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新生猪肠道对聚乙烯吡咯烷酮的吸收

The absorption of polyvinyl pyrrolidone by the new-born pig intestine.

作者信息

Hardy R N

出版信息

J Physiol. 1969 Oct;204(3):633-51. doi: 10.1113/jphysiol.1969.sp008936.

Abstract
  1. The intestinal absorption of [(131)I]polyvinyl pyrrolidone of mean mol. wt. 160,000 (K. 60) and 40,000 (K. 30) after oral administration has been measured in unsuckled conscious pigs less than 20 hr old. Absorption was assessed by the measurement of the concentration of [(131)I]PVP in venous blood during the 6 hr after feeding and also by the distribution at the end of the experiment of [(131)I]PVP between homogenates of the alimentary tract and homogenates of the rest of the animal.2. The concentration of [(131)I]PVP in the peripheral blood after feeding was dependent upon the mol. wt. of the polymer, when comparable amounts had been absorbed from the intestine. PVP K. 60 attained higher blood concentrations than PVP K. 30 and the blood concentrations of PVP K. 60 were close to the values to be expected if all the material which had left the intestine had remained in the blood. The lower blood concentrations found when PVP K. 30 was fed were associated with the disappearance of labelled solute from the gut and were thus the consequence of the relatively rapid escape of labelled solute from the plasma after absorption had taken place.3. The ability of the intestine to absorb [(131)I]PVP K. 60 declined progressively after birth but did not terminate abruptly unless the animal was fed colostrum. In unsuckled animals the rate and extent of absorption at 3 hr was much greater than at 20 hr after birth, but some absorption was still present at least 65 hr after birth.4. The transfer of PVP K. 60 to the peripheral blood was dependent upon factors in sow colostrum, since significant absorption did not occur when PVP was fed in water or simple salt solutions.5. The factors which accelerated absorption were present in colostrum from the goat, cow and ewe as well as that from the sow; they remained in the whey, but, in contrast to the factors which accelerate absorption in the calf, were largely inactivated by boiling. Similarly, neither phosphate, lactate, pyruvate, nor lower volatile fatty acid salts, which were effective in the calf, accelerated absorption in the pig.6. The absorption of [(131)I]PVP K. 30 was found to be much less dependent upon the composition of the solvent than the absorption of [(131)I]PVP K. 60, although absorption was most rapid when PVP K. 30 was fed in colostrum.
摘要
  1. 对出生不到20小时未吮乳的清醒仔猪口服平均分子量为160,000(K.60)和40,000(K.30)的[(131)I]聚乙烯吡咯烷酮后的肠道吸收情况进行了测定。通过测定喂食后6小时静脉血中[(131)I]PVP的浓度,以及在实验结束时[(131)I]PVP在消化道匀浆和动物其他部位匀浆之间的分布来评估吸收情况。

  2. 当从肠道吸收的量相当时,喂食后外周血中[(131)I]PVP的浓度取决于聚合物的分子量。PVP K.60达到的血药浓度高于PVP K.30,并且PVP K.60的血药浓度接近如果所有离开肠道的物质都留在血液中所预期的值。喂食PVP K.30时发现的较低血药浓度与标记溶质从肠道消失有关,因此是吸收发生后标记溶质从血浆中相对快速逸出的结果。

  3. 肠道吸收[(131)I]PVP K.60的能力在出生后逐渐下降,但除非给动物喂食初乳,否则不会突然终止。在未吮乳的动物中,出生后3小时的吸收速率和程度远大于出生后20小时,但至少在出生后65小时仍有一些吸收。

  4. PVP K.60向外周血的转运取决于母猪初乳中的因素,因为当PVP用水或简单盐溶液喂食时不会发生显著吸收。

  5. 加速吸收的因素存在于山羊、奶牛和母羊以及母猪的初乳中;它们保留在乳清中,但与加速小牛吸收的因素不同,通过煮沸基本上会失活。同样,在小牛中有效的磷酸盐、乳酸盐、丙酮酸盐或低级挥发性脂肪酸盐在猪中都不会加速吸收。

  6. 发现[(131)I]PVP K.30的吸收比[(131)I]PVP K.60的吸收对溶剂组成的依赖性小得多,尽管当PVP K.30在初乳中喂食时吸收最快。

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