This dual output nature of aNPY actions represents an intriguing example of feedforward signaling. As elements of neural circuit design, feedforward pathways are instances Capmatinib in vivo in

which the inputs and outputs of Neuron X are themselves directly connected. Feedforward pathways are termed coherent when both the indirect pathway to the output (via Neuron X) and the direct pathway (by-passing Neuron X) share the same sign. Coherent feedforward pathways may provide coordination among circuit elements that have divergent inputs and common outputs (Jarrell et al., 2012). Modeling studies suggest that in transcriptional networks, they can provide subtle temporal learn more variation in the control of target genes (Mangan and Alon, 2003). Additional studies of the Aplysia feeding CPGs support the hypothesis that neuropeptide modulation of behavior features extensive feedforward mechanisms ( Jing et al., 2010; Wu et al., 2010). A novel neuropeptide (called ATRP) provides a striking

additional example of a feedforward mechanism being used for compensation ( Jing et al., 2010). ATRP acts centrally on the feeding CPG to accelerate the ingestion program, and does so by reducing the protraction phase. This action could conceivably compromise the ingestion program, because reducing the protraction phase would shorten the time available for protractor muscle contractions (and thus weaken them). However, there is feedforward aspect to ATRP actions: the same ATRP peptide is released directly onto the muscle by its motorneuron to act peripherally, and this second (local) action increases the

rate of muscle contraction ( Figure 1B). Thus, peptide modulation of behavior Tolmetin coordinates action at several synaptic levels, and is well-described by a feedforward design in the neuropeptide modulation of neuronal circuitry. The best characterized example of neuropeptide-modulated behavior in C. elegans nematode worms is food-related aggregation (or clumping). Some wild-type strains (including the commonly used N2 strain) forage on a lawn of bacteria in solitary fashion, whereas others aggregate into clumps of worms; this aggregation is termed “social” ( de Bono and Bargmann, 1998). The genetic basis for this naturally occurring behavioral polymorphism has been identified as a single amino acid polymorphism in the npr-1 gene, which encodes a member of the neuropeptide Y receptor (NPYR family) ( de Bono and Bargmann, 1998). Worm strains bearing null mutant alleles of npr-1 are social, as are those bearing the partial loss-of-function allele encoding the 215Phe isoform (found in all the social strains), whereas strains bearing the allele encoding the 215Val isoform (including N2) are solitary ( de Bono and Bargmann, 1998).