The contractile effect of histamine, as well as the H1 receptor popula
tion and H2 receptor-mediated cAMP production, were measured in cardia
c tissue from control normal and autoimmune myocarditis mice. Histamin
e triggered positive chronotropy and negative inotropy at high concent
rations in both control and autoimmune auricles, H2 receptors being th
e most important mediator of these responses. In contrast, in atria fr
om autoimmune myocarditis mice, histamine at lower concentrations caus
ed positive inotropy and negative chronotropy. These effects, not veri
fied in the normal control atria, are mediated by H1 receptors. The ex
pression of H2 and H1 receptors mediating the cardiac response to hist
amine was evaluated through histamine-stimulated cAMP level and bindin
g of [H-3] mephyramine, respectively. Both control and autoimmune myoc
ardium were able to increase cAMP levels, an effect that was inhibited
by H2 antagonist drug. The amount of cAMP was significantly higher in
control myocardium than in those from autoimmune ones. Saturable bind
ing of [H-3] mephyramine occurs in autoimmune myocardium, with distinc
t high and low affinity binding sites. In control myocardium non-satur
able binding was detected. These results suggest that H1 and H2 recept
ors coexist in heart from autoimmune myocarditis mice, whereas only H2
receptors are present in myocardium from control mice. The presence o
f H1 receptors in autoimmune myocardium could be an important factor i
n the regulation of its physiological behaviour.