The physiological effects of selected classical transmitters and FMRFamide-related peptides (FaRPs) on dispersed muscle
fibres from the marine turbellarian, Procerodes littoralis have been examined. Confocal scanning laser microscopy coupled
with fluorescein isothiocyanate (FITC) or tetramethylrhodamine (TRITC)-labelled phalloidin revealed a highly developed
body wall muscle system with circular, longitudinal and diagonal layers of muscle fibres. Dispersed muscle fibres
contracted when depolarized by exposure to extracellular media with elevated K+ (15–100 mM) in a
concentration-dependent manner, with a maximal response of 87% achieved at [ges ] 75 mM. 5-Hydroxytryptamine (5-HT) induced
concentration-dependent muscle contraction between 0·01 and 1000 μM, with 10 μM producing a near maximal contraction
response of 75%. Acetylcholine (ACh) had less pronounced excitatory effects (0·01–1000 μM), inducing contraction of
only 32% of the fibres at 100 μM. The flatworm FMRFamide-related peptides (FaRPs), GYIRFamide, YIRFamide and
GNFFRFamide each had concentration-dependent myocontractile effects, indicating the occurrence of at least 1 FaRP
receptor on P. littoralis muscle fibres. At 10 μM peptide, GNFFRFamide induced contractions in < 40% of the muscle
fibres examined, whereas YIRFamide and GYIRFamide induced contraction in 70 and 75%of muscle fibres, respectively.
The order of potency of the peptides was: GYIRFamide > YIRFamide > GNFFRFamide. Pre-incubation of the muscle
fibres in 5 μM 5-HT significantly reduced the responses to GYIRFamide, YIRFamide and 5-HT, while the responses to
high K+ remained unaltered. Muscle fibres pre-incubated in GYIRFamide (0·1 μM) were also less responsive to 5-HT but
not to ACh and high-K+. The GYIRFamide analogue, GYIRdFamide, did not induce muscle contraction (0·01–100 μM)
per se, but when co-applied with the myoactive peptides GYIRFamide, YIRFamide or GNFFRFamide, it significantly
blocked their ability to elicit contractions. This suggests that the peptides tested may act via a common muscle-based
neuropeptide receptor. GYIRdFamide did not alter the contractile effects of high K+, 5-HT or ACh. Collectively, these
results indicate that FaRPs, 5-HT and ACh all have the potential to cause muscle contraction in flatworms and that
5-HT and FaRPs alter muscle sensitivity to each other, but do not influence the ability of flatworm muscle fibres to
contract.