Grant: Operating Grant: SickKids-CIHR-IHDCYH New Investigator Grants
University of Toronto
$0.00
Early Development of the Social Brain: Implications for Autism
EF 2018-19
Résumé
Social behaviour, including how we communicate and interact with peers, is at once necessary for
survival and intrinsic to our identity. Neurodevelopmental disorders featuring social deficits, such as
autism spectrum disorders (ASD), have their onset in early childhood, and lead to devastating
consequences to children which often last their lifetime. Multiple lines of research point to conserved
brain regions associated with social processing, such as prefrontal cortex, ventral tegmental area, and
nucleus accumbens, as also being implicated in ASD symptomatology. Still, the biological mechanisms
underlying the contribution of these brain regions to ASD onset and progression is unclear. Remarkably,
even though ASD has its onset during early life, very little is known about how social brain circuits
function during early development to support the emergence of social behaviour, and even less about
how this maturation is affected in ASD patients.
Here, we will use a combination of optogenetics and electrophysiology to (1) elucidate the maturation
of synaptic transmission within isolated brain circuits underlying social behaviour, and (2) determine
how this activity is altered in an animal model of ASD. This circuit-based approach will advance our
understanding of the biological mechanisms of ASD in three ways. First, it will identify biological factors
critically necessary to support social function, which might be disrupted in ASD and other
neurodevelopmental disorders marked by social deficits. Second, examining circuit activity in a model of
ASD will pave the way to the development of novel age- and circuit-based therapeutic approaches and
diagnostic tools to combat this devastating disorder. Third, this will identify critical periods in which
social brain circuits are more susceptible to external influence. Targeting clinical interventions to these
critical periods of increased plasticity will maximize their impact on child health, significantly improving
the lives of ASD patients and their families.
Programme
Operating Grant: SickKids-CIHR-IHDCYH New Investigator Grants
Bénéficiaire
Emplacement
Ontario, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database
Tel que publié
Id
395743
Name
Arruda Carvalho Maithe
Region
Ontario
Country
Canada
Orgtype
Institution Paid; Research Institution
Partnername
Hospital for Sick Children Foundation
Prcname2
Special Cases
Projecttitle
Early Development of the Social Brain: Implications for Autism
Programtype2
Operating Grants
Orgnameinp2
University of Toronto
Cihramount2
$0
Cihrequipment2
$0
Programname2
Operating Grant: SickKids-CIHR-IHDCYH New Investigator Grants
Keyworddelim
N/A
Abstract
Social behaviour, including how we communicate and interact with peers, is at once necessary for
survival and intrinsic to our identity. Neurodevelopmental disorders featuring social deficits, such as
autism spectrum disorders (ASD), have their onset in early childhood, and lead to devastating
consequences to children which often last their lifetime. Multiple lines of research point to conserved
brain regions associated with social processing, such as prefrontal cortex, ventral tegmental area, and
nucleus accumbens, as also being implicated in ASD symptomatology. Still, the biological mechanisms
underlying the contribution of these brain regions to ASD onset and progression is unclear. Remarkably,
even though ASD has its onset during early life, very little is known about how social brain circuits
function during early development to support the emergence of social behaviour, and even less about
how this maturation is affected in ASD patients.
Here, we will use a combination of optogenetics and electrophysiology to (1) elucidate the maturation
of synaptic transmission within isolated brain circuits underlying social behaviour, and (2) determine
how this activity is altered in an animal model of ASD. This circuit-based approach will advance our
understanding of the biological mechanisms of ASD in three ways. First, it will identify biological factors
critically necessary to support social function, which might be disrupted in ASD and other
neurodevelopmental disorders marked by social deficits. Second, examining circuit activity in a model of
ASD will pave the way to the development of novel age- and circuit-based therapeutic approaches and
diagnostic tools to combat this devastating disorder. Third, this will identify critical periods in which
social brain circuits are more susceptible to external influence. Targeting clinical interventions to these
critical periods of increased plasticity will maximize their impact on child health, significantly improving
the lives of ASD patients and their families.
Competitiondate
201804
Approvedterm2
3 yrs 0 mth
Pinamesdelim
Arruda Carvalho, Maithe
Approvedterm
3 ans 0 mois