Bomsztyk K, Calalb M B
Division of Nephrology, University of Washington, Seattle 98195.
J Clin Invest. 1988 May;81(5):1455-61. doi: 10.1172/JCI113476.
To evaluate the effect of luminal bicarbonate on calcium reabsorption, rat proximal tubules were perfused in vivo. Perfusion solution contained mannitol to reduce water flux to zero. Total Ca concentration was measured by atomic absorption spectrometry, Ca ion concentration in the tubule lumen (CaL2+) and the peritubular capillary (CaP2+), and luminal pH (pHL) with ion-selective microelectrodes and transepithelial voltage (VTE) with conventional microelectrodes. When tubules were perfused with buffer-free Cl-containing solution, net Ca absorption (JCa) averaged 3.33 pmol/min. Even though VTE was 1.64 mV lumen-positive, CaL2+, 1.05 mM, did not fall below the concentration in the capillary blood, 1.07 mM. When 27 mM of Cl was replaced with HCO3, there was luminal fluid acidification. Despite a decrease in VTE and CaL2+, JCa increased to 7.13 pmol/min, indicating that the enhanced JCa could not be accounted for by the reduced electrochemical gradient, delta CCa. When acetazolamide or an analogue of amiloride was added to the HCO3 solution, JCa was not different from the buffer-free solution, suggesting that HCO3-stimulated JCa may be linked to acidification. To further test this hypothesis, we used 27 mM Hepes as the luminal buffer. With Hepes there was luminal fluid acidification and JCa was not different from the buffer-free solution but delta CCa was significantly reduced, indicating enhanced active calcium transport. We conclude from the results of the present study that HCO3 stimulates active Ca absorption, a process that may be linked to acidification-mediated HCO3 absorption.
为评估管腔碳酸氢盐对钙重吸收的影响,对大鼠近端小管进行体内灌注。灌注液中含有甘露醇以使水通量降至零。通过原子吸收光谱法测量总钙浓度、小管腔(CaL2+)和肾小管周围毛细血管(CaP2+)中的钙离子浓度,使用离子选择性微电极测量管腔pH(pHL),使用传统微电极测量跨上皮电压(VTE)。当用不含缓冲液的含氯溶液灌注小管时,净钙吸收(JCa)平均为3.33 pmol/分钟。尽管VTE为1.64 mV管腔阳性,但CaL2+(1.05 mM)并未降至毛细血管血中浓度(1.07 mM)以下。当27 mM的Cl被HCO3取代时,出现管腔液酸化。尽管VTE和CaL2+降低,但JCa增加至7.13 pmol/分钟,这表明增强的JCa不能用降低的电化学梯度δCCa来解释。当向HCO3溶液中加入乙酰唑胺或氨氯地平类似物时,JCa与不含缓冲液的溶液无差异,这表明HCO3刺激的JCa可能与酸化有关。为进一步验证该假设,我们使用27 mM的HEPES作为管腔缓冲液。使用HEPES时出现管腔液酸化,JCa与不含缓冲液的溶液无差异,但δCCa显著降低,表明活性钙转运增强。我们从本研究结果得出结论,HCO3刺激活性钙吸收,这一过程可能与酸化介导的HCO3吸收有关。