Sister of P-glycoprotein expression in different tissues

被引:25
作者
Török, M
Gutmann, H
Fricker, G
Drewe, J
机构
[1] Univ Basel Hosp, Div Gastroenterol, CH-4031 Basel, Switzerland
[2] Univ Basel Hosp, Dept Clin Pharmacol, CH-4031 Basel, Switzerland
[3] Inst Pharmaceutics & Biopharmacy, Heidelberg, Germany
关键词
sister of P-glycoprotein; multidrug resistance proteins; tissue distribution; polymerase chain reaction;
D O I
10.1016/S0006-2952(98)00357-8
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Sister of P-glycoprotein (spgp) is a gene that is closely related to the P-glycoprotein family (Pgps). This class of proteins belongs to the superfamily of ATP-binding cassette transporters and is known for its involvement in pharmacological drug interactions. Therefore, this study investigated the distribution of spgp expression in different tissues known for their high levels of Pgps expression such as brain, liver, kidney, small-and large-gut mucosa. Analysis was done by using the reverse transcription-polymerase chain reaction. In addition to a high expression in the liver, we were able to demonstrate a significant spgp expression in brain grey cortex, small- and large-gut mucosa. Although Pgps are expressed in the kidney and brain capillary endothelial cells, no expression of spgp was detected in these tissues, which might indicate that spgp has no function in the blood-brain barrier and is not involved in the renal excretion of drugs. (C) 1999 Elsevier Science Inc.
引用
收藏
页码:833 / 835
页数:3
相关论文
共 19 条
[1]   Duplication and evolution of the P-glycoprotein genes in pig [J].
Childs, S ;
Ling, V .
BIOCHIMICA ET BIOPHYSICA ACTA-GENE STRUCTURE AND EXPRESSION, 1996, 1307 (02) :205-212
[2]  
CHILDS S, 1995, CANCER RES, V55, P2029
[3]   P-GLYCOPROTEIN STRUCTURE AND EVOLUTIONARY HOMOLOGIES [J].
CROOP, JM .
CYTOTECHNOLOGY, 1993, 12 (1-3) :1-32
[4]   Role of P-glycoprotein as a secretory mechanism in quinidine absorption from rat small intestine [J].
Emi, Y ;
Tsunashima, D ;
Ogawara, K ;
Higaki, K ;
Kimura, T .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1998, 87 (03) :295-299
[5]   Relevance of p-glycoprotein for the enteral absorption of cyclosporin A: In vitro in vivo correlation [J].
Fricker, G ;
Drewe, J ;
Huwyler, J ;
Gutmann, H ;
Beglinger, C .
BRITISH JOURNAL OF PHARMACOLOGY, 1996, 118 (07) :1841-1847
[6]   The sister of P-glycoprotein represents the canalicular bile salt export pump of mammalian liver [J].
Gerloff, T ;
Stieger, B ;
Hagenbuch, B ;
Madon, J ;
Landmann, L ;
Roth, J ;
Hofmann, AF ;
Meier, PJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (16) :10046-10050
[7]   BIOCHEMISTRY OF MULTIDRUG-RESISTANCE MEDIATED BY THE MULTIDRUG TRANSPORTER [J].
GOTTESMAN, MM ;
PASTAN, I .
ANNUAL REVIEW OF BIOCHEMISTRY, 1993, 62 :385-427
[8]   VARIOUS METHODS OF ANALYSIS OF MDR-1/P-GLYCOPROTEIN IN HUMAN COLON CANCER CELL-LINES [J].
HERZOG, CE ;
TREPEL, JB ;
MICKLEY, LA ;
BATES, SE ;
FOJO, AT .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1992, 84 (09) :711-716
[9]   TRANSPORT OF BILE-ACIDS IN A HUMAN INTESTINAL EPITHELIAL-CELL LINE, CACO-2 [J].
HIDALGO, IJ ;
BORCHARDT, RT .
BIOCHIMICA ET BIOPHYSICA ACTA, 1990, 1035 (01) :97-103
[10]   Evidence for P-glycoprotein-modulated penetration of morphine-6-glucuronide into brain capillary endothelium [J].
Huwyler, J ;
Drewe, J ;
Klusemann, C ;
Fricker, G .
BRITISH JOURNAL OF PHARMACOLOGY, 1996, 118 (08) :1879-1885