Bridging the interval: Theory and neurobiology of trace conditioning
Open accessAbstract
An early finding in the behavioral analysis of learning was that conditioned responding weakens as the conditioned stimulus (CS) and unconditioned stimulus (US) are separated in time. This "trace" conditioning effect has been the focus of years of research in associative learning. Theoretical accounts of trace conditioning have focused on mechanisms that allow associative learning to occur across long intervals between the CS and US. These accounts have emphasized degraded contingency effects, timing mechanisms, and inhibitory learning. More recently, study of the neurobiology of trace conditioning has shown that even a short interval between the CS and US alters the circuitry recruited for learning. Here, we review some of the theoretical and neurobiological mechanisms underlying trace conditioning with an emphasis on recent studies of trace fear conditioning. Findings across many studies have implications not just for how we think about time and conditioning, but also for how we conceptualize fear conditioning in general, suggesting that circuitry beyond the usual suspects needs to be incorporated into current thinking about fear, learning, and anxiety.
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Hippocampal damage impairs trace conditioning in humans, rabbits and rats.
“For example, hippocampal damage impairs trace conditioning in humans, rabbits and rats (Bangasser et al. 2006; Raybuck and Lattal 2014; McEchron et al. 1998; Moyer et al. 2015).”
From Unlimited Associative Learning and the origins of consciousness: a primer and some predictions (2020) · cites this paper as Raybuck and Lattal 2014
The Hippocampus section reports that hippocampal lesions disrupt trace fear learning, and the References identify lesion studies in rats and trace eyeblink conditioning in rabbits. The passages about humans discuss similar mechanisms and brain activity, but do not report that hippocampal damage impairs trace conditioning in humans. (LLM, conf=0.87)
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References 136 · Cited by 114
- Authors
- Raybuck, J. D., & Lattal, K. M.
- Affiliations
- Oregon Health & Science University (US)
- Corresponding author
- Raybuck, Jonathan D.
- Lattal, K. Matthew
- Venue
- Behavioural Processes
- Publisher
- Elsevier BV
- Published
- 2014-01
- Volume
- 101
- Pages
- 103-111
- ISSN
- 0376-6357 (ISSN-L)
- PMC
- PMC3943893
- OpenAlex
- W2099621229
- Cited by
- 114
- References
- 136
- Citations by year
- 2026: 8 · 2025: 12 · 2024: 14 · 2023: 11 · 2022: 4 · 2021: 10 · 2020: 9 · 2019: 9 · 2018: 8 · 2017: 9 · 2016: 6 · 2015: 5 · 2014: 9
- FWCI
- 0.57
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Behavioural Processes (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institute of Mental Health (MH077111, R01MH077111)
- National Institute on Drug Abuse (DA018165, F32DA031537, R01DA025922, T32DA007262, DA 025922, DA031537, P50DA018165, DA007262)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
- Keywords
- trace conditioning, trace fear conditioning, associative learning, neuroscience of learning, inhibitory learning, timing mechanism, fear conditioning, anxiety, neural circuits
- MeSH terms
- Animals, Association Learning, Brain, Conditioning, Classical, Fear, Psychological Theory
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