Skip to main content
Log in

Tolerance to oral H2-receptor antagonists

  • Original Articles
  • Published:
Digestive Diseases and Sciences Aims and scope Submit manuscript

Abstract

The acid-inhibitory action of H2-receptor antagonists was shown to decrease after one to two weeks of dosing in healthy volunteers. This tolerance was evaluated in three randomized, placebo-controlled trials with the H2-receptor antagonists famotidine, 40 mg given after the evening meal for 28 days; ranitidine, 300 mg four times a day for seven days followed by 300 mg at night until day 28; and ranitidine, 300 mg three times a day vs 300 mg at night for 14 days. Continuous 24-hr pH monitoring with glass electrodes was performed under fed conditions. The median 24-hr pH decreased from 3.2 on day 1 with famotidine 40 mg to 1.9 on day 28 (P<0.0012). After seven days of dosing with ranitidine 300 mg four times a day the median 24-hr pH dropped from 5.0 on day 1 to 3.0 on day 7 (P<0.001) and then to 2.2 with ranitidine 300 mg at night on day 28. With ranitidine 300 mg three times a day the median 24-hr pH fell from 4.3 on day 1 to 2.4 on day 14 (P< 0.0005). With ranitidine 300 mg at night the respective pH values were 2.5 and 1.8 (P< 0.003). Tolerance to H2-receptor antagonists given in a single evening dose was only evident during the night, whereas tolerance occurred throughout the day and night with the three- and four-times-a-day regimens. A large increase in the interindividual variability of pH response was seen during the nighttime.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Institutional subscriptions

Similar content being viewed by others

References

  1. Sewing KF, Hagie L, Ippoliti AF, Isenberg JI, Samloff IM, Sturdevant RAL: Effect of one month treatment with cimetidine on gastric secretion and serum gastrin and pepsinogen levels. Gastroenterology 74:376–379, 1978

    Google Scholar 

  2. Meyrick Thomas JU, Misiewicz JJ, Cook AR, Hill MJ, Smith PLR, Walters CL, Forster JK, Martin LE, Woodings DF: Effect of one year's treatment with ranitidine and of truncal vagotomy on gastric contents. Gut 28:726–738, 1987

    PubMed  Google Scholar 

  3. Prichard PJ, Jones DB, Yeomans ND, Mihaly GW, Smallwood RA, Louis WJ: The effectiveness of ranitidine in reducing gastric acid-secretion decreases with continued therapy. Br J Clin Pharmacol 22:663–668, 1986

    PubMed  Google Scholar 

  4. Frislid K, Aadland E, Berstad A: Augmented postprandial gastric acid secretion due to exposure to ranitidine in healthy subjects. Scand J Gastroenterol 21:119–122, 1986

    PubMed  Google Scholar 

  5. Jones DB, Howden CW, Burget DW, Silletti C, Hunt RH: Alteration of H2-receptor sensitivity in duodenal ulcer patients after maintenance treatment with an H2-receptor antagonist. Gut 29:890–893, 1988

    PubMed  Google Scholar 

  6. Wilder-Smith CH, Halter F, Ernst T, Gennoni M, Zeyen B, Varga L, Röhmel JJ, Merki HS: Rapid reduction of acid suppression of H2-receptor antagonists. Aliment Pharmacol Ther 1990 (in press)

  7. Jones DB, Howden CW, Burget DW, Kerr GD, Hunt RH: Acid suppression in duodenal ulcer. Gut 28:1120–1128, 1987

    PubMed  Google Scholar 

  8. Holm SA: A simple sequentially rejective multiple test procedure. Scand J Stat 6:65–70, 1979

    Google Scholar 

  9. Johnson NJ, Boyd EJS, Mills JG, Wood JR: Acute treatment of reflux oesophagitis: A multicentre trial to compare 150 mg ranitidine bd with 300 mg ranitidine qds. Aliment Pharmacol Ther 3:259–267, 1989

    PubMed  Google Scholar 

  10. Merki HS, Halter F, Wilder-Smith CH, Allemann P, Witzel L, Kempf M, Roehmel JJ, Walt RP: The effect of food on H2-receptor blockade in normal subjects and duodenal ulcer patients. Gut 31:148–150, 1990

    PubMed  Google Scholar 

  11. Gespach C, Emami S: Histamine H2-receptors and gastric cells.In Frontiers in Histamine Research. CR Ganellin, JC Schwartz (eds). Oxford, Pergamon Press, 1985, pp 265–274

    Google Scholar 

  12. Aadland E, Berstad A, Semb LS: Effect of cimetidine on pentagastrin-stimulated gastric secretion in healthy man. Scand J Gastroenterol 12:501–506, 1977

    PubMed  Google Scholar 

  13. Konturek SJ, Obtulowicz W, Kwiecien N, Kopp B, Oleksy J: Dynamics of gastric acid inhibition by ranitidine in duodenal ulcer patients. Digestion 22:119–125, 1988

    Google Scholar 

  14. Barbezat GO, Bank S: Effect of prolonged cimetidine therapy on gastric acid secretion. Gut 19:151–154, 1987

    Google Scholar 

  15. Aadland E, Berstad A: Effect of cimetidine on pentagastrin-stimulated gastric acidity and pepsin secretion before and after 6 weeks of cimetidine treatment. Scand J Gastroenterol 13:193–197, 1978

    PubMed  Google Scholar 

  16. Mihaly GW, Jones DB, Anderson JA, Smallwood RA, Louis WJ: Pharmacokinetic studies of cimetidine and ranitidine before and after treatment in peptic ulcer patients. Br J Clin Pharmacol 17:109–111, 1984

    PubMed  Google Scholar 

  17. Lanzon-Miller S, Pounder RE, Hamilton MR, Chronos NAF, Ball S, Mercieca JE, Olausson M, Cederberg C: Twenty-four hour intragastric acidity and plasma gastrin concentration in healthy subjects and patients with duodenal or gastric ulcer, or pernicious anaemia. Aliment Pharmacol Ther 1:225–237, 1987

    PubMed  Google Scholar 

  18. Lind T, Cederberg C, Forssell H, Olausson M, Olbe L: Relationship between reduction of gastric acid secretion and plasma gastrin concentration during omeprazole treatment. Scand J Gastroenterol 23:1259–1266, 1988

    PubMed  Google Scholar 

  19. Lanzon-Miller S, Pounder RE, Hamilton MR, Ball S, Chronos NAF, Raymond F, Olausson M, Cederberg C: Twenty-four hour intragastric acidity and plasma gastrin concentration before and during treatment with either ranitidine or omeprazole. Aliment Pharmacol Ther 1:239–251, 1987

    PubMed  Google Scholar 

  20. McGuigan J: Inhibition of Hydrogen-Potassium-stimulated adenosine triphosphatase: effects on acid secretion, plasma gastrin and the gastric mucosa. Gastroenterology 97:1045–1048, 1989

    PubMed  Google Scholar 

  21. Stockbrugger R, Larsson LI, Lundqvist G, Angervall L: Antral gastrin cells and serum gastrin in achlorhydria. Scand J Gastroenterol 12:209–213, 1977

    PubMed  Google Scholar 

  22. Koop H, Willemer S, Steinbach F, Eissele R, Tuch K, Arnold R: Influence of chronic drug-induced achlorhydria by substituted benzimidazoles on the endocrine stomach of rats. Gastroenterology 92:406–413, 1987

    PubMed  Google Scholar 

  23. Arnold R, Hillse MV, Neuhof CH, Schwarting H, Becker HD, Creutzfeld EW: Antral gastrin-producing G-cells and somatostatin-producing D-cells in different states of gastric acid secretion. Gut 23:285–291, 1982

    PubMed  Google Scholar 

  24. Bertaccini G, Coruzzi G: Regulation of receptors on parietal cells on acid secretion. Scand J Gastroenterol 23(suppl 146):22–33, 1988

    Google Scholar 

  25. Johnson LR: Regulation of gastrointestinal growth. World J Surg 3:477–487, 1979

    PubMed  Google Scholar 

  26. Bertaccini G: Receptors involved in the regulation of gastric acid secretion. S Afr Med J 74:3–14, 1988

    Google Scholar 

  27. Burget DW, Chiverton SG, Hunt RH: Is there an optimal degree of acid suppression for healing duodenal ulcer? Gut (in press)

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Wilder-Smith, C.H., Ernst, T., Gennoni, M. et al. Tolerance to oral H2-receptor antagonists. Digest Dis Sci 35, 976–983 (1990). https://doi.org/10.1007/BF01537246

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF01537246

Key words

Navigation