induction and persistence of SCE-inducing damage in human lymphocytes exposed to vinyl acetate and acetaldehyde in vitro. , 1985, Mutation research.

[19]  M. Andersen,et al.  Physiologically based modeling of vinyl acetate uptake, metabolism, and intracellular pH changes in the rat nasal cavity. , 1997, Toxicology and applied pharmacology.

[20]  J. Kuykendall,et al.  Cytotoxicity and DNA-protein crosslink formation in rat nasal tissues exposed to vinyl acetate are carboxylesterase-mediated. , 1993, Toxicology and applied pharmacology.

[21]  C B Frederick,et al.  Application of a hybrid computational fluid dynamics and physiologically based inhalation model for interspecies dosimetry extrapolation of acidic vapors in the upper airways. , 1998, Toxicology and applied pharmacology.

[22]  H. Järventaus,et al.  Sister-chromatid exchanges induced by vinyl esters and respective carboxylic acids in cultured human lymphocytes. , 1992, Mutation research.

[23]  L. Rhomberg,et al.  Quantitative estimation of the genetic risk associated with the induction of heritable translocations at low‐dose exposure: Ethylene oxide as an example , 1990, Environmental and molecular mutagenesis.

[24]  A. Dahl,et al.  Metabolic capacity of nasal tissue interspecies comparisons of xenobiotic-metabolizing enzymes. , 1997, Mutation research.

[25]  W. Pulsinelli,et al.  Acid-induced death in neurons and glia , 1991, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[26]  T. Morita,et al.  Evaluation of clastogenicity of formic acid, acetic acid and lactic acid on cultured mammalian cells. , 1990, Mutation research.

[27]  P. J. Hilton,et al.  Relationship between intracellular proton buffering capacity and intracellular pH. , 1992, Kidney international.

[28]  R. Miller,et al.  Chronic toxicity and oncogenicity bioassay of inhaled ethyl acrylate in Fischer 344 rats and B6C3F1 mice. , 1985, Drug and chemical toxicology.

[29]  M E Andersen,et al.  A biologically based risk assessment for vinyl acetate-induced cancer and noncancer inhalation toxicity. , 1999, Toxicological sciences : an official journal of the Society of Toxicology.

[30]  R. Sarangapani,et al.  Analysis of Vinyl Acetate Metabolism in Rat and Human Nasal Tissues by an in Vitro Gas Uptake Technique , 1998 .

[31]  J. Mccormick,et al.  Acetaldehyde‐induced mutation at the hprt Locus in Human Lymphocytes In Vitro , 1990, Environmental and molecular mutagenesis.

[32]  F J Ballard,et al.  Production and utilization of acetate in mammals. , 1974, The Biochemical journal.

[33]  T. Keku,et al.  Studies of pHi in rabbit esophageal basal and squamous epithelial cells in culture. , 1992, Gastroenterology.

[34]  R. Sarangapani,et al.  High-affinity nasal extraction of vinyl acetate vapor is carboxylesterase dependent. , 1999, Inhalation toxicology.

[35]  A. Natarajan,et al.  Induction of chromosomal aberrations in peripheral lymphocytes of human blood in vitro, and of SCEs in bone-marrow cells of mice in vivo by ethanol and its metabolite acetaldehyde. , 1979, Mutation research.

[36]  B. Epe,et al.  Synthesis and genotoxicity of acetoxyoxirane, the epoxide of vinyl acetate. , 1986, Journal of biochemical toxicology.

[37]  J. Morris,et al.  A physiologically based pharmacokinetic model for nasal uptake and metabolism of nonreactive vapors. , 1993, Toxicology and applied pharmacology.

[38]  B. Lambert,et al.  DNA cross-links in human leucocytes treated with vinyl acetate and acetaldehyde in vitro. , 1985, Mutation research.

[39]  H. Bolt,et al.  Vinyl acetate, a structural analog of vinyl carbamate, fails to induce enzyme-altered foci in rat liver. , 1986, Carcinogenesis.

[40]  T. Morita,et al.  Clastogenicity of low pH to various cultured mammalian cells. , 1991, Mutation research.

[41]  A. Koestner,et al.  Chronic toxicity and oncogenicity of inhaled methyl acrylate and n-butyl acrylate in Sprague-Dawley rats. , 1991, Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association.

[42]  K. Morgan,et al.  Biochemical quantitation and histochemical localization of carboxylesterase in the nasal passages of the Fischer-344 rat and B6C3F1 mouse. , 1987, Toxicology and applied pharmacology.

[43]  Julia S. Kimbell,et al.  COMPUTATIONAL FLUID DYNAMICS SIMULATIONS OF INSPIRATORY AIRFLOW IN THE HUMAN NOSE AND NASOPHARYNX , 1998 .

[44]  V. Frighi,et al.  Na+/H+ antiport and buffering capacity in human polymorphonuclear and mononuclear leucocytes. , 1991, Clinical science.

[45]  K. Morgan,et al.  Histochemical localization of aldehyde dehydrogenase in the respiratory tract of the Fischer-344 rat. , 1986, Toxicology and applied pharmacology.

[46]  H. Bolt,et al.  Vinyl acetate: DNA-binding assay in vivo. , 1985, Toxicology Letters.

[47]  R. Miller,et al.  Propylene glycol monomethyl ether acetate (PGMEA) metabolism, disposition, and short-term vapor inhalation toxicity studies. , 1984, Toxicology and applied pharmacology.