H2-receptor antagonists are scavengers of oxygen radicals

Eur J Clin Invest. 1994 Jul;24(7):476-81. doi: 10.1111/j.1365-2362.1994.tb02378.x.


Potential oxygen radical scavenging properties of the H2-receptor antagonists cimetidine, ranitidine and famotidine were investigated. These drugs, although ineffective against superoxide anion and hydrogen peroxide, can scavenge hydroxyl radical (OH.) with a very high rate constant, which is about tenfold higher than that of the specific scavenger mannitol for famotidine (1.7 x 10(10) mol-1 s-1) and cimetidine (1.6 x 10(10) mol-1 s-1), ranitidine displaying a rate constant of 7.5 x 10(9) mol-1 s-1. These OH. savenging effects are significant beginning from 10, 28 and 100 mumol l-1 concentration for famotidine, cimetidine and ranitidine, respectively, thus suggesting that the drugs may effectively act as OH. scavengers in vivo especially in the gastric lumen. Only cimetidine can apparently bind and inactivate iron, which further emphasizes its antioxidant capacity. Moreover, all drugs, even at 10 mumol l-1 concentration, show powerful scavenging effects on hypochlorous acid and monochloramine, which are cytotoxic oxidants arising from inflammatory cells, such as neutrophils. These data suggest that some therapeutical effects of H2-receptor antagonists in peptic ulcer may also be related to their antiradical-antioxidant capacity, and that these drugs could potentially be used in other disease entities characterized by free radical-mediated oxidative stress in vivo.

MeSH terms

  • Chloramines / metabolism*
  • Cimetidine / metabolism*
  • Famotidine / metabolism*
  • Free Radical Scavengers / metabolism*
  • Hydroxyl Radical / metabolism*
  • Hypochlorous Acid / metabolism*
  • Oxidative Stress / drug effects
  • Ranitidine / metabolism*


  • Chloramines
  • Free Radical Scavengers
  • Hydroxyl Radical
  • Famotidine
  • Hypochlorous Acid
  • Cimetidine
  • Ranitidine
  • chloramine