INTERACTION OF THE ANTIINFLAMMATORY SELENOORGANIC COMPOUND EBSELEN WITH ACID-SECRETION IN ISOLATED PARIETAL-CELLS AND GASTRIC H+/K+-ATPASE

被引:27
作者
BEIL, W
STAAR, U
SEWING, KF
机构
[1] Abteilung Allgemeine Pharmakologie, Medizinische Hochschule, Hannover
关键词
D O I
10.1016/0006-2952(90)90229-E
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The effects of the anti-inflammatory seleno-organic compound ebselen on gastric H+/K+-ATPase, H+/K+-ATPase-mediated proton transport and on parietal cell HCl production was studied. Ebselen inhibited K+-stimulated ATPase activity in leaky gastric membranes (ic50:0.15 μM) and H+/ K+-ATPase-mediated proton transport in intact gastric membrane vesicles (ic50:0.7μM). Histamine- and dibutyryl-cAMP-stimulated HCl production in isolated and enriched guinea-pig parietal cells was inhibited with an ic50 value of 12 μM. The mercaptan dithioerythritol and the nucleotide ATP prevents the H+/K+-ATPase against inactivation and dithioerythritol was found to restore already inhibited enzyme activity and ATPase mediated H+ transport. Furthermore, dithioerythritol could prevent ebselen-induced inhibition of HCl production in the parietal cell preparation. It is concluded that ebselen inhibits acid secretion in the parietal cell by interference with SH groups of the gastric proton pump, the H+/K+-ATPase. Therefore ebselen can be regarded as an anti-inflammatory drug for which in vitro anti-secretory properties can be demonstrated. © 1990.
引用
收藏
页码:1997 / 2003
页数:7
相关论文
共 20 条
[11]   A NOVEL BIOLOGICALLY-ACTIVE ORGANOSELENIUM COMPOUND .3. EFFECTS OF PZ-51 (EBSELEN) ON GLUTATHIONE-PEROXIDASE AND SECRETORY ACTIVITIES OF MOUSE MACROPHAGES [J].
PARNHAM, MJ ;
KINDT, S .
BIOCHEMICAL PHARMACOLOGY, 1984, 33 (20) :3247-3250
[12]   SELENOORGANIC COMPOUNDS AND THE THERAPY OF HYDROPEROXIDE-LINKED PATHOLOGICAL CONDITIONS [J].
PARNHAM, MJ ;
GRAF, E .
BIOCHEMICAL PHARMACOLOGY, 1987, 36 (19) :3095-3102
[13]  
SACHS G, 1976, J BIOL CHEM, V251, P7690
[14]   A NOVEL BIOLOGICALLY-ACTIVE SELENO-ORGANIC COMPOUND .5. INHIBITION BY EBSELEN (PZ-51) OF RAT PERITONEAL NEUTROPHIL LIPOXYGENASE [J].
SAFAYHI, H ;
TIEGS, G ;
WENDEL, A .
BIOCHEMICAL PHARMACOLOGY, 1985, 34 (15) :2691-2694
[15]   STUDIES ON (K+ + H+)-ATPASE .2. ROLE OF SULFHYDRYL-GROUPS IN ITS REACTION-MECHANISM [J].
SCHRIJEN, JJ ;
VANGRONINGENLUYBEN, WAHM ;
DEPONT, JJHHM ;
BONTING, SL .
BIOCHIMICA ET BIOPHYSICA ACTA, 1981, 640 (02) :473-486
[16]   EFFECT OF SUBSTITUTED BENZIMIDAZOLES ON ACID-SECRETION IN ISOLATED AND ENRICHED GUINEA-PIG PARIETAL-CELLS [J].
SEWING, KF ;
HARMS, P ;
SCHULZ, G ;
HANNEMANN, H .
GUT, 1983, 24 (06) :557-560
[17]  
STEKHOVEN FS, 1981, PHYSIOL REV, V61, P1
[18]   CYTOPROTECTION IN GASTROINTESTINAL PHARMACOLOGY [J].
SZABO, S ;
SZELENYI, I .
TRENDS IN PHARMACOLOGICAL SCIENCES, 1987, 8 (04) :149-154
[19]   A NOVEL BIOLOGICALLY-ACTIVE ORGANOSELENIUM COMPOUND .2. ACTIVITY OF PZ-51 IN RELATION TO GLUTATHIONE-PEROXIDASE [J].
WENDEL, A ;
FAUSEL, M ;
SAFAYHI, H ;
TIEGS, G ;
OTTER, R .
BIOCHEMICAL PHARMACOLOGY, 1984, 33 (20) :3241-3245
[20]   GLUTATHIONE-PEROXIDASE ACTIVITY OF D,L-SELENO-CYSTINE AND SELENOCYSTAMINE [J].
YASUDA, K ;
WATANABE, H ;
YAMAZAKI, S ;
TODA, S .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1980, 96 (01) :243-249