Difference between revisions of "2014 Group Project 7"

From Embryology
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==Current research models and findings==
 
==Current research models and findings==
  
 
===Current Research===
 
 
Most previous studies describe overall growth of brain based upon ''in utero'' imaging studies with the use of magnetic resonance imaging (MRI) and ultrasound; however, complicated folding of the cortex in adult brain is due to different rates of regional tissue growth. In the following study, maps of local variation in tissue expansion are created for the first time in the living fetal human brain, in order to examine how structural complexity emerges in fetal brain.
 
{|
 
|-bgcolor="ECCEF5"
 
|
 
 
[[Image:Cerebral_Brain_Image.jpg|400x400px|frame|Local growth pattern of cerebral brain tissue]]
 
 
'''Local tissue growth patterns underlying normal fetal human brain gyrification quantified in utero'''<ref name=PMID21414909><pubmed>21414909</pubmed></ref>
 
 
Recent development in fetal MRI motion correction and computational image analysis techniques were employed in this study to help with the understanding of the patterns of local tissue growth. These techniques were applied to 40 normal fetal human brains in the period of primary sulcal formation (20–28 gestational weeks). This time period covers a developmental stage from the point at which only few primary sulci have developed until the time at which most of the primary sulci have formed, but before the emergence of secondary sulci on MRI. This developmental period is also important clinically, since the clinical MRI scans are also performed at this gestational age. Therefore it is important to describe the normal growth patterns in this period in order to be able to recognise abnormalities in the formation of sulci and gyri.
 
 
Techniques mentioned previously were utilised to quantify tissue locations in order to map the tissues that were expanding with a higher or lower growth rate than the overall cerebral growth rate. It was found that relatively higher growth rates were detected in the formation of precentral and postcentral gyri, right superior temporal gyrus, and opercula whereas slower growth rates were found in the germinal matrix and ventricles. Additionally, analysis of the cortex illustrated greater volume increases in parietal and occipital regions compared to the frontal lobe. It was also found that gyrification was more active after 24 gestational weeks. These maps of the fetal brain were used to create a three-dimensional model of developmental biomarkers with which abnormal development in human brain can be compared.
 
|}
 
 
{|
 
|-bgcolor="CED8F6"
 
|The following are recent studies that use a similar model to what was described above:
 
 
'''Mapping Longitudinal Hemispheric Structural Asymmetries of the Human Cerebral Cortex From Birth to 2 Years of Age'''
 
<ref><pubmed> 23307634 </pubmed></ref>
 
 
* In this study longitudinal cortical hemispheric asymmetries were mapped in infants using surface-based morphometry of magnetic resonance images
 
 
* Some of the findings of this study:
 
 
-Sexual dimorphisms of cortical asymmetries are present at birth with males having larger sizes of asymmetries.
 
 
-The left supra marginal gyrus is much more posterior compared to the right supra marginal gyrus at birth and this position difference increases for    both males and females by 2 years of age.
 
 
-The right superior temporal parieto-occipital sulci are significantly larger and deeper than those in the left hemisphere while the left planum temporale is significantly larger and deeper than that in the right hemisphere at all 3 ages.
 
 
* It was concluded in this study that early hemispheric structural asymmetries are inherent and gender related.
 
|}
 
{|
 
|-bgcolor="ECCEF5"
 
|
 
'''Sexually Dimorphic White Matter Geometry Abnormalities in Adolescent Onset Schizophrenia'''
 
<ref><pubmed> 23307635 </pubmed></ref>
 
 
* In this study, they investigate the geometry of inter-hemispheric white matter connections in patients with schizophrenia with a particular focus on sexual differences in white matter connection.
 
 
* They find a correlation between the sex-dependent abnormality in the geometry of white matter connecting the two hemispheres and the severity of schizophrenia
 
 
|}
 
{|
 
|-bgcolor="CED8F6"
 
|
 
'''Asymmetry of White Matter Pathways in Developing Human Brains'''
 
<ref><pubmed> 24812082 </pubmed></ref>
 
 
* The use of high-angular resolution diffusion imaging tractography has allowed the above article to investigate the emergence of asymmetry of white matter pathways in fetal brains typically being less than 3 years of age comparable to adult brains over 40 years of age. Furthermore, the high spatial resolution generated from the use of this imaging technique provides a detailed image in order to shed some light on the irregular spatial pattern of white matter systems and whether primary associative functions form before higher cognitive functions. This is essentially important in the application of learning difficulties at a youthful age due to improved and revised understanding on cognitive development in children.
 
 
* It was found that the emergence of asymmetry of white matter pathways in children less than 3 years of age specifically the association of higher order cognitive functions (arcuate fasciculus) was not observed however the emergence of the ILF pathway in FA occurred. Hence asymmetry while present in prenatal development, a more resilient and sturdy asymmetry develops at a later age.
 
 
* The study however was unable to use a wider range of age intervals for brains obtained (only up to 3 years) and hence was unable to investigate the asymmetry of white matter pathways during important periods further. 
 
|}
 
{|
 
|-bgcolor="ECCEF5"
 
|
 
'''Cortical Overgrowth in Fetuses With Isolated Ventriculomegaly'''
 
<ref><pubmed> 23508710 </pubmed></ref>
 
 
* The condition fetal ventriculomegaly is characterised by dilation of lateral ventricles whilst sharing associations with other malformations. It was hypothesised that using relative brain overgrowth as marked measure of altered brain development is due to the occurrence of ventriculomegaly and to evaluate this brain overgrowth through the use of magnetic resonance imaging (MRI) of fetuses isolated with enlarged ventricles (3rd and 4th ventricles as well as cerebrospinal fluid). Furthermore, significant changes to thalamic volumes, basal ganglia and white matter did not occur between cohorts.
 
 
* The study found that there was a sufficient increase in brain volume (overgrowth) of fetuses that had ventriculomegaly in comparison to controls. Also, larger lateral ventricle volumes were yielded with fetuses with ventriculomegaly assessed via 2-dimensional movement of the atrial diameter (ultrasound and MRi) as well as a larger total brain tissue volume. This provides support for the hypothesis  in that brain overgrowth can be used as a marked measure for ventriculomegaly with results showing that overgrowth was not localised in one region but across both hemispheres and thus lead to a neural deficit in children (altered neural connectivity).
 
 
* Hence, this study has assisted in the improved understanding of the effects of ventriculomegaly on cognition, language and behaviour in children.
 
|}
 
 
===Future Research===
 
  
 
===Current Research===  
 
===Current Research===  
Line 340: Line 267:
 
* Some of the findings of this study:
 
* Some of the findings of this study:
  
-Sexual dimorphisms of cortical asymmetries are present at birth with males having larger sizes of asymmetries.
+
** Sexual dimorphisms of cortical asymmetries are present at birth with males having larger sizes of asymmetries.
  
-The left supra marginal gyrus is much more posterior compared to the right supra marginal gyrus at birth and this position difference increases for    both males and females by 2 years of age.
+
** The left supra marginal gyrus is much more posterior compared to the right supra marginal gyrus at birth and this position difference increases for    both males and females by 2 years of age.
  
-The right superior temporal parieto-occipital sulci are significantly larger and deeper than those in the left hemisphere while the left planum temporale is significantly larger and deeper than that in the right hemisphere at all 3 ages.
+
** The right superior temporal parieto-occipital sulci are significantly larger and deeper than those in the left hemisphere while the left planum temporale is significantly larger and deeper than that in the right hemisphere at all 3 ages.
  
 
* It was concluded in this study that early hemispheric structural asymmetries are inherent and gender related.
 
* It was concluded in this study that early hemispheric structural asymmetries are inherent and gender related.
Line 385: Line 312:
 
* Post-mortem studies have demonstrated that NAA is produced in neurons, transported into white matter and broken down into aspartate and acetate in oligodendrocytes. <ref><pubmed>17275978</pubmed></ref> NAA catabolism is thus closely related to the metabolism of myelin, since it provides a crucial source of acetate which is necessary for the formation of myelin from lipid.
 
* Post-mortem studies have demonstrated that NAA is produced in neurons, transported into white matter and broken down into aspartate and acetate in oligodendrocytes. <ref><pubmed>17275978</pubmed></ref> NAA catabolism is thus closely related to the metabolism of myelin, since it provides a crucial source of acetate which is necessary for the formation of myelin from lipid.
 
* Therefore due to abnormal myelin biosynthesis in schizophrenia, brain tissues can be examined by <sup>1</sup>H-MRS studies as long as the targeted brain region involves a single tissue type (white matter) that provides the necessary information regarding the catabolic cycle of NAA.
 
* Therefore due to abnormal myelin biosynthesis in schizophrenia, brain tissues can be examined by <sup>1</sup>H-MRS studies as long as the targeted brain region involves a single tissue type (white matter) that provides the necessary information regarding the catabolic cycle of NAA.
 
  
 
|}
 
|}

Revision as of 01:27, 24 October 2014

2014 Student Projects
2014 Student Projects: Group 1 | Group 2 | Group 3 | Group 4 | Group 5 | Group 6 | Group 7 | Group 8
The Group assessment for 2014 will be an online project on Fetal Development of a specific System.

This page is an undergraduate science embryology student and may contain inaccuracies in either description or acknowledgements.

Neural - CNS

Introduction

The Central Nervous System (CNS) is a complex network of neurons which are responsible for the sending, recieving and integration of information from all parts of the body, serving as the processing center of the bodies nervous system. The CNS controls all bodily functions (sensory and motor), consisting of 2 main organs; The Brain and Spinal Cord.

The brain is the body's control center consisting of 3 main components; Forebrain, Midbrain and Hindbrain. The forebrain functions in receiving and processing sensory information, thinking, perception, and control of motor functions as well as containing essential structures; Hypothalamus and Thalamus, which are responsible in motor control, autonomic function control and the relaying of sensory information. The Midbrain along with the Hindbrain together form the brain-stem and are both important in auditory and visual responses

The spinal cord is a cylindrical shaped structure composes of nerve fiber bundles which is connected to the brain via the brain-stalk formed from the Midbrain and Hindbrain, running through the spinal canal in the vertebrae (in animals) from the neck to the lower back. The spinal cord plays the important role of transmitting information from bodily organs and external stimuli to the brain and acts as a channel to send important signals to other parts of the body. The nerve bundles in the Spinal cord are divided into ascending bundles, which transmits sensory information from the body to the brain, and descending bundle, which transmits motor function information from the brain to the body.

Before fetal period, neurulation occurs that ectoderm forms initial structure of the CNS and folds upon itself to form neural tube towards the end of week 3. The head portion becomes the brain, which further differentiates into forebrain, midbrain and hindbrain, while the middle portion becomes the brain stem. Around week 5, neural tube differentiates into the proencephalon (forebrain), the mesencephalon (midbrain) and the rhombencephalon (hindbrain). By week 7, the prosencephalon divides into the telencephalon and the diencephalon, while the rhombencephalon divides into the metencephalon and the myelencephalon. The formation of these 2 additional structures creates 5 primary units that will become the mature brain.

In this website, CNS development during the fetal period, including cellular processes and brain development will be discussed. Current research models and findings, and historic findings will be stated. The abnormalities associated to CNS during fetal period, and neural defects that occur during embryonic period and contribute in fetal development will be discussed.

Development during fetal period

Cellular process

In developing CNS, there are 4 major cellular processes, including cell proliferation, cell migration, cell differentiation and cell death. They are a cascade of events that the earlier occurring process may influence the subsequently occurring ones, but a late-occurring event cannot influence the earlier ones.

Schematic representation of the timeline of human neural development.jpg

A simplified timeline of human neural development (modified) [1]

This simplified graph shows a timeline for major events of neural development that occur during fetal and postnatal periods. These events, which are summarized in the following table, are broadly classified by cell multiplication, cell migration, growth and differentiation and angiogenesis:

Major Events Descriptions
Cell multiplication
  • Neurons are proliferated and generated from neural stem cells and progenitor cells (precursor cells) in a process known as neurogenesis in 2nd trimester.
  • Cell death and Gliogenesis (glial cells (such as astrocytes) deriving from multipotent neural stem cells) occur in the 3rd trimester.
  • Local gliogenesis continues postnatally.
Cell migration
  • Neuronal migration is maximised during 2nd trimester while glial migration is maximised during 3rd trimester
Growth and differentiation
  • Axonal and dendritic arborisation (fine branching structures at the end of nerve fibers) appear by the end of fetal period.
  • Synaptogenesis (formation of synapses) and electrical activity is maximised in 3rd trimester (and continued postnatally).
  • Cell death due to over-innervation can be observed in late fetal and postnatal period.
  • Myelination occurs in late fetal and postnatal period (vast majority of postnatal growth in brain is due to myelination).
Angiogenesis
  • Oxidative metabolism can be seen in late fetal period.
  • Capillary networks develop postnatally.

1. cell proliferation

Image of coronal sections of somatosensory cortex of E20 rat showing boundaries between the ventricular zone (VZ), inner subventricular zone (iSVZ) and outer SVZ (oSVZ) [2]
  • This process is responsible for the formation of neurons and glia.
  • Begins around 40th embryonic day and is almost complete around the 6th month of gestation [3]
  • Location: occurs in germinal matrix that comprised of ventricular and subventricular proliferative zones of cells.
  1. Ventricular zone: This is the proliferative zone that appears first which is a pseudostratified columnar epithelium [4]. In some part if the developing CNS, this is the only proliferative zone and therefore it is assume that ventricular zone produces all of the cell types. For example, in the hippocampus, all of the neurons of the major subdivisions (areas CA1, CA2 and CA3) are derived from the ventricular zone. There is substantial movement of the nuclei as they move through the cell cycle [5]. The nuclei move between the ventricular surface and the border of the ventricular zone with the subventricular zone [6].
  2. Subventricular zone: This is the second proliferative zone that appears in some parts of the developing CNS. Most of the glia for most of the brain are produced in this zone, therefore it is important to the adult brain [7]. In some parts of the brain, there is the production of a significant number of neurons in this zone [8]. For example, the subventricular zone contributes large number of cells to the neocortex, which is the youngest structure in the brain [9]. In contrast to ventricular zone, the proliferating cells do not move through the cell cycle.



2. cell migration

Passive cell displacement and outside-to-inside spatiotemporal gradient [10]
Active cell migration and inside-to-outside spatiotemporal gradient [10]
  • This is the process that influences the final cell position by migrating the cells produced from the two ventricular zones.
  • The postmitotic young neurons migrate from the proliferation site to their ultimate position in two different ways.
  1. Passive cell displacement: Moving of cells in this way does not require active locomotor activity. In some parts of the developing CNS, the postmitotic neurons that only move a very short distance from the border of proliferative zone are displaced outward by newly produced cells (figure). This results in an “outside-to-inside” spatiotemporal gradient that the earliest generated neurons are located farthest away from the proliferative zone, where the youngest generated ones are located closest to the zone. This pattern can be found in the thalamus [11], hypothalamus [12], spinal cord [13], dentate gyrus of the hippocampal formation [14] and many regions of the brainstem.
  2. Active migration: This requires the active participation of the moving cell for its displacement which neurons move at a greater distance and the migrating young neuron bypasses the previously generated cell (figure). This results in an “inside-to-outside” spatiotemporal gradient. This pattern can be found in well-laminated structure including cerebral cortex and several subcortical areas [14].



Image of interneurons migration and interactions with radial glia in the developing cerebral cortex [15]



3. cell differentiation[10]

  • This is the process begins after the migration of neuronal and glial cells to the final positions and it is responsible for the generation of a wide variety of cells in the adult CNS. During the differentiation, each neuron grows out its axon and dendrites.
  • Time: starts about the 25th month of gestation until adolescence
  • The axons do not grow directly to their final targets, but they transiently innervate areas and cells in two ways that the connections cannot be found in adult brain. These two types of transient connections are not mutually exclusive and can be found within a single population of cells.
  1. Divergent transient connections: one neuron innervates more cells than normal which will be eliminated by the reduction of projection area.
  2. Convergent transient connections: several neurons innervate one target neuron where only one of these neuronal connections is found in adult.


4. cell death (apoptosis)

  • This is the process where elimination of transient connections occurs and two mechanisms, axonal retraction and neuronal pruning [10], are involved.
  1. Axonal retraction: The transient connections are removed by the recession of the collaterals of the neuron’s axon or by the shrinking of the terminal arborisation of the axon.
  2. Neuronal pruning: The transient connections are removed through a selective cell death that neurons die due to the failing to establish projections.
  • Critical for appropriate brain development


Brain Development

  • The human brain development begins in the 3rd gestational week with the start marked by differentiation of the neural progenitor cells. By the end of the embryonic period in gestation week 9 (GW9), the basic structures of the brain and CNS are established as well as the major parts of the Central and Peripheral nervous systems being defined [16]
  • The early fetal period (mid-gestation) is a critical period in the development of the neocortex, as well as the formation of vital cortical neurons which are vital in the brain processing information


During Fetal Period

Increase in size of of brain and ventricles [17]
Increase in size of brain fissure [17]
  • The gross morphology of the developing brain undergoes striking change during this time, beginning as a smooth structure and gradually developing the characteristic mature pattern of gyral and sulcal folding.
  • The brain development begins rostral in GW8, proceeding caudally until it is complete at GW22 [18]
  • The formation of Secondary Sulci is between GW30-35, while the formation of of Tertiary Sulci begins during GW36 and into the postnatal period.
  • Different population of neurons form grey matter structures in many regions of the brain including hindbrain and spinal column, cerebellum, midbrain structure and the neocortex
  • Neurons, after production, migrate away from the proliferative regions of the VZ, the neurons that will form the neocortex migrate in an orderly fashion forming the 6 layered neocortical mantle
  • The major fibre pathways make up the brain white matter
  • AS development proceeds, the brain becomes larger and the primary mode of neuronal migration from the VZ changes.


Neuron Production

  • The human brain contains billions of neurons which are produced by mid-gestation; during fetal development [19]
  • Processes of Neuronal production is initiated by first increasing the size of the Neural progenitor cell population within the body, these cells are mitotic in nature and are capable of forming new cells.
  • Initially (from the end of gastrulation through to embryonic day 42), the neural progenitor cell population is increased greatly when the progenitor cells divide through 'symmetrical' mode of cell division. Multiple repeats of the cell division occurs throughout this period. This 'symmetrical' division method brings about the formation of 2 new identical neural progenitor cells
  • Mode of cell division changes from a symmetrical cell division type to an 'asymmetrical' cell division from the beginning of E42. This asymmetrical cell division forms 2 different cell types; one Neural progenitor & one Neuron [20]
  • Newly formed Neural progenitor cells remains to undergo more processes of cell division whereas the newly formed neuron moves into position in the developing neocortex


Neuron Migration [21]

Outlined above was a broad summary on neuron migration. Neuron migration in the cortex will be covered below in more detail.

  • The ventricular zone (VZ) is where the majority of neurons migrate radially out and into the neocortex. The type of migration utilised here is referred to as somal translocation where the neuron cell body translocates out of the VZ and into the outer brain region with the nucleus moving across the cytoplasm and into the outer brain region.
  • With increasing brain size, somal translocation is no longer efficient for neuronal migration out of VZ. Since greater distances are evident, radial glial guides are adopted to allow the migration of neurons to continue. Similar to somal translocation, these cell populations establish a scaffolding system where neurons can attach to (basal process occurs) and then move into the developing cortical plate. These cell populations are comprised of neural progenitor cells and are therefore able to support mass neuron migration.
  • Another mode of transport utilised by neurons situated within a second zone of the ventral telencephalon is referred to as tangential migration. The neurons here migrate tangentially to the cortical mantle whilst adopting different signalling pathways (guidance molecules) as opposed to radial migration. As a result of neuronal migration, a 6-layered structure forms within the developing neocortex.
  • Once completion of the pre-plate has occurred, two regions are formed and which are the subplate (SP) and th marginal zone (MZ).In between these two regions, the cortical plate arises as well. Earliest neuron arrival forms the deepest layer of the cortex; cortical layer 6. More superficial layers of the cortex will develop with continuous cell migration. It is important to note that a specific cell class is located within the MZ in which are the Cajal-Retzius cells (CR). CR's are important for correct neuron positioning within the cortical layers as well as having an inhibitory effect on neuron migration. Rheelin, a molecular signal produced by the CR's is important here as it stops neurons from migrating and signals them to up their corresponding positions.


Folding: sulcation and gyration

Simplified external lateral (left) view of the brain growth
  • During the fifth and sixth month of gestation, the smooth cortex begins to fold by sulcation and gyration. [22]
  1. Sulcation: This is the development of sulci, including primary and secondary. The formation of primary sulci involve the appearance of shallow grooves on the surface of the brain, which then become more deeply infolded, while the formation of secondary sulci is due to the development of side branches of the primary ones [23].
  2. Gyration: This is the development of gyrus that occurs during late during fetal development until the end of the pregnancy or after birth [23]. This process is the formation of tertiary sulci, which is the formation of other side branches of the secondary sulci [23].
Weeks of gestation Visible anatomical details
20-21 smooth, with the impression of "lissencephalic" brain; wide Sylvian fissures; visible interhemispheric fissure and parieto-occipital fissure
22-23 beginning of calcarine and hippocampal fissures and of callosal sulci
24-25 smooth cerebral cortex surface; visible shallow grooves in the central sulci, interparietal sulci and superior temporal sulci; start of opercularization of Sylvian fissures; presence of calcarine fissures and cingular sulci
26 presence of central and collateral sulci
27 presence of marginal and precentral sulci
28 presence of postcentral and intraparietal sulci
29 presence of superior and inferior frontal sulci; narrower Sylvian fissure; clear corpus callosum; bright white matter; dark cortical ribbon
30-31 beginning of infolding of cortex which is first apparent in the occipital lobe; narrower ventricular system and subarachnoid spaces
32 presence of superior and inferior temporal sulci
33 presence of external occipitotemporal sulci
34-35 close to final shape of gyration; compactly and extensively folded cortex
36-37 completed opercularization of Sylvian fissures; narrow pericerebral fluid spaces; dark subcortical fibres and corona radiata
38-40 dark posterior limbs of internal capsules

table of the process of sulcation and gyration [24]

Spinal Cord Development

The spinal cord is formed from parts of the neural tube during embryonic and fetal development

Meninges Development

Historical Research and Findings

Historical knowledge, predating when modern research techniques were made available, in understanding and studying the Central Nervous structure of humans and other animals were gathered by various investigations by Pathologists, Anatomists, Physiologists from the early 1800’s.

Year Research and Findings
1824 Luigi Rolando first discovered a method to study Central Nervous system structures via cutting chemically hardened pieces of brain tissue into thin sections for microscopical observations [25]
1833 Robert Remak discovers that the brain tissue is cellular. Ehrenberg discovers that it is also fibrillar
1842 Rolando’s method of observing CNS structures was perfected by Benedikt Stilling by cutting series of consecutive slices of the same tissue, this allowed the ability to trace nerve tracts and establish spacial relations
1858 Joseph von Gerlach brings forth a new process to differentiate between the different microstructures in the brain by treating the sample to a solution of ‘Carmine’.

This solution made the sample no longer appear homogenous under the lens but able to be differentiable to its components

1889 Camille Golgi comes forth with the procedure of impregnating hardened brain tissues with silver nitrate solution which resulted in the staining of nerve cells.

Possibility to trace cellular prolongations definitely to their termini now present. Ramon y Cajal announces his discoveries.

Old theory of union of nerve cells into an endless mesh-work is discarded altogether, the new theory of isolated nerve elements ‘theory of neurons’ is fully established in its place [26]

HOW DO WE REFERENCE BOOKS? A History of Science by Henry Smith Williams, M.D., LL.D. assisted by Edward H. Williams, M.D. (1904)

Current research models and findings

Current Research

Most previous studies describe overall growth of brain based upon in utero imaging studies with the use of magnetic resonance imaging (MRI) and ultrasound; however, complicated folding of the cortex in adult brain is due to different rates of regional tissue growth. In the following study, maps of local variation in tissue expansion are created for the first time in the living fetal human brain, in order to examine how structural complexity emerges in fetal brain.

Local tissue growth patterns underlying normal fetal human brain gyrification quantified in utero[27]

Recent development in fetal MRI motion correction and computational image analysis techniques were employed in this study to help with the understanding of the patterns of local tissue growth. These techniques were applied to 40 normal fetal human brains in the period of primary sulcal formation (20–28 gestational weeks). This time period covers a developmental stage from the point at which only few primary sulci have developed until the time at which most of the primary sulci have formed, but before the emergence of secondary sulci on MRI. This developmental period is also important clinically, since the clinical MRI scans are also performed at this gestational age. Therefore it is important to describe the normal growth patterns in this period in order to be able to recognise abnormalities in the formation of sulci and gyri.

Techniques mentioned previously were utilised to quantify tissue locations in order to map the tissues that were expanding with a higher or lower growth rate than the overall cerebral growth rate. It was found that relatively higher growth rates were detected in the formation of precentral and postcentral gyri, right superior temporal gyrus, and opercula whereas slower growth rates were found in the germinal matrix and ventricles. Additionally, analysis of the cortex illustrated greater volume increases in parietal and occipital regions compared to the frontal lobe. It was also found that gyrification was more active after 24 gestational weeks. These maps of the fetal brain were used to create a three-dimensional model of developmental biomarkers with which abnormal development in human brain can be compared.

The following recent studies use a similar model to what was described above:

Mapping Longitudinal Hemispheric Structural Asymmetries of the Human Cerebral Cortex From Birth to 2 Years of Age [28]

  • In this study longitudinal cortical hemispheric asymmetries were mapped in infants using surface-based morphometry of magnetic resonance images
  • Some of the findings of this study:
    • Sexual dimorphisms of cortical asymmetries are present at birth with males having larger sizes of asymmetries.
    • The left supra marginal gyrus is much more posterior compared to the right supra marginal gyrus at birth and this position difference increases for both males and females by 2 years of age.
    • The right superior temporal parieto-occipital sulci are significantly larger and deeper than those in the left hemisphere while the left planum temporale is significantly larger and deeper than that in the right hemisphere at all 3 ages.
  • It was concluded in this study that early hemispheric structural asymmetries are inherent and gender related.

Asymmetry of White Matter Pathways in Developing Human Brains [29]

  • The use of high-angular resolution diffusion imaging tractography has allowed the above article to investigate the emergence of asymmetry of white matter pathways in fetal brains typically being less than 3 years of age comparable to adult brains over 40 years of age. Furthermore, the high spatial resolution generated from the use of this imaging technique provides a detailed image in order to shed some light on the irregular spatial pattern of white matter systems and whether primary associative functions form before higher cognitive functions. This is essentially important in the application of learning difficulties at a youthful age due to improved and revised understanding on cognitive development in children.
  • It was found that the emergence of asymmetry of white matter pathways in children less than 3 years of age specifically the association of higher order cognitive functions (arcuate fasciculus) was not observed however the emergence of the ILF pathway in FA occurred. Hence asymmetry while present in prenatal development, a more resilient and sturdy asymmetry develops at a later age.
  • The study however was unable to use a wider range of age intervals for brains obtained (only up to 3 years) and hence was unable to investigate the asymmetry of white matter pathways during important periods further.

In the following studies new models and imaging techniques have been employed to gain a better understanding of the changes in brains of patients with schizophrenia

Sexually Dimorphic White Matter Geometry Abnormalities in Adolescent Onset Schizophrenia [30]

  • In this study, they investigate the geometry of inter-hemispheric white matter connections in patients with schizophrenia with a particular focus on sexual differences in white matter connection.
  • They find a correlation between the sex-dependent abnormality in the geometry of white matter connecting the two hemispheres and the severity of schizophrenia

Moreover, in the following study, a neuroimaging technique known as Proton Magnetic Resonance Spectroscopy (1H-MRS) is used to examine the brain of patients with schizophrenia.

Multimodal neuroimaging of frontal white matter microstructure in early phase schizophrenia: the impact of early adolescent cannabis use [31]

The 1H-MRS volume of interest is placed parallel to the AC-PC line (AC =anterior commissure, PC = posterior commissure). [32]
  • The neurochemical used in this technique is N-acetylaspartate (NAA), a free amino acid that has a peak resonance at 2.02 ppm on the spectral profile in the 1H-MRS of human brain.
  • In vivo concentration levels of NAA are higher in white matter compared to gray matter.
  • Post-mortem studies have demonstrated that NAA is produced in neurons, transported into white matter and broken down into aspartate and acetate in oligodendrocytes. [33] NAA catabolism is thus closely related to the metabolism of myelin, since it provides a crucial source of acetate which is necessary for the formation of myelin from lipid.
  • Therefore due to abnormal myelin biosynthesis in schizophrenia, brain tissues can be examined by 1H-MRS studies as long as the targeted brain region involves a single tissue type (white matter) that provides the necessary information regarding the catabolic cycle of NAA.

References

  1. Report of the Workshop on Acute Perinatal Asphyxia in Term Infants, U.S. Department of Health and Human Services, Public Health Service, National Institutes of Health, National Institute of Child Health and Human Development, NIH Publication No. 96-3823, March 1996.
  2. <pubmed>22272298</pubmed>
  3. <pubmed>4203033</pubmed>
  4. <pubmed>5414696</pubmed>
  5. <pubmed>7204662</pubmed>
  6. <pubmed>12764033</pubmed>
  7. <pubmed>8523077</pubmed>
  8. <pubmed>9712307</pubmed>
  9. <pubmed>1713238</pubmed>
  10. 10.0 10.1 10.2 10.3 <pubmed>10532616</pubmed>
  11. <pubmed>489804</pubmed>
  12. <pubmed>5029133</pubmed>
  13. <pubmed>4407392</pubmed>
  14. 14.0 14.1 <pubmed>17533671</pubmed>
  15. <pubmed>17726524</pubmed>
  16. <pubmed>21042938</pubmed>
  17. 17.0 17.1 <pubmed>19339620</pubmed>
  18. <pubmed>560818</pubmed>
  19. <pubmed>8361683</pubmed>
  20. <pubmed>12764028 </pubmed>
  21. <pubmed>21042938</pubmed>
  22. <pubmed>21571694</pubmed>
  23. 23.0 23.1 23.2 <pubmed>11158907</pubmed>
  24. <pubmed>20608424</pubmed>
  25. <pubmed>7472570</pubmed>
  26. <Pubmed>17490748</pubmed>
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