FxRIamide regulates the oscillatory activity in the olfactory center of the terrestrial slug Limax.

The terrestrial slug Limax acquires odor-aversion memory. The procerebrum is the secondary olfactory center in the brain of Limax, and functions as the locus of the memory formation and storage. The change in the local field potential oscillation in the procerebrum reflects the information processing of the learned odor. However, it is not fully understood what factors, intrinsic or extrinsic in the procerebrum, alter the oscillatory activity and how it is regulated. In the present study, we found that FxRIamide (Phe-x-Arg-Ile-NH2), which was previously identified as a myomodulatory peptide in the gastropod Fusinus ferrugineus, downregulates the oscillatory frequency of the local field potential oscillation in the procerebrum of Limax. FxRIamide peptides were encoded by two distinct transcripts, which exhibit partially overlapping expression patterns in the brain. Immunohistochemical staining revealed a scattered distribution of FxRIamide-expressing neurons in the cell mass layer of the procerebrum, in addition to the ramified innervation of FxRIamidergic neurons in the neuropile layers. Down-regulation of the oscillatory frequency of the local field potential was explained by the inhibitory effects of FxRIamide on the bursting neurons, which are the kernels of the local field potential oscillation in the procerebrum. Our study revealed the previously unidentified role of FxRIamide peptides in the network of interneurons of Limax, and these peptides may play a role in the mnemonic functions of the procerebrum.

RFamidergic neurons in the olfactory centers of the terrestrial slug Limax.

BACKGROUND: The terrestrial slug Limax has long been used as a model for the study of olfactory information processing and odor learning. Olfactory inputs from the olfactory epithelium are processed in the tentacular ganglion and then in the procerebrum. Glutamate and acetylcholine are the major neurotransmitters used in the procerebrum. Phe-Met-Arg-Phe-NH2 (FMRFamide) has been shown to be involved in the regulation of the network activity of the procerebrum. Although there are thought to be various RFamide family peptides other than FMRFamide that are potentially recognized by anti-FMRFamide antibody in the central nervous system of mollusks, identifying the entire repertoire of RFamide peptides in Limax has yet to be achieved. METHODS: In the present study, we made a comprehensive search for RFamide peptide-encoding genes from the transcriptome data of Limax, and identified 12 genes. The expression maps of these RFamide genes were constructed by in situ hybridization in the cerebral ganglia including the procerebrum, and in the superior/inferior tentacles. RESULTS: Ten of 12 genes were expressed in the procerebrum, and nine of 12 genes were expressed in the tentacular ganglia. Gly-Ser-Leu-Phe-Arg-Phe-NH2 (GSLFRFamide), which is encoded by two different genes, LFRFamide1 (Leu-Phe-Arg-Phe-NH2-1) and LFRFamide2 (Leu-Phe-Arg-Phe-NH2-2), decreased the oscillatory frequency of the local field potential oscillation in the procerebrum when exogenously applied in vitro. We also found by immunohistochemistry that the neurons expressing pedal peptide send efferent projections from the procerebrum back to the tentacular ganglion. CONCLUSION: Our findings suggest the involvement of a far wider variety of RFamide family peptides in the olfactory information processing in Limax than previously thought.