Literature DB >> 7840420

The neocortex. An overview of its evolutionary development, structural organization and synaptology.

R Nieuwenhuys1.   

Abstract

By way of introduction, an outline is presented of the origin and evolutionary development of the neocortex. A cortical formation is lacking in amphibians, but a simple three-layered cortex is present throughout the pallium of reptiles. In mammals, two three-layered cortical structures, i.e. the prepiriform cortex and the hippocampus, are separated from each other by a six-layered neocortex. Still small in marsupials and insectivores, this "new" structure attains amazing dimensions in anthropoids and cetaceans. Neocortical neurons can be allocated to one of two basic categories: pyramidal and nonpyramidal cells. The pyramidal neurons form the principal elements in neocortical circuitry, accounting for at least 70% of the total neocortical population. The evolutionary development of the pyramidal neurons can be traced from simple, "extraverted" neurons in the amphibian pallium, via pyramid-like neurons in the reptilian cortex to the fully developed neocortical elements designated by Cajal as "psychic cells". Typical mammalian pyramidal neurons have the following eight features in common: (1) spiny dendrites, (2) a stout radially oriented apical dendrite, forming (3) a terminal bouquet in the most superficial cortical layer, (4) a set of basal dendrites, (5) an axon descending to the subcortical white matter, (6) a number of intracortical axon collaterals, (7) terminals establishing synaptic contacts of the round vesicle/asymmetric variety, and (8) the use of the excitatory aminoacids glutamate and/or aspartate as their neurotransmitter. The pyramidal neurons constitute the sole output and the largest input system of the neocortex. They form the principal targets of the axon collaterals of other pyramidal neurons, as well as of the endings of the main axons of cortico-cortical neurons. Indeed, the pyramidal neurons constitute together a continuous network extending over the entire neocortex, justifying the generalization: the neocortex communicates first and foremost within itself. The typical pyramidal neurons represent the end stage of a progressive evolutionary process. During further development many of these elements have become transformed by reduction into various kinds of atypical or aberrant pyramidal neurons. Interestingly, none of the six morphological characteristics, mentioned above under 1-6, has appeared to be unassailable; pyramidal neurons lacking spines, apical dendrites, long axons and intracortical axon collaterals etc. have all been described. From an evolutionary point of view the typical pyramidal neurons represent not only the principal neocortical elements, but also the source of various excitatory local circuit neurons. The spiny stellate cells, which are abundant in highly specialized primary sensory areas, form a remarkable case in point.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1994        PMID: 7840420     DOI: 10.1007/bf00187291

Source DB:  PubMed          Journal:  Anat Embryol (Berl)        ISSN: 0340-2061


  143 in total

1.  The organization of chromatic and spatial interactions in the primate striate cortex.

Authors:  D Y Ts'o; C D Gilbert
Journal:  J Neurosci       Date:  1988-05       Impact factor: 6.167

2.  Synaptic connections of callosal projection neurons in the vibrissal region of mouse primary motor cortex: an electron microscopic/horseradish peroxidase study.

Authors:  L L Porter; E L White
Journal:  J Comp Neurol       Date:  1986-06-22       Impact factor: 3.215

3.  Excitatory transmitter amino acid-containing neurons in the rat visual cortex: a light and electron microscopic immunocytochemical study.

Authors:  I Dori; M Petrou; J G Parnavelas
Journal:  J Comp Neurol       Date:  1989-12-08       Impact factor: 3.215

4.  Relationships between horizontal interactions and functional architecture in cat striate cortex as revealed by cross-correlation analysis.

Authors:  D Y Ts'o; C D Gilbert; T N Wiesel
Journal:  J Neurosci       Date:  1986-04       Impact factor: 6.167

5.  Dendritic morphology and axon collaterals of corticotectal, corticopontine, and callosal neurons in layer V of primary visual cortex of the hooded rat.

Authors:  L E Hallman; B R Schofield; C S Lin
Journal:  J Comp Neurol       Date:  1988-06-01       Impact factor: 3.215

6.  An electron microscopic study of the types and proportions of neurons in the cortex of the motor and visual areas of the cat and rat.

Authors:  D A Winfield; K C Gatter; T P Powell
Journal:  Brain       Date:  1980-06       Impact factor: 13.501

7.  Smooth and sparsely-spined stellate cells in the visual cortex of the rat: a study using a combined Golgi-electron microscopic technique.

Authors:  A Peters; A Fairén
Journal:  J Comp Neurol       Date:  1978-09-01       Impact factor: 3.215

8.  A new procedure for examining Golgi impregnated neurons by light and electron microscopy.

Authors:  A Fairén; A Peters; J Saldanha
Journal:  J Neurocytol       Date:  1977-06

9.  Intracortical distribution of axonal collaterals of pyramidal tract cells in the cat motor cortex.

Authors:  P Landry; A Labelle; M Deschênes
Journal:  Brain Res       Date:  1980-06-09       Impact factor: 3.252

10.  Bipolar neurons in rat visual cortex: a combined Golgi-electron microscope study.

Authors:  A Peters; L M Kimerer
Journal:  J Neurocytol       Date:  1981-12
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  68 in total

Review 1.  Neurons of layer I and their significance in the embryogenesis of the neocortex.

Authors:  V E Okhotin; S G Kalinichenko
Journal:  Neurosci Behav Physiol       Date:  2004-01

Review 2.  Evolution of columns, modules, and domains in the neocortex of primates.

Authors:  Jon H Kaas
Journal:  Proc Natl Acad Sci U S A       Date:  2012-06-20       Impact factor: 11.205

3.  Bistable network behavior of layer I interneurons in auditory cortex.

Authors:  Elliott B Merriam; Theoden I Netoff; Matthew I Banks
Journal:  J Neurosci       Date:  2005-06-29       Impact factor: 6.167

4.  Studies of stimulus parameters for seizure disruption using neural network simulations.

Authors:  William S Anderson; Pawel Kudela; Jounhong Cho; Gregory K Bergey; Piotr J Franaszczuk
Journal:  Biol Cybern       Date:  2007-07-07       Impact factor: 2.086

Review 5.  Neuronal functional diversity and collective behaviors: a scientific case.

Authors:  Walter G Sannita
Journal:  Cogn Process       Date:  2009-01-10

6.  Neuronal functional diversity and collective behaviors.

Authors:  Walter G Sannita
Journal:  J Biol Phys       Date:  2008-09-07       Impact factor: 1.365

Review 7.  Normal development of brain circuits.

Authors:  Gregory Z Tau; Bradley S Peterson
Journal:  Neuropsychopharmacology       Date:  2010-01       Impact factor: 7.853

8.  Combinations of AMPA receptor subunit expression in individual cortical neurons correlate with expression of specific calcium-binding proteins.

Authors:  M Kondo; R Sumino; H Okado
Journal:  J Neurosci       Date:  1997-03-01       Impact factor: 6.167

9.  Predicting single-neuron activity in locally connected networks.

Authors:  Feraz Azhar; William S Anderson
Journal:  Neural Comput       Date:  2012-07-30       Impact factor: 2.026

10.  Phase-dependent stimulation effects on bursting activity in a neural network cortical simulation.

Authors:  William S Anderson; Pawel Kudela; Seth Weinberg; Gregory K Bergey; Piotr J Franaszczuk
Journal:  Epilepsy Res       Date:  2009-01-29       Impact factor: 3.045

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