Literature DB >> 28017854

The effects of neonatal amygdala or hippocampus lesions on adult social behavior.

Eliza Bliss-Moreau1, Gilda Moadab2, Anthony Santistevan2, David G Amaral3.   

Abstract

The present report details the final phase of a longitudinal evaluation of the social behavior in a cohort of adult rhesus monkeys that received bilateral neurotoxic lesions of the amygdala or hippocampus, or sham operations at 2 weeks of age. Results were compared to previous studies in which adult animals received amygdala lesions and were tested in a similar fashion. Social testing with four novel interaction partners occurred when the animals were between 7 and 8 years of age. Experimental animals interacted with two male and two female partners in two conditions - one in which physical access was restricted (the constrained social access condition) and a second in which physical access was unrestricted (the unconstrained social access condition). Across conditions and interaction partners, there were no significant effects of lesion condition on the frequency or duration of social interactions. As a group, the hippocampus-lesioned animals generated the greatest number of communicative signals during the constrained social access condition. Amygdala-lesioned animals generated more frequent stress-related behaviors and were less exploratory. Amygdala and hippocampus-lesioned animals demonstrated greater numbers of stereotypies than control animals. Subtle, lesion-based differences in the sequencing of behaviors were observed. These findings suggest that alterations of adult social behavior are much less prominent when damage to the amygdala occurs early in life rather than in adulthood.
Copyright © 2016 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Amygdala; Development; Hippocampus; Macaca mulatta; Rhesus macaque; Social behavior

Mesh:

Substances:

Year:  2016        PMID: 28017854      PMCID: PMC5423538          DOI: 10.1016/j.bbr.2016.11.052

Source DB:  PubMed          Journal:  Behav Brain Res        ISSN: 0166-4328            Impact factor:   3.332


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