Roche C, Bellaton C, Pansu D, Miller A, Bronner F
Am J Physiol. 1986 Sep;251(3 Pt 1):G314-20. doi: 10.1152/ajpgi.1986.251.3.G314.
Vitamin D-replete (+D) and vitamin D-deficient (-D) rats received by intraperitoneal injection varying amounts of 1,25-dihydroxyvitamin D3, and 4 h (+D) or 9 h (-D) later everted duodenal sacs were prepared to evaluate active calcium transport, i.e., the amount of calcium found in the serosal fluid. At the same time, duodenal calcium-binding protein (CaBP) content was measured. Calcium transport was a close positive function of CaBP content. It was not detectable when CaBP content was zero and increased linearly without plateauing as CaBP content increased to 100 nmol calcium bound/g mucosa. Trifluoperazine (TFP) inhibited active calcium transport in a concentration-dependent manner. Experiments using vesicles prepared from brush-border or basolateral membranes indicated that TFP inhibited the calcium-extrusion process, with virtually no effect on calcium entry. It is concluded that vitamin D exerts its major regulation of active calcium transport in the rat duodenum via CaBP on transport steps beyond brush-border entry.
给维生素 D 充足(+D)和维生素 D 缺乏(-D)的大鼠腹腔注射不同剂量的 1,25 - 二羟维生素 D3,4 小时后(+D 组)或 9 小时后(-D 组)制备外翻十二指肠囊,以评估活性钙转运,即浆膜液中钙的含量。同时,测定十二指肠钙结合蛋白(CaBP)含量。钙转运与 CaBP 含量呈密切正相关。当 CaBP 含量为零时无法检测到钙转运,随着 CaBP 含量增加至 100 nmol 钙结合/克黏膜,钙转运呈线性增加且无平台期。三氟拉嗪(TFP)以浓度依赖性方式抑制活性钙转运。使用从刷状缘膜或基底外侧膜制备的囊泡进行的实验表明,TFP 抑制钙的外排过程,对钙的内流几乎没有影响。得出的结论是,维生素 D 通过 CaBP 对大鼠十二指肠中活性钙转运的主要调节作用发生在刷状缘进入之外的转运步骤。