A Methodology for Studying Social Stimulus Functions in Children

Author(s):  
William H. Redd ◽  
Andrew S. Winston ◽  
Edward K. Morris
Keyword(s):  
2009 ◽  
Vol 27 (4) ◽  
pp. 287-306 ◽  
Author(s):  
Karen Louise Smith ◽  
Masashi Crete-Nishihata ◽  
Thecla Damianakis ◽  
Ronald M. Baecker ◽  
Elsa Marziali

2021 ◽  
Author(s):  
Julia Pinho ◽  
Vincent T. Cunliffe ◽  
Giovanni Petri ◽  
Rui Oliveira

Group living animals can use social and asocial cues to predict the presence of a reward or a punishment in the environment through associative learning. The degree to which social and asocial learning share the same mechanisms is still a matter of debate, and, so far, studies investigating the neuronal basis of these two types of learning are scarce and have been restricted to primates, including humans, and rodents. Here we have used a Pavlovian fear conditioning paradigm in which a social (fish image) or an asocial (circle image) conditioned stimulus (CS) have been paired with an unconditioned stimulus (US=food), and we have used the expression of the immediate early gene c-fos to map the neural circuits associated with social and asocial learning. Our results show that the learning performance is similar with social (fish image) and asocial (circle image) CSs. However, the brain regions involved in each learning type are distinct. Social learning is associated with an increased expression of c-fos in olfactory bulbs, ventral zone of ventral telencephalic area, ventral habenula and ventromedial thalamus, whereas asocial learning is associated with a decreased expression of c-fos in dorsal habenula and anterior tubercular nucleus. Using egonetworks, we further show that each learning type has an associated pattern of functional connectivity across brain regions. Moreover, a community analysis of the network data reveals four segregated functional submodules, which seem to be associated with different cognitive functions involved in the learning tasks: a generalized attention module, a visual response module, a social stimulus integration module and a learning module. Together, these results suggest that, although there are localized differences in brain activity between social and asocial learning, the two learning types share a common learning module and social learning also recruits a specific social stimulus integration module. Therefore, our results support the occurrence of a common general-purpose learning module, that is differentially modulated by localized activation in social and asocial learning.


2011 ◽  
pp. 331-383
Author(s):  
Daniel Katz ◽  
Richard L. Schanck

2019 ◽  
Vol 9 (1) ◽  
Author(s):  
Uwe Mayer ◽  
Orsola Rosa-Salva ◽  
Jasmine L. Loveland ◽  
Giorgio Vallortigara

1945 ◽  
Vol 36 (6) ◽  
pp. 344-351 ◽  
Author(s):  
C. Mitchell

2007 ◽  
Vol 87 (3) ◽  
pp. 341-348 ◽  
Author(s):  
Arthur Tomie ◽  
Kandia Lewis ◽  
Jodi Curiotto ◽  
Larissa A. Pohorecky

2020 ◽  
Vol 14 ◽  
Author(s):  
Fernanda Teixeira Ribeiro ◽  
Marcia Ivany Silva de Serro-Azul ◽  
Fernanda Beraldo Lorena ◽  
Bruna Pascarelli Pedrico do Nascimento ◽  
Alexandre José Tavolari Arnold ◽  
...  

The early life status epilepticus (SE) causes high anxiety and chronic socialization abnormalities, revealed by a low preference for social novelty and deficit in social discrimination. This study investigated the involvement of the endocannabinoid system on the sociability in this model, due to its role in social motivation regulation. Male Wistar rats at postnatal day 9 were subjected to pilocarpine-induced neonatal SE and controls received saline. From P60 the groups received vehicle or JZL195 2 h before each behavioral test to increase endocannabinoids availability. In the sociability test, animals subjected to neonatal SE exhibited impaired sociability, characterized by social discrimination deficit, which was unaffected by the JZL195 treatment. In contrast, JZL195-treated control rats showed low sociability and impaired social discrimination. The negative impact of JZL195 over the sociability in control rats and the lack of effect in animals subjected to neonatal SE was confirmed in the social memory paradigm. In this paradigm, as expected for vehicle-treated control rats, the investigation toward the same social stimulus decreased with the sequential exposition and increased toward a novel stimulus. In animals subjected to neonatal SE, regardless of the treatment, as well as in JZL195-treated control rats, the investigation toward the same social stimulus was significantly reduced with no improvement toward a novel stimulus. Concerning the locomotion, the JZL195 increased it only in control rats. After behavioral tests, brain tissues of untreated animals were used for CB1 receptor quantification by Elisa and for gene expression by RT-PCR: no difference between control and experimental animals was noticed. The results reinforce the evidence that the early SE causes chronic socialization abnormalities, revealed by the low social interest for novelty and impaired social discrimination. The dual FAAH/MAGL inhibitor (JZL195) administration before the social encounter impaired the social interaction in intact rats with no effect in animals subjected to early-life seizures.


2017 ◽  
pp. 92-99
Author(s):  
B. K. Kanthamani
Keyword(s):  

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