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      Single amino acids in sucrose rewards modulate feeding and associative learning in the honeybee

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          Abstract

          Highlights

          • The mouthparts are more sensitive to amino acids in sucrose solution than the antennae.

          • Pre-feeding with sucrose solutions containing single amino acids reduces learning performance and feeding.

          • Iso-leucine was rewarding in sucrose solution whereas methionine was aversive.

          • Nutritional state modulated how bees responded to solutions containing proline or phenylalanine.

          Abstract

          Obtaining the correct balance of nutrients requires that the brain integrates information about the body’s nutritional state with sensory information from food to guide feeding behaviour. Learning is a mechanism that allows animals to identify cues associated with nutrients so that they can be located quickly when required. Feedback about nutritional state is essential for nutrient balancing and could influence learning. How specific this feedback is to individual nutrients has not often been examined. Here, we tested how the honeybee’s nutritional state influenced the likelihood it would feed on and learn sucrose solutions containing single amino acids. Nutritional state was manipulated by pre-feeding bees with either 1 M sucrose or 1 M sucrose containing 100 mM of isoleucine, proline, phenylalanine, or methionine 24 h prior to olfactory conditioning of the proboscis extension response. We found that bees pre-fed sucrose solution consumed less of solutions containing amino acids and were also less likely to learn to associate amino acid solutions with odours. Unexpectedly, bees pre-fed solutions containing an amino acid were also less likely to learn to associate odours with sucrose the next day. Furthermore, they consumed more of and were more likely to learn when rewarded with an amino acid solution if they were pre-fed isoleucine and proline. Our data indicate that single amino acids at relatively high concentrations inhibit feeding on sucrose solutions containing them, and they can act as appetitive reinforcers during learning. Our data also suggest that select amino acids interact with mechanisms that signal nutritional sufficiency to reduce hunger. Based on these experiments, we predict that nutrient balancing for essential amino acids during learning requires integration of information about several amino acids experienced simultaneously.

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          Most cited references55

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          Pathogenic bacteria induce aversive olfactory learning in Caenorhabditis elegans.

          Food can be hazardous, either through toxicity or through bacterial infections that follow the ingestion of a tainted food source. Because learning about food quality enhances survival, one of the most robust forms of olfactory learning is conditioned avoidance of tastes associated with visceral malaise. The nematode Caenorhabditis elegans feeds on bacteria but is susceptible to infection by pathogenic bacteria in its natural environment. Here we show that C. elegans modifies its olfactory preferences after exposure to pathogenic bacteria, avoiding odours from the pathogen and increasing its attraction to odours from familiar nonpathogenic bacteria. Particular bacteria elicit specific changes in olfactory preferences that are suggestive of associative learning. Exposure to pathogenic bacteria increases serotonin in ADF chemosensory neurons by transcriptional and post-transcriptional mechanisms. Serotonin functions through MOD-1, a serotonin-gated chloride channel expressed in sensory interneurons, to promote aversive learning. An increase in serotonin may represent the negative reinforcing stimulus in pathogenic infection.
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            A chemosensory gene family encoding candidate gustatory and olfactory receptors in Drosophila.

            A novel family of candidate gustatory receptors (GRs) was recently identified in searches of the Drosophila genome. We have performed in situ hybridization and transgene experiments that reveal expression of these genes in both gustatory and olfactory neurons in adult flies and larvae. This gene family is likely to encode both odorant and taste receptors. We have visualized the projections of chemosensory neurons in the larval brain and observe that neurons expressing different GRs project to discrete loci in the antennal lobe and subesophageal ganglion. These data provide insight into the diversity of chemosensory recognition and an initial view of the representation of gustatory information in the fly brain.
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              A neural circuit mechanism integrating motivational state with memory expression in Drosophila.

              Behavioral expression of food-associated memory in fruit flies is constrained by satiety and promoted by hunger, suggesting an influence of motivational state. Here, we identify a neural mechanism that integrates the internal state of hunger and appetitive memory. We show that stimulation of neurons that express neuropeptide F (dNPF), an ortholog of mammalian NPY, mimics food deprivation and promotes memory performance in satiated flies. Robust appetitive memory performance requires the dNPF receptor in six dopaminergic neurons that innervate a distinct region of the mushroom bodies. Blocking these dopaminergic neurons releases memory performance in satiated flies, whereas stimulation suppresses memory performance in hungry flies. Therefore, dNPF and dopamine provide a motivational switch in the mushroom body that controls the output of appetitive memory.
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                Author and article information

                Contributors
                Journal
                J Insect Physiol
                J. Insect Physiol
                Journal of Insect Physiology
                Elsevier
                0022-1910
                1879-1611
                1 October 2014
                October 2014
                : 69
                : 41-48
                Affiliations
                Institute of Neuroscience, Newcastle University, Newcastle upon Tyne NE1 7RU, United Kingdom
                Author notes
                [* ]Corresponding author. Tel.: +44 0191 208 6667. jeri.wright@ 123456ncl.ac.uk
                Article
                S0022-1910(14)00079-1
                10.1016/j.jinsphys.2014.05.004
                4194351
                24819203
                30b97c6e-0c88-440e-9082-dd6dd6c3a75e
                © 2014 The Authors
                History
                Categories
                Article

                Animal science & Zoology
                honeybee,amino acids,olfactory learning,nutrient balancing,gustation
                Animal science & Zoology
                honeybee, amino acids, olfactory learning, nutrient balancing, gustation

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