The Journal of Neuroscience, 1999, 0:RC18:1-5
RAPID COMMUNICATION
Exposing Rats to a Predator Blocks Primed Burst Potentiation in
the Hippocampus In Vitro
Michael H.
Mesches1,
Monika
Fleshner2,
Karen L.
Heman1,
Gregory M.
Rose1, and
David M.
Diamond3
1 Department of Pharmacology, University of Colorado
Health Sciences Center, Denver, Colorado 80262, 2 Department of Kinesiology and Applied Physiology,
University of Colorado, Boulder, Colorado 80309, and
3 Departments of Psychology and Pharmacology and
Neuroscience Program, University of South Florida, and Medical Research
Service, Veterans Administration Medical Center, Tampa, Florida 33620
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.
Key words:
psychological stress; neuronal plasticity; memory; LTP; hippocampus; fear
Copyright © 1999 Society for Neuroscience 0270-6474/99/$05.00/0