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Open AccessJournal ArticleDOI

Conditioning-specific membrane changes of rabbit hippocampal neurons measured in vitro

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TLDR
These experiments demonstrate the feasibility of analyzing cellular mechanisms of associative learning in mammalian brain with the in vitro brain slice technique and conditioning-induced biophysical alteration of the CA1 pyramidal cell must be stored by mechanisms intrinsic to the hippocampal slice.
Abstract
Intracellular recordings were made from hippocampal CA1 pyramidal neurons within brain slices of nictitating membrane conditioned, pseudoconditioned, and naive adult male albino rabbits. All neurons included (26 conditioned, 26 pseudoconditioned, and 28 naive) had stable penetration and at least 60 mV action potential amplitudes. Mean input resistances were approximately equal to 60 mu omega for the three groups. A marked reduction in the afterhyperpolarization (AHP) following an impulse was apparent for conditioned (x = -0.98 mV) as compared to the pseudoconditioned (x = -1.7 mV) and naive (x = -2.0 mV) neurons. The AHP has been attributed previously to activation of a Ca2+-dependent outward K+ current. The distribution of AHP amplitudes for the conditioned group included a new lower range of values for which there was little overlap with the other groups. The conditioning-specific reduction of AHP may be due to reduction of ICa2+-K+ as shown previously for conditioned Hermissenda neurons. This conditioning-induced biophysical alteration of the CA1 pyramidal cell must be stored by mechanisms intrinsic to the hippocampal slice and cannot be explained as a consequence of changes of presynaptic input arising elsewhere in the brain. Our experiments demonstrate the feasibility of analyzing cellular mechanisms of associative learning in mammalian brain with the in vitro brain slice technique.

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Long-term potentiation.

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The neurobiology of learning and memory

TL;DR: Probably applications of this new understanding of the neural bases of learning and memory range from education to the treatment of learning disabilities to the design of new artificial intelligence systems.
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The other side of the engram: experience-driven changes in neuronal intrinsic excitability.

TL;DR: The evidence for persistent changes in intrinsic neuronal excitability — what the authors will call intrinsic plasticity — that is produced by training in behaving animals and by artificial patterns of activation in brain slices and neuronal cultures is considered.
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Cognitive neuroscience of human memory

TL;DR: Evidence is reviewed about which brain regions mediate specific kinds of procedural memory, including sensorimotor, perceptual, and cognitive skill learning; perceptual and conceptual repetition priming; and several forms of conditioning.
Journal ArticleDOI

Hippocampectomy disrupts trace eye-blink conditioning in rabbits.

TL;DR: The authors conclude that the HPC encodes a temporal relationship between CS and UCS, and when the trace interval is long enough (e.g., 500 ms), that theHPC is necessary for associative learning of the conditioned eye-blink response.
References
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BookDOI

Neural Mechanisms in Behavior

TL;DR: This volume is the edited version of a symposium held at the University of Texas, Austin, in March, 1978, partly to mark the thirtieth anniversary of the famous Hixon Symposium on Cerebral Mechanisms in Behavior, organized by Lloyd Jefftess.
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