Developmental changes in synaptic distribution in arcuate nucleus neurons

J Neurosci. 2015 Jun 3;35(22):8558-69. doi: 10.1523/JNEUROSCI.0058-15.2015.

Abstract

Neurons coexpressing neuropeptide Y, agouti-related peptide, and GABA (NAG) play an important role in ingestive behavior and are located in the arcuate nucleus of the hypothalamus. NAG neurons receive both GABAergic and glutamatergic synaptic inputs, however, the developmental time course of synaptic input organization of NAG neurons in mice is unknown. In this study, we show that these neurons have low numbers of GABAergic synapses and that GABA is inhibitory to NAG neurons during early postnatal period. In contrast, glutamatergic inputs onto NAG neurons are relatively abundant by P13 and are comparatively similar to the levels observed in the adult. As mice reach adulthood (9-10 weeks), GABAergic tone onto NAG neurons increases. At this age, NAG neurons received similar numbers of inhibitory and EPSCs. To further differentiate age-associated changes in synaptic distribution, 17- to 18-week-old lean and diet-induced obesity (DIO) mice were studied. Surprisingly, NAG neurons from lean adult mice exhibit a reduction in the GABAergic synapses compared with younger adults. Conversely, DIO mice display reductions in the number of GABAergic and glutamatergic inputs onto NAG neurons. Based on these experiments, we propose that synaptic distribution in NAG neurons is continuously restructuring throughout development to accommodate the animals' energy requirements.

Keywords: NAG neurons; arcuate; development; obesity; synaptic inputs.

Publication types

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

MeSH terms

  • 2-Amino-5-phosphonovalerate / pharmacology
  • 6-Cyano-7-nitroquinoxaline-2,3-dione / pharmacology
  • Age Factors
  • Animals
  • Animals, Newborn
  • Arcuate Nucleus of Hypothalamus / cytology*
  • Arcuate Nucleus of Hypothalamus / growth & development*
  • Excitatory Amino Acid Antagonists / pharmacology
  • Excitatory Postsynaptic Potentials / drug effects
  • Excitatory Postsynaptic Potentials / genetics
  • Female
  • Inhibitory Postsynaptic Potentials / drug effects
  • Inhibitory Postsynaptic Potentials / genetics
  • Lysine / analogs & derivatives
  • Lysine / metabolism
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Neurons / physiology*
  • Neuropeptide Y / genetics
  • Neuropeptide Y / metabolism
  • Sodium Channel Blockers / pharmacology
  • Synapses / drug effects
  • Synapses / genetics
  • Synapses / physiology*
  • Tetrodotoxin / pharmacology
  • Vesicular Inhibitory Amino Acid Transport Proteins / metabolism
  • gamma-Aminobutyric Acid / pharmacology

Substances

  • Excitatory Amino Acid Antagonists
  • Neuropeptide Y
  • Sodium Channel Blockers
  • Vesicular Inhibitory Amino Acid Transport Proteins
  • Tetrodotoxin
  • gamma-Aminobutyric Acid
  • 6-Cyano-7-nitroquinoxaline-2,3-dione
  • 2-Amino-5-phosphonovalerate
  • biocytin
  • Lysine