Abstract

Trace conditioning is a form of associative learning that can be induced by presenting a conditioned stimulus (CS) and an unconditioned stimulus (US) following each other, but separated by a temporal gap. This gap distinguishes trace conditioning from classical delay conditioning, where the CS and US overlap. To bridge the temporal gap between both stimuli and to form an association between CS and US in trace conditioning, the brain must keep a neural representation of the CS after its termination—a stimulus trace. Behavioral and physiological studies on trace and delay conditioning revealed similarities between the two forms of learning, like similar memory decay and similar odor identity perception in invertebrates. On the other hand differences were reported also, like the requirement of distinct brain structures in vertebrates or disparities in molecular mechanisms in both vertebrates and invertebrates. For example, in commonly used vertebrate conditioning paradigms the hippocampus is necessary for trace but not for delay conditioning, and Drosophila delay conditioning requires the Rutabaga adenylyl cyclase (Rut-AC), which is dispensable in trace conditioning. It is still unknown how the brain encodes CS traces and how they are associated with a US in trace conditioning. Insects serve as powerful models to address the mechanisms underlying trace conditioning, due to their simple brain anatomy, behavioral accessibility and established methods of genetic interference. In this review we summarize the recent progress in insect trace conditioning on the behavioral and physiological level and emphasize similarities and differences compared to delay conditioning. Moreover, we examine proposed molecular and computational models and reassess different experimental approaches used for trace conditioning.

Highlights

  • Actions may have delayed, rather than immediate consequences

  • In commonly used vertebrate conditioning paradigms the hippocampus is necessary for trace but not for delay conditioning, and Drosophila delay conditioning requires the Rutabaga adenylyl cyclase (Rut-AC), which is dispensable in trace conditioning

  • We noted some differences in the features of trace conditioning between different studies

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Summary

INTRODUCTION

Rather than immediate consequences. If you have ever woken up with a terrible headache the morning after drinking too much tequila, you probably had a feeling of nausea the time you encountered the taste and smell of tequila and may have refrained from drinking it. The model by Yarali et al (2012) refers to aversive olfactory learning in Drosophila melanogaster and is based on the mechanism of coincidence detection by an adenylyl cyclase (AC) It suggests that slowly decaying Ca2+ transient in the presynaptic neuron, elicited by the CS, could function as a stimulus trace. When the odor-induced Ca2+ influx shortly preceded the US-induced G protein activation (Gα∗) as in delay conditioning, the formation of the AC∗/Gα∗ complex was transiently accelerated This led to increased cAMP production resulting in potentiation of synaptic output in these particular KCs. In trace conditioning where the CS is already gone upon US arrival, the coincidence could be achieved by residual Ca2+ transient in the cell. It is evident that the suitability of the US for conditioning paradigms depends on the responsiveness of the animal (Pavlov, 1927)

CONCLUSIONS
Erlernen einer Farbe an einer künstlichen Futterstelle durch
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