Searched for: school:SOM
Department/Unit:Neuroscience Institute
The CA3 "backprojection" to the dentate gyrus
Scharfman, Helen E
The hippocampus is typically described in the context of the trisynaptic circuit, a pathway that relays information from the perforant path to the dentate gyrus, dentate to area CA3, and CA3 to area CA1. Associated with this concept is the assumption that most hippocampal information processing occurs along the trisynaptic circuit. However, the entorhinal cortex may not be the only major extrinsic input to consider, and the trisynaptic circuit may not be the only way information is processed in hippocampus. Area CA3 receives input from a variety of sources, and may be as much of an 'entry point' to hippocampus as the dentate gyrus. The axon of CA3 pyramidal cells targets diverse cell types, and has commissural projections, which together make it able to send information to much more of the hippocampus than granule cells. Therefore, CA3 pyramidal cells seem better designed to spread information through hippocampus than the granule cells. From this perspective, CA3 may be a point of entry that receives information which needs to be 'broadcasted,' whereas the dentate gyrus may be a point of entry that receives information with more selective needs for hippocampal processing. One aspect of the argument that CA3 pyramidal cells have a widespread projection is based on a part of its axonal arbor that has received relatively little attention, the collaterals that project in the opposite direction to the trisynaptic circuit, 'back' to the dentate gyrus. The evidence for this 'backprojection' to the dentate gyrus is strong, particularly in area CA3c, the region closest to the dentate gyrus, and in temporal hippocampus. The influence on granule cells is indirect, through hilar mossy cells and GABAergic neurons of the dentate gyrus, and appears to include direct projections in the case of CA3c pyramidal cells of ventral hippocampus. Physiological studies suggest that normally area CA3 does not have a robust excitatory influence on granule cells, but serves instead to inhibit it by activating dentate gyrus GABAergic neurons. Thus, GABAergic inhibition normally controls the backprojection to dentate granule cells, analogous to the way GABAergic inhibition appears to control the perforant path input to granule cells. From this perspective, the dentate gyrus has two robust glutamatergic inputs, entorhinal cortex and CA3, and two 'gates,' or inhibitory filters that reduce the efficacy of both inputs, keeping granule cells relatively quiescent. When GABAergic inhibition is reduced experimentally, or under pathological conditions, CA3 pyramidal cells activate granule cells reliably, and do so primarily by disynaptic excitation that is mediated by mossy cells. We suggest that the backprojection has important functions normally that are dynamically regulated by nonprincipal cells of the dentate gyrus. Slightly reduced GABAergic input would lead to increased polysynaptic associative processing between CA3 and the dentate gyrus. Under pathological conditions associated with loss of GABAergic interneurons, the backprojection may support reverberatory excitatory activity between CA3, mossy cells, and granule cells, possibly enhanced by mossy fiber sprouting. In this case, the backprojection could be important to seizure activity originating in hippocampus, and help explain the seizure susceptibility of ventral hippocampus
PMCID:1986638
PMID: 17765742
ISSN: 0079-6123
CID: 76103
Correlative learning : a basis for brain and adaptive systems
Chen, Zhe; Haykin, Simon; Eggermont, Jos J; Becker, Suzanna
Hoboken, N.J. : Wiley-Interscience, 2007
Extent: xxvi, 448 p. ; 24 cm.
ISBN: 0470044888
CID: 3631372
Representation of hand kinematics during prehension in posterior parietal cortex (PPC) [Meeting Abstract]
Chen, Jessie; Debowy, DJ; Babu, KS; Ghosh, S; Gardner, EP
ORIGINAL:0007461
ISSN: 1558-3635
CID: 162618
An empirical quantitative EEG analysis for evaluating clinical brain death
Chen, Zhe; Cao, Jianting
In this paper, we apply qualitative tools and quantitative analysis for the EEG recordings of 23 adult patients. Specifically, independent component analysis (ICA) was applied to separate independent source components, followed by spectrum analysis. In terms of quantitative EEG analysis, we use several complexity measures to evaluate the differences between two groups of patients: the subjects in deep coma, and the subjects who were prejudged as brain death. For the first time, we report statistically significant differences of quantitative statistics in such a clinical study. The empirical results reported in this paper suggest some promising directions and valuable clues for clinical practice.
PMID: 18002846
ISSN: 1557-170x
CID: 3632552
A Bayesian Model of Conditioned Perception
Stocker, Alan A; Simoncelli, Eero P
We argue that in many circumstances, human observers evaluate sensory evidence simultaneously under multiple hypotheses regarding the physical process that has generated the sensory information. In such situations, inference can be optimal if an observer combines the evaluation results under each hypothesis according to the probability that the associated hypothesis is correct. However, a number of experimental results reveal suboptimal behavior and may be explained by assuming that once an observer has committed to a particular hypothesis, subsequent evaluation is based on that hypothesis alone. That is, observers sacrifice optimality in order to ensure self-consistency. We formulate this behavior using a conditional Bayesian observer model, and demonstrate that it can account for psychophysical data from a recently reported perceptual experiment in which strong biases in perceptual estimates arise as a consequence of a preceding decision. Not only does the model provide quantitative predictions of subjective responses in variants of the original experiment, but it also appears to be consistent with human responses to cognitive dissonance.
PMCID:4199208
PMID: 25328364
ISSN: 1049-5258
CID: 1931332
Hilar mossy cells: functional identification and activity in vivo
Henze, Darrell A; Buzsaki, Gyorgy
Network oscillations are proposed to provide the framework for the ongoing neural computations of the brain. Thus, an important aspect of understanding the functional roles of various cell classes in the brain is to understand the relationship of cellular activity to the ongoing oscillations. While many studies have characterized the firing properties of cells in the hippocampal network including granule cells, pyramidal cells and interneurons, information about the activity of dentate mossy cells in the intact brain is scant. Here we review the currently available information and describe biophysical properties and network-related firing patterns of mossy cells in vivo. These new observations will assist in the extracellular identification of this unique cell type and help elucidate their functional role in behaving animals
PMID: 17765720
ISSN: 0079-6123
CID: 148935
The dentate gyrus: fundamental neuroanatomical organization (dentate gyrus for dummies)
Amaral, David G; Scharfman, Helen E; Lavenex, Pierre
The dentate gyrus is a simple cortical region that is an integral portion of the larger functional brain system called the hippocampal formation. In this review, the fundamental neuroanatomical organization of the dentate gyrus is described, including principal cell types and their connectivity, and a summary of the major extrinsic inputs of the dentate gyrus is provided. Together, this information provides essential information that can serve as an introduction to the dentate gyrus--a 'dentate gyrus for dummies.'
PMCID:2492885
PMID: 17765709
ISSN: 0079-6123
CID: 76104
Modafinil enhances thalamocortical activity through electronic coupling [Meeting Abstract]
Urbano Fj; Leznik E; Llinas R
ORIGINAL:0006284
ISSN: 1558-3635
CID: 75351
Performance accuracy and error correction of skilled musicians [Meeting Abstract]
Chen, Jessie; Moore, GP; Woollacott, M; Pologe, S
ORIGINAL:0007462
ISSN: 1558-3635
CID: 162619
Effect of T-817MA on MPP+ and amyloid B induced axonal mitochondria transport impairment in vitro [Meeting Abstract]
Hirata K; Nakagawa M; Sugimori M; Llinas R
ORIGINAL:0006286
ISSN: 1558-3635
CID: 75353