Exposing Rats to a Predator Blocks Primed Burst Potentiation in the Hippocampus In Vitro
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This study evaluated the effects of acute psychological stress (cat exposure) in adult male rats on electrophysiological plasticity subsequently assessed in the hippocampus in vitro. Two physiological models of memory were studied in CA1 in each recording session: (1) primed burst potentiation (PBP), a low-threshold form of plasticity produced by a total of five physiologically patterned pulses; and (2) long-term potentiation (LTP), a suprathreshold form of plasticity produced by a train of 100 pulses. Three groups of rats were studied: (1) undisturbed rats in their home cage (home cage); (2) rats placed in a chamber for 75 min (chamber); and (3) rats placed in a chamber for 75 min in close proximity to a cat (chamber/stress). At the end of the chamber exposure period, blood samples were obtained, and the hippocampus was prepared for in vitro recordings. Only the chamber/stress group had elevated (stress) levels of corticosterone. The major finding was that PBP, but not LTP, was blocked in the chamber/stress group. Thus, the psychological stress experienced by the rats in response to cat exposure resulted in an inhibition of plasticity, which was localized to the intrinsic circuitry of the hippocampus. This work provides novel observations on the effects of an ethologically relevant stressor on PBP in vitro and of the relative insensitivity of LTP to being modulated by psychological stress. We discuss the relevance of these electrophysiological findings to our behavioral work showing that predator stress impairs spatial memory.
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Stress or stress-related neuromodulators block LTP produced by relatively weak (primed burst or theta burst) tetanizing stimulation, but stress has no effect on LTP produced by stronger forms of tetanizing stimulation.
“Moreover, in electrophysiological studies, stress or stress-related neuromodulators have been shown to block LTP produced by relatively weak (primed burst or theta burst) tetanizing stimulation, but stress has been shown to have no effect on LTP produced by stronger forms of tetanizing stimulation (Corradetti et al. [283]; Mesches et al. [51]; Diamond et al. [139]; Alfarez et al. [152]; Vouimba et”
From The Temporal Dynamics Model of Emotional Memory Processing: A Synthesis on the Neurobiological Basis of Stress-Induced Amnesia, Flashbulb and Traumatic Memories, and the Yerkes-Dodson Law (2007) · cites this paper as Mesches et al. [51]
The Abstract reports that predator stress in adult male rats blocked primed burst potentiation but not LTP induced by a 100-pulse train; Figures 2–3 report the same comparison. The broader claim that stress has no effect with stronger stimulation is not established: the Discussion notes that other studies found stress effects on LTP, and this study did not test theta-burst stimulation or stress-related neuromodulators. (LLM, conf=0.86)
Experimental — accuracy not yet measuredStress blocked the induction of PB potentiation in vivo and in vitro.
“and blocked the induction of PB potentiation in vivo (Diamond et al. [139]; Vouimba et al. [140]) and in vitro (Mesches et al. [51]).”
From The Temporal Dynamics Model of Emotional Memory Processing: A Synthesis on the Neurobiological Basis of Stress-Induced Amnesia, Flashbulb and Traumatic Memories, and the Yerkes-Dodson Law (2007) · cites this paper as Mesches et al. [51]
Animal studies show that stress exposure can suppress synaptic and structural plasticity underlying information storage in the hippocampus.
“animal studies have shown that stress exposure can lead to a suppression of synaptic and structural plasticity underlying information storage in the hippocampus (Mesches et al. 1999;Diamond et al. 2005).”
From Stress administered prior to encoding impairs neutral but enhances emotional long-term episodic memories. (2007) · cites this paper as Mesches et al. 1999
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Self-citation
- Authors
- Mesches, M. H., Fleshner, M., Heman, K. L., Rose, G. M., & Diamond, D. M.
- Affiliations
- University of Colorado Health (US)
- University of Colorado Boulder (US)
- United States Department of Veterans Affairs (US)
- Venue
- The Journal of Neuroscience
- Publisher
- Society for Neuroscience
- Published
- 1999-07-15
- Volume
- 19
- Issue
- 14
- Pages
- RC18-RC18
- ISSN
- 0270-6474 (ISSN-L)
- 1529-2401
- PMC
- PMC6783102
- OpenAlex
- W1599181452
- Cited by
- 276
- References
- 48
- Citations by year
- 2026: 1 · 2024: 1 · 2023: 1 · 2022: 1 · 2021: 9 · 2020: 1 · 2019: 3 · 2018: 5 · 2017: 7 · 2016: 10 · 2015: 1 · 2014: 5 · 2013: 7 · 2012: 5
- FWCI
- 10.93
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Journal of Neuroscience (publishedVersion, cc-by-nc-sa)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Digital Commons - University of South Florida (University of South Florida) (submittedVersion)
- Funders
- Office of Naval Research (N00014)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Behavioral Neuroscience › Stress Responses and Cortisol
- Keywords
- predator stress, cat exposure, long-term potentiation, hippocampal plasticity, CA1, corticosterone, acute psychological stress, spatial memory
- MeSH terms
- Action Potentials, Animals, Cats, Corticosterone, Fear, Hippocampus, Male, Memory, Stress, Psychological, Rats, Sprague-Dawley, Long-Term Potentiation, Rats
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
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