Caffeine, which stimulates intracellular Ca2+ release channels known as ryanodine receptor (RyR) channels, induces
contraction of individual muscle fibres dissociated from the trematode Schistosoma mansoni, and the turbellarians Dugesia
tigrina and Procerodes littoralis. Caffeine is much more potent on S. mansoni fibres (EC50 0·7 mM) than those from D.
tigrina or P. littoralis (3·2 mM and 4·6 mM, respectively). These caffeine-induced contractions are blocked by ryanodine,
confirming the presence of functional RyR channels in these flatworm muscles. However, the contractions are not blocked
by typical RyR channel blockers ruthenium red or neomycin, indicating that there may be important pharmacological
differences between the RyR channels in this early-diverging phylum and those of later animals. These studies demonstrate
that RyR channels are present in the muscle of these flatworms, and that the sarcoplasmic reticulum stores sufficient Ca2+ to support contraction.