Favus M J, Angeid-Backman E, Breyer M D, Coe F L
Am J Physiol. 1983 Feb;244(2):G111-5. doi: 10.1152/ajpgi.1983.244.2.G111.
Bidirectional steady-state calcium fluxes were measured in vitro under short-circuited conditions in segments of rat duodenum and descending colon. The calcium-activated ATPase (Ca-ATPase) inhibitor trifluoperazine (TFP, 0.1 mM) reduced net calcium absorption in both tissues by decreasing the absorptive flux from mucosa to serosa (Jm leads to s) without consistently altering the secretory flux from serosa to mucosa. 1,25-Dihydroxyvitamin D3 administration (50 ng/day for 4 days) increased net calcium absorption by increasing Jm leads to s, and TFP reduced Jm leads to s to the same extent across tissues from vehicle- or 1,25-dihydroxyvitamin D3-treated animals. Na-K-ATPase inhibitors ouabain and ethacrynic acid both reduced short-circuit current without affecting calcium fluxes. These data suggest that Ca-ATPase, located in the basolateral membrane of intestinal epithelial cells, plays a role in the transepithelial transport of calcium. More general effects of TFP on intestinal epithelium may also contribute to the reduction in calcium fluxes. Duodenal and descending colon calcium transport appears independent of transcellular sodium transport mediated by Na-K-ATPase.
在短路条件下,对大鼠十二指肠和降结肠段进行体外双向稳态钙通量测量。钙激活ATP酶(Ca-ATP酶)抑制剂三氟拉嗪(TFP,0.1 mM)通过降低从黏膜到浆膜的吸收通量(Jm→s),减少了两种组织中的净钙吸收,而未持续改变从浆膜到黏膜的分泌通量。给予1,25-二羟维生素D3(50 ng/天,共4天)通过增加Jm→s提高了净钙吸收,并且TFP在来自未处理或1,25-二羟维生素D3处理动物的组织中同等程度地降低了Jm→s。钠钾ATP酶抑制剂哇巴因和依他尼酸均降低了短路电流,但不影响钙通量。这些数据表明,位于肠上皮细胞基底外侧膜的Ca-ATP酶在钙的跨上皮转运中起作用。TFP对肠上皮的更广泛作用也可能导致钙通量的降低。十二指肠和降结肠的钙转运似乎独立于由钠钾ATP酶介导的跨细胞钠转运。