» Articles » PMID: 33994956

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

Overview
Date 2021 May 17
PMID 33994956
Citations 3
Authors
Affiliations
Soon will be listed here.
Abstract

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.

Citing Articles

Complement Component 5 (C5) Deficiency Improves Cognitive Outcome After Traumatic Brain Injury and Enhances Treatment Effects of Complement Inhibitors C1-Inh and CR2-Crry in a Mouse Model.

Chen M, Edwards S, Maskey D, Woodruff T, Tomlinson S, Reutens D Neurotrauma Rep. 2023; 4(1):663-681.

PMID: 37908321 PMC: 10615070. DOI: 10.1089/neur.2023.0024.


Emotional- and cognitive-like responses induced by social defeat stress in male mice are modulated by the BNST, amygdala, and hippocampus.

da Costa V, Ramirez J, Ramirez S, Avalo-Zuluaga J, Baptista-de-Souza D, Canto-de-Souza L Front Integr Neurosci. 2023; 17:1168640.

PMID: 37377628 PMC: 10291097. DOI: 10.3389/fnint.2023.1168640.


Dynamic θ Frequency Coordination within and between the Prefrontal Cortex-Hippocampus Circuit during Learning of a Spatial Avoidance Task.

Dickson C, Holmes G, Barry J eNeuro. 2022; 9(2).

PMID: 35396256 PMC: 9034755. DOI: 10.1523/ENEURO.0414-21.2022.

References
1.
Jay T, Glowinski J, Thierry A . Selectivity of the hippocampal projection to the prelimbic area of the prefrontal cortex in the rat. Brain Res. 1989; 505(2):337-40. DOI: 10.1016/0006-8993(89)91464-9. View

2.
Herman J, Cullinan W, Young E, Akil H, Watson S . Selective forebrain fiber tract lesions implicate ventral hippocampal structures in tonic regulation of paraventricular nucleus corticotropin-releasing hormone (CRH) and arginine vasopressin (AVP) mRNA expression. Brain Res. 1992; 592(1-2):228-38. DOI: 10.1016/0006-8993(92)91680-d. View

3.
Broadbent N, Squire L, Clark R . Spatial memory, recognition memory, and the hippocampus. Proc Natl Acad Sci U S A. 2004; 101(40):14515-20. PMC: 521976. DOI: 10.1073/pnas.0406344101. View

4.
Ferbinteanu J, Ray C, McDonald R . Both dorsal and ventral hippocampus contribute to spatial learning in Long-Evans rats. Neurosci Lett. 2003; 345(2):131-5. DOI: 10.1016/s0304-3940(03)00473-7. View

5.
Potvin O, Allen K, Thibaudeau G, Dore F, Goulet S . Performance on spatial working memory tasks after dorsal or ventral hippocampal lesions and adjacent damage to the subiculum. Behav Neurosci. 2006; 120(2):413-22. DOI: 10.1037/0735-7044.120.2.413. View