Titi Monkeys as a Novel Non-Human Primate Model for the Neurobiology of Pair Bonding

Yale J Biol Med. 2017 Sep 25;90(3):373-387. eCollection 2017 Sep.

Abstract

It is now widely recognized that social bonds are critical to human health and well-being. One of the most important social bonds is the attachment relationship between two adults, known as the pair bond. The pair bond involves many characteristics that are inextricably linked to quality of health, including providing a secure psychological base and acting as a social buffer against stress. The majority of our knowledge about the neurobiology of pair bonding comes from studies of a socially monogamous rodent, the prairie vole (Microtus ochrogaster), and from human imaging studies, which inherently lack control. Here, we first review what is known of the neurobiology of pair bonding from humans and prairie voles. We then present a summary of the studies we have conducted in titi monkeys (Callicebus cupreus)-a species of socially monogamous New World primates. Finally, we construct a neural model based on the location of neuropeptide receptors in the titi monkey brain, as well as the location of neural changes in our imaging studies, with some basic assumptions based on the prairie vole model. In this model, we emphasize the role of visual mating stimuli as well as contributions of the dopaminergic reward system and a strong role for the lateral septum. This model represents an important step in understanding the neurobiology of social bonds in non-human primates, which will in turn facilitate a better understanding of these mechanisms in humans.

Keywords: dopamine; opioids; oxytocin; pair bond; prairie vole; relationships; social monogamy; vasopressin.

Publication types

  • Review
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Analgesics, Opioid / metabolism
  • Animals
  • Arvicolinae / metabolism*
  • Dopamine / metabolism
  • Neurobiology / methods*
  • Oxytocin / metabolism
  • Pair Bond*
  • Primates
  • Vasopressins / metabolism

Substances

  • Analgesics, Opioid
  • Vasopressins
  • Oxytocin
  • Dopamine