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Histamine2 (H2)-Receptor Antagonists in the Treatment of Urticaria

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Summary

Urticaria may develop in response to a number of stimuli such as allergic reactions, drugs, cold, pressure, stings and, most interestingly, neuropsychological upheavals. Classical treatment has utilised H1-receptor antagonists, in view of the fact that histamine released from local mast cells acts on H1-receptors on the vasculature and participates in the pathophysiology of this syndrome. More recently, H2-receptor antagonists have also been tried, alone or in combination, with encouraging results. The question still remains why H2-receptor antagonists should have any beneficial effect since H2-receptors are mostly present on exocrine cells and on T-suppressor lymphocytes, where they are stimulatory, or mast cells, where they are auto-inhibitory. Possible explanations may include the ratio of H1- to H2-receptors on local vasculature and the effect of H2-antagonists on responses elicited through nervous system activity via cholinergic or neuropeptidergic neurons. Finally, evidence is presented that certain tricyclic H-receptor antagonists may have powerful inhibitory effects on secretion from both peripheral and central nervous system mast cells, as well as from neurons. The possible role of H3-receptors in this process is also discussed.

At present, the available evidence does not justify the routine use of H2-antagonists in the treatment of urticaria.

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    Theoharis C. Theoharides (Director of Medical Pharmacology)

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Theoharides, T.C. Histamine2 (H2)-Receptor Antagonists in the Treatment of Urticaria. Drugs 37, 345–355 (1989). https://doi.org/10.2165/00003495-198937030-00004

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