TY - JOUR
T1 - A comprehensive assay of social motivation reveals sex-specific roles of autism-associated genes and oxytocin
AU - Maloney, Susan E.
AU - Sarafinovska, Simona
AU - Weichselbaum, Claire
AU - McCullough, Katherine B.
AU - Swift, Raylynn G.
AU - Liu, Yating
AU - Dougherty, Joseph D.
N1 - Funding Information:
We would like to thank Dr. John Constantino for guidance; Drs. Adrian Gomez, Kyle Parker, Ream Al-Hasani, and Daniel Castro for operant paradigm training; Kyle Kneipkamp for assistance designing and creating custom chambers; and Drs. Elena Minakova and Kayla Nygaard for surgery training. This work was generously supported by the NICHD P50HD103525 (IDDRC@WUSTL), NIMH R01MH107515-05 and R01MH124808 (J.D.D.), and the Autism Science Foundation (22-007 to S.S.).
Publisher Copyright:
© 2023 The Authors
PY - 2023/6/26
Y1 - 2023/6/26
N2 - Social motivation is critical to the development of typical social functioning. Social motivation, specifically one or more of its components (e.g., social reward seeking or social orienting), could be relevant for understanding phenotypes related to autism. We developed a social operant conditioning task to quantify effort to access a social partner and concurrent social orienting in mice. We established that mice will work for access to a social partner, identified sex differences, and observed high test-retest reliability. We then benchmarked the method with two test-case manipulations. Shank3B mutants exhibited reduced social orienting and failed to show social reward seeking. Oxytocin receptor antagonism decreased social motivation, consistent with its role in social reward circuitry. Overall, we believe that this method provides a valuable addition to the assessment of social phenotypes in rodent models of autism and the mapping of potentially sex-specific social motivation neural circuits.
AB - Social motivation is critical to the development of typical social functioning. Social motivation, specifically one or more of its components (e.g., social reward seeking or social orienting), could be relevant for understanding phenotypes related to autism. We developed a social operant conditioning task to quantify effort to access a social partner and concurrent social orienting in mice. We established that mice will work for access to a social partner, identified sex differences, and observed high test-retest reliability. We then benchmarked the method with two test-case manipulations. Shank3B mutants exhibited reduced social orienting and failed to show social reward seeking. Oxytocin receptor antagonism decreased social motivation, consistent with its role in social reward circuitry. Overall, we believe that this method provides a valuable addition to the assessment of social phenotypes in rodent models of autism and the mapping of potentially sex-specific social motivation neural circuits.
KW - CP: Neuroscience
KW - Shank3b
KW - autism
KW - behavioral assay
KW - mice
KW - operant conditioning
KW - oxytocin
KW - sex differences
KW - sociability
KW - social motivation
UR - http://www.scopus.com/inward/record.url?scp=85162920383&partnerID=8YFLogxK
U2 - 10.1016/j.crmeth.2023.100504
DO - 10.1016/j.crmeth.2023.100504
M3 - Article
C2 - 37426756
AN - SCOPUS:85162920383
SN - 2667-2375
VL - 3
JO - Cell Reports Methods
JF - Cell Reports Methods
IS - 6
M1 - 100504
ER -