Lippe G, Andersen K J, Schjönsby H
Scand J Gastroenterol. 1977;12(1):109-14.
Pancreatic extract (PE) reduced the uptake of rat intrinsic factor (IF)-bound 57CoB12 by perfused rat intestinal segments (p is less than 0.02) as well as by isolated rat intestinal brush borders (p is less than 0.01). The inhibition was concentration-dependent. Preincubation of the brush borders with PE recular weight of the 57CoB12-IF complex, as well as the uptake of the complex by isolated intestinal brush borders, was unchanged after prolonged preincubation with PE. PE also inhibited the uptake of glucose by perfused intestinal segments (p is less than 0.01), but the morphology and idsaccharidase activity (p is greater than 0.5) of the intestinaleptihelium was unaltered. The results indicate that the inhibition may be due to interaction between the intestinal epithelium and PE.
胰腺提取物(PE)降低了灌注大鼠肠段对大鼠内因子(IF)结合的57CoB12的摄取(p<0.02),以及分离的大鼠肠刷状缘对其的摄取(p<0.01)。这种抑制作用呈浓度依赖性。用PE预孵育刷状缘后,57CoB12 - IF复合物的分子量以及分离的肠刷状缘对该复合物的摄取,在与PE长时间预孵育后未发生变化。PE还抑制了灌注肠段对葡萄糖的摄取(p<0.01),但肠上皮的形态和二糖酶活性未改变(p>0.5)。结果表明,这种抑制作用可能是由于肠上皮与PE之间的相互作用所致。