Literature DB >> 7814692

Patterning of the neocortical projections from the raphe nuclei in perinatal rats: investigation of potential organizational mechanisms.

C A Bennett-Clarke1, M H Hankin, M J Leslie, N L Chiaia, R W Rhoades.   

Abstract

Serotoninergic (5-HT) fibers in the cerebral cortex of perinatal rats have a pattern that coincides with the boundaries of primary sensory areas and within the primary somatosensory cortex form the rattunculus. This patterned immunoreactivity (IR) appears about 60 hours after birth and disappears between postnatal days (P-) 12 and 15. Three experiments were carried out to evaluate mechanisms that might underlie the precise patterning of the 5-HT-IR. Retrograde labelling with fluorescent tracers in perinatal rats revealed only a coarse rostrocaudal topography in the raphe-cortical projection and the existence of raphe cells projecting to multiple cortical locations. Thus, a precise point-to-point, raphe-cortical projection does not underlie the patterned cortical 5-HT-IR. Ablation of the thalamus prior to the age at which patterned 5-HT-IR could be seen in the developing cortex caused a complete loss of patterned immunoreactivity. This suggests that 5-HT fibers may require the presence of thalamocortical axons to achieve the pattern observed in normal animals. Serotoninergic raphe neurons transplanted to the cortices of newborn rats exhibited extensive axonal outgrowth, but did not form a somatotopic pattern. This result also suggests that specific spatiotemporal interactions between growing 5-HT and thalamocortical axons may be necessary for the somatotopic patterning of the former fibers.

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Mesh:

Year:  1994        PMID: 7814692     DOI: 10.1002/cne.903480209

Source DB:  PubMed          Journal:  J Comp Neurol        ISSN: 0021-9967            Impact factor:   3.215


  10 in total

Review 1.  Regulation of gap junction coupling in the developing neocortex.

Authors:  B Rörig; B Sutor
Journal:  Mol Neurobiol       Date:  1996-06       Impact factor: 5.590

2.  Area-specific regulation of gamma-aminobutyric acid type A receptor subtypes by thalamic afferents in developing rat neocortex.

Authors:  J Paysan; A Kossel; J Bolz; J M Fritschy
Journal:  Proc Natl Acad Sci U S A       Date:  1997-06-24       Impact factor: 11.205

Review 3.  Insights into the complex influence of 5-HT signaling on thalamocortical axonal system development.

Authors:  Esmee S B van Kleef; Patricia Gaspar; Alexandre Bonnin
Journal:  Eur J Neurosci       Date:  2012-05       Impact factor: 3.386

4.  Modeling early cortical serotonergic deficits in autism.

Authors:  Carolyn B Boylan; Mary E Blue; Christine F Hohmann
Journal:  Behav Brain Res       Date:  2006-10-10       Impact factor: 3.332

5.  Barrel pattern formation requires serotonin uptake by thalamocortical afferents, and not vesicular monoamine release.

Authors:  A M Persico; E Mengual; R Moessner; F S Hall; R S Revay; I Sora; J Arellano; J DeFelipe; J M Gimenez-Amaya; M Conciatori; R Marino; A Baldi; S Cabib; T Pascucci; G R Uhl; D L Murphy; K P Lesch; F Keller; S F Hall
Journal:  J Neurosci       Date:  2001-09-01       Impact factor: 6.167

6.  Decreased cortical serotonin in neonatal rabbits exposed to endotoxin in utero.

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7.  Postnatal growth defects in mice with constitutive depletion of central serotonin.

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Journal:  ACS Chem Neurosci       Date:  2012-12-15       Impact factor: 4.418

Review 8.  Developmental effects of SSRIs: lessons learned from animal studies.

Authors:  Xenia Borue; John Chen; Barry G Condron
Journal:  Int J Dev Neurosci       Date:  2007-07-07       Impact factor: 2.457

9.  Postsynaptic deregulation in GAP-43 heterozygous mouse barrel cortex.

Authors:  Emily A Kelly; Marie-Eve Tremblay; James S McCasland; Ania K Majewska
Journal:  Cereb Cortex       Date:  2009-11-13       Impact factor: 5.357

10.  Subbarrel patterns in somatosensory cortical barrels can emerge from local dynamic instabilities.

Authors:  Bard Ermentrout; Daniel J Simons; Peter W Land
Journal:  PLoS Comput Biol       Date:  2009-10-16       Impact factor: 4.475

  10 in total

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