Abstract
4,4′-Methylenedianiline (DAPM) is an aromatic amine used in the synthesis of polyurethanes and epoxy resins. Acute exposure to DAPM produces hepatobiliary toxicity in humans as well as animal models. However, the toxic effects of intermittent DAPM exposure have not been explored. We treated male and female rats with 25 mg DAPM/kg or vehicle once per week for 17–22 wk. Though concentric fibrosis around bile ducts of the liver was noted, vascular medial hyperplasia was also prominent. Morphometric analysis of histologic sections revealed that in male rats, vessel wall area increased relative to lumen area in hepatic arteries by 22 wk. However, in female rats, wall areas of both hepatic and pulmonary arteries increased relative to lumen area by 17 wk. In both male and female rats, increased wall thickness was localized to the medial layer; no intimal changes were noted. In vitro treatment of vascular smooth muscle cells (VSMC) with 25–100 μM DAPM resulted in increased DNA synthesis and VSMC proliferation. To test whether the observed alterations in cell cycle control involved VSMC-mediated metabolism of DAPM to electrophilic intermediates, cells were treated with DAPM or DAPM plus 50 μM N-acetylcysteine (NAC). Coincubation with NAC afforded dramatic protection against DAPM-induced VSMC proliferation. Though DAPM had no appreciable effect on levels of reduced glutathione, oxidized glutathione, or oxidant production, DAPM increased glutathione-S-transferase activity in VSMC. These data indicate that DAPM can initiate VSMC proliferation, possibly via VSMC-mediated metabolism of DAPM to reactive intermediates.
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References
Dempsey, D.J., Phaneuf, M.D., Bide, M.J., Szycher, M., Quist, W.C., and Logerfo, F.W. (1998). Synthesis of a novel small diameter polyurethane vascular graft with reactive binding sites. ASAIO J. 44:M506-M510.
Feng, L.J. and Amini, S.B. (1999). Analysis of risk factors associated with rupture of silicone gel breast implants. Plast. Reconstr. Surg. 104:955–963.
IARC. (1986). IARC Monographs on the Evaluation of Carcinogenic Risk of Chemicals to Humans. Vol. 39, Lyon, France, pp. 347–365.
Moore, W.M. (1978). Methylenedianiline, in Kirkothmer Encyclopedia of Chemical Technology (Mark, H.F., Othmer, D.F., Overberger, C.G., and Seaborg, G.T., eds.), Wiley, New York, pp. 338–348.
Brookes, L.J., Neale, J.M., and Pieroni, D.R. (1979). Acute myocardiopathy following tripathway exposure to methyl-enedianiline. JAMA 242:1527–1528
Kopelman, H., Scheuer, P.J., and Williams, R. (1966). The liver lesion of the Epping jaundice. Q. J. Med. 35:553–565.
Kanz, M.F., Gunasena, G.H., Kaphalia, L., Hammond, D.K., and Syed, Y.A. (1998). A minimally toxic dose of methylene dianiline injures biliary epithelial cells in rats. Toxicol. Appl. Pharmacol. 150:414–426.
Dalene, M., Jakobsson, K., Rannug, A., Skarping, G., and Hagmar, L. (1996). MDA in plasma as a biomarker of exposure to pyrolysed MDI-based polyurethane: correlations with estimated cumulative dose and geonotype for N-acetylation. Int. Arch. Occup. Environ. Health 68:165–169.
Kautiainen, A., Wachtmeister, C.A., and Ehrenberg, L. (1998). Characterization of hemoglobin adducts from a 4, 4′-methylenedianiline metabolite evidently produced by peroxidative oxidation in vivo. Chem. Res. Toxicol. 11: 614–621.
Do Luu, H.M. and Hutter, J.C. (2000). Pharmacokinetic modeling of 4,4′-methylenedianiline released from reused polyurethane dialyzer potting materials. J. Biomed. Mater. Res. 53:276–286.
Shintani, H. and Nakamura, A. (1989). Analysis of a carcinogen, 4,4′-methylenedianiline, from thermosetting polyurethane during sterilization. J. Anal. Toxicol. 13:354–357.
Brennan, M.B. (1999). Knitting textile chemistry to medicine. Chem. Eng. News 77:33–36.
Wilkinson, S.L. (1998). Seeking clarity on breast implants. Chem. Eng. News 76:53–54.
Chamley, J.H., Campbell, G.R., McConnell, J.D., and Groschel-Stewart, U. (1977). Comparison of vascular smooth muscle cells from adult human, monkey and rabbit in primary culture and in subculture. Cell. Tissue Res. 177:503–522.
Huong, P.L., Kolk, A.H., Eggelte, T.A., Verstijnen, C.P., Gilis, H., and Henddriks, J.T. (1991). Measurement of antigen specific lymphocyte proliferation using 5-bromo-deoxyuridine incorporation. An easy and low cost alternative to radioactive thymidine incorporation. J. Immunol. Methods 140:243–248.
Tietze, F. (1969). Enzymic method for quantitative determination of nanogram amounts of total and oxidized glutathione: applications to mammalian blood and other tissues. Anal. Biochem 27:248–254.
O’Donovan, D.J., Katkin, J.P., Tamura, T., Smith, C.V., and Welty, S.E. (2000). Attenuation of hyperoxia-induced growth inhibition in H441 cells by gene transfer of mitochondrially targeted glutathione reductase. Am. J. Respir. Cell. Mol., Biol. 22:732–738.
Royall, J.A. and Ischiropoulos, H. (1993). Evaluation of 2′7′-dichlorofluorescin and dihydrorhodamine 123 as fluorescent probes for intracellular H2O2 in cultured endothelial cells. Arch. Biochem. Biophys 302:338–355.
Ischiropoulos, H., Gow, A., Thom, S.R., Kooy, N.W., Royall, J.A., and Crow, J.P. (1999). Detection of reactive nitrogen species using 2,7-dichlorodihydrofluoresce in and dihydrorhodamine 123. Methods Enzymol. 301: 367–373.
Cao, A., Hardej, D., Trombetta, L.D., Trush, M.A., and Li, Y. (2003). Induction of cellular glutathione and glutathione-S-transferase by 3H-1,2-dithiole-3-thione in rat aortic smooth muscle A10 cells: protection against acrolein-induced toxicity. Atherosclerosis 166:291–301.
Bailie, M.B., Mullaney, T.P., and Roth, R.A. (1993). Characterization of acute 4,4′-methylene dianiline hepatotoxicity in the rat. Environ. Health Perspect. 101:130–133.
Haber, M.M., Marboe, C.C., and Genoglio, J.J. Jr. (1991). Vasculitis in drug reactions and serum sickness, in Systemic Vascultides (Churg, A. and Churg, J., eds.), Igaku-Shoin, New York, pp. 305–325.
Drory, V.E. and Korczyn, A.D. (1993). Hypersensitivity vasculitis and systemic lupus erythematosus induced by anticonvulsants. Clin. Neuropharmacol. 16:19–29.
Mitchell, G.G., Magnusson, A.R., and Weiler, J.M. (1983). Cimetidine-induced cutaneous vasculitis. Am. J. Med. 75:875–876.
Jennette, J.C. and Falk, R.J. (1997). Small-vessel vasculitis. N. Engl. J. Med. 337:1512–1523.
Dugas, T.R., Santa Cruz, V., Liu, H., and Kanz, M.F. (2001). Evaluation of the gender differences in 4, 4′-methylenedianiline toxicity, distribution, and effects on biliary parameters. J. Toxicol. Environ. Health A 62: 467–483.
Cocker, J., Boobis, A.R., and Davies, D.S. (1988). Determination of the N-acetyl metabolites of 4,4′-methylene dianiline and 4,4′-methylene-bis(2-chloroaniline) in urine. Biomed. Environ. Mass Spectrom. 17:161–167.
Morgott, D.A., Weber, W.W., and Cornish, H.H. (1984). In vivo biotransformation of methylenedianiline (MDA) in the rat and rabbit. The Toxicologist 4:8.
Bailey, E., Brooks, A.G., Bird, I., Farmer, P.B., and Street, B. (1990). Monitoring exposure to 4,4′-methylenedianiline by the gas chromatography-mass spectrometry determination of adducts to hemoglobin. Anal. Biochem. 190: 176–181.
Marnett, L.J. (1990). Prostaglandin synthase-mediated metabolism of carcinogens and a potential role for peroxyl radicals as reactive intermediates. Environ. Health Perspect. 88:5–12.
Zenser, T.V., Mattammal, M.B., Armbrecht, H.J., and Davis, B.B. (1980). Benzidine binding to nucleic acids mediated by the peroxidative activity of prostaglandin endoperoxide synthetase. Cancer Res. 40:2839–2845.
Zhao, W., Parrish, A.R., and Ramos, K.S. (1998). Constitutive and inducible expression of cytochrome P450IA1 and P450IB1 in human vascular endothelial and smooth muscle cells. In Vitro Cell. Dev. Biol. Anim. 34:671–673.
Marnett, L.J., Reed, G.A., and Dennison, D.J. (1978). Prostaglandin synthetase dependent activation of 7,8-dihydro-7,8-dihydroxy-geno(a) pyrene to mutagenic derivativies. Biochem. Biophys. Res. Commun. 82:210–216.
Kim, H.-Y., Rhim, T., Choi, I., and Kim, S.-S. (2001). N-Acetylcysteine induces cell cycle arrest in hepatic stellate cells through its reducing activity. J. Biol. chem. 276: 40591–40598.
Sjodin, K., Nilsson, E., Hallberg, A., and Tunek, A. (1989). Metabolism of N-acetyl-L-cysteine: some structural requirements for the deacetylation and consequences for the oral bioavailability. Biochem. Pharmacol. 38:3981–3985.
Huxtable, R.J. (1990). Activation and pulmonary toxicity of pyrrolizidine alkaloids. Pharmacol. Ther. 47:371–389.
Lafranconi, W.M. and Huxtable, R.J. (1984). Hepatic metabolism and pulmonary toxicity of monocrotaline using isolated perfused liver and lung. Biochem. Pharmacol. 33: 2479–2484.
Estep, J.E., Lame, M.W., Morin, D., Jones, A.D., Wilson, D.W., and Segall, H.J. (1991). [14C] Monocrotaline kinetics and metabolism in the rat. Drug. Metab. Dispos. 19:135–139.
Yost, G.S., Buckpitt, A.R., Roth, R.A., and McLemore, T.L. (1989). mechanisms of lung injury by systemically administered chemicals. Toxicol. Appl. Pharmacol. 101:179–195.
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Dugas, T.R., Kanz, M.F., Hebert, V.Y. et al. Vascular medial hyperplasia following chronic, intermittent exposure to 4,4′-methylenedianiline. Cardiovasc Toxicol 4, 85–96 (2004). https://doi.org/10.1385/CT:4:1:85
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DOI: https://doi.org/10.1385/CT:4:1:85
Key Words
- Methylenedianiline
- glutathione
- vascular smooth muscle cells
- proliferation
- glutathione-S-transferase