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. 2009 Jun 17;31(4):332–341. doi: 10.1159/000216544

Table 2.

Effects in later life of postnatal day 1 exposure to a single injection of OT (oxytocin, low dose = 3 or 6 μg; high dose = 12 or 24 μg), or OT antagonist (OTA, 0.3 ng) in prairie voles

Neonatal treatment OT (low dose), males OT (low dose), females OT (high dose), females OTA, males OTA, females
Anxiety (EPM) ↓ 3 μg NC NC NC NC
Alloparental behavior ↑ 3 μg NC 1 NC
Pair-bond formation ↑ 3 μg ↑ 6 μg ↓ 12–24 μg NC NC
OT-ir, PVN NC ↑ 3 μg NA NC
AVP-ir, PVN NC NC NA
OTR NC NC NA NC NC
AVP V1aR 3 μg ∗∗ 3 μg NA ∗∗∗ ∗∗∗∗

See table 1 for other abbreviations. In comparison to either saline or handled controls (which did not differ from each other).

↑ = Significant increase; ↓ = significant decrease.

In neonatal OT (3 μg) group males,

Effects of higher doses of OT for males are available only for pair-bond formation. While a 3-μg dose facilitated pair-bonding in males [Bales and Carter, 2003b], males given a 6-μg dose showed no pair-bond, and a 12-μg dose reinstated the bond [Carter et al., 2008].

1

Trend to increase.

AVP V1a R was increased in the ventral pallidum and cingulate cortex (CgCtx), and in females,

∗∗

reduced in the medial preoptic area (mPOA), bed nucleus of the stria terminalis (BNST), lateral septum (LS), CgCtx and medial thalamus. In the neonatal OTA (0.3 μg) male group

∗∗∗

AVP V1aR was reduced in the mPOA, BNST and lateral septum, and in the female group, it was

∗∗∗∗

reduced in BNST and CgCtx.