TY - JOUR
T1 - Conditioned social preference, but not place preference, produced by intranasal oxytocin in female mice
AU - Kosaki, Yutaka
AU - Watanabe, Shigeru
N1 - Funding Information:
The authors declare no conflict of interest. This research was supported by grants from Japan Society for the Promotion of Science (JSPS) Grantin-aid for Scientific Research on Innovative Area (25118001) awarded to Shigeru Watanabe, and by JSPS Grant-in-aid for Scientific Research Activity Start-up (26885079) awarded to Yutaka Kosaki.
Publisher Copyright:
© 2016 American Psychological Association.
PY - 2016/4/1
Y1 - 2016/4/1
N2 - Oxytocin (OT) has been implicated in a variety of mammalian reproductive and social behaviors, and the use of intranasal OT for clinical purposes is on the rise. However, basic actions of OT, including the rewarding or reinforcing properties of the drug, are currently not fully understood. In this study, the authors investigated whether intranasally administered OT has different reinforcing properties for social and nonsocial stimuli and whether such effects are variable between male and female subjects. Conditioned social preference (CSP) and conditioned place preference (CPP) paradigms were used to examine social and nonsocial reinforcing properties of OT. In CSP, the presence of a same-sex unfamiliar conspecific was repeatedly paired with intranasal OT, while a different conspecific was associated with saline. The reinforcing effect of OT was assessed in a postconditioning choice test under a drug-free condition. In CPP, the 2 conspecifics were replaced with nonsocial black and white compartments. The authors found that intranasal OT (12 μg) in females supported the formation of CSP (Experiment 1) but not CPP (Experiment 3). Neither CSP (Experiment 2) nor CPP (Experiment 4) was formed in males. Extended conditioning with higher dose OT (36 μg), however, abolished the initial CSP in females and produced an aversion to the OT-paired stimulus mouse. Experiment 5 indicated that it was the repeated administrations rather than the higher dose that produced the abolition of the original preference. Overall, the current results demonstrate for the first time a sex- and stimulus-dependent reinforcing property of intranasal OT in mice.
AB - Oxytocin (OT) has been implicated in a variety of mammalian reproductive and social behaviors, and the use of intranasal OT for clinical purposes is on the rise. However, basic actions of OT, including the rewarding or reinforcing properties of the drug, are currently not fully understood. In this study, the authors investigated whether intranasally administered OT has different reinforcing properties for social and nonsocial stimuli and whether such effects are variable between male and female subjects. Conditioned social preference (CSP) and conditioned place preference (CPP) paradigms were used to examine social and nonsocial reinforcing properties of OT. In CSP, the presence of a same-sex unfamiliar conspecific was repeatedly paired with intranasal OT, while a different conspecific was associated with saline. The reinforcing effect of OT was assessed in a postconditioning choice test under a drug-free condition. In CPP, the 2 conspecifics were replaced with nonsocial black and white compartments. The authors found that intranasal OT (12 μg) in females supported the formation of CSP (Experiment 1) but not CPP (Experiment 3). Neither CSP (Experiment 2) nor CPP (Experiment 4) was formed in males. Extended conditioning with higher dose OT (36 μg), however, abolished the initial CSP in females and produced an aversion to the OT-paired stimulus mouse. Experiment 5 indicated that it was the repeated administrations rather than the higher dose that produced the abolition of the original preference. Overall, the current results demonstrate for the first time a sex- and stimulus-dependent reinforcing property of intranasal OT in mice.
KW - Intranasal administration
KW - Mice
KW - Oxytocin
KW - Reinforcing property
KW - Selective association
KW - Sex difference
KW - Social preference
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U2 - 10.1037/bne0000139
DO - 10.1037/bne0000139
M3 - Article
C2 - 26890248
AN - SCOPUS:84958211387
SN - 0735-7044
VL - 130
SP - 182
EP - 195
JO - Behavioral Neuroscience
JF - Behavioral Neuroscience
IS - 2
ER -