El'kina V A, Rozanov A Ia
Fiziol Zh (1994). 1996;42(5-6):72-80.
Calcium chloride injected intramuscularly to white mice in the therapeutical dose of 50 mM/kg, influences considerably distribution, proteidization, enterohepatic recycling level, elimination from the blood, excretion with urine and catabolism of 14C-biotin injected simultaneously in the physiological dose of 0.5 mM/kg. CaCl2 decreases and retards inflow of the 14C-biotin general radio-label to the analyzed tissues and organs, with the simultaneous increase of its proteidization in the same tissues. At the same time permeability of histohematic barriers of these tissues for 14C-biotin under the CaCl2 effect falls markedly. Calcium chloride increases the level of complete catabolism of 14C-biotin to 14CO2 by 51% 480 min after their simultaneous injection. A conclusion is made that calcium introduced as CaCl2 in the mentioned dose inhibits enterohepatic recycling of 14C-biotin in the white mice organism with the simultaneous of 14C-biotin assimilation in the analyzed tissues.
以50 mM/kg的治疗剂量向小白鼠肌肉注射氯化钙,会显著影响同时以0.5 mM/kg的生理剂量注射的14C-生物素的分布、蛋白质化、肠肝循环水平、血液清除、尿液排泄及分解代谢。氯化钙会减少并延缓14C-生物素总放射性标记流入被分析的组织和器官,同时其在相同组织中的蛋白质化增加。与此同时,在氯化钙作用下,这些组织的组织血液屏障对14C-生物素的通透性显著下降。同时注射氯化钙和14C-生物素480分钟后,氯化钙使14C-生物素完全分解代谢为14CO2的水平提高了51%。得出的结论是,以上述剂量作为氯化钙引入的钙会抑制小白鼠体内14C-生物素的肠肝循环,同时抑制14C-生物素在被分析组织中的同化作用。