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大鼠小肠在体内和体外对蔗糖的吸收

Sucrose absorption by the rat small intestine in vivo and in vitro.

作者信息

Davidson R E, Leese H J

出版信息

J Physiol. 1977 May;267(1):237-48. doi: 10.1113/jphysiol.1977.sp011810.

Abstract
  1. The absorption of glucose and fructose derived from sucrose has been studied using in vitro and in vivo loops of the rat jejunum.2. At low sucrose concentrations (1 and 10 mM) glucose appeared in the serosal compartment of the in vitro preparation at a faster rate than fructose, but at high sucrose concentrations (50 and 100 mM) the rates of serosal transfer of the two sugars were similar. Glucose and fructose appeared in the mucosal compartment, with the rate of fructose appearance exceeding that of glucose, at all the sucrose concentrations studied.3. Phlorizin (5 x 10(-5)M) added to the mucosal medium of the in vitro preparation abolished the serosal transfer of glucose derived from 50 mM sucrose, and reduced that of fructose by 75%.4. In the absence of sodium ions, the in vitro preparation failed to transfer glucose and fructose derived from 50 mM sucrose, into the serosal compartment.5. Glucose was actively accumulated in the whole gut wall of the in vivo preparation to concentrations higher than those in the plasma at 50 and 100 mM, but not at 10 mM sucrose concentrations. Fructose was also actively accumulated to about half the extent of glucose, but reached tissue concentrations greater than those in the plasma, at each sucrose concentration.6. The whole wall concentrations of glucose and fructose derived from sucrose added to the lumen continued to rise when the blood supply to the in vivo preparation was terminated.7. No increase in the in vivo whole wall concentrations of glucose and fructose were detected when sucrose was added to the lumen together with concentrations of glucose sufficient to saturate the monosaccharide transport systems.8. The results favour the view that disaccharide hydrolysis and resulting hexose transfer are sequential, separate events.
摘要
  1. 利用大鼠空肠的体外和体内肠袢研究了蔗糖衍生的葡萄糖和果糖的吸收情况。

  2. 在低蔗糖浓度(1和10 mM)下,体外制剂浆膜腔中葡萄糖出现的速率比果糖快,但在高蔗糖浓度(50和100 mM)下,两种糖的浆膜转运速率相似。在所研究的所有蔗糖浓度下,葡萄糖和果糖都出现在黏膜腔中,果糖出现的速率超过葡萄糖。

  3. 添加到体外制剂黏膜培养基中的根皮苷(5×10⁻⁵M)消除了源自50 mM蔗糖的葡萄糖的浆膜转运,并使果糖的转运减少了75%。

  4. 在没有钠离子的情况下,体外制剂无法将源自50 mM蔗糖的葡萄糖和果糖转运到浆膜腔中。

  5. 在体内制剂中,葡萄糖在50和100 mM蔗糖浓度下会在整个肠壁中主动积累,浓度高于血浆中的浓度,但在10 mM蔗糖浓度下不会。果糖也会主动积累,程度约为葡萄糖的一半,但在每个蔗糖浓度下,其组织浓度都高于血浆中的浓度。

  6. 当体内制剂的血液供应终止时,添加到肠腔中的蔗糖衍生的葡萄糖和果糖的全壁浓度继续上升。

  7. 当蔗糖与足以饱和单糖转运系统的葡萄糖浓度一起添加到肠腔中时,未检测到体内葡萄糖和果糖的全壁浓度增加。

  8. 这些结果支持这样一种观点,即二糖水解和由此产生的己糖转运是相继发生的、独立的事件。

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