Literature DB >> 16855099

Responses to affective stimuli in monkeys with entorhinal or perirhinal cortex lesions.

Martine Meunier1, Laetitia Cirilli, Jocelyne Bachevalier.   

Abstract

Recent efforts to define the functions of the primate rhinal (entorhinal and perirhinal) cortical areas have focused on their interaction with the hippocampus in the mediation of normal memory. Less is known on the functional meaning of their strong connections to the amygdala, a key substrate for emotion. A previous study (Meunier and Bachevalier, 2002) showed evidence that complete rhinal ablations yield changes in monkeys' behavioral responses to affectively salient stimuli. Here, we studied monkeys with separate entorhinal or perirhinal ablations in the same paradigm, where responses were triggered by four stimuli: an unfamiliar human, a conspecific stimulus, a toy snake, and a familiar (generally rewarded) junk object. The two separate lesions produced similar changes, and each replicated the effects of complete rhinal lesions (i.e., attenuated affiliation and enhanced defense). Failure to modulate responses based on previous experience (i.e., memory difficulties) may explain these affective changes. This interpretation does not account, however, for the sparing of some memory-dependent modulations of defense, nor for the lack of correlation between the animals' affective changes and their own recognition memory performance. Alternatively, rhinal damage may introduce a negative bias in the risk assessment of affectively salient stimuli, a proposal more compatible with Gray and McNaughton's (2000) anxiety-centered view of medial temporal functions, than with prominent mnemonic/perceptual functional models of the hippocampal/rhinal duo. Reconciling the two perspectives may improve our understanding of rhinal functions.

Entities:  

Mesh:

Year:  2006        PMID: 16855099      PMCID: PMC6674284          DOI: 10.1523/JNEUROSCI.1949-06.2006

Source DB:  PubMed          Journal:  J Neurosci        ISSN: 0270-6474            Impact factor:   6.167


  9 in total

1.  Neonatal perirhinal cortex lesions impair monkeys' ability to modulate their emotional responses.

Authors:  Nathan S Ahlgrim; Jessica Raper; Emily Johnson; Jocelyne Bachevalier
Journal:  Behav Neurosci       Date:  2017-10       Impact factor: 1.912

2.  Brain enlargement and increased behavioral and cytokine reactivity in infant monkeys following acute prenatal endotoxemia.

Authors:  Auriel A Willette; Gabriele R Lubach; Rebecca C Knickmeyer; Sarah J Short; Martin Styner; John H Gilmore; Christopher L Coe
Journal:  Behav Brain Res       Date:  2010-12-27       Impact factor: 3.332

3.  Long-term effects of neonatal medial temporal ablations on socioemotional behavior in monkeys (Macaca mulatta).

Authors:  Ludise Malkova; Mortimer Mishkin; Stephen J Suomi; Jocelyne Bachevalier
Journal:  Behav Neurosci       Date:  2010-12       Impact factor: 1.912

4.  Impact of amygdala, orbital frontal, or hippocampal lesions on threat avoidance and emotional reactivity in nonhuman primates.

Authors:  Christopher J Machado; Andy M Kazama; Jocelyne Bachevalier
Journal:  Emotion       Date:  2009-04

5.  Entorhinal cortex inhibits medial prefrontal cortex and modulates the activity states of electrophysiologically characterized pyramidal neurons in vivo.

Authors:  Ornella Valenti; Anthony A Grace
Journal:  Cereb Cortex       Date:  2008-07-16       Impact factor: 5.357

6.  Behavioral and hormonal reactivity to threat: effects of selective amygdala, hippocampal or orbital frontal lesions in monkeys.

Authors:  Christopher J Machado; Jocelyne Bachevalier
Journal:  Psychoneuroendocrinology       Date:  2008-07-22       Impact factor: 4.905

7.  Structural connections support emotional connections: Uncinate Fasciculus microstructure is related to the ability to decode facial emotion expressions.

Authors:  Bethany M Coad; Mark Postans; Carl J Hodgetts; Nils Muhlert; Kim S Graham; Andrew D Lawrence
Journal:  Neuropsychologia       Date:  2017-11-06       Impact factor: 3.139

8.  Behavioral and neuroanatomical abnormalities in pleiotrophin knockout mice.

Authors:  Jason W Krellman; Henry H Ruiz; Veronica A Marciano; Bracha Mondrow; Susan D Croll
Journal:  PLoS One       Date:  2014-07-07       Impact factor: 3.240

9.  Tactile modulation of memory and anxiety requires dentate granule cells along the dorsoventral axis.

Authors:  Chi Wang; Hui Liu; Kun Li; Zhen-Zhen Wu; Chen Wu; Jing-Ying Yu; Qian Gong; Ping Fang; Xing-Xing Wang; Shu-Min Duan; Hao Wang; Yan Gu; Ji Hu; Bing-Xing Pan; Mathias V Schmidt; Yi-Jun Liu; Xiao-Dong Wang
Journal:  Nat Commun       Date:  2020-11-27       Impact factor: 14.919

  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.