Human peptide transporters: therapeutic applications

被引:39
作者
Nielsen, CU
Brodin, B
Jorgensen, FS
Frokjaer, S
Steffansen, B
机构
[1] Royal Danish Sch Pharm, Dept Pharmaceut, DK-2100 Copenhagen, Denmark
[2] Royal Danish Sch Pharm, Dept Med Chem, DK-2100 Copenhagen, Denmark
关键词
beta-lactams; angiotensin converting enzyme (ACE) inhibitors; bestatin; bisphosphonates; carrier-mediated drug delivery; cephalosporins; di/tripeptide transporter; drug absorption; hPepT1; hPepT2; oligopeptide transporter; renin inhibitors; thrombin inhibitors; valacyclovir; valgancyclovir;
D O I
10.1517/13543776.12.9.1329
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Peptide transporters are epithelial solute carriers. Their functional role has been characterised in the small intestine and proximal tubules, where they are involved in absorption of dietary peptides and peptide reabsorption, respectively. Currently, two peptide transporters, PepT1 and PepT2, which possess transport activity, have been identified. The transporters are not drug targets per se, but due to uniquely broad substrate specificity they have proven to be relevant in drug therapy at the level of drug transport. Therapeutic agents such as orally active beta-lactam antibiotics, bestatin, prodrugs of acyclovir and gancyclovir have oral bioavailabilities, which are largely a result of their interaction with PepT1. The transporters have therefore received considerable attention in relation to drug delivery. The aim of the present review is to highlight structural requirements for binding to peptide transporters, as well as their role in drug delivery and in potential future drug design and targeted tissue delivery of peptides and peptidomimetics.
引用
收藏
页码:1329 / 1350
页数:22
相关论文
共 185 条
[1]   EVIDENCE FOR ACTIVE TRANSPORT OF DIPEPTIDE GLYCYLSARCOSINE BY HAMSTER JEJUNUM IN-VITRO [J].
ADDISON, JM ;
BURSTON, D ;
MATTHEWS, DM .
CLINICAL SCIENCE, 1972, 43 (06) :907-&
[2]   Renal assimilation of oligopeptides: Physiological mechanisms and metabolic importance [J].
Adibi, SA .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 1997, 272 (05) :E723-E736
[3]   The oligopeptide transporter (Pept-1) in human intestine: Biology and function [J].
Adibi, SA .
GASTROENTEROLOGY, 1997, 113 (01) :332-340
[5]   CHEMICAL ASPECTS OF SELECTIVE TOXICITY [J].
ALBERT, A .
NATURE, 1958, 182 (4633) :421-423
[6]  
ALPERS DH, 1986, FASEB J, V45, P2261
[7]  
Amasheh S, 1996, FASEB J, V10, P465
[8]   A THEORETICAL BASIS FOR A BIOPHARMACEUTIC DRUG CLASSIFICATION - THE CORRELATION OF IN-VITRO DRUG PRODUCT DISSOLUTION AND IN-VIVO BIOAVAILABILITY [J].
AMIDON, GL ;
LENNERNAS, H ;
SHAH, VP ;
CRISON, JR .
PHARMACEUTICAL RESEARCH, 1995, 12 (03) :413-420
[9]   UTILIZATION OF PEPTIDE CARRIER SYSTEM TO IMPROVE INTESTINAL-ABSORPTION - TARGETING PROLIDASE AS A PRODRUG-CONVERTING ENZYME [J].
BAI, JPF ;
HU, M ;
SUBRAMANIAN, P ;
MOSBERG, HI ;
AMIDON, GL .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1992, 81 (02) :113-116
[10]   PGLU-L-DOPA-PRO - A TRIPEPTIDE PRODRUG TARGETING THE INTESTINAL PEPTIDE TRANSPORTER FOR ABSORPTION AND TISSUE ENZYMES FOR CONVERSION [J].
BAI, JPF .
PHARMACEUTICAL RESEARCH, 1995, 12 (07) :1101-1104