Literature DB >> 8263229

Postnatal development of the cholecystokinin innervation of monkey prefrontal cortex.

K M Oeth1, D A Lewis.   

Abstract

Although the structure and function of primate prefrontal cortex undergo substantial modifications during postnatal development, relatively little is known about the maturation of neurotransmitter systems in these cortical regions. In the primate brain, cholecystokinin is present in the greatest concentrations in prefrontal regions. Thus, in this study, we used immunohistochemical techniques to investigate the postnatal development of the cholecystokinin innervation of monkey prefrontal cortex. In animals aged 4 days through adult, cholecystokinin immunoreactivity was present in nonpyramidal neurons that appeared to represent at least two distinct cell types. The most common type was a vertically oval bitufted neuron, located in layers II-superficial III, which typically had a radially descending axon that gave rise to short collaterals in layer IV. Another frequently observed cell type was a larger multipolar neuron located in the superficial half of layer III. The axon of these neurons branched locally in the vicinity of the cell body. The greatest density of cholecystokinin-containing neurons and processes was present in monkeys less than 1 month of age. The density of immunoreactive structures in every prefrontal region then progressively declined with increasing age, with the most marked changes occurring during the first postnatal year. As a result, the density of labeled neurons in adult monkeys was less than one-third of that in neonatal monkeys. However, labeled structures were significantly more dense in some ventromedial and orbital regions than in dorsal regions of the prefrontal cortex in neonatal, but not in older animals. In all animals, cholecystokinin-containing neurons were present in highest density in layers II-superficial III, and labeled terminal fields were observed in layers II, IV, and VI. In animals less than 1 month of age, fascicles of radial fibers traversed through layers III and V, whereas in animals 1 to 3 months of age, individual radial fibers rather than fiber bundles were present in layers III and V. In addition, immunoreactive pericellular arrays, which appeared to surround unlabeled nonpyramidal cells, were present in layers V and VI and the subcortical white matter in the youngest monkeys. Although many aspects of the cholecystokinin innervation of monkey prefrontal cortex remain constant during postnatal life, the distinct developmental changes in the cholecystokinin innervation of these regions suggest that it may play an important role in the maturation of the cortical circuitry that mediates the acquisition of certain cognitive abilities.

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Year:  1993        PMID: 8263229     DOI: 10.1002/cne.903360307

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


  13 in total

1.  Lamina-specific alterations in cortical GABA(A) receptor subunit expression in schizophrenia.

Authors:  Monica Beneyto; Andrew Abbott; Takanori Hashimoto; David A Lewis
Journal:  Cereb Cortex       Date:  2010-09-15       Impact factor: 5.357

2.  An automated segmentation methodology for quantifying immunoreactive puncta number and fluorescence intensity in tissue sections.

Authors:  Kenneth N Fish; Robert A Sweet; Anthony J Deo; David A Lewis
Journal:  Brain Res       Date:  2008-09-03       Impact factor: 3.252

3.  GABA-Synthesizing Enzymes in Calbindin and Calretinin Neurons in Monkey Prefrontal Cortex.

Authors:  Brad R Rocco; Robert A Sweet; David A Lewis; Kenneth N Fish
Journal:  Cereb Cortex       Date:  2015-03-30       Impact factor: 5.357

Review 4.  Cortical basket cell dysfunction in schizophrenia.

Authors:  Allison A Curley; David A Lewis
Journal:  J Physiol       Date:  2012-01-04       Impact factor: 5.182

5.  Conserved interneuron-specific ErbB4 expression in frontal cortex of rodents, monkeys, and humans: implications for schizophrenia.

Authors:  Jörg Neddens; Kenneth N Fish; Ludovic Tricoire; Detlef Vullhorst; Alon Shamir; Wonjae Chung; David A Lewis; Chris J McBain; Andrés Buonanno
Journal:  Biol Psychiatry       Date:  2011-06-12       Impact factor: 13.382

6.  Relationship of cannabinoid CB1 receptor and cholecystokinin immunoreactivity in monkey dorsolateral prefrontal cortex.

Authors:  S M Eggan; D S Melchitzky; S R Sesack; K N Fish; D A Lewis
Journal:  Neuroscience       Date:  2010-06-11       Impact factor: 3.590

7.  Differential distribution of proteins regulating GABA synthesis and reuptake in axon boutons of subpopulations of cortical interneurons.

Authors:  Kenneth N Fish; Robert A Sweet; David A Lewis
Journal:  Cereb Cortex       Date:  2011-03-21       Impact factor: 5.357

8.  Cannabinoid CB1 receptor immunoreactivity in the prefrontal cortex: Comparison of schizophrenia and major depressive disorder.

Authors:  Stephen M Eggan; Samuel R Stoyak; Christopher D Verrico; David A Lewis
Journal:  Neuropsychopharmacology       Date:  2010-06-16       Impact factor: 7.853

Review 9.  Postnatal developmental trajectories of neural circuits in the primate prefrontal cortex: identifying sensitive periods for vulnerability to schizophrenia.

Authors:  Gil D Hoftman; David A Lewis
Journal:  Schizophr Bull       Date:  2011-05       Impact factor: 9.306

10.  Development of cannabinoid 1 receptor protein and messenger RNA in monkey dorsolateral prefrontal cortex.

Authors:  Stephen M Eggan; Yoshito Mizoguchi; Samuel R Stoyak; David A Lewis
Journal:  Cereb Cortex       Date:  2009-08-24       Impact factor: 5.357

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