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Induction of micronuclei following exposure to methylene di-phenyl diisocyanate: potential genotoxic metabolites.

Zhong-BZ; Siegel-PD

Toxicol Sci 2000 Nov; 58(1):102-108

http://dx.doi.org/10.1093/toxsci/58.1.102

20020871

Methylene di-phenyl diisocyanate (MDI) is used to make polyurethane products. The predominant occupational disease attributed to diisocyanates, including MDI, is asthma; however, the potential for genotoxicity has also been of concern. Diisocyanates are very reactive compounds that can undergo nonenzymatic hydrolysis to form methylenedianiline (MDA), or react under physiological conditions with primary amines to form ureas and/or with thiols to form labile thiol acid esters. MDA is a carcinogen in animals and a suspected carcinogen in humans. Brown Norway rats (BNR) were exposed to either 7 or 113 mg/m(3) MDI aerosol for 1 h/week x3 weeks and sacrificed 1 week later. Micronuclei (MN) formation was assessed from bone marrow polychromatic erythrocytes (PCE). A dose-dependent increase in the frequency of micronucleated polychromatic erythrocytes (MN-PCEs) was noted. In vitro exposure of Chinese hamster lung fibroblasts (V79) to MDA or MDI-thiol conjugates, but not to MDI, significantly increased the frequency of MN. MDI-thiol conjugate-exposed cell cultures did not have detectable levels of MDA. A significant increase in the number of V79 cells in metaphase, as well as the number of cells with precipitants within both the cytoplasm and nuclei, were noted in MDI-glutathione-exposed cultures. The results of this study indicate that MDI aerosol exposure can cause MN formation through either the hydrolysis of MDI to MDA or possibly the formation of thiol conjugates.

Genotoxic-effects; Occupational-exposure; Occupational-diseases; Bronchial-asthma; Physiological-factors; Amines; Thiols; Esters; Carcinogens; Laboratory-animals; Animals; Animal-studies; In-vitro-studies; Cell-cultures; Aerosols

Analystical Services Branch, M/S L4218, HELD, NIOSH, 1095 Willowdale Road, Morgantown, WV 26505-2888

TOSCF2

101-77-9

20001101

Journal Article

pds3@cdc.gov

2001

1

1096-6080

HELD

Toxicological Sciences

WV