Abstract. Testosterone‐4‐14C (2430 pmol, 0.48 μM) was incubated aerobically in 67 mM phosphate buffer pH 7.4 with homogenates and minces of salivary glands from male dogs. Extracted radiosteroids were resolved by thin‐layer chromatography on silica gel, removed and quantitated. Substantially higher NAD+‐dependent 17 β‐hydroxy‐C19‐steroid oxidoreductase activity was found in submaxillary gland homogenates than in similar parotid‐gland preparations. Preliminary evidence is presented that the enzyme activity per unit wet weight of the minced submaxillary gland is decreased in the 2‐week male castrate, in the absence of any recognizable histologic changes in the gland. Testosterone metabolism by canine salivary glands is thus oxidative, contrasting with the reductive 17 β‐hydroxysteroid pathway characteristic of androgen‐dependent organs such as the prostate, and is more extensive than in this accessory sex tissue. Our findings suggest that the canine salivary glands are not target organs for circulating male hormone.