The fine structure of tuft cells in the main excretory duct of rat submandibular gland was investigated using the high pressure freezing and freeze substitution (HPF-FS) method and compared with that seen with both conventional chemical fixation (CF) method and en bloc treatment with ruthenium red. Some MEDs also were subjected to histochemistry for lectins. The apical vesicles and tubules of tuft cells observed by TEM after the HPF-FS method were different ill shape from those treated by CF. With the first method, these vesicles and tubules, which may represent sections of a tubular system, appeared more slender and filled with a material of moderate density. A prominent glycocalyx covering the microvillar plasma membrane was observed in tuft cells processed both with the HPF-FS method and with ruthenium red. The surface of microvilli and the tubulo-vesicular structures of these cells exhibited the same soybean agglutinin (SBA) reactivity, suggesting a relationship between them.