scholarly journals Transient Inactivation of the Medial Prefrontal Cortex and Ventral Hippocampus Impairs Active Place Avoidance Retrieval on a Rotating Arena

2021 ◽  
Vol 15 ◽  
Author(s):  
Daniela Cernotova ◽  
Ales Stuchlik ◽  
Jan Svoboda

It is well known that communication between the medial prefrontal cortex (mPFC) and the ventral hippocampus (vHPC) is critical for various cognitive and behavioral functions. However, the exact role of these structures in spatial coordination remains to be clarified. Here we sought to determine the involvement of the mPFC and the vHPC in the spatial retrieval of a previously learned active place avoidance task in adult male Long-Evans rats, using a combination of unilateral and bilateral local muscimol inactivations. Moreover, we tested the role of the vHPC-mPFC pathway by performing combined ipsilateral and contralateral inactivations. Our results showed not only bilateral inactivations of either structure, but also the combined inactivations impaired the retrieval of spatial memory, whereas unilateral one-structure inactivations did not yield any effect. Remarkably, muscimol injections in combined groups exerted similar deficits, regardless of whether the inactivations were contralateral or ipsilateral. These findings confirm the importance of these structures in spatial cognition and emphasize the importance of the intact functioning of the vHPC-mPFC pathway.

2009 ◽  
Vol 24 (S1) ◽  
pp. 1-1
Author(s):  
J. Svoboda ◽  
K. Blahna ◽  
P. Telensky ◽  
J. Bures ◽  
A. Stuchlik

One of key features of cognitive processing in both humans and animals is to select relevant stimuli. Several rodent spatial paradigms proved to be useful in biological psychiatric research. A place avoidance task has been previously used in animal model of cognitive deficits in psychosis.Here we present modifications of the place avoidance paradigm, assessing the ability of selecting appropriate cues at various levels of task complexity. Moreover, we present a pilot experiment showing an effect of lesion to medial prefrontal cortex (mPFC) on those tasks. Generally, the place avoidance apparatus consists of a circular arena elevated 1m above the floor. Rats are trained to avoid an unmarked forbidden sector, entering which is punished by mild footshocks. The sector can be defined with respect to the room or arena frame, which can be dissociated by arena rotation. Moreover, we studied an ability of rats to avoid the place defined by salient rotating object.The results showed that animals with mPFC lesion were capable of avoiding a place defined either by distal of by proximal cues, similarly as controls. However, both control and mPFC-lesioned rats had difficulties to avoid a place surrounding moving salient object. The performance increased whenever the rat was passively rotated with the arena, suggesting that vestibular stimulation enhanced the directed attention to an object. The poster will discuss the present findings and outline the future directions with emphasis on their utilization in animal models of neuropsychiatric disorders.Supported by GACR grants 309/07/0341 and 309/06/1231.


2020 ◽  
Vol 3 ◽  
Author(s):  
M. Regina Barron ◽  
William Truitt

The social interaction habituation (SI-hab) protocol has been used to demonstrate that rats acquire Social Familiarity-induced Anxiolysis (SoFiA), a form of safety learning where rats display anxiolysis in the presence of a familiar conspecific. SoFiA acquisition and expression can be simplified into four different constructs: social memory, anxiety, safety learning and anxiolysis. The neural circuitry of SoFiA; however, has not been fully identified. As a step towards elucidating the SoFiA neural circuitry we are identifying the role of projections from the ventral hippocampus (vHIP) to the medial prefrontal cortex (mPFC) in SoFiA acquisition.   Prior work from our lab has shown that the mPFC is needed for acquisition and expression of SoFiA. The mPFC may be the location of convergence of anxiety and social memory processing, making it a loci for safety learning. The goal of the current work is to identify the inputs to the mPFC that are pivotal for SoFiA acquisition. vHIP has been implicated in social memory and projects to the mPFC leading to the hypothesis that SoFiA acquisition requires vHIP projections to mPFC.  This hypothesis will be tested via intersectional genetics where neural tracts are selectively targeted through viruses. One virus is introduced at the soma of the neuron, and another is introduced at the end of the axon. The first virus, adeno-associated virus 8 (AAV8) will contain Cre-dependent code for an inhibitory DREADD (designer receptors exclusively activated by designer drugs.) The second virus, canine adenovirus 2 (CAV2) is picked up by axon terminals and transported to the soma where it will express Cre. Unfortunately, the uptake and transport of these viruses require specific receptors and the vHIP-mPFC pathway has poor CAV2 uptake. CAV2 levels will be increased by the introduction of Coxsackievirus and Adenovirus receptor (CAR) via AAV8 two weeks prior to CAV2-Cre injection.  


2006 ◽  
Vol 96 (4) ◽  
pp. 2134-2138 ◽  
Author(s):  
Akinori Ishikawa ◽  
Shoji Nakamura

The ventral hippocampus (VH) may have an important role in spatial memory processes and emotional behaviors through connections with the medial prefrontal cortex (mPFC) and amygdala. Although the mPFC and amygdala receive afferent projections from the VH, it has not been determined whether the individual VH neurons project to both the mPFC and the amygdala. In this study, antidromic responses to the mPFC and amygdala stimulation were evoked in single VH neurons. In addition, VH neurons were retrogradely double-labeled with fluorescent tracers injected in the mPFC and amygdala. VH neurons projecting to both the mPFC and amygdala were predominantly located in the subiculum and CA1 and bifurcated near or at the soma. Our anatomical and electrophysiological evidence for the presence of VH neurons projecting to both the mPFC and amygdala provides a previously unrecognized pathway from the hippocampus that simultaneously activates the mPFC and amygdala.


2017 ◽  
Vol 42 (8) ◽  
pp. 1715-1728 ◽  
Author(s):  
Gustavo Morrone Parfitt ◽  
Robin Nguyen ◽  
Jee Yoon Bang ◽  
Afif J Aqrabawi ◽  
Matthew M Tran ◽  
...  

2019 ◽  
Author(s):  
Eun Hye Park ◽  
Kally C. O’Reilly ◽  
David Taborga ◽  
Kyndall Nicholas ◽  
Armaan S Ahmed ◽  
...  

ABSTRACTCognitive control tasks require that the subject use one class of information and ignore another competing class of information. In prior work, we used an active place avoidance task on a rotating arena that requires rodent subjects to avoid shock by using information about their location in the stationary room and ignore information about their location on the rotating floor. During the task, the discharge of hippocampus neurons alternates judiciously between representing stationary and rotating locations according to the proximity of shock, demonstrating cognitive control directly in the neural representations of hippocampal discharge. The central role of the medial prefrontal cortex (mPFC) in cognitive control is well established in the primate literature, and largely accepted in the rodent literature because mPFC damage causes deficits in tasks that may require cognitive control, as inferred, typically from the task design. Here we test whether rat mPFC lesion impairs the active place avoidance task that requires cognitive control in order to test the “central-computation” hypothesis in which the mPFC is hypothesized to be essential for the computations required for cognitive control. Although ibotenic acid lesion of the mPFC was effective and caused alterations in the coordination of metabolic activity, including the dorsal hippocampus to the dorsal subiculum, its output structure, nonetheless the lesion did not impair active place avoidance. These data support an alternative “local computation” hypothesis: the computations required for cognitive control can occur locally in brain networks independently of the mPFC as a central computational locus for cognitive control.SIGNIFICANCE STATEMENTThe medial prefrontal cortex (mPFC) is considered to be crucial for cognitive control of information, operating with winner-take-all dynamics that allows subjects to make judicious choices in the presence of alternatives. Alternatively, cognitive control may also result from computations in neural circuits such as hippocampus, with a neural architecture for winner-take-all computations. We investigated whether mPFC lesion impairs an active place avoidance task that is demonstrated to require cognitive control that is observed in hippocampus place cell spike train dynamics. We produced mPFC lesions with brain-wide consequences that reduced resting-state coordination of metabolic activity within hippocampus and related areas. Nonetheless mPFC lesion did not impair the active place avoidance task, demonstrating that cognitive control does not always depend on mPFC.


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