Abstract Nitric oxide plays a crucial role in multiple physiological processes in salivary glands, yet its precise cellular sources in human glandular tissues remain insufficiently characterized. This study investigated the distribution and subcellular localization of neuronal nitric oxide synthase (nNOS) in human parotid and submandibular gland tissue samples obtained from surgical biopsies and autopsies, using both light and electron-microscope immunohistochemistry. In both gland types, nNOS was consistently observed in serous secretory cells and the ductal epithelium, whereas mucous cells showed no immunoreactivity. Ductal cell staining was heterogeneous, with some cells displaying intense labeling and others remaining unstained. Nerve fibers containing the enzyme were rare within the gland parenchyma. Ultrastructural analysis revealed the enzyme within secretory granules and small cytoplasmic vesicles of serous cells, as well as in the apical and basal cytoplasm, mitochondria, and nuclei of ductal epithelial cells. These findings provide the first ultrastructural evidence of nNOS in secretory and ductal cells of human major salivary glands. The selective localization in serous cells, absence in mucous cells, and limited nitrergic innervation suggest a substantial parenchymal contribution to nitric oxide production. This distribution indicates that nitric oxide regulates saliva formation, composition, and intracellular signaling and could play a broader role in oral physiology and disease.
Isola et al. (Sun,) studied this question.