Chapter 8 The development of the rat prefrontal cortex : Its size and development of connections with thalamus, spinal cord and other cortical areas

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This chapter focuses on the development of the rat prefrontal cortex (PFC). It also describes the size and development of connections with the thalamus, spinal cord and, other cortical areas. It also explores whether or not the prefrontal cortex has a later or prolonged development in comparison with other cortical areas. The pre- and postnatal development of the rat cerebral cortex is also reviewed in the chapter. The cortical areas that attain an adult-like myelinization pattern prior to birth all belong to sensoric/motoric areas. The development of the cortical layers, ingrowth of thalamic and dopaminergic fibers, follow a scheme of development that is comparable to that of other cortical areas. Only the volumetric development seems to point to a delayed maturation of the prefrontal areas, especially the orbital PFC. Reciprocal projection from the prefrontal cortex to the mediodorsal thalamus is largely formed during the second week of postnatal life. A way to monitor the development of the PFC is to measure its increase in size during the first postnatal months.

References (69)

  • B. Kolb et al.

    Sparing of function in rats with early prefrontal cortex lesions

    Brain Res.

    (1978)
  • C.M. Leonard

    The prefrontal cortex of the rat. I. Cortical projection of the mediodorsal nucleus. II. Efferent connections

    Brain Res.

    (1969)
  • D.D.M. O'Leary et al.

    Occipital cortical neurons with transient pyramidal tract axons extend and maintain collaterals to subcortical but not intracortical targets

    Brain Res.

    (1985)
  • D.D.M. O'Leary et al.

    A transient pyramidal tract projection from the visual cortex in the hamster and its removal by selective collateral elimination

    Dev. Brain Res.

    (1986)
  • D.D.M. O'Leary et al.

    Evidence that the early postnatal restriction of the callosal projection is due to the elimination of axonal collaterals rather than to the death of neurons

    Dev. Brain Res.

    (1981)
  • J.G. Parnavelas et al.

    The growth of nonpyramidal neurons in the visual cortex of the rat: a morphometric study

    Brain Res.

    (1980)
  • F. Valverde et al.

    Transitory population of cells in the temporal cortex of kittens

    Dev. Brain Res.

    (1987)
  • D. Wahlsten

    Prenatal schedule of appearance of mouse brain commissures

    Dev. Brain Res.

    (1981)
  • D.D.M. O'Leary et al.

    Occipital cortical neurons with transient pyramidal tract axons extend and maintain collaterals to subcortical but not intracortical targets

    Brain Res.

    (1985)
  • R.M. Beckstead

    An autoradiographic examination of corticocortical- and subcortical projections of the mediodorsal projection (prefrontal) cortex in the rat

    J. Comp. Neurol.

    (1979)
  • J.J.M. Chun et al.

    Transient cells of the developing mammalian telencephalon are peptide-immunoreactive neurons

    Nature

    (1987)
  • J.E. Crandal et al.

    Axon strata of the cerebral wall in embryonic mice

    Dev. Brain Res.

    (1984)
  • C. Dehay et al.

    Transient projections from the fronto-parietal and temporal cortex to areas 17, 18 and 19 in the kitten

    Exp. Brain Res.

    (1984)
  • A. Diamond et al.

    Comparison of human infants and rhesus monkeys on Piaget's AB task: Evidence for dependence of dorsolateral prefrontal cortex

    Exp. Brain Res.

    (1989)
  • J.T. Eayrs et al.

    Postnatal development of the cerebral cortex in the rat

    J. Anat.

    (1959)
  • P. Flechsig

    Developmental (myelogenetic) localisation of the cerebral cortex in the human subject

    Lancet

    (1901)
  • P.S. Goldman

    Developmental determinants of cortical plasticity

    Acta Neurobiol. Exp.

    (1972)
  • P.S. Goldman-Rakic et al.

    Prenatal removal of frontal association cortex in the fetal rhesus monkey: Anatomical and functional consequences in postnatal life

    Brain Res.

    (1978)
  • M.H. Hankin et al.

    Mechanisms in axonal guidance. The problem of intersecting fiber systems

  • D. Heumann et al.

    Postnatal development of the mouse cerebral neocortex. II. Quantitative cytoarchitectonics of visual and auditory areas

    J. Hirnforsch.

    (1976)
  • G.M. Innocenti

    Growth and reshaping of axons in the establishment of visual callosal connections

    Science

    (1981)
  • G.M. Innocenti

    General organization of callosal connections in the cerebral cortex

  • A. Kalsbeek, De J.P. Bruin, C., M.G. Feenstra, P. and H.B.M. Uylings, (1990) Age-dependent effects of lesioning the...
  • H.P. Killackey et al.

    Ontogenetic change in the distibution of callosal projecting neurons in the postcentral gyrus of the fetal rhesus monkey

    J. Comp. Neurol.

    (1986)
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