COMPARISON OF ACID INHIBITION BY EITHER ORAL HIGH-DOSE RANITIDINE OR OMEPRAZOLE

被引:71
作者
HURLIMANN, S [1 ]
ABBUHL, B [1 ]
INAUEN, W [1 ]
HALTER, F [1 ]
机构
[1] UNIV HOSP BERN, INSELSPITAL, GASTROINTESTINAL UNIT, CH-3010 BERN, SWITZERLAND
关键词
D O I
10.1111/j.1365-2036.1994.tb00278.x
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background: High-dose once daily oral omeprazole dosing can inhibit acid secretion almost completely but several days elapse before maximum efficacy is established. The acid inhibitory effect obtained with high doses of a histamine H-2-receptor antagonist is built up rapidly but has the tendency to fade-the term 'tolerance' has been applied to characterize this phenomenon. Methods: To obtain more information on the dynamics of acid inhibition during prolonged dosing, we compared the acid suppressory effects of oral high-dose omeprazole with high-dose ranitidine. Twenty-eight healthy volunteers were randomly assigned to a 2-week dosing with omeprazole or ranitidine in a double-blind, double-dummy, parallel-group study design. Omeprazole was given as 1 capsule of 40 mg mane and ranitidine as 2 tabs of 150 mg q.d.s. The median 24-h pH, daytime pH and night-time pH were measured by ambulatory continuous 24-h pH metry on days -8, -6, 1, 2, 7 and 14. Results: High reproducibility was observed for the two baseline acidity measurements. Ranitidine exerted its peak acid suppressant effect on day 1 of dosing; the degree of acid inhibition faded from day 2 to 7, with no significant change thereafter. The decline in antisecretory activity was more pronounced during the day than the night. In contrast, acid inhibition by omeprazole increased throughout the first week, and antisecretory activity was stable thereafter. Despite the considerable differences in median intragastric pH values at the end of the 14-day study, plasma gastrin levels were elevated to a similar degree with both medications. Conclusions: This study confirms the 'tolerance' phenomenon previously observed with high-dose histamine H-2-receptor antagonist dosing. The dynamics with which it occurs exclude a typical exaggerated first-dose response. Prolonged high-dose histamine H-2-receptor dosing compromises the feedback mechanism regulating gastrin release, whilst this is maintained during dosing with omeprazole.
引用
收藏
页码:193 / 201
页数:9
相关论文
共 49 条
[1]   ADAPTATION AND RENEWAL OF THE ENDOCRINE STOMACH [J].
ARNOLD, R ;
FRANK, M ;
SIMON, B ;
EISSELE, R ;
KOOP, H .
SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY, 1992, 27 :20-27
[2]   ROLE OF GASTRIC-ACID SUPPRESSION IN THE TREATMENT OF GASTROESOPHAGEAL REFLUX DISEASE [J].
BELL, NJV ;
HUNT, RH .
GUT, 1992, 33 (01) :118-124
[3]  
Bertaccini G, 1988, S Afr Med J, V74 Suppl, P3
[4]   REGULATION OF RECEPTORS ON PARIETAL-CELLS ON ACID-SECRETION [J].
BERTACCINI, G ;
CORUZZI, G .
SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY, 1988, 23 :22-33
[5]   RECIPROCAL REGULATION OF ANTRAL GASTRIN AND SOMATOSTATIN GENE-EXPRESSION BY OMEPRAZOLE-INDUCED ACHLORHYDRIA [J].
BRAND, SJ ;
STONE, D .
JOURNAL OF CLINICAL INVESTIGATION, 1988, 82 (03) :1059-1066
[6]   IS THERE AN OPTIMAL DEGREE OF ACID SUPPRESSION FOR HEALING OF DUODENAL-ULCERS - A MODEL OF THE RELATIONSHIP BETWEEN ULCER HEALING AND ACID SUPPRESSION [J].
BURGET, DW ;
CHIVERTON, SG ;
HUNT, RH .
GASTROENTEROLOGY, 1990, 99 (02) :345-351
[7]   COMPARISON OF ONCE-DAILY INTRAVENOUS AND ORAL OMEPRAZOLE ON PENTAGASTRIN-STIMULATED ACID-SECRETION IN DUODENAL-ULCER PATIENTS [J].
CEDERBERG, C ;
LIND, T ;
ROHSS, K ;
OLBE, L .
DIGESTION, 1992, 53 (3-4) :171-178
[8]   EFFECT OF INTRAVENOUS AND ORAL OMEPRAZOLE ON 24-HOUR INTRAGASTRIC ACIDITY IN DUODENAL-ULCER PATIENTS [J].
CEDERBERG, C ;
THOMSON, ABR ;
MAHACHAI, V ;
WESTIN, JA ;
KIRDEIKIS, P ;
FISHER, D ;
ZUK, L ;
MARRIAGE, B .
GASTROENTEROLOGY, 1992, 103 (03) :913-918
[9]   EFFECT OF ONCE DAILY INTRAVENOUS AND ORAL OMEPRAZOLE ON 24-HOUR INTRAGASTRIC ACIDITY IN HEALTHY-SUBJECTS [J].
CEDERBERG, C ;
ROHSS, K ;
LUNDBORG, P ;
OLBE, L .
SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY, 1993, 28 (02) :179-184
[10]   EFFECT OF GASTRIN RECEPTOR BLOCKADE ON ENDOCRINE-CELLS IN RATS DURING ACHLORHYDRIA [J].
EISSELE, R ;
PATBERG, H ;
KOOP, H ;
KRACK, W ;
LORENZ, W ;
MCKNIGHT, AT ;
ARNOLD, R .
GASTROENTEROLOGY, 1992, 103 (05) :1596-1601