Chow S L, Hollander D
Lipids. 1978 Apr;13(4):239-45. doi: 10.1007/BF02533662.
The kinetics of initial cholesterol uptake by everted rat proximal and distal small intestinal sacs were evaluated in vitro. The mucosal incubation solution consisted of 0.05 mM cholesterol solubilized in 4.8 mM sodium taurocholate micellar solution at pH 7.4 Experiments were performed at temperatures from 26 to 38 C. The rate of cholesterol uptake followed a linear relationship when plotted against time indicating an apparent zero-order kinetics mechanism for initial uptake. An Arrhenius plot of the results of uptake versus temperature remained linear over the entire range of temperatures studied. The large free energy of activation (20 kcal/mole) suggests that an energy barrier for cholesterol uptake exists at the enterocyte luminal cell membrane and may be an important limiting step in cholesterol uptake. It is proposed that a transient association between cholesterol and a component of the enterocyte luminal cell membrane is formed during initial uptake of cholesterol. The transient association may be an activated complex formed with proteins present at or within the luminal enterocyte cell membrane.
在体外评估了外翻大鼠近端和远端小肠囊对初始胆固醇摄取的动力学。黏膜孵育溶液由在pH 7.4的4.8 mM牛磺胆酸钠胶束溶液中溶解的0.05 mM胆固醇组成。实验在26至38℃的温度下进行。当绘制胆固醇摄取速率与时间的关系图时,呈现线性关系,表明初始摄取存在明显的零级动力学机制。在研究的整个温度范围内,摄取结果与温度的阿伦尼乌斯图保持线性。较大的活化自由能(20千卡/摩尔)表明在肠上皮细胞腔面膜处存在胆固醇摄取的能量屏障,这可能是胆固醇摄取的一个重要限制步骤。有人提出,在胆固醇初始摄取过程中,胆固醇与肠上皮细胞腔面膜的一个成分形成了瞬时缔合。这种瞬时缔合可能是与存在于肠上皮细胞腔面膜处或膜内的蛋白质形成的活化复合物。