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Glucose metabolism in the mucosa of the small intestine. Changes of hexokinase activity during perfusion of the proximal half of rat small intestine

机译:小肠粘膜中的葡萄糖代谢。大鼠小肠近端灌注过程中己糖激酶活性的变化

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摘要

1. The effect of perfusion on the activities of hexokinase and lactate dehydrogenase was studied in the proximal half of the small intestine of fed and starved rats. 2. Perfusion of preparations from starved rats with a medium containing glucose caused a significant increase in hexokinase activity of the particle-free supernatant. The increase in activity was observed as early as 5min after the start of perfusion and persisted for up to 66min of perfusion. No increase in hexokinase activity of the particle-free supernatant was observed when a medium containing mannitol was used. As a further control, preparations from fed rats were perfused under the same conditions. With the medium containing glucose, the hexokinase activity of the particle-free supernatant remained unchanged during the first 15min of perfusion and thereafter fell gradually until, after 66min of perfusion, 73% of the original activity was retained. 3. The activity of lactate dehydrogenase in the particle-free supernatant prepared from the proximal half of the untreated small intestine of starved rats was significantly lower than in corresponding preparations from fed animals. However, it did not change significantly on perfusion with media containing either mannitol or glucose. 4. The distribution of hexokinase activity between total particulate fraction and particle-free supernatant was measured in preparations from starved rats after perfusion for 5–10min. In preparations that had not been perfused the ratio of hexokinase activity in total particulate fraction/particle-free supernatant was significantly higher in starved than in fed animals. After perfusion with a medium containing glucose, the total homogenate activity had not changed significantly, whereas the ratio of hexokinase activity in total particulate fraction/particle-free supernatant decreased significantly and approached the value obtained with fed animals. 5. The results agree with the view that the glucose-dependent increase of hexokinase activity in the soluble cell compartment as observed in vivo and in vitro in the intestinal mucosa of starved rats is brought about by a release of hexokinase activity from a particulate subcellular structure(s).
机译:1.在饱食和饥饿的大鼠小肠近端研究了灌注对己糖激酶和乳酸脱氢酶活性的影响。 2.用含葡萄糖的培养基灌注饥饿的大鼠的制剂导致无颗粒上清液的己糖激酶活性显着增加。早在灌注开始后5分钟就观察到了活性的增加,并且持续了长达66分钟的灌注。当使用含有甘露醇的培养基时,未观察到无颗粒的上清液中的己糖激酶活性没有增加。作为进一步的对照,在相同条件下灌注来自饲喂大鼠的制剂。在含葡萄糖的培养基中,无颗粒上清液的己糖激酶活性在灌注的前15分钟内保持不变,然后逐渐下降,直到灌注66分钟后,保留了原始活性的73%。 3.从饥饿的大鼠未经处理的小肠的近半部分制备的无颗粒上清液中的乳酸脱氢酶活性显着低于饲喂动物的相应制剂中的水平。但是,在灌注含有甘露醇或葡萄糖的培养基时,其变化不明显。 4.在饥饿5-10分钟后,从饥饿的大鼠的制剂中测量总颗粒级分和无颗粒上清液之间己糖激酶活性的分布。在未灌注的制剂中,饥饿动物中总颗粒级分/无颗粒上清液中己糖激酶活性的比率明显高于喂食动物。用含葡萄糖的培养基灌注后,总匀浆活性没有显着变化,而总颗粒级分/无颗粒上清液中己糖激酶活性的比率则显着下降,并接近饲喂动物获得的值。 5.结果与以下观点相一致,即饥饿和饥饿的肠粘膜在体内和体外观察到的可溶性细胞室中己糖激酶活性的葡萄糖依赖性增加是由己糖激酶活性从颗粒状亚细胞结构中释放引起的。 (s)。

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