Aerosolized oxytocin increases cerebrospinal fluid oxytocin in rhesus macaques

• Authors: Meera E. Modi, Emory University; Fawn Connor-Stroud, Emory University; Rainer Landgraf, Max Planck Institute of Psychiatry; Larry Young, Emory University; Lisa Parr, Emory University
• Journal Title: Psychoneuroendocrinology
• Volume: Volume 45
• Publisher: Elsevier | 2014-07-01, Pages 49-57
• Type of Work: Article | Post-print: After Peer Review
• Publisher DOI: http://doi.org/10.1016/j.psyneuen.2014.02.011
• Subjects: Biology, Neuroscience; Biology, Zoology; Psychology, Cognitive
• Keywords: Science & Technology; Life Sciences & Biomedicine; Endocrinology & Metabolism; Neurosciences; Psychiatry; Neurosciences & Neurology; Oxytocin; Vasopressin; Social cognition; Intranasal; Autism; Rhesus monkey; INTRANASAL OXYTOCIN; PLASMA OXYTOCIN; VASOPRESSIN; NASAL; BRAIN; RELEASE; BLOOD; NEUROPEPTIDES; INTRANUCLEAR; ATTENTION

Abstract

Intranasal (IN) administration is a widely used method for examining the effect of oxytocin (OT) on social behavior and cognition in healthy subjects and psychiatric populations. IN-OT in humans enhances trust, emotional perception, and empathetic behavior and is under investigation as a potential pharmacotherapy to enhance social functioning in a variety of neuropsychiatric disorders, including autism spectrum disorders (ASD). Nonhuman primates (NHP) are an important model for understanding the effect of OT on social cognition, its neural mechanisms, and the development of IN-OT as a pharmacotherapy for treating social deficits in humans. However, NHP and even some human populations, such as very young infants and children, cannot easily follow the detailed self-administration protocol used in the majority of human IN-OT studies. Therefore, we evaluated the efficacy of several OT-administration routes for elevating central OT concentrations in rhesus macaques. First, we examined the effect of IN and intravenous (IV) routes of OT administration on concentrations of OT and vasopressin (AVP) in plasma and lumbar CSF. Second, we examined these same measures in monkeys after an aerosolized (AE) OT delivery route. All three administration routes significantly increased plasma OT concentrations, but only the AE-OT route significantly increased concentrations of CSF OT. No route affected concentrations of AVP in plasma or CSF. This study confirms that the AE route is the most effective method for increasing central OT concentrations in monkeys, and may also be an effective route, alternative to IN, for administering OT to some human populations.