Localization of 11/β-Hydroxysteroid Dehydrogenase: Specific Protector of the Mineralocorticoid Receptor in Mammalian Olfactory Mucosa

Abstract

The enzyme 11/β-hydroxysteroid dehydrogenase (11β HSD) plays a major role in the protection of the mineralocorticoid (type 1) receptor. The cellular mechanism of aldosterone selectivity relies on the coexpression of mineralocorticoid receptors and 11β HSD in the same cells. In the current study, 11β HSD activity was localized in the mammalian olfactory mucosa by a histochemical technique which links steroid metabolism with the deposition of formazan. The histochemical reaction results from oxidation of the synthetic substrate β-hydroxyandrostenedione and is dependent on nicotine-adenine dinucleotide (NAD). This demonstrates the presence of a dehydrogenase activity separate from the nicotineamide-adenine dinucleotide phosphate (NADP)-dependent 11βHSD. In the olfactory mucosa, the presence of NAD-dependent 11βHSD activity is localized to the sustentacular cells and acinar cells of Bowman's glands. No definite NAD-dependent activity was demonstrated in the olfactory receptor neurons. These data suggest that mineralocorticoid receptors present in acinar cells and sustentacular cells are aldosterone selective.

Key Words:

• Bowman's gland
• Na/K-ATPase
• ion transport
• mineralocorticoids
• glucocorticoids