Bushinsky D A, Krieger N S, Geisser D I, Grossman E B, Coe F L
Am J Physiol. 1983 Aug;245(2):F204-9. doi: 10.1152/ajprenal.1983.245.2.F204.
Bone mineral is thought to decompose during acute and chronic metabolic acidosis and thereby contribute to buffering of the acid load. We cultured neonatal mouse calvariae for 3 h and found calcium efflux from bone when the medium pH was below 7.40, calcium influx into bone when the pH was above 7.40, and no net flux at pH 7.40. The calcium flux varied to the same extent when medium pH was altered by a primary change in the medium bicarbonate concentration or in the partial pressure of carbon dioxide. Calcium and proton fluxes were inversely correlated (r = -0.713, P less than 0.001), and the slope of the linear regression indicated that between 16 and 21 neq of proton entered the calvariae in exchange for each neq of calcium that left. In 24-h cultures, acid medium also caused net calcium efflux from bone, and alkaline medium caused net influx. PTH increased calcium efflux at acid but not at alkaline medium pH. Sodium azide resulted in net influx of calcium into bone at all values of medium pH. Calcium release by cultured calvariae in response to low medium pH is associated with proton buffering; over 3 h the stoichiometry indicates that little buffering is due to the dissolution of calcium-containing crystals. Effects of medium pH on calcium release are amplified by PTH, and calcium efflux can be prevented by the metabolic inhibitor sodium azide.
人们认为,在急性和慢性代谢性酸中毒期间,骨矿物质会分解,从而有助于缓冲酸负荷。我们将新生小鼠颅骨培养3小时,发现当培养基pH低于7.40时,钙从骨中流出;当pH高于7.40时,钙流入骨中;在pH 7.40时无净通量。当通过改变培养基碳酸氢盐浓度或二氧化碳分压来改变培养基pH时,钙通量的变化程度相同。钙通量和质子通量呈负相关(r = -0.713,P < 0.001),线性回归斜率表明,每有1个钙当量离开颅骨,就有16至21个质子当量进入颅骨进行交换。在24小时培养中,酸性培养基也会导致骨中钙的净流出,碱性培养基则会导致净流入。甲状旁腺激素(PTH)在酸性而非碱性培养基pH条件下会增加钙的流出。叠氮化钠在所有培养基pH值下都会导致钙净流入骨中。培养的颅骨因培养基低pH而释放钙与质子缓冲有关;在3小时内,化学计量关系表明几乎没有缓冲是由于含钙晶体的溶解。培养基pH对钙释放的影响会被PTH放大,代谢抑制剂叠氮化钠可以阻止钙的流出。