Ilundain A, Alcalde A I, Barcina Y, Larralde J
Biochim Biophys Acta. 1985 Aug 8;818(1):67-72. doi: 10.1016/0005-2736(85)90139-7.
The involvement of Ca2+ in the theophylline action on sugar transport was investigated in isolated rat small intestinal mucosa. Theophylline significantly increased cell water free sugar accumulation and reduced mucosal to serosal sugar fluxes both in the presence and absence of calcium, but the effects of theophylline were significantly less in calcium free media. In theophylline untreated tissues, calcium-deprived bathing solutions decreased tissue galactose accumulation and increased mucosal to serosal sugar flux. The calcium-channel blocker verapamil produced similar effects on intestinal galactose transport to those induced by low extracellular calcium activity. RMI 12330A and the calmodulin antagonist trifluoperazine abolished the theophylline-effects on intestinal galactose transport. Both drugs also affected sugar transport in basal conditions. These studies suggest that calcium might modulate sugar permeability across the basolateral boundary of rat enterocytes, and that its effect may be mediated by calmodulin.
在离体大鼠小肠黏膜中研究了钙离子在茶碱对糖转运作用中的参与情况。无论有无钙离子存在,茶碱均能显著增加细胞内游离糖的积累,并减少黏膜到浆膜的糖通量,但在无钙培养基中,茶碱的作用明显减弱。在未用茶碱处理的组织中,剥夺钙的浴液会降低组织半乳糖的积累,并增加黏膜到浆膜的糖通量。钙通道阻滞剂维拉帕米对肠道半乳糖转运产生的影响与低细胞外钙活性所诱导的影响相似。RMI 12330A和钙调蛋白拮抗剂三氟拉嗪消除了茶碱对肠道半乳糖转运的作用。这两种药物在基础条件下也会影响糖转运。这些研究表明,钙可能调节大鼠肠上皮细胞基底外侧边界的糖通透性,其作用可能由钙调蛋白介导。