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The  Hûman  Brain's
The Electronic Brain
Anatõmical
A r c h i t e c t û r e
By Ther°al L. Bynum, M.D.

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      The Human Brain:   Unchanged for over
40,000 Years!

      Much about Man's brain remains a puzzle.
The Brain   Packed within this oversized Pecan, no larger than a grapefruit, are well over 100 billion neurons!



      The Anatomical and Functional Organization of the adult human brain is at the least difficult to grasp.   This is because of the complicated clustering of nuclei and the intricate pathways of their axons.   It is perhaps easier to understand the nervous system and its organization by examining the way it has developed
Phylogenetically!



   The Nervous System Developed In
Four General Steps:

      1)  Initially the nervous system was just a simple tube, or Spinal Cord, which received sensory fibers from the different segments of the body and sent motor fibers back to them.

      2)  Later, one end of the cord became specialized, responding to special features of the outside world, and in so doing made up the primative brain - the Brain Stem.

      3)  Then the front and the hind ends of the Brain Stem sprouted two new, large structures.   Cerebral Hemispheres developed in front, to become the initiators of movement;  at the rear, developed the Cerebellum, to become the coordinator of movement.   These final additions completed the mammalian brain.

      4)  The mammalian brain continued to develop and evolved into the Human Brain.

(SeeSee Divisions Of The Nervous SystemFigure B )



The Spinal Cord

      In privitive animals (and also in the first weeks of mammalian embryonic development) some of the outer (ectodermal) cells of the dorsal (upper) surface of the body formed a trough running the length of the body;  the upper edges of the trough folded to form a tube (the percursor of the adult mammalian spinal cord).

      At this stage of development the body and the cord were arranged in segments, with sensory receptors in the body sending input to the dorsal portion of the cord, while the cord sent axons from its ventral (underside) portion to control muscles in each of the segments.   This primitive system provided the basis of the somatic sensory system (skin and muscle senses),  and the ventral portion provided the neural basis for movement. !



The Brain Stem

      The front end of the spinal cord increaced its neural and functional specialization during evolution, forming an Encephalon (Greek for Head) or brain.   The formation of the Brain probably occurred because the first vertibrates were mobile and found it easier to travel mostly in one direction;  thus, it was adaptive to have special sensory analysis take place at the end that goes first.

      The front end then formed three enlargements or vesicles.   The cells surrounding each multiplied to form centers that were specialized for receiving and responding to particular features of the outside world.
   The front enlargement, the Prosencephalon (forebrain), became specialized mainly for the sense of smell (and taste).
   The second enlargement, the Mesencephalon (midbrain), became specialized for vision and hearing;  making perception of the distant environment possible.
   The posterior enlargement, the Rhombencephalon (hindbrain), became specialized for equilibrium and balance;  giving the animal better perception of its place in its immediate environment. !



The Mammalian Brain

      The brain continued to develop primarily at its first and third segments.   The Prosencephalon developed to form two major new divisions: the Telencephalon (endbrain) , and Diencephalon (between-brain).   The most significant addition in the telencephalon was the Cerebral Hemispheres, which functionally became the level of highest control for behavior.
   The Rhombencephalon also divided to form two major new divisions:   the Metencephalon (across-brain), and the Myelencephalon (spinal-brain).   The feature distingusihing the development of the metencephalon in mammals was the growth of the Cerebellum, which became the coordinating center for all movement. !



The Human Brain

      The human brain evolved from the mammalian brain with very little change in its basic design, with the exception that in humans the Cerebral Hemispheres and Cerebellum have grown markedly larger than those found in other mammals.   There was an increase in lateralization of function within the brain (ie, a function is restricted to one half of the brain), associated with an increase in EQ.   Also, there was an increase in the number of distinct anatomical and functional subregions within the Neocortex as it expanded in volume. !

      Each Cerebral Hemisphere is identical in cellular structure and relative size, and expands up, out and over from the midbrain, masking most of the other regions of the brain.   Their functions justify their relative colossal size, for within the cerebral hemispheres is the seat of our creative intelligence and memory - places where we perceive, remember, think, dream, experience pleasure, anticipate the future, and make decisions. !

      The primitive spinal cord had the form of a tube with a hollow center.   The central core of the brain stem and the mammalian brain remains hollow.   This hollow cavity is filled with a substance called Cerebral Spinal Fluid (CSF), which is produced by the Choricoid Plexus, a specialized cluster of glial cells found within the cavity.   These cavities are larger in some portions of its length than in others - The enlargements are called Ventricles (Latin for belly).   In the mammalian brain there are four ventricles, numbered I thru IV. !



      The Human Brain grows from the top end of the spinal cord.   It can be divided into three parts:
   the Forebrain (formed mostly by two identical Cerebral Hemispheres);
the Midbrain (the top of the Brain Stem); and
the Hindbrain (formed by the Cerebellum and the remaining parts of the Brain Stem).



      The Cerebral Cortex   (also referred to as the Neocortex), makes up 70% of the CNS and anatomically consists of two large virtually identical Cerebral Hemispheres united by the Corpus Callosum (a fibrous band of tissue which carries over 200 million nerve tracts from one hemisphere to the other).
      The surface of the Neocortex is composed almost entirely of a tight mat of dendrites which extend to the surface from their neural cells in the lower layers of the cortex.   The functional aspect of the Cerebral Cortex near the surface of all the convolutions of the brain, is a thin layer of neurons (the Plexiform Layer I) 2 to 5 millimeters in thickness. !

      The NeöCortical Layers :    On the basis of their slightly different cytoarchitectonic specificities, Neurohistologists have divided the Neocortex into almost 100 different areas.   There are, however, Six Major Layers of cells which are present in all of these different areas (except the Hippocampus and Limbic regions which possess only three).
      These cellular layers within the Neocortex can be separated into two basic groups based upon their function:   The outer four layers receive axons in from other brain areas( Afferents);  The two inner layers ( V-Ganglionic and VI-Fusiform ) send axons out to other brain areas ( Efferents ). The Çytoarchitecture of the brain is Identical in Both Hemispheres

(SeeSee Divisions Of CortexFigure C )


On the basis of their anatomical shape, neurons within the Neocortex may be further categorized into two main types:

Pyramidal  &  Stellate.

      Pyramidal Cells;   neurons generally shaped like pyramids, represent the major efferents of the Cerebral Cortex and are found within Layer II (External Granular), Layer III (External Pyramidal),The Pyramidal Cell and Layer V (Ganglionic Layer).   Pyramidal cells of Layer V are the largest in size and project to the Brainstem and Spinal Cord.   Those in Layers II and III project to other regions of the Neocortex.

      Stellate Cells   are star-shaped cells which are interneurons and represent a collection of different types on neural cells, which are named largely on the basis of the configuration of their axons and dendrites.
   Stellate Cells are found within all of the layers of the Neocortex, but the greatest concentration of them is within Layer IV (Internal Granular Layer),The Stellate Cell and esepecially within the sensory cortex.   Stellate cells receive afferent neuronal axons from subcortical structures, as well as providing interconnections between the cortical afferent and efferent neurons.


      Afferent Neurons (neurons which send axons into the Neocortex) are of two general types:

Specific  &  Nonspecific.

      Specific Afferents   are those neurons that terminate in relatively discrete regions of the cortex, usually involving only one or two layers.   These include projections from the Thalamus as well as those from the Amygdala.   Most of these projections terminate in the more superficial layers of the cortex.  The Specific Afferent Neurons are utilized especially in Left Hemispheric Cognition

      Nonspecific Afferents   are those neurons that terminate diffusely over large regions of the cortex, in some cases over all of the cortex.   The norepinephrinergic projections from the Brainstem, the cholinergic projections from the basal forebrain, and the projections from certain Thalamic nuclei are examples of nonspecific afferents.   Nonspecific afferent neurons often terminate in many if not all of the layers of the Neocortex and presumably serve some general function so as to the enhance ongoing cortical activities. The Nonspecific Afferent Neurons are utilized especially in Right Hemispheric Cognition


      The various regions of the Neocortex are interrelated by three types of axon projections:
   (1) Associational fibers - long and short fibers which project between one gyrus and another,
   (2) Projection fibers - between one lobe and lower centers, and
   (3) Commisural fibers - interhemispheric connections between one hemisphere and the other.

(SeeSee Axon ProjectionsFigure D )


      The Thalamus :    Our brain is an extremely large memory storehouse.   It never functions alone however, but always in association with the lower centers of the nervous system.
   Deep within the cerebrum lie other forebrain structures.   One of the most important components of which is the Thalamus, located within the middle of the brain directly above the Brain Stem.   All areas of the Neocortex have direct afferent and efferent connections with the Thalamus.   The Thalamus transfers all information from the sensory organs (except olfaction) to the Neocortex, and sends all of the instructions from the Neocortex out to the body'smuscles.  !

      The Thalamus is divided into two functional areas, dorsal and ventral.
   The ventral Thalamus provides a general input into the Neocortex that may modulate the activity of the Neocortex.    The Dorsal Thalamus, (or Thalamus proper), is composed of a number of nuclei, each of which projects to a specific area of the Neocortex.    These nuclei receive input from the body's different sensory systems or from other brain areas.   The Lateral Geniculate Body (LGB) receives the visual projections, the Medial Geniculate Body (MGB) receives auditory projections, and the Ventral-Posterior-Lateral nuclei (VPL) receive touch, pressure, pain, and temperature projections from the body.

      In turn, the LGB projects to area 17, the MGB projects to area 41, and the VPL nuclei projects to Brodmann's areas 1, 2, and 3.   A large area of the posterior secondary and tertiary cortex sends projections to and receives projections back from the Pulvinar (P).   Some of the subcortical motor nuclei, such as the Globus Pallidus, Substantia Nigra, and Dentate nucleus, project to the Ventral-Anterior and Ventral-Lateral nuclei (VA and VL), and these areas project to primary motor area 4 and secondary motor area 5.   The Dorsal Medial nucleus (DM) receives projections from the Amygdaloid complex, Temporal Neocortex, and Caudate nucleus and projects to the remainder of the Frontal Lobe. The Neocortex is often thought of as being an Outgrowth of the Thalamus

      The Hypothalamus :    Below the Thalamus, lies a nerve cluster called the Hypothalamus, which acts as an essential coordinator of the CNS, playing a crucial role in our emotions, and controlling basic life processes.   It is the Hypothalamus which acts as the head ganglion of the internal milieu and the chief coordinator of human instincts and drives. The Hypothalamus Choreographs many of our Instinctual Thoughts

      The Basal Ganglia :   Crowning the Thalamus is the Basal Ganglia, four neuronal clusters that help to regulate the body's movements.   This structure overlaps the Limbic System which largely controls emotions and behavior, along with the circuitry for Short-Term Memory.   The Basal Ganglia and Limbic System both share a nerve knot known as the Amygdala , the oblation of which can produce inappropriate emotional behavior in man at the least and manifest at its worst as alexithymia ! See Short Term Memory


      The Reticular Activating System :    Arousal and attentional mechanisms located deep within the brain tend to activate regions of both hemispheres symmetrically.  
   One of the principle sources of signals to excite the outer dendritic layer of the Neocortex is the generalized Thalamocortical fibers of the Reticular Formation (the brain's arousal system).
   Diffuse electrical stimulation in the mesencephalic and pontine portions of the Reticular Formation causes immediate and marked activation of the Neocortex.   Extending upward into the cerebrum from the mesencephalic reticular formation are multiple diffuse pathways that terminate in all areas in the diencephlon and the cerebrum.   This entire system is called the Reticular Activating System (RAS).
   Consciousness requires both arousal and mental content.   The anatomic substrate includes both the Neocortex, and the Reticular Activating System. The RAS is our Main Source for Alertness



See The Hûman Brain's
Functiõnal Architecture of the Brain
"Functiõnal  Architecture"



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