Socio-emotional behaviour in a VTAshSHANK3 mouse model of ASD
Détails
Télécharger: Mémoire no 4385 M. Pantone.pdf (872.82 [Ko])
Etat: Public
Version: Après imprimatur
Licence: Non spécifiée
Etat: Public
Version: Après imprimatur
Licence: Non spécifiée
Document(s) secondaire(s)
Télécharger: Mémoire no 4385 Annexes M. Pantone.pdf (85.99 [Ko])
Etat: Public
Version: de l'auteur⸱e
Licence: Non spécifiée
Etat: Public
Version: de l'auteur⸱e
Licence: Non spécifiée
ID Serval
serval:BIB_F74AE7810819
Type
Mémoire
Sous-type
(Mémoire de) maîtrise (master)
Collection
Publications
Institution
Titre
Socio-emotional behaviour in a VTAshSHANK3 mouse model of ASD
Directeur⸱rice⸱s
BELLONE C.
Codirecteur⸱rice⸱s
TZANOULINOU S.
Détails de l'institution
Université de Lausanne, Faculté de biologie et médecine
Statut éditorial
Acceptée
Date de publication
2017
Langue
anglais
Nombre de pages
36
Résumé
Social deficits and stereotyped repetitive behaviours are the two core features of autistic
spectrum disorders (ASDs) and animal models of these disorders can prove as valuable tools to
investigate their mechanisms and causes. Here, we aimed first to better characterize rewarding
aspects of social interaction in a three chambers task. Then, we developed a shorter protocol to
perform social conditioning place preference (sCPP) and tested the requirement of the conditioning
sessions to promote a sCPP by using a group of mice that underwent a trial where the contingencies
were not kept between associations of stimuli and chamber. As social interaction can be aversive too,
we developed the first protocol of social aversion place preference (sCPA) using an aggressive social
stimulus. Finally, we tested the two core domains of ASDs and anxiety that is often comorbid in these
disorders in a mouse model (shShank3) in which SHANK3 was downregulated specifically in the
ventral tegmental area (VTA) that plays a key role in social motivation. Even thought a bidirectional
social interaction is not required to promote a social preference it seems to be crucial to sustain and
improve a reciprocal motivation, which will facilitate a stable long-term relationship. Our sCPP and
sCPA protocols showed the relevance of the conditioning sessions and are time sparing. ShShank3
mice displayed social interaction deficits and repetitive behaviour but did not show any increased
anxiety compared with controls.
spectrum disorders (ASDs) and animal models of these disorders can prove as valuable tools to
investigate their mechanisms and causes. Here, we aimed first to better characterize rewarding
aspects of social interaction in a three chambers task. Then, we developed a shorter protocol to
perform social conditioning place preference (sCPP) and tested the requirement of the conditioning
sessions to promote a sCPP by using a group of mice that underwent a trial where the contingencies
were not kept between associations of stimuli and chamber. As social interaction can be aversive too,
we developed the first protocol of social aversion place preference (sCPA) using an aggressive social
stimulus. Finally, we tested the two core domains of ASDs and anxiety that is often comorbid in these
disorders in a mouse model (shShank3) in which SHANK3 was downregulated specifically in the
ventral tegmental area (VTA) that plays a key role in social motivation. Even thought a bidirectional
social interaction is not required to promote a social preference it seems to be crucial to sustain and
improve a reciprocal motivation, which will facilitate a stable long-term relationship. Our sCPP and
sCPA protocols showed the relevance of the conditioning sessions and are time sparing. ShShank3
mice displayed social interaction deficits and repetitive behaviour but did not show any increased
anxiety compared with controls.
Mots-clé
ASDs, VTA, SHANK3
Création de la notice
06/09/2018 10:59
Dernière modification de la notice
08/09/2020 6:11