use-an-eight-arm-radial-water-maze-to-assess-working-reference-memory

Use of an Eight-arm Radial Water Maze to Assess Working and Reference Memory Following Neonatal Brain Injury

Working and reference memory are commonly assessed using the land based radial arm maze.&#160;However, this paradigm requires pretraining, food ...

Rhode Island College

Rodent studies using cortical removal techniques, ranging from transient deactivation to surgical ablation of cortex, reveal the importance of auditory cortical integrity in detecting short silent gaps in white noise (2-15 ms). Processing limits for longer gaps under decorticate conditions in rats remain unknown. Determining the temporal threshold for subcortical resolution of gaps in noise could, however, shed light on both normal hierarchical processing of acoustic temporal stimuli, as well as the etiology of processing anomalies following developmental cortical disruption. To address these important issues, we assessed whether intact rats, as well as those with induced developmental cortical disruptions (microgyria) could resolve silent gaps of 20-100 ms in duration when embedded in white noise, during functional deactivation of auditory cortex. Results showed that both intact rats, as well as those with cortical malformations resulting from early focal disruptions of neuronal migration could resolve silent gaps of 100-ms duration under cortical deactivation (KCl). However, only intact rats could reliably detect 75-ms gaps, suggesting possible subcortical anomalies in subjects with early cortical disturbances.

Detection of silent gaps in white noise following cortical deactivation in rats.

In humans the hippocampus plays a role in both episodic memory and spatial navigation. Similar findings have been shown in other animals including monkeys and rats. The relationship between the processing of episodic and spatial related inputs within the hippocampus remains a puzzle. One approach to understanding how the hippocampus processes information is to examine how hippocampal cell activity corresponds to environmental experience. Hippocampal pyramidal cells can alter their spatial tuning (re-map) in response to changes in task demands. The degree to which this re-mapping is related to contextual/episodic information or to changes in spatial navigation/trajectories is unclear. The current study was designed to examine cell activity under two conditions that differed in contextual information without alterations in the goal-directed trajectories taken by the animals. Adult and aged rats were trained to do an alternation task on a fixed pathway [J. A. Oler et al. (2005)Neuroscience, 131, 1-12]. The animals ran this pathway during either 'safe' or 'unsafe' (a tone indicating a shock region) trials, with hesitation during 'unsafe' trials providing a clear behavioral measure of discrimination between these two conditions. Relatively few place cells displayed re-mapping between the two conditions. We propose that the principle source of re-mapping in the dorsal hippocampus is changes in the animal's trajectories rather than behavioral context. Possible reasons why so few cells responded to the change in context are discussed.

Does the dorsal hippocampus process navigational routes or behavioral context? A single-unit analysis.

Theta and gamma rhythms synchronize neurons within and across brain structures. Both rhythms are widespread within the hippocampus during exploratory behavior and rapid-eye-movement (REM) sleep. How synchronous are these rhythms throughout the hippocampus? The present study examined theta and gamma coherence along the septotemporal (long) axis of the hippocampus in rats during REM sleep, a behavioral state during which theta signals are unaffected by external sensory input or ongoing behavior. Unilateral entorhinal cortical inputs are thought to play a prominent role in the current generation of theta, whereas current generation of gamma is primarily due to local GABAergic neurons. The septal 50% (4-5 mm) of the dentate gyrus (DG) receives a highly divergent, unilateral projection from any focal point along a lateral band of entorhinal neurons near the rhinal sulcus. We hypothesized that theta coherence in the target zone (septal DG) of this divergent entorhinal input would not vary, while gamma coherence would significantly decline with distance in this zone. However, both theta and gamma coherence decreased significantly along the long axis in the septal 50% of the hippocampus across both DG and CA1 electrode sites. In contrast, theta coherence between homotypic (e.g., DG to DG) sites in the contralateral hemisphere ( approximately 3-5 mm distant) were quite high ( approximately 0.7-0.9), much greater than theta coherence between homotypic sites 3-5 mm distant ( approximately 0.4-0.6) along the long axis. These findings define anatomic variation in both rhythms along the longitudinal axis of the hippocampus, indicate the bilateral CA3/mossy cell projections are the major determinant of theta coherence during REM, and demonstrate that theta coherence varies as a function of anatomical connectivity rather than physical distance. We suggest CA3 and entorhinal inputs interact dynamically to generate theta field potentials and advance the utility of theta and gamma coherence as indicators of hippocampal dynamics.

Theta and gamma coherence along the septotemporal axis of the hippocampus.

Theta (6-12 Hz) field potentials and the synchronization (coherence) of these potentials present neural network indices of hippocampal physiology. Theta signals within the hippocampal formation may reflect alterations in sensorimotor integration, the flow of sensory input, and/or distinct cognitive operations. While the power and coherence of theta signals vary across lamina within the septal hippocampus, limited information is available about variation in these indices across the septotemporal (long) or areal axis. The present study examined the relationship of locomotor speed to theta indices at CA1 and dentate gyrus (DG) sites across the septotemporal axis as well as in the entorhinal cortex. Our findings demonstrate the dominant relationship of speed to theta indices at septal sites. This relationship diminished systematically with distance from the septal pole of the hippocampus at both CA1 and DG sites. While theta power at entorhinal sites varied in relation to speed, there were no differences across the areal axis of the entorhinal cortex. Locomotor speed was also related to changes in theta coherence along the septotemporal axis as well as between the hippocampus and entorhinal cortex. In addition to the speed-related variation, we observed a decrease in theta power at more temporal hippocampal sites over repeated behavioral testing within a single day that was not observed at septal sites. The results outline a dynamic and distributed pattern of network activity across the septotemporal axis of the hippocampus in relation to locomotor speed and recent past experience.

Septotemporal variation in dynamics of theta: speed and habituation.

Theta (4-12 Hz) and gamma (40-100 Hz) field potentials represent the interaction of synchronized synaptic input onto distinct neuronal populations within the hippocampal formation. Theta is quite prominent during exploratory activity, locomotion, and REM sleep. Although it is generally acknowledged that theta is coherent throughout most of the hippocampus, there is significant variability in theta, as well as gamma, coherence across lamina at any particular septotemporal level of the hippocampus. Larger differences in theta coherence are observed across the septotemporal (long) axis. We have reported that during REM sleep there is a decrease in theta coherence across the long axis that varies with the topography of CA3/mossy cell input rather than the topography of the prominent entorhinal input. On the basis of differences in the rat's behavior as well as the activity of neuromodulatory inputs (e.g., noradrenergic and serotonergic), we hypothesized that theta coherence across the long axis would be greater during locomotion than REM sleep and exhibit a pattern more consistent with the topography of entorhinal inputs. We examined theta and gamma coherence indices at different septotemporal and laminar sites during distinct theta states: locomotion during maze running, REM sleep, following acute treatment with a θ-inducing cholinomimetic (physostigmine) and for comparison during slow-wave sleep. The results demonstrate a generally consistent pattern of theta and gamma coherence across the septotemporal axis of the hippocampus that is quite indifferent to sensory input and overt behavior. These results are discussed with regards to the neurobiological mechanisms that generate theta and gamma and the growing body of evidence linking theta and gamma indices to memory and other cognitive functions.

Theta and gamma coherence across the septotemporal axis during distinct behavioral states.

The hippocampal theta signal reflects moment-to-moment variation in the synchrony of synaptic input to hippocampal neurons. Consistent with the topography of hippocampal afferents, the synchrony (coherence) of the theta signal varies across the septotemporal axis. Septotemporal variation in the theta signal can also be observed in relation to ongoing and past experience. Thus there is a systematic decrease in the relationship between locomotor speed and theta power across the septotemporal axis, septal hippocampus exhibiting the strongest relationship. Conversely, theta in temporal hippocampus decrements over repeated behavioral experience (running episodes), while theta in the septal hippocampus does not. Ketamine is an N-methyl-D-aspartate (NMDA) antagonist that can decrease theta power. The present study examined whether ketamine treatment could alter theta coherence across the long axis independent of changes in locomotor behavior. Rats were well trained to navigate a linear runway and outfitted with electrodes at different septotemporal positions within CA1. Locomotor behavior and theta coherence and power were examined after administration of 2.5 and 10 mg/kg ketamine. Ketamine (2.5 mg/kg) decreased theta coherence between distant CA1 electrode sites without altering running speed or theta power. Both doses of ketamine also blunted and reversed the decrement in theta power observed at midseptotemporal and temporal electrodes over repeated run sessions. The results demonstrate the sensitivity of global network synchronization to relatively low doses of ketamine and septotemporal differences in the influence of ketamine on hippocampal dynamics in relation to past experience.

Ketamine disrupts theta synchrony across the septotemporal axis of the CA1 region of hippocampus.

Hippocampal theta (6-10 Hz) and gamma (25-50 Hz and 65-100 Hz) local field potentials (LFPs) reflect the dynamic synchronization evoked by inputs impinging upon hippocampal neurons. Novel experience is known to engage hippocampal physiology and promote successful encoding. Does novelty synchronize or desynchronize theta and/or gamma frequency inputs across the septotemporal (long) axis of the hippocampus (HPC)? The present study tested the hypothesis that a novel spatial environment would alter theta power and coherence across the long axis. We compared theta and gamma LFP signals at individual (power) and millimeter distant electrode pairs (coherence) within the dentate gyrus (DG) and CA1 region while rats navigated a runway (1) in a familiar environment, (2) with a modified path in the same environment and (3) in a novel space. Locomotion in novel space was related to increases in theta and gamma power at most CA1 and DG sites. The increase in theta and gamma power was concurrent with an increase in theta and gamma coherence across the long axis of CA1; however, there was a significant decrease in theta coherence across the long axis of the DG. These findings illustrate significant shifts in the synchrony of entorhinal, CA3 and/or neuromodulatory afferents conveying novel spatial information to the dendritic fields of CA1 and DG targets across the long axis of the HPC. This shift suggests that the entire theta/gamma-related input to the CA1 network, and likely output, receives and conveys a more coherent message in response to novel sensory experience. Such may contribute to the successful encoding of novel sensory experience.

Article	Year
Detection of silent gaps in white noise following cortical deactivation in rats. Neuroreport\| PubMed ID: 18463508	2008
Does the dorsal hippocampus process navigational routes or behavioral context? A single-unit analysis. The European journal of neuroscience\| PubMed ID: 18671742	2008
Theta and gamma coherence along the septotemporal axis of the hippocampus. Journal of neurophysiology\| PubMed ID: 19118111	2009
Septotemporal variation in dynamics of theta: speed and habituation. Journal of neurophysiology\| PubMed ID: 21411562	2011
Theta and gamma coherence across the septotemporal axis during distinct behavioral states. Hippocampus\| PubMed ID: 21748821	2012
Ketamine disrupts theta synchrony across the septotemporal axis of the CA1 region of hippocampus. Journal of neurophysiology\| PubMed ID: 23114214	2013
Novel space alters theta and gamma synchrony across the longitudinal axis of the hippocampus. Frontiers in systems neuroscience\| PubMed ID: 23805081	2013

Stephanie C. Penley

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