Neurological
histology:
-
Neurons
make up the tissue of the nervous system. They are highly specialized for
impulse conduction to control muscle activity, think, and regulate glands
-
The
central
nervous system is divided into the afferent (sensory) and efferent
(motor) systems. The efferent system is then broken into the somatic nervous
system, which controls voluntary muscular contractions, and the autonomic
nervous system which is involuntary. The ANS is divided into the sympathetic
and parasympathetic nervous systems
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Neuroglia
serve as special supporting cells in the nervous system, also called glial
cells (glia=glue). Glial cells are generally smaller than neurons,
but outnumber them by five to ten times. Many of the glial cells form a
supporting network by twining around nerve cells are lining certain structures
in the brain and spinal cord. A few glial cells also have specialized functions.
Some produce a phospholipid covering, called the myelin sheath, around
the axons of neurons. These myelin sheaths speed the impulse conduction
rate and insulate fibers. Certain glial cells are phagocystic. Of clinical
interest, neuroglia are a common source of tumor (gliomas), which account
for some forty-five percent of intercranial tumors. There are four types
of glial cells:
-
astrocytes--
as the name suggests, these cells are star-shaped, with many processes.
Protoplasmic astrocytes are found in gray matter in the central nervous
system. Fibrous astrocytes are located in white matter in the central nervous
system. They form a supporting network in the brain and spinal cord, as
well as attack neurons to their blood vessels
-
oligodendrocytes--
resemble astrocytes, but with fewer and shorter processes. The lend support
to semirigid connective tissue rows between neurons in the brain and spinal
cord and produce myelin sheathing for neurons of the central nervous system
-
microglia--
small cells with only a few processes, derived from monocytes. Mostly,
these cells are stationary, but may migrate to the site of an injury. Microglia
are also called brain macrophages. Microglia are phagocystic
-
ependyma
(ependymocytes)-- these are epithelial cells arranged in a simple layer,
ranging from squamous to columnar. Many ependyma are ciliated. This epithelium
forms a continuous lining for the ventricles of the brain and central canal
of the spinal cord, and probably assist in circulation of cerebrospinal
fluid
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Neurons
are the nerve cells responsible for the conduction of impulses. They are
made up of three distinct parts:
-
cell
body, soma, or perikaryon-- contains a well defined nucleus and nucleolus
surrounded by a granular cytoplasm. The cytoplasm contains all of the typical
cellular organelles. Many neurons also have inclusions such as lipofuscin,
yellowish in color, and may be a by-product of lysosomal activities. This
lipofuscin grows in amount as we age. The chromatophilic substance, or
Nissl bodies, is an orderly arrangement of rough endoplasmic reticulum.
The proteins from these Nissl bodies are used to restore peripheral nerve
fibers. Neurofibrils are long, slender fibers composed of microtubules.
Neurofibrils assume the task of supporting the cell and transporting nutrients.
Mature neurons do not have mitotic potential
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dendrites--
carries impulses towards the cell body. They are the shorter of the two
extensions of the cell body. Neurons usually have several main dendrites.
Dendrites typically contain chromatophilic substance and typical organelles
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axon,
axis cylinder-- a single long, thin process of the neuron originating from
a small, conical elevation-- the axon hillock. The axoplasm houses no chromatophilic
substance, and thus cannot synthesize proteins. The axon is surrounded
by a plasma membrane known as the axolemma. Axons can range in length from
a millimeter to a meter. Branches of the axon are called axon collaterals.
The axon and it's collaterals terminate in axon terminals, or telodendria.
The axon terminals expand into synaptic bulbs. These bulbs contain membrane-enclosed
sac referred to as synaptic vesicles
Neurons
have two main types of intracellular systems for transporting synthesized
material from the cell. The slower of the two is axoplasmic flow. It moves
axoplasm in only one direction; from the cell body, down the axon for regeneration,
restoration and replenishing the axon. The faster is called axonal transport.
It conveys materials on both directions, possibly along tracks formed by
microtubules and filaments. Axonal transport moves various organelle secretions
that form the neurolemma, synaptic endbulbs and contents and membrane of
the synaptic vesicles
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The
axons of many neurons are wrapped in a segmented myelin sheath. The cells
of this sheath are neurolemmocytes, or Schwann cells. They secrete the
white phospholipid covering that speeds the rate of impulse conduction.
To make the myelin sheath, the neurolemmocyte wrapped itself about the
axon, and spirals about it. The spiraling squeezed most all of the cytoplasm
and organelles, including the nucleus, to the outside, stopping when there
is about twenty to thirty layers of it's phospholipid membrane embrace
the axon. The part of the cell membrane which encloses the cytoplasm and
organelles of the Schwann cell is called the neurolemma. Myelin is responsible
for 'white' matter in the brain, nerves and spinal cord. The neurolemma
is only found in the peripheral nervous system. Gaps in the myelin sheath
are neurofibral nodes, or nodes of Ravier. Unmyelated axons are also sometimes
wrapped in neurolemmocytes, but without the multiple layers. The central
nervous system has fewer neurofibral nodes, and uses oligodendrocytes to
aid in myelation. The unfinished process of myelation in an infant accounts
for it's slower reaction time
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Neurons
can be categorized by form and function:
-
multipolar
neurons-- have several dendrites and one axon. Most of the neurons in the
brain and spinal cord are of this type
-
bipolar
neurons-- have one dendrite and one axon. Found in the retina of the eye,
inner ear, and olfactory area
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unipolar
neurons-- have on process, which splits into two branches. The central
branch acts as the axon, the peripheral, a dendrite. Originate as bipolars
in the fetus. Unipolar neurons are found in the posterior (sensory) root
ganglia of spinal nerves
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sensory,
afferent neurons-- usually unipolar
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exteroceptors--
provide information about the outside world. Located near the surface of
the body
free,
naked nerve endings-- touch receptor
tactile,
Merkel's discs-- touch receptors, deep epidermal
corpuscles
of touch, Meissner's corpuscles-- touch receptors, deep dermal
type
II cutaneous mechanoreceptors, end organs of Ruffini-- receptors for heavy,
continuous touch. Located usually more deep to the other touch receptors
lamellated,
Pacinian corpuscles-- pressure receptors
nociceptors--
pain receptors. Actually the branching ends of certain sensory neurons
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visceroceptors--
provide information about the internal environment
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proprioceptors--
provide information about position and movement
muscle
spindles-- delicate skeletal muscle receptors
tendon
organs, Golgi tendon organs-- receptors at the junction between a tendon
and muscle
joint
kinesthetic receptors-- similar in structure to type II mechanoreceptors
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motor,
efferent neurons-- convey impulses from the brain to to effectors (glands,
organ, muscles)
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association,
connecting, or interneuron neurons-- carry information from sensory neurons
to the brain and spinal cord. Examples of association neurons are stellate
cells, cells of Martinotti, horizontal cells of Cajal, and pyramidal cells.
All are found in the cerebral cortex. Granule cells and Purkinje cells
are association cells in the cerebellum. Up to ninety percent of neurons
in the body are association neurons
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The
sodium-potassium pump keeps a -70 millivolt resting potential of the plasma
membrane. The concentration of sodium outside the cell is much greater
then that on the inside. The opposite is true of potassium on the inside
of the cell. The outside of the membrane keeps a positive charge. On the
inside are potassium, calcium, and negatively charged, nondiffusable proteins
to keep a negative charge. The ability of the cells to respond to stimulus
is it's excitability. If a stimulus of adequate strength, a threshold stimulus,
is applied, the membrane become permeable to sodium ions. The potential
moved from -70 towards 0, then to a positive value. This loss of polarization
is called depolarization, and begins at -69 millivolts. The high point
of the depolarization is at about 30 millivolts. This action moves like
a wave down the neuron. Once the events of depolarization have taken place,
it is said that an action potential, or nerve impulse, has been initiated.
By the time the depolarization has moved to another point, the previous
has begun repolarization. The sodium-potassium pump restores the resting
potential. The period directly after depolarization in which the cell cannot
generate another action potential is called the refractory period, which
may last up to 0.4 milliseconds. Threshold stimulus can be either one strong
stimulus, several smaller ones from different dendrites, or several smaller
in direct succession from one dendrite. When the depolarization reached
the end of the axon, the influx of sodium sets the calcium ions on the
synaptic vesicles in the presynaptic end bulb. They then release neurotransmitters
across the synaptic cleft to the postsynaptic neuron. The acetylcholine
is disassembled by acetylcholinesterase and sent back to the presynaptic
neuron after the depolarization has moved on
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In
myelinated neurons, the impulse jumps from one neurofibral node to the
next, greatly increasing the rate of impulse conduction. The speed of conduction
depends on temperature, the diameter of the nerve fiber, and the presence
of myelin. Cold is applied to painful areas because it slows the painful
nerve impulses
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