A mechanism for rapid neurosteroidal regulation of parenting behaviour

Proc Biol Sci. 2014 Jul 7;281(1786):20140239. doi: 10.1098/rspb.2014.0239.

Abstract

While systemic steroid hormones are known to regulate reproductive behaviour, the actual mechanisms of steroidal regulation remain largely unknown. Steroidogenic enzyme activity can rapidly modulate social behaviour by influencing neurosteroid production. In fish, the enzyme 11β-hydroxysteroid dehydrogenase (11β-HSD) synthesizes 11-ketotestosterone (KT, a potent teleost androgen) and deactivates cortisol (the primary teleost glucocorticoid), and both of these steroid hormones can regulate behaviour. Here, we investigated the role of neurosteroidogenesis in regulating parenting in a haremic bidirectionally hermaphroditic fish, Lythrypnus dalli, where males provide all requisite parental care. Using an in vitro assay, we found that an 11β-HSD inhibitor, carbenoxolone (CBX), reduced brain and testicular KT synthesis by 90% or more. We modulated neurosteroid levels in parenting males via intracerebroventricular injection of CBX. Within only 20 min, CBX transiently eliminated parenting behaviour, but not other social behaviour, suggesting an enzymatic mechanism for rapid neurosteroidal regulation of parenting. Consistent with our proposed mechanism, elevating KT levels rescued parenting when paired with CBX, while cortisol alone did not affect parenting. Females paired with the experimental males opportunistically consumed unattended eggs, which reduced male reproductive success by 15%, but some females also exhibited parenting behaviour and these females had elevated brain KT. Brain KT levels appear to regulate the expression of parenting behaviour as a result of changes in neural 11β-HSD activity.

Keywords: androgen; cortisol; fish; fitness; glucocorticoid; reproduction.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • 11-beta-Hydroxysteroid Dehydrogenases / antagonists & inhibitors
  • Animals
  • Carbenoxolone / pharmacology
  • Enzyme Inhibitors / pharmacology
  • Female
  • Hydrocortisone / antagonists & inhibitors
  • Male
  • Maternal Behavior / drug effects
  • Maternal Behavior / physiology*
  • Neurosecretory Systems / drug effects
  • Neurosecretory Systems / physiology*
  • Paternal Behavior / drug effects
  • Paternal Behavior / physiology*
  • Perciformes / physiology*
  • Testosterone / analogs & derivatives
  • Testosterone / antagonists & inhibitors

Substances

  • Enzyme Inhibitors
  • Testosterone
  • 11-beta-Hydroxysteroid Dehydrogenases
  • 11-ketotestosterone
  • Carbenoxolone
  • Hydrocortisone