Toxicity to rats of methanol‐fueled engine exhaust inhaled continuously for 28 days

Abstract

Fischer 344 rats were exposed to three concentrations of exhaust generated by an M85 methanol‐fueled engine (methanol with 15% gasoline) without catalyst for 8 h/d, 7 d/wk for 7, 14, 21, or 28 d. Concentration‐ and time‐dependent yellowing of the fur was prominent in all treated groups. Concentration‐dependent increases in the erythrocyte count, hematocrit, hemoglobin concentration, formaldehyde in plasma, and carboxyhemoglobin in the erythrocytes, and decrease in serum alkaline phosphatase activity were seen after all exposure periods. Histopathologically, lesions were found in the nasal cavity and lungs after 7 d of exposure. Squamous metaplasia of the respiratory epithelium of level 1 (level of the posterior edge of the upper incisor teeth) lining of the nasoturbinate andlor maxilloturbinate and infiltration of neutrophils into the submucosa, and decreases of Clara cells in the terminal bronchiolus and of cilia in the bronchiolar epithelium, were observed in the high‐concentration group (carbon monoxide, 94 ppm; formaldehyde, 6.9 ppm; methanol, 17.9 ppm; nitrogen oxides, 52.7 ppm; nitrogen dioxide, 10.6 ppm). The histopathological extents of several lesions increased slightly with the exposure time. Slight squamous metaplasia and hyperplasia of the respiratory epithelium at level 1 were also observed in the medium‐concentration group (one in three of the high‐concentration group). No histopathological changes were found in the olfactory epithelium of the nasal cavity. In the low‐concentration group (one in nine of the high‐concentration group), no marked histopathological changes in these organs were observed. These results may suggest that the lesions observed in the nasal cavity of rats exposed to methanol‐fueled engine exhaust were mainly caused by formaldehyde, although other components in the exhaust also may have affected nasal cavity andlor lungs to less extent.