Nesting behavior is associated with VIP expression and VIP-Fos colocalization in a network-wide manner

Horm Behav. 2015 Mar:69:68-81. doi: 10.1016/j.yhbeh.2014.12.010. Epub 2015 Jan 5.

Abstract

Many species, including humans, engage in a series of behaviors that are preparatory to the arrival of offspring. Such "nesting behaviors" are of obvious importance, but relevant neuroendocrine mechanisms remain little studied. We here focus on the potential roles of vasoactive intestinal polypeptide (VIP) in the performance of appetitive and consummatory nesting behaviors in male and female zebra finches (Taeniopygia guttata). Using combined immunocytochemistry for Fos and in situ hybridization for VIP, we now show that many VIP cell groups show increased transcriptional activity in response to nest building in male and female zebra finches. Particularly strong data come from the preoptic area (medial preoptic area and medial preoptic nucleus), where VIP-Fos co-expression correlates positively with three different measures of nesting behavior, as does the number of VIP-expressing cells. Remarkably, we find that VIP mRNA and/or VIP-Fos co-expression is correlated with nesting behavior in virtually every brain area that we examined, including the medial amygdala (anterior and posterior), medial bed nucleus of the stria terminalis, medial preoptic area, medial preoptic nucleus, anterior hypothalamus, ventromedial hypothalamus, periaqueductal gray complex (central gray and nucleus intercollicularis), and ventral tegmental area. Near-significant effects are also obtained in the tuberoinfundibular hypothalamus. Although most correlations are positive, negative correlations are observed for the VIP cell group of the anterior hypothalamus, a population that selectively promotes aggression, and also the periaqueductal gray complex. These data demonstrate a network-wide relationship between peptide production and social behavior that is, to our knowledge, unparalleled by other peptidergic modulators.

Keywords: Hypothalamus; Medial amygdala; Nest building; Parental care; Periaqueductal gray; Preoptic area; Vasoactive intestinal polypeptide; Zebra finch.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Aggression / physiology
  • Animals
  • Brain / metabolism*
  • Female
  • Humans
  • Immunohistochemistry
  • Male
  • Nerve Net / metabolism*
  • Nesting Behavior / physiology*
  • Proto-Oncogene Proteins c-fos / metabolism
  • Social Behavior
  • Songbirds / metabolism
  • Songbirds / physiology*
  • Tissue Distribution
  • Vasoactive Intestinal Peptide / metabolism*

Substances

  • Proto-Oncogene Proteins c-fos
  • Vasoactive Intestinal Peptide