Gallium nitrate inhibits bone resorption and collagen synthesis in neonatal mouse calvariae

• Published in: Journal of bone and mineral research Vol. 6; no. 10; p. 1121
• Main Authors: Lakatos, P, Mong, S, Stern, P H
• Format: Journal Article
• Language: English
• Published: United States 01.10.1991
• Subjects: Animals; Bone and Bones - drug effects; Bone and Bones - metabolism; Bone Resorption - drug therapy; Calcitriol - pharmacology; Calcium - metabolism; Collagen - biosynthesis; Dose-Response Relationship, Drug; Gallium - pharmacology; Gallium - therapeutic use; Glucuronidase - metabolism; Interleukin-1 - pharmacology; Mice; Organ Culture Techniques; Parathyroid Hormone - pharmacology; Peptide Fragments - pharmacology; Teriparatide; Thyroxine - pharmacology
• ISSN: 0884-0431
• DOI: 10.1002/jbmr.5650061014

Gallium nitrate (GN) is an agent used in the treatment of hypercalcemia. To more fully characterize the direct actions of GN on bone, we examined its effects on medium calcium, medium beta-glucuronidase (beta-GLU), and collagen synthesis in control and hormone-stimulated neonatal (4-6 days) mouse calvariae in vitro. GN (10 micrograms/ml) inhibited parathyroid hormone-stimulated (PTH; 1 nM) calcium release. A 24 h preincubation with 10 micrograms/ml of GN was required for complete inhibition; partial inhibition was seen with 12 h preincubation; 1, 3, or 6 h was inadequate. A dose-response study showed that with 24 h preincubation, 5, 3, and 1 microgram/ml of GN inhibited 81, 62, and 0% of PTH-induced calcium release. The effects of GN on the release of beta-GLU generally paralleled those on the release of calcium except that 10 micrograms/ml of GN stimulated beta-GLU release. Collagen synthesis was inhibited 50% by 3 micrograms/ml of GN, whereas noncollagen protein synthesis was unaffected. With PTH + GN no further decrease was observed. When GN was withdrawn from the medium after 24 h of preincubation, the inhibitory effect on calcium release and beta-GLU activity, but not on collagen synthesis, persisted through the 72 h of culture. GN also inhibited the resorption elicited by thyroxine (1 microM) and interleukin-1 beta (10 nM) but not by 1,25-dihydroxyvitamin D3 (30 pM). Our results indicate that GN is a powerful inhibitor of bone resorption in neonatal mouse calvariae even at low doses.