Suppr超能文献

关于氨基酸对无尾两栖类小肠上皮单糖输出抑制作用的研究。

Studies on amino acid inhibition of monosaccharide exit from anuran small intestinal epithelium.

作者信息

Boyd C A

出版信息

J Physiol. 1979 Sep;294:195-210. doi: 10.1113/jphysiol.1979.sp012925.

Abstract
  1. The effect of the addition of amino acids to the intestinal lumen upon the movement of the monosaccharide alpha-methyl-D-glucopyranoside (alpha MG) from the preloaded epithelium into the blood and into the lumen of the vascularly perfused frog small intestine has been studied. 2. The neutral hydrophobic amino acids tryptophan, leucine, phenylalanine, tyrosine, isoleucine, valine, norleucine and cycloleucine all rapidly inhibit the exit of alpha MG out of the epithelium into the vascular bed. They stimulate backflux of the sugar from the epithelium into the lumen to a very much smaller extent. 3. L-Leucine is a more effective inhibitor of alpha MG exit into the blood than is D-leucine. Near-maximal inhibition of alpha MG exit is seen with 10 mM-L-leucine in the intestinal lumen. 4. The addition of leucine (10 mM) to the lumen of the intestine preloaded with alpha MG approximately halves the rate constant for alpha MG washout into the blood from 12.6 +/- 1.7 (4) x 10(-3) to 5.5 +/- 1.4 (4) x 10(-3) min-1, without appreciably altering the pool of monosaccharide in the tissue. The inhibitory effect of L-leucine upon alpha MG exit into the blood is not abolished by the presence of phlorizin (5 x 10(-5) M) in the intestinal lumen. 5. The complex pattern of inhibition of alpha MG transfer from the lumen to the blood observed upon the addition of L-leucine to the lumen is consistent with the finding that the amino acid inhibits the exit of the monosaccharide out of the epithelium into the blood in addition to any inhibitory effect upon sugar entry across the brush border. 6. It is suggested that alpha MG may be a substrate for a proposed transport system for neutral hydrophobic amino acids which, it is suggested, is present in the basolateral membrane of the epithelial cell.
摘要
  1. 研究了向肠腔添加氨基酸对单糖α-甲基-D-吡喃葡萄糖苷(αMG)从预先加载的上皮细胞进入血液以及进入血管灌注的青蛙小肠肠腔的转运的影响。2. 中性疏水氨基酸色氨酸、亮氨酸、苯丙氨酸、酪氨酸、异亮氨酸、缬氨酸、正亮氨酸和环亮氨酸都能迅速抑制αMG从上皮细胞进入血管床。它们对糖从上皮细胞回流到肠腔的刺激作用要小得多。3. L-亮氨酸比D-亮氨酸更有效地抑制αMG进入血液。在肠腔中加入10 mM-L-亮氨酸可观察到对αMG进入血液的近乎最大程度的抑制。4. 向预先加载αMG的肠腔中添加亮氨酸(10 mM),可使αMG冲刷进入血液的速率常数从12.6±1.7(4)×10⁻³降至5.5±1.4(4)×10⁻³ min⁻¹,约减半,而不会明显改变组织中单核糖类的总量。肠腔中存在根皮苷(5×10⁻⁵ M)时,L-亮氨酸对αMG进入血液的抑制作用不会消除。5. 向肠腔中添加L-亮氨酸后观察到的αMG从肠腔向血液转运的复杂抑制模式与以下发现一致:除了对糖跨刷状缘进入的任何抑制作用外,氨基酸还抑制单糖从上皮细胞进入血液。6. 有人提出,αMG可能是一种推测的中性疏水氨基酸转运系统的底物,该转运系统被认为存在于上皮细胞的基底外侧膜中。

相似文献

本文引用的文献

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验