Research report
An in vivo electrophysiological study of the ontogeny of excitatory and inhibitory processes in the rat hippocampus

https://doi.org/10.1016/0165-3806(89)90113-2Get rights and content

Abstract

Although several studies have compared hippocampal slices from young vs adult rats, a systematic in vivo characterization of the ontogeny of electrophysiologic responses in this structure has not been done. The current report describes the postnatal development of excitatory and inhibitory responses in the CA1 region of the hippocampus in rats 7–65 days of age. Under urethane anesthesia, a recording electrode was placed in one CA1 region to measure extracellular population spikes elicited by stimulation of the contralateral CA3 region. Age-related changes in the maximal population spike amplitude, the voltage required to elicit a half-maximal amplitude spike, the width at half-maximal spike amplitude, and latency to onset of the population spike (‘conduction velocity’) were monitored as parameters describing excitatory processes in the hippocampus. A paired-pulse paradigm was used to quantify the ontogeny of inhibitory processes. In younger animals, population spikes were broader, smaller in amplitude, and required higher stimulus intensities to be elicited. After postnatal (PN) day 14, excitability (voltage to elicit half-maximal population spike) and spike width were at fully mature levels. Maximal spike amplitudes were also smaller in rats younger than PN14, but not thereafter. The conduction velocity parameter steadily increased during development. In contrast, no evidence of inhibition was found prior to PN18, after which it steadily increased to reach adult levels by PN28. These results indicate that, in the rat hippocampus, excitatory processes are well established or fully mature within 2 weeks following birth, whereas the maturation of inhibitory processes to adult levels is not achieved until several weeks later.

References (37)

  • P.A. Schwartzkroin et al.

    Development of kitten hippocampal neurons

    Brain Res.

    (1977)
  • O.C. Snead et al.

    Ontogeny of cortical and subcortical electroencephalographic events in unrestrained neonatal and infant rats

    Exp. Neurol.

    (1983)
  • P.T.-N. Wong et al.

    Postnatal changes of GABAergic and glutamatergic parameters

    Dev. Brain Res.

    (1981)
  • H.C. Agrawal et al.

    Postnatal changes in free amino acid pool of rat brain

    J. Neurochem.

    (1966)
  • B.E. Alger et al.

    Feedforward dendritic inhibition in rat hippocampal pyramidal cells studied in vitro

    J. Physiol. (Lond.)

    (1982)
  • P. Andersen et al.

    Unit analysis of hippocampal population spikes

    Exp. Brain Res.

    (1971)
  • P. Andersen et al.

    Location of postsynaptic inhibitory synapses on hippocampal pyramids

    J. Neurophysiol.

    (1964)
  • J.B. Angevine

    Time of neuron origin in the hippocampal region. An autoradiographic study in the mouse

    Exp. Neurol.

    (1965)
  • Cited by (96)

    • Age and sex-dependent differences in activity, plasticity and response to stress in the dentate gyrus

      2013, Neuroscience
      Citation Excerpt :

      Maturation includes an expansion of the molecular cell layer of the dentate gyrus by approximately 50% during rat juvenility and adolescence. Concomitant with this expansion, dendritic length increases and, notably, the number of dendritic segments decreases (Rihn and Claiborne, 1990), resulting in a functionally mature network (Michelson and Lothman, 1989). On a molecular level, age-related changes were reported for several receptors (Insel et al., 1990; Monyer et al., 1994; Kirson and Yaari, 1996; Rissman et al., 2006).

    • Functional and morphological changes in the dentate gyrus after experimental status epilepticus

      2008, Seizure
      Citation Excerpt :

      Post-synaptically, enhanced expression and altered function of glutamate receptors30,31 or changes in sodium or calcium currents32,33 could be responsible for the change observed in vivo. In keeping with the current results, a reduced discharge latency of evoked potentials in vivo has been seen in the context of increased excitability in the dentate gyrus.34–36 We conclude from this finding that in vivo changes in PS latencies may be used as parameters to assess excitability in this structure.

    • New drugs in the treatment of epilepsy in children

      2005, Current Problems in Pediatric and Adolescent Health Care
    View all citing articles on Scopus
    View full text