Literature DB >> 7638220

Functional anatomy of human eyeblink conditioning determined with regional cerebral glucose metabolism and positron-emission tomography.

C G Logan1, S T Grafton.   

Abstract

Relative cerebral glucose metabolism was examined with positron-emission tomography (PET) as a measure of neuronal activation during performance of the classically conditioned eyeblink response in 12 young adult subjects. Each subject received three sessions: (i) a control session with PET scan in which unpaired presentations of the tone conditioned stimulus and corneal airpuff unconditioned stimulus were administered, (ii) a paired training session to allow associative learning to occur, and (iii) a paired test session with PET scan. Brain regions exhibiting learning-related activation were identified as those areas that showed significant differences in glucose metabolism between the unpaired control condition and well-trained state in the 9 subjects who met the learning criterion. Areas showing significant activation included bilateral sites in the inferior cerebellar cortex/deep nuclei, anterior cerebellar vermis, contralateral cerebellar cortex and pontine tegmentum, ipsilateral inferior thalamus/red nucleus, ipsilateral hippocampal formation, ipsilateral lateral temporal cortex, and bilateral ventral striatum. Among all subjects, including those who did not meet the learning criterion, metabolic changes in ipsilateral cerebellar nuclei, bilateral cerebellar cortex, anterior vermis, contralateral pontine tegmentum, ipsilateral hippocampal formation, and bilateral striatum correlated with degree of learning. The localization to cerebellum and its associated brainstem circuitry is consistent with neurobiological studies in the rabbit model of eyeblink classical conditioning and neuropsychological studies in brain-damaged humans. In addition, these data support a role for the hippocampus in conditioning and suggest that the ventral striatum may also be involved.

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Year:  1995        PMID: 7638220      PMCID: PMC41367          DOI: 10.1073/pnas.92.16.7500

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  35 in total

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Authors:  K J Worsley; A C Evans; S Marrett; P Neelin
Journal:  J Cereb Blood Flow Metab       Date:  1992-11       Impact factor: 6.200

2.  Rapid automated algorithm for aligning and reslicing PET images.

Authors:  R P Woods; S R Cherry; J C Mazziotta
Journal:  J Comput Assist Tomogr       Date:  1992 Jul-Aug       Impact factor: 1.826

3.  Double dissociation of fornix and caudate nucleus lesions on acquisition of two water maze tasks: further evidence for multiple memory systems.

Authors:  M G Packard; J L McGaugh
Journal:  Behav Neurosci       Date:  1992-06       Impact factor: 1.912

4.  Conditioning using a cerebral cortical conditioned stimulus is dependent on the cerebellum and brain stem circuitry.

Authors:  B J Knowlton; R F Thompson
Journal:  Behav Neurosci       Date:  1992-06       Impact factor: 1.912

5.  Cerebellar cortex lesions disrupt learning-dependent timing of conditioned eyelid responses.

Authors:  S P Perrett; B P Ruiz; M D Mauk
Journal:  J Neurosci       Date:  1993-04       Impact factor: 6.167

6.  Cerebellum: essential involvement in the classically conditioned eyelid response.

Authors:  D A McCormick; R F Thompson
Journal:  Science       Date:  1984-01-20       Impact factor: 47.728

7.  Hippocampectomy selectively disrupts discrimination reversal conditioning of the rabbit nictitating membrane response.

Authors:  T W Berger; W B Orr
Journal:  Behav Brain Res       Date:  1983-04       Impact factor: 3.332

8.  Hippocampectomy disrupts trace eye-blink conditioning in rabbits.

Authors:  J R Moyer; R A Deyo; J F Disterhoft
Journal:  Behav Neurosci       Date:  1990-04       Impact factor: 1.912

9.  Classical conditioning after temporal lobe lesions in man: impairment in conditional discrimination.

Authors:  I Daum; S Channon; C E Polkey; J A Gray
Journal:  Behav Neurosci       Date:  1991-06       Impact factor: 1.912

10.  Hippocampus, context, and conditioning.

Authors:  S Penick; P R Solomon
Journal:  Behav Neurosci       Date:  1991-10       Impact factor: 1.912

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  48 in total

Review 1.  Programs of gene expression during the laying down of memory formation as revealed by DNA microarrays.

Authors:  Sebastiano Cavallaro; Velia Dagata; Daniel L Alkon
Journal:  Neurochem Res       Date:  2002-10       Impact factor: 3.996

2.  fMRI of the conscious rabbit during unilateral classical eyeblink conditioning reveals bilateral cerebellar activation.

Authors:  Michael J Miller; Nan-kuei Chen; Limin Li; Brian Tom; Craig Weiss; John F Disterhoft; Alice M Wyrwicz
Journal:  J Neurosci       Date:  2003-12-17       Impact factor: 6.167

3.  Impaired delay and trace eyeblink conditioning in school-age children with fetal alcohol syndrome.

Authors:  Sandra W Jacobson; Mark E Stanton; Neil C Dodge; Mariska Pienaar; Douglas S Fuller; Christopher D Molteno; Ernesta M Meintjes; H Eugene Hoyme; Luther K Robinson; Nathaniel Khaole; Joseph L Jacobson
Journal:  Alcohol Clin Exp Res       Date:  2010-11-12       Impact factor: 3.455

4.  Amygdala-hippocampal involvement in human aversive trace conditioning revealed through event-related functional magnetic resonance imaging.

Authors:  C Büchel; R J Dolan; J L Armony; K J Friston
Journal:  J Neurosci       Date:  1999-12-15       Impact factor: 6.167

5.  Functional mapping of human learning: a positron emission tomography activation study of eyeblink conditioning.

Authors:  T A Blaxton; T A Zeffiro; J D Gabrieli; S Y Bookheimer; M C Carrillo; W H Theodore; J F Disterhoft
Journal:  J Neurosci       Date:  1996-06-15       Impact factor: 6.167

Review 6.  Eyeblink classical conditioning differentiates normal aging from Alzheimer's disease.

Authors:  D S Woodruff-Pak
Journal:  Integr Physiol Behav Sci       Date:  2001 Apr-Jun

7.  Intracellular correlates of acquisition and long-term memory of classical conditioning in Purkinje cell dendrites in slices of rabbit cerebellar lobule HVI.

Authors:  B G Schreurs; P A Gusev; D Tomsic; D L Alkon; T Shi
Journal:  J Neurosci       Date:  1998-07-15       Impact factor: 6.167

8.  Hippocampal, but not amygdala, activity at encoding correlates with long-term, free recall of nonemotional information.

Authors:  M T Alkire; R J Haier; J H Fallon; L Cahill
Journal:  Proc Natl Acad Sci U S A       Date:  1998-11-24       Impact factor: 11.205

9.  Amygdala activity at encoding correlated with long-term, free recall of emotional information.

Authors:  L Cahill; R J Haier; J Fallon; M T Alkire; C Tang; D Keator; J Wu; J L McGaugh
Journal:  Proc Natl Acad Sci U S A       Date:  1996-07-23       Impact factor: 11.205

10.  Functional magnetic resonance imaging of early visual pathways in dyslexia.

Authors:  J B Demb; G M Boynton; D J Heeger
Journal:  J Neurosci       Date:  1998-09-01       Impact factor: 6.167

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