Neonatal melanocortin receptor agonist treatment reduces play fighting and promotes adult attachment in prairie voles in a sex-dependent manner.
Neonatal melanocortin receptor agonist treatment reduces play fighting and promotes adult attachment in prairie voles in a sex-dependent manner.
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DOI:
10.1016/j.neuropharm.2014.05.041
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发表时间:
2014-10
影响因子:
4.7
通讯作者:
Young LJ
中科院分区:
文献类型:
--
作者:
Barrett CE;Modi ME;Zhang BC;Walum H;Inoue K;Young LJ
The melanocortin receptor (MCR) system has been studied extensively for its role in feeding and sexual behavior, but effects on social behavior have received little attention. α-MSH interacts with neural systems involved in sociality, including oxytocin, dopamine, and opioid systems. Acute melanotan-II (MTII), an MC3/4R agonist, potentiates brain oxytocin (OT) release and facilitates OT-dependent partner preference formation in socially monogamous prairie voles. Here we examined the long-term impact of early-life MCR stimulation on hypothalamic neuronal activity and social development in prairie voles. Male and female voles were given daily subcutaneous injections of 10 mg/kg MTII or saline between postnatal days (PND) 1-7. Neonatally-treated males displayed a reduction in initiated play fighting bouts as juveniles compared to control males. Neonatal exposure to MTII facilitated partner preference formation in adult females, but not males, after a brief cohabitation with an opposite-sex partner. Acute MTII injection elicited a significant burst of the immediate early gene EGR-1 immunoreactivity in hypothalamic OT, vasopressin, and corticotrophin releasing factor neurons, when tested in PND 6-7 animals. Daily neonatal treatment with 1 mg/kg of a more selective, brain penetrant MC4R agonist, PF44687, promoted adult partner preferences in both females and males compared with vehicle controls. Thus, developmental exposure to MCR agonists lead to a persistent change in social behavior, suggestive of structural or functional changes in the neural circuits involved in the formation of social relationships.
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影响因子:
2.9
作者:
Carter, C. Sue;Boone, Ericka M.;Bales, Karen L.
通讯作者:
Bales, Karen L.
影响因子:
3
作者:
ACKER, GR;BERRAN, J;STRAND, FL
通讯作者:
STRAND, FL
影响因子:
3.6
作者:
CHAMPNEY, TF;SAHLEY, TL;SANDMAN, CA
通讯作者:
SANDMAN, CA
影响因子:
3
作者:
ARLETTI, R;BENELLI, A;BERTOLINI, A
通讯作者:
BERTOLINI, A
影响因子:
4.1
作者:
Dhillo, WS;Small, CJ;Bloom, SR
通讯作者:
Bloom, SR