Inhibitory action of YJA2-379, a new proton pump inhibitor of Helicobacter pylori growth and urease

被引:8
作者
Woo, TW [1 ]
Chang, MS [1 ]
Chung, YK [1 ]
Kim, KB [1 ]
Sohn, SK [1 ]
Kim, SG [1 ]
Choi, WS [1 ]
机构
[1] Yung Jin Pharmaceut Co Ltd, Ctr Res & Dev, Pharmacol & Toxicol Lab, Hwasung Kun 445850, Kyunggi Do, South Korea
关键词
YJA20379; omeprazole; Helicobacter pylori; agar dilution method; urease;
D O I
10.1007/BF03216745
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The activities of two types of antiulcer agents against 9 strains of Helicobacter pylori (H. pylori) were determined by the agar dilution method. The antiulcer agents were YJA20379, a newly synthesized proton pump inhibitor developed by Yung-Jin Pharmaceutical company, and omeprazole. Both compounds were found to have significant activities against this organism. The MIC values of YJA20379 and omeprazole were 11.7 and 31.25 mu g/ml, respectively. In addition, the inhibitory potency of bath compounds was investigated on H. pylori urease which is believed to be an important colonization and virulence factor in the pathogenesis of gastritis and peptic ulcers. These compounds dose-dependently inhibited urease extracted with distilled water and their IC50 values were 16.4 x 10(-5) M and 14.3 x 10(-5) M, respectively. In addition, a pH-dependent study to determine whether inhibitory potency would be activated by acid condition was performed. It was found that unlike omeprazole, YJA20379 was not affected by acid condition. To determine the inhibition pattern and optimal concentration of substrate, kinetics were evaluated at various pH levels (pH 5.0, 7.0, and 8.5). The data show that YJA20379 noncompetitively inhibited H. pylori urease and K-m/K-i values were 0.96 mM/60 mu M (pH 5.0), 0.56 mM/141.5 mu M (pH 7.0), and 1.94 mM/34 mu M (pH 8.5), respectively. Based on data obtained, it is concluded that YJA20379 is a significant inhibitor of H. pylori growth and urease and therefore, taking these results into consideration, YJA20379 might be a beneficial therapy for gastritis and peptic ulcers induced by H. pylori.
引用
收藏
页码:6 / 11
页数:6
相关论文
共 26 条
[1]   RESPONSE OF CAMPYLOBACTER-PYLORIDIS TO ANTIBIOTICS, BISMUTH AND AN ACID-REDUCING AGENT INVITRO - AN ULTRASTRUCTURAL-STUDY [J].
ARMSTRONG, JA ;
WEE, SH ;
GOODWIN, CS ;
WILSON, DH .
JOURNAL OF MEDICAL MICROBIOLOGY, 1987, 24 (04) :343-350
[2]   HELICOBACTER-PYLORI AND THE PATHOGENESIS OF GASTRODUODENAL INFLAMMATION [J].
BLASER, MJ .
JOURNAL OF INFECTIOUS DISEASES, 1990, 161 (04) :626-633
[3]  
EBERHARDT R, 1990, REV INFECT DIS, V12, pS115
[4]  
GIASTI G, 1974, MEHTODS ENZYMATIC AN, V4, P1791
[5]   TRANSFER OF CAMPYLOBACTER-PYLORI AND CAMPYLOBACTER-MUSTELAE TO HELICOBACTER GEN-NOV AS HELICOBACTER-PYLORI COMB-NOV AND HELICOBACTER MUSTELAE COMB-NOV, RESPECTIVELY [J].
GOODWIN, CS ;
ARMSTRONG, JA ;
CHILVERS, T ;
PETERS, M ;
COLLINS, MD ;
SLY, L ;
MCCONNELL, W ;
HARPER, WES .
INTERNATIONAL JOURNAL OF SYSTEMATIC BACTERIOLOGY, 1989, 39 (04) :397-405
[6]   THE MINIMUM INHIBITORY AND BACTERICIDAL CONCENTRATIONS OF ANTIBIOTICS AND ANTIULCER AGENTS AGAINST CAMPYLOBACTER-PYLORIDIS [J].
GOODWIN, CS ;
BLAKE, P ;
BLINCOW, E .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1986, 17 (03) :309-314
[7]   CAMPYLOBACTER-PYLORI AND PEPTIC-ULCER DISEASE [J].
GRAHAM, DY .
GASTROENTEROLOGY, 1989, 96 (02) :615-625
[8]   EFFECT OF TREATMENT ON CAMPYLOBACTER-PYLORI IN PEPTIC DISEASE - A RANDOMIZED PROSPECTIVE TRIAL [J].
HUMPHREYS, H ;
BOURKE, S ;
DOOLEY, C ;
MCKENNA, D ;
POWER, B ;
KEANE, CT ;
SWEENEY, EC ;
OMORAIN, C .
GUT, 1988, 29 (03) :279-283
[9]  
KAWANO S, 1989, Gastroenterology, V96, pA252
[10]   SUSCEPTIBILITY OF CAMPYLOBACTER-PYLORIDIS TO 20 ANTIMICROBIAL AGENTS [J].
LAMBERT, T ;
MEGRAUD, F ;
GERBAUD, G ;
COURVALIN, P .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1986, 30 (03) :510-511