Literature DB >> 8622138

Conditioned and unconditioned stimuli increase frontal cortical and hippocampal acetylcholine release: effects of novelty, habituation, and fear.

E Acquas, C Wilson, H C Fibiger.   

Abstract

Recent evidence showing that basal forebrain cholinergic neurons with projections to the frontal cortex and hippocampus are activated by behaviorally salient stimuli suggests that these neurons are involved in arousal and/or attentional processes. We sought in the present experiments to test this hypothesis by examining whether unconditioned stimuli (a tone and flashing light) that normally increase cortical nad hippocampal acetylcholine (ACh) release would fail to do so after habituation (i.e., repeated presentation with no programmed consequences). In addition, the extent to which presentation of these stimuli would continue to increase ACh release when they had previously been paired with an aversive stimulus was investigated. Three experimental groups were used: habituation, novel stimuli, and conditioned fear. Subjects in each of these groups were placed in a training apparatus for twelve 200 min sessions. While the habituation group received extensive exposure to the tone and light during the training sessions, subjects in the novel stimuli group were placed in the apparatus but were never exposed to the tone or light during these sessions. The conditioned fear group was treated identically to the habituation group, with the addition that the tone and light were paired with footshock. On completion of these training schedules, all animals were implanted with microdialysis probes in the frontal cortex and hippocampus. Two days later, they were placed in the apparatus and the tone and light were presented to all subjects during microdialysis. In the novel stimuli group, the tone and light (unconditioned stimuli) produced significant increases in frontal cortical and hippocampal ACh release. Similarly, in the conditioned fear group, presentation of the tone and light (conditioned stimuli) also significantly increased ACh release in frontal cortex and hippocampus. In contrast, in the habituation group the tone and light failed to significantly enhance ACh release in either structure. During the test session, the tone and light elicited a variety of arousal- and fear-related behaviors in the novel stimuli and conditioned fear groups. In contrast, subjects in the habituation group generally failed to respond to these stimuli. These data indicate that cortically and hippocampally projecting basal forebrain cholinergic neurons are activated by conditioned and unconditioned stimuli that produce arousal in rats (novelty or conditioned fear). In contrast, presentation of these stimuli to habituated animals fails to enhance ACh release. These findings are consistent with a growing body of information indicating that ACh release in the cortex and hippocampus is reliably activated by behaviorally relevant stimuli. They also provide strong support for the hypothesis that cholinergic neurons in the basal forebrain are involved in arousal and/or attentional processes.

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Year:  1996        PMID: 8622138      PMCID: PMC6579062     

Source DB:  PubMed          Journal:  J Neurosci        ISSN: 0270-6474            Impact factor:   6.167


  56 in total

1.  Lesions of the dorsal hippocampal formation interfere with background but not foreground contextual fear conditioning.

Authors:  R G Phillips; J E LeDoux
Journal:  Learn Mem       Date:  1994 May-Jun       Impact factor: 2.460

2.  Distribution and organization of cholinergic neurons in the rat forebrain demonstrated by computer-aided data acquisition and three-dimensional reconstruction.

Authors:  J S Schwaber; W T Rogers; K Satoh; H C Fibiger
Journal:  J Comp Neurol       Date:  1987-09-15       Impact factor: 3.215

3.  Neuronal responses related to reinforcement in the primate basal forebrain.

Authors:  F A Wilson; E T Rolls
Journal:  Brain Res       Date:  1990-02-19       Impact factor: 3.252

4.  Hippocampal lesions disrupt decrements but not increments in conditioned stimulus processing.

Authors:  J S Han; M Gallagher; P Holland
Journal:  J Neurosci       Date:  1995-11       Impact factor: 6.167

5.  Increases in hippocampal and frontal cortical acetylcholine release associated with presentation of sensory stimuli.

Authors:  F M Inglis; H C Fibiger
Journal:  Neuroscience       Date:  1995-05       Impact factor: 3.590

6.  Further analysis of the cognitive effects of tetrahydroaminoacridine (THA) in Alzheimer's disease: assessment of attentional and mnemonic function using CANTAB.

Authors:  B J Sahakian; A M Owen; N J Morant; S A Eagger; S Boddington; L Crayton; H A Crockford; M Crooks; K Hill; R Levy
Journal:  Psychopharmacology (Berl)       Date:  1993       Impact factor: 4.530

7.  Acetylcholine permits long-term enhancement of neuronal responsiveness in cat primary somatosensory cortex.

Authors:  R Metherate; N Tremblay; R W Dykes
Journal:  Neuroscience       Date:  1987-07       Impact factor: 3.590

8.  Chronic lithium attenuates dopamine D1-receptor mediated increases in acetylcholine release in rat frontal cortex.

Authors:  E Acquas; H C Fibiger
Journal:  Psychopharmacology (Berl)       Date:  1996-05       Impact factor: 4.530

9.  Cholinergic activity in the rat hippocampus, cortex and striatum correlates with locomotor activity: an in vivo microdialysis study.

Authors:  J Day; G Damsma; H C Fibiger
Journal:  Pharmacol Biochem Behav       Date:  1991-04       Impact factor: 3.533

10.  Complementary roles for the amygdala and hippocampus in aversive conditioning to explicit and contextual cues.

Authors:  N R Selden; B J Everitt; L E Jarrard; T W Robbins
Journal:  Neuroscience       Date:  1991       Impact factor: 3.590

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  78 in total

1.  ERKI/II regulation by the muscarinic acetylcholine receptors in neurons.

Authors:  K Rosenblum; M Futter; M Jones; E C Hulme; T V Bliss
Journal:  J Neurosci       Date:  2000-02-01       Impact factor: 6.167

2.  Responses of cat motor cortex neurons to electrical stimulation of the base of the forebrain used as a conditioned signal for a reflex consisting of placing the forelimb on a support.

Authors:  V I Maiorov; S Lide
Journal:  Neurosci Behav Physiol       Date:  2000 Jul-Aug

3.  Differential acetylcholine release in the prefrontal cortex and hippocampus during pavlovian trace and delay conditioning.

Authors:  M Melissa Flesher; Allen E Butt; Brandee L Kinney-Hurd
Journal:  Neurobiol Learn Mem       Date:  2011-04-15       Impact factor: 2.877

4.  The effects of galantamine on nicotine withdrawal-induced deficits in contextual fear conditioning in C57BL/6 mice.

Authors:  Derek S Wilkinson; Thomas J Gould
Journal:  Behav Brain Res       Date:  2011-04-14       Impact factor: 3.332

Review 5.  Molecular signals into the insular cortex and amygdala during aversive gustatory memory formation.

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Journal:  Cell Mol Neurobiol       Date:  2004-02       Impact factor: 5.046

6.  A disinhibitory microcircuit for associative fear learning in the auditory cortex.

Authors:  Johannes J Letzkus; Steffen B E Wolff; Elisabeth M M Meyer; Philip Tovote; Julien Courtin; Cyril Herry; Andreas Lüthi
Journal:  Nature       Date:  2011-12-07       Impact factor: 49.962

7.  Cholinergic modulation of the resonance properties of stellate cells in layer II of medial entorhinal cortex.

Authors:  James G Heys; Lisa M Giocomo; Michael E Hasselmo
Journal:  J Neurophysiol       Date:  2010-05-05       Impact factor: 2.714

8.  Cortical cholinergic abnormalities contribute to the amnesic state induced by pyrithiamine-induced thiamine deficiency in the rat.

Authors:  Steven Anzalone; Ryan P Vetreno; Raddy L Ramos; Lisa M Savage
Journal:  Eur J Neurosci       Date:  2010-08-19       Impact factor: 3.386

9.  Intrinsic Mechanisms of Frequency Selectivity in the Proximal Dendrites of CA1 Pyramidal Neurons.

Authors:  Crescent L Combe; Carmen C Canavier; Sonia Gasparini
Journal:  J Neurosci       Date:  2018-08-03       Impact factor: 6.167

Review 10.  Cellular dynamical mechanisms for encoding the time and place of events along spatiotemporal trajectories in episodic memory.

Authors:  Michael E Hasselmo; Lisa M Giocomo; Mark P Brandon; Motoharu Yoshida
Journal:  Behav Brain Res       Date:  2009-12-16       Impact factor: 3.332

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