Regulation of PepT1 peptide transporter expression in the rat small intestine under malnourished conditions

被引:104
作者
Ihara, T [1 ]
Tsujikawa, T [1 ]
Fujiyama, Y [1 ]
Bamba, T [1 ]
机构
[1] Shiga Univ Med Sci, Dept Internal Med 2, Otsu, Shiga 5202152, Japan
关键词
PepT1; rat; small intestine; regulation; nutrition;
D O I
10.1159/000007736
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background and Aims: Many investigations suggested that peptide nutrition had a clinical advantage for nitrogen absorption. Recently, the cDNA encoding the H+/peptide cotransporter PepT1 was cloned. However, the regulatory mechanism of PepT1 expression under malnourished conditions has not been elucidated. The aim of this study was to clarify regulatory mechanisms of PepT1 expression. Methods: Sprague-Dawley rats were starved for 4 days, semistarved (50% amount of control) for 10 days, or given total parenteral nutrition (TPN) for 10 days. Rats with free feeding were used as control. Among those groups, the changes of PepT1 mRNA level in the jejunal mucosa and PepT1 protein density at the brush-border membranes were examined by Northern blot and by Western blot analysis, respectively. Results: Both starvation and TPN treatment caused a significant decrease in mucosal weight by 41 and 50% respectively. PepT1 mRNA level increased to 179% in the starved group and also to 161 and 164% in the TPN and semistarved groups, respectively. In contrast, sodium-dependent glucose transporter 1 mRNA expression showed no significant change. PepT1 protein density showed similar changes with the mRNA. Conclusions: PepT1 gene expression was significantly enhanced under the malnourished conditions in spite of atrophic changes of intestinal mucosa. Copyright (C) 2000 S. Karger AG, Basel.
引用
收藏
页码:59 / 67
页数:9
相关论文
共 37 条
[1]   The oligopeptide transporter (Pept-1) in human intestine: Biology and function [J].
Adibi, SA .
GASTROENTEROLOGY, 1997, 113 (01) :332-340
[2]  
ADIBI SA, 1974, GASTROENTEROLOGY, V67, P586
[4]   Deregulation of hexose transporter expression in Caco-2 cells by ras and polyoma middle T oncogenes [J].
BaronDelage, S ;
Mahraoui, L ;
Cadoret, A ;
Veissiere, D ;
Taillemite, JL ;
Chastre, E ;
Gespach, C ;
Zweibaum, A ;
Capeau, J ;
BrotLaroche, E ;
Cherqui, G .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 1996, 270 (02) :G314-G323
[5]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[6]   EXPRESSION OF AMINO-ACID AND PEPTIDE-TRANSPORT SYSTEMS IN RAT SMALL-INTESTINE [J].
CHEESEMAN, CI .
AMERICAN JOURNAL OF PHYSIOLOGY, 1986, 251 (05) :G636-G641
[7]   SINGLE-STEP METHOD OF RNA ISOLATION BY ACID GUANIDINIUM THIOCYANATE PHENOL CHLOROFORM EXTRACTION [J].
CHOMCZYNSKI, P ;
SACCHI, N .
ANALYTICAL BIOCHEMISTRY, 1987, 162 (01) :156-159
[8]   Hexose transporter expression in rat small intestine: Effect of diet on diurnal variations [J].
Corpe, CP ;
Burant, CF .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 1996, 271 (01) :G211-G216
[9]   ASSAY OF INTESTINAL DISACCHARIDASES [J].
DAHLQVIST, A .
ANALYTICAL BIOCHEMISTRY, 1968, 22 (01) :99-+
[10]   Function and molecular structure of brush border membrane peptide H+ symporters [J].
Daniel, H .
JOURNAL OF MEMBRANE BIOLOGY, 1996, 154 (03) :197-203