Abstract

We addressed the question how long salivary oxytocin levels remain elevated after intranasal administration, and whether it makes a difference when 16 or 24 IU of oxytocin administration is used. Oxytocin levels were measured in saliva samples collected from 46 female participants right before intranasal administration (at 9:30 a.m.) of 16 IU (n = 18) or 24 IU (n = 10) of oxytocin, or a placebo (n = 18), and each hour after administration, for 7 h in total. Oxytocin levels did not differ among conditions before use of the nasal spray. Salivary oxytocin levels in the placebo group showed high stability across the day. After oxytocin administration oxytocin levels markedly increased, they peaked around 1 h after administration, and were still significantly elevated 7 h after administration. The amount of oxytocin (16 or 24 IU) did not make a difference for oxytocin levels. The increase of oxytocin levels for at least 7 h shows how effective intranasal administration of oxytocin is. Our findings may raise ethical questions about potentially persisting behavioral effects after participants have left the lab setting. More research into the long-term neurological and behavioral effects of sniffs of oxytocin is urgently needed.

Highlights

  • Baseline OT levels were similar for the three groups, F (2, 45) = 0.28, p = 0.754, but at all time points after administration of either placebo or oxytocin (16 or 24 IU) participants in the oxytocin conditions showed much higher levels of salivary OT, see Figure 1B

  • Seven hours after administration the level of OT had not yet returned to baseline; it was still six to tenfold higher than OT levels observed in the placebo condition

  • In the placebo condition salivary OT levels were highly correlated over time, indicating an impressive individual stability of OT levels over the day

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Summary

Introduction

Intranasal oxytocin (OT) administration is used in numerous experimental studies to investigate the role of this neuropeptide in neural activation, information processing, and behavior (e.g., Insel, 1992; Carter, 2003; Parker et al, 2005; Feldman et al., 2007; Campbell, 2008; De Dreu et al, 2010; Naber et al, 2010; for reviews see Heinrichs et al, 2009; MacDonald and MacDonald, 2010; Bartz et al, 2011; Galbally et al, 2011; for a meta-analysis see Van IJzendoorn and Bakermans-Kranenburg, 2012). We examine the influence of 16 or 24 IU OT on salivary OT levels in the course of the day in a sample of healthy female participants. The study included 57 female participants who provided saliva samples right before, approximately

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