Long-term potentiation in the neonatal rat barrel cortex in vivo

J Neurosci. 2012 Jul 11;32(28):9511-6. doi: 10.1523/JNEUROSCI.1212-12.2012.

Abstract

Long-term potentiation (LTP) is important for the activity-dependent formation of early cortical circuits. In the neonatal rodent barrel cortex, LTP has been studied only in vitro. We combined voltage-sensitive dye imaging with extracellular multielectrode recordings to study whisker stimulation-induced LTP in the whisker-to-barrel cortex pathway of the neonatal rat barrel cortex in vivo. Single whisker stimulation at 2 Hz for 10 min induced an age-dependent expression of LTP in postnatal day (P) 0 to P14 rats, with the strongest expression of LTP at P3-P5. The magnitude of LTP was largest in the activated barrel-related column, smaller in the surrounding septal region, and no LTP could be observed in the neighboring barrel. Current source density analyses revealed an LTP-associated increase of synaptic current sinks in layer IV/lower layer II/III at P3-P5 and in the cortical plate/upper layer V at P0-P1. Our study demonstrates for the first time an age-dependent and spatially confined LTP in the barrel cortex of the newborn rat in vivo.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Afferent Pathways / physiology
  • Age Factors
  • Animals
  • Animals, Newborn
  • Biophysics
  • Electric Stimulation
  • Evoked Potentials, Somatosensory / physiology*
  • In Vitro Techniques
  • Long-Term Potentiation / physiology*
  • Neurons / physiology*
  • Patch-Clamp Techniques
  • Rats
  • Serotonin Plasma Membrane Transport Proteins / metabolism
  • Somatosensory Cortex / cytology*
  • Somatosensory Cortex / physiology
  • Statistics, Nonparametric
  • Vibrissae / innervation
  • Voltage-Sensitive Dye Imaging / methods

Substances

  • Serotonin Plasma Membrane Transport Proteins