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肠二肽水解部位。

Site of intestinal dipeptide hydrolysis.

作者信息

Wiseman G

出版信息

J Physiol. 1977 Dec;273(3):731-43. doi: 10.1113/jphysiol.1977.sp012120.

Abstract
  1. Sacs of everted small intestine of the hamster have been used to study the site of final hydrolysis of twelve dipeptides. 2. The results suggest that L-alanyl-glycine, glycyl-glycine, L-valyl-L-valine, L-alanyl-L-valine, L-valyl-L-alanine and L-prolyl-glycine are hydrolysed beyond the locus of the active transport mechanism for D-glucose, perhaps even within the cell. These may be designated class 1 (deep) dipeptides. 3. In contrast, superficial (perhaps even surface) hydrolysis seems to occur with L-alanyl-L-alanine, L-leucly-L-leucine, glycyl-L-alanine, L-alanyl-L-leucine, L-leucyl-L-alanine and glycyl-L-proline. These may be designated class 2 (superficial) dipeptides. 4. All the dipeptides were able to partially inhibit D-glucose active transport, the findings supporting the view that more than one mechanism may exist for the active absorption of the sugar.
摘要
  1. 仓鼠外翻小肠囊已被用于研究12种二肽的最终水解部位。2. 结果表明,L-丙氨酰甘氨酸、甘氨酰甘氨酸、L-缬氨酰-L-缬氨酸、L-丙氨酰-L-缬氨酸、L-缬氨酰-L-丙氨酸和L-脯氨酰甘氨酸在D-葡萄糖主动转运机制位点之外被水解,甚至可能在细胞内被水解。这些可被指定为1类(深度)二肽。3. 相比之下,L-丙氨酰-L-丙氨酸、L-亮氨酰-L-亮氨酸、甘氨酰-L-丙氨酸、L-丙氨酰-L-亮氨酸、L-亮氨酰-L-丙氨酸和甘氨酰-L-脯氨酸似乎发生表面(甚至可能是在表面)水解。这些可被指定为2类(表面)二肽。4. 所有二肽都能够部分抑制D-葡萄糖的主动转运,这些发现支持了这样一种观点,即糖的主动吸收可能存在不止一种机制。

相似文献

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Site of intestinal dipeptide hydrolysis.肠二肽水解部位。
J Physiol. 1977 Dec;273(3):731-43. doi: 10.1113/jphysiol.1977.sp012120.
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Glycyl-L-leucine transport in the rat small intestine.大鼠小肠中甘氨酰-L-亮氨酸的转运
Can J Physiol Pharmacol. 1982 Sep;60(9):1177-84. doi: 10.1139/y82-171.
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[Peptide interactions in the intestines of birds].[鸟类肠道中的肽相互作用]
Fiziol Zh SSSR Im I M Sechenova. 1983 Dec;69(12):1608-13.
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Dipeptide transport in isolated intestinal brush border membrane.分离的肠刷状缘膜中的二肽转运
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本文引用的文献

5
The active absorption of amino-acids by the intestine.肠道对氨基酸的主动吸收。
J Physiol. 1953 Aug;121(2):255-63. doi: 10.1113/jphysiol.1953.sp004945.
6
Effect of amino acids on sugar absorption.氨基酸对糖吸收的影响。
J Physiol. 1966 Sep;186(1):166-74. doi: 10.1113/jphysiol.1966.sp008026.

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