Intestinal transport and metabolism of glucose-conjugated kyotorphin and cyclic kyotorphin: metabolic degradation is crucial to intestinal absorption of peptide drugs-Reference-Cited by-同舟云学术

Intestinal transport and metabolism of glucose-conjugated kyotorphin and cyclic kyotorphin: metabolic degradation is crucial to intestinal absorption of peptide drugs

Published:2000-06 Issue:1 Volume:1475 Page:90-98
ISSN:0304-4165
Container-title:Biochimica et Biophysica Acta (BBA) - General Subjects
language:en
Short-container-title:Biochimica et Biophysica Acta (BBA) - General Subjects

Author:

Mizuma Takashi,Koyanagi Akihiro,Awazu Shoji

Publisher

Elsevier BV

Subject

Molecular Biology,Biochemistry,Biophysics

Reference20 articles.

1. Is intestinal peptide transport energized by a proton gradient?;Ganapathy;Am. J. Physiol.,1985

2. Expression cloning of a mammalian proton-coupled oligopeptide transporter;Fei;Nature,1994

3. A novel analgesic dipeptide from bovine brain is a possible Met-enkephalin releaser;Takagi;Nature,1979

4. Kyotorphin and D-kyotorphin stimulate Met-enkephalin release from striatum in vitro;Janicki;Neurosci. Lett.,1983

5. Regional distribution of a novel analgesic dipeptide kyotorphin (Tyr-Arg) in the rat brain and spinal cord;Ueda;Brain Res.,1980

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