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Raymond P. Kesner, Bridget L. Bolland, Manoli Dakis
Group A7: Snir Seitelbach, Dave Dudar, Scott Good, Katie Herdman, Monika Walerjan
Memory for Spatial Locations, Motor Memory for Spatial Locations, Motor Responses, and Objects: Triple Responses, and Objects: Triple
Dissociation among the Hippocampus, Dissociation among the Hippocampus, Caudate Nucleus, and Extrastriate Caudate Nucleus, and Extrastriate
Visual CortexVisual Cortex
OUTLINEINTRODUCTION
Overall Motive of the Experiment Background
Inadequate Research Adequate Research
METHOD Pros Cons
RESULTS & DISCUSSION CRITIQUES Hippocampus Lesions Caudate Nucleus Lesions Extrastriate Visual Cortex Lesions
NEXT STEPSREFERENCES
INTRODUCTIONOverall Motive of the Experiment
To prove there are multiple memory systems
Attribute Database Memory Model
Working & Declarative Memory
Model
Different neural substrates that mediate different attributes
Hippocampus exclusively codes all information (spatial, temporal, response, sensory-perceptual, or affect)
Snir Seitelbach
BACKGROUND Inadequate Research
“Equivalent impairment of spatial and nonspatial memory following damage to the hippocampus”
- Cave and Squire
• Our study claimed Cave and Squire thought humans with demonstrated hippocampal damage show deficits in spatial memory tasks
• Conclusion of study above: Hippocampus is not especially involved in spatial memory
Snir Seitelbach
BACKGROUND Inadequate Research
“A note on spatial-motor deficits in patients with Huntington’s disease: a test of a hypothesis”
- Potegal
In Our Study: labeled as a deficit in memory.Health Canada defines Huntington’s disease
as a neuronal degeneration disorder that involves functional deficit.
Snir Seitelbach
BACKGROUND Adequate Research
“Limbic lesions and the problem of stimulus-reinforcement associations”
- Jones & Mishkin
Hippocampal lesions in monkeys produce severe deficits in spatial location memory tasks
Snir Seitelbach
BACKGROUND Adequate Research
“The contributions of positions, direction and velocity to single unit activity in the hippocampus of freely moving rats”
- McNaughton, Barnes, & O’Keefe
In both monkeys and rodents many hippocampi cells increase their firing rate when an animal is located a specific place within a specific environment or is attempting to locate a stimulus in a particular location
Snir Seitelbach
METHOD
EXPERIMENT 1 EXPERIMENT 2 EXPERIMENT 3
Spatial Location Memory Task
Motor Response Memory Task
Visual Object Memory Task
Katie Herdman
METHODPros
The radial arm maze in Experiment 1 is an adequate method for testing spatial location memory as established by previous studies.Modification of Experiment 3 to allow for
direct comparisons with the same analogous procedures used in monkeys.
Katie Herdman
METHODPros
Verification of lesions to show consistent damage across all three experiments.
Katie Herdman
METHODCons
Sample size was small for each lesioned groups in each experiment.
The sample size was not the same for all lesioned groups.
Katie Herdman
METHODCons
Lesion verification showed damage to primary striate visual cortex, affecting rat’s vision during Experiment 3.
Katie Herdman
The Primary Visual Cortex
V1 is uniquely positioned as the primary distributor of most visual information that reaches other cortical areas
In absence of V1, visual signals still reach many extrastriate areas, but seem incapable of generating normal conscious experiences
(Tong, 2003)
Katie Herdman
METHODCons
Acid lesioning may be more preferable instead of electrolytic lesioning because it is more accurate
Kainic Acid
Katie Herdman
A Different Method for Lesioning
“In situ injection of kainic acid: a new method for selectively lesioning neural cell bodies while sparing axons of passage”
- Coyle, Molliver & KuharThese morphologic studies provide direct
evidence that injection of kainic acid in brain causes a selective degeneration of neurons will cell bodies in the area of the injection but spares axons that pass through or terminate in the injected area.
(Coyle et al., 1978)
Katie Herdman
RESULTS & DISCUSSION Critiques
Hippocampal Lesions: Mice unable to perform well in spatial memory tasks, but performed well on the other tasks.
This supports the attribute model.
Scott Good
RESULTS & DISCUSSION Critiques
Hippocampal Lesions: A recent study made an observation on the hippocampus’ function: it is only responsible for spatial memory.
This is a large generalization.
Scott Good
RESULTS & DISCUSSION Critiques
Hippocampal Lesions: the hippocampus is responsible for processing memory.
The rats were retested seconds-to-minutes after the learning process.
A longer wait would have showed deficits in all the experimental procedures.
Scott Good
RESULTS & DISCUSSION Critiques
Caudate Nucleus Lesions: responding do a visual stimulus requires egocentric knowledge of the location of the stimulus.
Many cells responsible for this cognitive ‘roadmap’ are found in the posterior parietal cortex, but this was not addressed.
Scott Good
RESULTS & DISCUSSION Critiques
Caudate Nucleus Lesions: Cells in the caudate nucleus respond to other stimuli such as smell, sound and sight.
Lesions in the caudate nucleus would affect these senses, most importantly the rat’s ability to see to respond.
Scott Good
RESULTS & DISCUSSION Critiques
Extrastriate Visual Cortex Lesions: mice had difficulty in non-matching to sample tasks
Evidence supports the attribute model
Scott Good
RESULTS & DISCUSSION Critiques
Extrastriate Visual Cortex Lesions: object recognition test should have had controls
Comparison to apperceptive agnosia is confusing
Role of hippocampus may have been underestimated for long term memory formation (Squire & Zola-Morgan, 1991)
Scott Good
NEXT STEPS…Less bias toward one specific model (Kessner
is the author of the study and the creator of the attribute model…hmmmm?)
A much larger sample size: study did not have a lot of power
More accurate lesioningMore scientific method for object-
discrimination task.
Snir Seitelbach
REFERENCES Cave, C.B. & Squire, L.R. (1991). Equivalent impairment of spatial and nonspatial memory
following damage to the human hippocampus. Hippocampus 1: 329-340. Coyle, J.T., Molliver, M.E., & Kuhar, M.J. (1978). In situ injection of kainic acid: a new method
for selectively lesioning neural cell bodies while sparing axons of passage. J Comp Neurol. 180 (2): 301-323
Firth, C. D. (2000). Abnormalities in the Awareness and Control of Action. Biological Sciences. 355 (1404): 1771-1788.
Howell, D. (2008). Fundamental Statistics for the Behavioural Sciences. Belmont, CA : Thomson/Wadsworth, 6th ed.
Jones, B. & Mishkin, M. (1972). Limbic lesions and the problem of stimulus reinforcement associations. Exp Neurol 36: 362-377.
McNaughton, B.L., Barnes, C.A., O’Keefe, J. (1983). The contribution of position, direction and velocity to single unit activity in the hippocampus of freely moving rats. Exp Brain Res 52: 41-49.
Milner, A. D. et. al. (1999). A Paradoxical Improvement of Misreaching in Optic Ataxia: New Evidence for Two Separate Neural Visual Systems for Visual Localization. Biological Sciences. 266 (1434): 2225-2229.
Squire, L.R. & Zola-Morgan, S. (1991). The medial temporal lobe memory system. Science. 253: 1380-1386.
Tong, F. (2003). Primary Visual Cortex and Visual Awareness. Neuroscience. 4, 219-229.
THANK YOU For Your TIME
and ATTENTION!