DECREASED POTASSIUM STIMULATES BONE-RESORPTION

Citation
Da. Bushinsky et al., DECREASED POTASSIUM STIMULATES BONE-RESORPTION, American journal of physiology. Renal, fluid and electrolyte physiology, 41(6), 1997, pp. 774-780
Citations number
32
Categorie Soggetti
Physiology
ISSN journal
03636127
Volume
41
Issue
6
Year of publication
1997
Pages
774 - 780
Database
ISI
SICI code
0363-6127(1997)41:6<774:DPSB>2.0.ZU;2-A
Abstract
Metabolic acidosis induces net calcium efflux (J(Ca)(+)) from cultured bone, in part, through an increase in osteoclastic resorption and a d ecrease in osteoblastic formation. In humans provision of base as pota ssium (K+) citrate, but not sodium (Na+) citrate, reduces urine Ca (U- Ca), and oral KHCO3 decreases bone resorption and Uc, in postmenopausa l women. Potassium deprivation alone leads to an increase in U-Ca. To determine whether decreased extracellular K+ concentration ([K+]) at a constant pH, P-CO2, and [HCO2-] alters J(Ca)(+) and bone cell activit y, we measured J(Ca)(+), osteoblastic collagen synthesis, and osteocla stic beta-glucuronidase release from neonatal mouse calvariae cultured for 48 h in medium of varying [K+]. Calvariae were cultured in contro l medium (approximate to 4 mM [K+]) or medium with mildly low K+ (MLK, approximate to 3 mM: [K+]), very low K+ (VLK, approximate to 2 mM [K]), or extremely low K+ (ELK, approximate to 1 mM [K+]) (n greater tha n or equal to 9 in each group). Compared with control, ELK, but not ML K or VLK, resulted in a marked increase in J(Ca)(+) and an increase in beta-glucuronidase release and a decrease in collagen synthesis. J(Ca )(+), was correlated directly with medium beta-glucuronidase activity and inversely with collagen synthesis. To determine whether the reduct ion in medium [K+] was associated with a decrease in intracellular pH (pH(i)), we measured pH(i) in MC3T3-E1 cells, a mouse osteoblastic cel l line. Incubation in 1 mM [K+] led to a significant decrease in pH(i) compared with 3 mM [K+]. Thus incubation in a reduced [K+] medium sti mulates J(Ca)(+) and osteoclastic enzyme release and inhibits osteobla stic collagen synthesis, which may be mediated by a reduction in bone cell pH.