Activation of state-regulating neurochemical systems in newborn and embryonic chicks

Neuroscience. 2016 Dec 17:339:219-234. doi: 10.1016/j.neuroscience.2016.09.048. Epub 2016 Oct 4.

Abstract

Coordinated activity in different sets of widely-projecting neurochemical systems characterize waking (W) and sleep (S). How and when this coordination is achieved during development is not known. We used embryos and newborns of a precocial bird species (chickens) to assess developmental activation in different neurochemical systems using cFos expression, which has been extensively employed to examine cellular activation during S and W in adult mammals. Similarly to adult mammals, newborn awake chicks showed significantly higher cFos expression in W-active hypocretin/orexin (H/O), serotonergic Dorsal Raphe, noradrenergic Locus Coeruleus and cholinergic Laterodorsal and Pedunculopontine Tegmental (Ch-LDT/PT) neurons when compared to sleeping chicks. cFos expression was significantly correlated both between these systems, and with the amount of W. S-active melanin-concentrating hormone (MCH) neurons showed very low cFos expression with no difference between sleeping and awake chicks, possibly due to the very short duration of S episodes. In embryonic chicks, cFos expression was low or absent across all five systems at embryonic day (E) 12. Unexpectedly, a strong activation was seen at E16 in H/O neurons. The highest activation of Ch-LDT/PT (also S-active) and MCH neurons was seen at E20. These data suggest that maturation of arousal systems is achieved soon after hatching, while S-control networks are active in late chick embryos.

Keywords: cFos; chick embryo; newborn chick; sleep; waking; widely-projecting neurochemical systems.

MeSH terms

  • Acetylcholine / metabolism
  • Animals
  • Avian Proteins / metabolism
  • Blotting, Western
  • Chick Embryo
  • Chickens
  • Hypothalamic Hormones / metabolism
  • Immunohistochemistry
  • Melanins / metabolism
  • Mesencephalon / cytology
  • Mesencephalon / growth & development*
  • Mesencephalon / metabolism*
  • Microscopy, Fluorescence
  • Neurons / cytology
  • Neurons / metabolism*
  • Norepinephrine / metabolism
  • Orexins / metabolism
  • Pituitary Hormones / metabolism
  • Proto-Oncogene Proteins c-fos / metabolism
  • Random Allocation
  • Serotonin / metabolism
  • Sleep / physiology*
  • Sleep Deprivation / metabolism
  • Sleep Deprivation / pathology
  • Wakefulness / physiology*

Substances

  • Avian Proteins
  • Hypothalamic Hormones
  • Melanins
  • Orexins
  • Pituitary Hormones
  • Proto-Oncogene Proteins c-fos
  • Serotonin
  • melanin-concentrating hormone
  • Acetylcholine
  • Norepinephrine