» Articles » PMID: 25451454

Anisomycin Administered in the Olfactory Bulb and Dorsal Hippocampus Impaired Social Recognition Memory Consolidation in Different Time-points

Overview
Journal Brain Res Bull
Specialty Neurology
Date 2014 Dec 3
PMID 25451454
Citations 12
Authors
Affiliations
Soon will be listed here.
Abstract

To identify an individual as familiar, rodents form a specific type of memory named social recognition memory. The olfactory bulb (OB) is an important structure for social recognition memory, while the hippocampus recruitment is still controversial. The present study was designed to elucidate the OB and the dorsal hippocampus contribution to the consolidation of social memory. For that purpose, we tested the effect of anisomycin (ANI), which one of the effects is the inhibition of protein synthesis, on the consolidation of social recognition memory. Swiss adult mice with cannulae implanted into the CA1 region of the dorsal hippocampus or into the OB were exposed to a juvenile during 5 min (training session; TR), and once again 1.5 h or 24 h later to test social short-term memory (S-STM) or social long-term memory (S-LTM), respectively. To study S-LTM consolidation, mice received intra-OB or intra-CA1 infusion of saline or ANI immediately, 3, 6 or 18 h after TR. ANI impaired S-LTM consolidation in the OB, when administered immediately or 6h after TR. In the dorsal hippocampus, ANI was amnesic only if administered 3 h after TR. Furthermore, the infusion of ANI in either OB or CA1, immediately after training, did not affect S-STM. Moreover, ANI administered into the OB did not alter the animal's performance in the buried food-finding task. Altogether, our results suggest the consolidation of S-LTM requires both OB and hippocampus participation, although in different time points. This study may help shedding light on the specific roles of the OB and dorsal hippocampus in social recognition memory.

Citing Articles

Autistic behavior is a common outcome of biallelic disruption of PDZD8 in humans and mice.

Pantiru A, Van de Sompele S, Ligneul C, Chatelain C, Barrea C, Lerch J Mol Autism. 2025; 16(1):14.

PMID: 40016860 PMC: 11866840. DOI: 10.1186/s13229-025-00650-8.


Tetrandrine alleviates inflammation and neuron apoptosis in experimental traumatic brain injury by regulating the IRE1α/JNK/CHOP signal pathway.

Liu H, He S, Li C, Wang J, Zou Q, Liao Y Brain Behav. 2022; 12(12):e2786.

PMID: 36377337 PMC: 9759135. DOI: 10.1002/brb3.2786.


The Influence of Social Isolation on Social Orientation, Sociability, Social Novelty Preference, and Hippocampal Parvalbumin-Expressing Interneurons in Peripubertal Rats - Understanding the Importance of Meeting Social Needs in Adolescence.

Potrebic M, Pavkovic Z, Puskas N, Pesic V Front Behav Neurosci. 2022; 16:872628.

PMID: 35592640 PMC: 9113078. DOI: 10.3389/fnbeh.2022.872628.


A Temporal Activity of CA1 Neurons Underlying Short-Term Memory for Social Recognition Altered in PTEN Mouse Models of Autism Spectrum Disorder.

Chai A, Chen X, Xu X, Zhang N, Li M, Li J Front Cell Neurosci. 2021; 15:699315.

PMID: 34335191 PMC: 8319669. DOI: 10.3389/fncel.2021.699315.


The mTORC1 inhibitor rapamycin and the mTORC1/2 inhibitor AZD2014 impair the consolidation and persistence of contextual fear memory.

MacCallum P, Blundell J Psychopharmacology (Berl). 2020; 237(9):2795-2808.

PMID: 32601986 DOI: 10.1007/s00213-020-05573-1.