Lecture 1: Intro Terminology, Neurohistology Flashcards

BLOCK 1: BASIC ORGANIZATION OF THE NERVOUS SYSTEM, BLOOD SUPPLY, AND MENINGES BLOCK 2: CRANIAL NERVES, CROSS SECTIONAL ANATOMY OF THE BRAIN, ORGANIZATION OF THE FOREBRAIN BLOCK 3: SENSORY SYSTEM AND NEUROMUSCULAR JUNCTION BLOCK 4: MOTOR SYSTEM, HYPOTHALAMUS, AND LIMBIC SYSTEM,

1
Q

The brain weighs approximately ___

A

3 lbs (1400 gm)

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2
Q

The brain represents ____ of total body weight

A

2-3%

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3
Q

The brain accounts for ____ of total energy consumption.

A

20%

Of this 20%, 60-80% supports communication among neurons and glia rather than the brain’s response to external stimuli.

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4
Q

The brain contains several billion very fragile neurons which, if put end to end, would make a cable several thousand miles long

A

Estimated synaptic connections as high as a hundred trillion

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5
Q

Approximately ____ of the human genome is involved in nervous system function

A

one half

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6
Q

The brain directs all motor activity, somatic as well as autonomic

A

The brain directs all motor activity – voluntary as well as involuntary

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7
Q

The brain receives far more _____ compared to ____ produced.

A

The brain receives far more sensory inputs compared to motor outputs produced.

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8
Q

Approximately ____ Americans are afflicted with neurological, communicative, or behavioral disorders and the majority are _____.

A

Approximately 50 million Americans are afflicted with neurological, communicative, or behavioral disorders and the majority are chronic.

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9
Q

Third leading cause of death

after heart disease and cancer

A

Cerebral vascular disease (stroke)

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10
Q

____ of deaths occurring during the first year of life are caused by congenital malformations of the CNS.

A

40% of deaths occurring during the first year of life are caused by congenital malformations of the CNS.

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11
Q

What disease is estimated to afflict one quarter of the population who live to age 85 years?

A

Alzheimer’s disease

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12
Q

CENTRAL NERVOUS SYSTEM

A

Brain

Spinal Cord

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13
Q

PERIPHERAL NERVOUS SYSTEM

A

12 pairs of cranial nerves -arise from brainstem

31 pairs of spinal nerves –arise from spinal cord

Ganglia

Axons that enter or leave the brain and spinal cord form nerves that are part of the PNS. This includes 12 pairs of cranial nerves arising from the brainstem and 31 pairs of spinal nerves arising from the spinal cord. Another structure found in the peripheral nervous system are ganglia.

Peripheral nerves are generally collections of axons on their way to or from places such as skin, muscle, or internal organs, accompanied by glial and connective tissue sheaths. Many of these axons have cell bodies that also reside in the PNS, and these somata are typically clustered in ganglia at predictable sites along the nerve

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14
Q

GANGLIA

A

Ganglia = Greek for Tumor; anything gathered into a ball

Ganglia are structures located outside the CNS that contain neurons. An example is a dorsal root ganglion located immediately adjacent to the spinal cord.

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15
Q

Dorsal Root ganglia

A

the small swellings located bilaterally at the level of each intervertebral foramen.

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16
Q

NUCLEUS

A

NUCLEUS = Collection of neurons within brain or spinal cord (i.e., within the CNS)

Whereas a ganglion is a collection of neurons in the periphery, a nucleus is a collection of neurons within the CNS.

Specialized areas of gray matter.

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17
Q

Myelin

A

the lipid membrane that surrounds the axons of neurons.

Myelin– plasma membrane of oligodendrocyte or Schwann cell that forms multiple wraps around segments of the axon.

Myelin extends for short distances. Gaps between wraps are called Nodes of Ranvier

Spiral wrappings of Schwann cell (PNS) or oligodendrocyte (CNS) membranes around axons, interrupted periodically by nodes of Ranvier. Myelin forms a low-capacitance insulating coating around axons, greatly increasing their conduction velocities by allowing saltatory conduction.

mammalian

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18
Q

Dorsal

A

toward the top of the head

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19
Q

ventral

A

toward the neck

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20
Q

horizontal plane

A

transverse plane

the brain is cut from rostral to caudal for the forebrain which is dorsal to ventral for the brainstem.

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21
Q

coronal plane

A

is a cut from dorsal to ventral for the forebrain

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22
Q

sagittal plane

A

divides down the middle into two halves.

Sections taken adjacent to the mid-sagittal cut are referred to as parasagittal.

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23
Q

The brain may be divided into 6 regions

A

. 4 regions are collectively referred to as the brainstem. Starting caudally these are: The Medulla which is a direct continuation of the spinal cord. The Pons (this is latin for Bridge as it has the appearance of which). the cerebellum (little brain). The Midbrain which is the smallest part of the brainstem. The diencephalon which is the transition between the brainstem and the cerebral cortex. This is the area where the flexure between the brainstem and the cerebral cortex referred to preciously occurs. Finally, the largest part of the brain is the telencehalon or forebrain. It consists of the massive cerebral cortex and several nuclei that are buried deep within the telencephalon. These are referred to as subcortical nuclei

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24
Q

TELENCEPHALON

A

FOREBRAIN

Cerebral cortex and subcortical nuclei (e.g., Basal Ganglia).

The largest part of the brain. It consists of the cerebral cortex and several nuclei that are buried deep within the cortical mantle. These are referred to as subcortical nuclei.

This is what most people think about when you say “the brain”. Two prominent fissures are evident. The Central Sulcus extends from dorsal to ventral, beginning at about the midpoint of the cerebral cortex. The Lateral Sulcus extends from rostral to caudal. These deep sulci help divide the cortex into lobes: **the Frontal lobe, ** the Parietal lobe, ** The temporal lobe, and the **Occipital lobe.

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25
Q

DIENCEPHALON

A

Encephalon is Greek for “in the head/brain” Diencephalon means “in-between brain,” signifying this part of the CNS lies between the cerebral hemispheres and the brainstem.

Composed of the Thalamus & Hypothalamus

the transition between the brainstem and the cerebral cortex

Most of the diencephalon is covered by the telencephalon or cerebral cortex. It extends from the mammillary bodies to the optic chiasm.

Only a small portion of the diencephalon is evident from the ventral view. Structures that can be seen include the **mammillary bodies which form the posterior border of the diencephalon, and *** the optic nerve. At this point, some of the axons traveling in the optic nerves arising from the right and the left eye cross the midline and continue to visual centers in the cerebral cortex as the optic tract. The point of crossing is called the optic chiasm.

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26
Q

Medulla

A

Direct Rostral extension of the Spinal cord

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27
Q

Pons

A

Latin for Bridge, as it has the appearance of one

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28
Q

Midbrain

A

the smallest part of the brainstem

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29
Q

Order of these buggers

A

spine &raquo_space; mudulla&raquo_space; pons &raquo_space; midbrain &raquo_space; diencephalon&raquo_space; telencephalon

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30
Q

Bumps on the brain

A

(hillocks, tubercles, colliculi, gyri, peduncles, brachium, eminence)

generally indicate the location of underlying nuclei or fiber tracts

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31
Q

Grooves

A

(fissures, sulci, raphe)

divide brain into different regions or represent a midline division of the brain.

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32
Q

Cut off nerves are central portions of ______ that emerge from the medulla, pons, midbrain and diencephalon

A

Cut off nerves are central portions of cranial nerves that emerge from the medulla, pons, midbrain and diencephalon

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33
Q

VENTRAL MEDULLA

A

Cylindrical in shape and continuous with the spinal cord

Is located ventral to the cerebellum.

Numerous cranial nerves arise from the lateral aspect of the medulla bilaterally.

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34
Q

the optic nerve

A

Cranial nerve II

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35
Q

central sulcus

A

extends from dorsal to ventral, beginning at about the midpoint of the cerebral cortex.

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36
Q

Lateral Sulcus extends from rostral to caudal.

A

extends from rostral to caudal.

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37
Q

Sulci/ Fissures

A

depressions between gyri

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38
Q

Gyri

A

elevated ridges of tissue

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39
Q

2 prominent fiber tracts are evident:

A

corpus callosum and fornix

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40
Q

Neuron

A

the Functional Unit of the Nervous System
the Functional Unit of the Nervous System

Information-processing and signaling cell.

Neurons are anatomically and functionally polarized, with electrical signals traveling in only one direction under ordinary physiological circumstances.

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41
Q

Neuron Anatomy

A
Cell Body (Soma, Perikaryon) 
Fills the metabolic needs.

Dendrites (Spines)
Receive info from other neurons via the synapse.

Axon: neurons usually have only one.
Hillock – origin of axon from soma
Initial Segment – segment of axon just before first myelin wrap.
Terminals – ending of axon which usually divides into multiple branches.

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42
Q

synapse

A

Connections between neurons

May be excitatory or inhibitory

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43
Q

GLIAL CELL TYPES

A

Oligodendrocytes

Schwann cells

Microglia

Glial stem cells

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44
Q

OLIGODENDROCYTE

A

Myelinates axons within the CNS.

Each oligodendrocyte may wrap more than 1 axon.

45
Q

Nodes of Ranvier

A

Gap between myelin wraps

46
Q

SCHWANN CELL

A

Myelinates axons in the periphery.

Myelin sheaths, sheaths of unmyelinated axons, satellite cells

1 Schwann cell forms a single wrap on one axon.

Most PNS glial cells are variants of the Schwann cell. Some Schwann cells are flattened out as satellite cells that surround the neuronal cell bodies in PNS ganglia. Most, however, envelop axons as they travel through peripheral nerves.

Schwann cells have been implicated in several other functions, including facilitating the regrowth of axons after peripheral nerve injury, helping to regulate extracellular ionic concentrations around neurons and their processes, and collaborating with neurons in some developmental and metabolic processes.

47
Q

Anterograde Transport

A

– Amino acids.

Inject radioactive amino acid into a region and neurons take it up and transport it to their axon terminals where it can be visualized.

48
Q

Retrograde Transport

A

– Horseradish peroxidase, microspheres

Inject tracer into area of axon terminals. Terminals take it up and transport it retrogradely to their cells of origin where it can be visualized.

49
Q

Cellular And Molecular Approaches For Studying Connectivity And Molecular Identity Of Nerve Cells:
Antibodies

A

Antibodies to specific proteins/neurotransmitters can be used to identify populations of neurons.

50
Q

Cellular And Molecular Approaches For Studying Connectivity And Molecular Identity Of Nerve Cells:
Genetic Probes

A

Genetic Probes can be used to identify specific populations of neurons. Example: a section of the cerebellum can be labeled with a probe for a specific gene that is only expressed in one type of neuron in the cerebellum.

51
Q

Physiological Recording

A

Stimulate in one area and record in another.

Example: skin is touched and recording is made from primary sensory cortex to determine if the region in which the recording electrode is placed receives input from the stimulated part of the forearm.

52
Q

Physiological Techniques for Studying Connectivity Between Nerve Cells

A

Reporter gene that codes for visualizable substance (e.g., GFP) is inserted in a genome and is under the control of a cell type-specific promoter (DNA sequence that turns gene “on”). Reporter is only activated in specific cell types that express the gene. Here Dorsal Root Ganglion cells are activated and the distribution of their processes in the periphery and in the CNS are apparent.

53
Q

Cerebrum

A

Composed of the 2 cerebral hemispheres and the diencephalon.

54
Q

Longitudinal Fissure

A

Divides the 2 hemispheres of the Cerebrum.

55
Q

Does the brainstem include the cerebellum?

A

NO!

56
Q

Multipolar

A

Describes a neuron having more than 2 dendrites and/or axons

57
Q

Bipolar

A

Describes a neuron having just 2 dendrites and/or axons

58
Q

Dendrites

A

The tapered extensions of the cell body that collect info from other neurons.

Major organelles: cytoskeleton, mitochondria

provide a great increase in the surface area available for synaptic inputs

The principal but not the only site of synaptic inputs. The dendrites of many neurons have their own extensions, dendritic spines, that may be favored sites for modifying the strength of synapses.

59
Q

Soma

A

Cell body.
Synthesizes macromolecules and integrates electrical signals.

Major organelles: Nucleus, Golgi apparatus, Nissle substance, cytoskeleton, mitochondria

60
Q

Axon

A

Conducts info to other neurons.
Single, cylindrical.
May be many centimeters long.
May be myelinated or unmylinated.

Major organelles: mitochondria, transport vesicles, cytoskeleton,

The single, cylindrical appendage used by most neurons to conduct action potentials away from the soma and toward axon terminals that make synaptic endings on other neurons.

61
Q

Axon Terminals

a.k.a., synaptic endings

A

Vesicle-filled. Close to the parts of other neurons.

Most are axodendritic or axosomatic.

Major organelles: mitochondria, synaptic vesicles

62
Q

Sensory Neurons

A

Are directly sensitive to various stimuli (like touch or temperature change), or receive direct connections from nonneuronal receptor cells.

unipolar

Sensory axons are located in the dorsal root ganglia of spinal nerves, and enter the spinal cord and divide into a large number of branches, most of which terminate on neuronal processes in the spinal gray matter.

63
Q

Motor Neuron

A

End directly on muscles, glands, or other neurons in PNS ganglia.

multipolar

Motor axons are located in the spinal gray matter, leave the spinal cord and enter spinal nerves.

64
Q

Interneuron

A

In the broadest sense of the term, neurons that are located entirely within the CNS and interconnect other neurons. However, the term is usually used to refer to small local-circuit neurons.

65
Q

projection neuron

A

Have long axons that connect different areas (e.g., corticospinal neurons).

66
Q

Golgi Stain

A

The Golgi stain reveals the shapes of the arborizations of cortical neurons by completely staining a small percentage of them.

For many years, the major technique available for studying the shapes & sizes of neurons was Golgi staining, a method that infiltrates all the processes of a small percentage of neurons with heavy metals, causing them to stand out from an unstained or counterstained background.

One drawback of Golgi staining is that it stains a subset of neurons indiscriminately, revealing relatively little about the function of an individual cell.

67
Q

Astrocytes

A

Greek for “star cell”

2nd major category of CNS glial cells.

Adult astrocytes fall into 2 broad classes—protoplasmic astrocytes, found in gray matter, and fibrous astrocytes, found in white matter. (A third type of astrocyte, called radial glia, is present during development and forms a scaffolding that helps guide growing axons.) Despite their somewhat different appearances, protoplasmic and fibrous astrocytes have basically similar characteristics. Astrocytes have a well-developed cytoskeleton that is dominated by intermediate filaments but also includes microtubules and actin filaments, consistent with a role as structural support elements in the CNS. In addition, some astrocyte processes have enlarged end-feet that are applied either to the surface of CNS capillaries or to the surface of the CNS itself; other processes abut neurons, dendrites, synaptic endings, and nodes of Ranvier. This carpeting of otherwise exposed surfaces with astrocyte processes underlies the role of these cells in the regulation of extracellular ionic concentrations and in the transfer of metabolites to and from neurons. Finally, astrocytes are a major part of the limited armamentarium available to the CNS in responding to injury; they hypertrophy, increase their production of intermediate filaments, and form dense, gliotic scars.

68
Q

Gray Matter

A

Area that’s dense with cell bodies and dendrites.

Is actually pinkish-gray because of the rich blood supply.

Gray matter contains motor neurons, the endings of incoming sensory axons and long descending tracts, local interneurons, and projection neurons whose axons enter long ascending tracts.

  • Nuclei are specialized areas of gray matter.
  • A cortex is made of gray matter (e.g., cerebral and cerebellar cortices)
69
Q

cortex

A

A cortex is made of gray matter (e.g., cerebral and cerebellar cortices).

It’s an area where gray matter forms a layered surface that covers some part of the CNS.

70
Q

Names for white matter

A

tract, fasciculus, funiculus, lemniscus, peduncle.

These are mostly descriptive terms that also make sense. Fasciculus and funiculus mean “little bundle” and “string,” respectively. Lemniscus means “ribbon” and is used for tracts that are flattened out in cross section. Peduncle means “little foot” and is used for a site where axons funnel down into a compact bundle.

71
Q

White matter

A

Refers to areas where there is a predominance of axons.

Many axons have a myelin sheath that is mostly lipid and has a fatty, white appearance.

White matter contains long descending tracts (from the brainstem and cerebrum), long ascending tracts (to the brainstem, cerebellum, and cerebrum), and local axons interconnecting different spinal levels.

72
Q

Tract Naming

A

Many tracts have two-part names that provide information about the nature of the tract.

The first part of the name refers to the location of the neuronal cell bodies from which these axons originate, and the second part refers to the site where they terminate.

A spinocerebellar tract is a collection of axons with cell bodies in the spinal cord and synaptic endings in the cerebellum.

73
Q

Ribosomes

A

stud the surface of the rough endoplasmic reticulum and float freely in the cytoplasm between the cisternae.

are stained intensely by basic dyes, appearing by light microscopy as clumps called Nissl bodies or Nissl substance

74
Q

Nissl bodies

A

Clumps of rough endoplasmic reticulum that are prominent in the cell bodies and proximal dendrites of neurons.

75
Q

long descending tracts

A

from the brainstem and cerebrum

76
Q

long ascending tracts

A

to the brainstem, cerebellum, and cerebrum

77
Q

cytoskeleton

A

Organelles are embedded in a network of filamentous protein polymers that extend throughout the neuron and its processes, collectively constituting the neuronal cytoskeleton

78
Q

Microtubules

A

Cylindrical assembly of 13 strands of tubulin polymers. Microtubules are major cytoskeletal components, and serve as the “railroad tracks” for fast axonal transport.

Cylindrical assemblies, about 25 nm in diameter, of 13 strands (protofilaments) of protein arranged around a hollow core.

Each protofilament is a polymer of the protein tubulin; an assortment of additional proteins associated with the microtubules links them to one another, to other cytoskeletal elements, and to various organelles as they travel toward or away from the cell body.

79
Q

Neurofilaments

A

A ropelike assembly of protein polymers; one of three major cytoskeletal components. Neurofilaments aggregate into neurofibrils after some preparation methods, and can be stained and seen microscopically.

the neuron’s version of the intermediate filaments found in most cells, are multiply twisted, assemblies of strands of polymers involving at least 3 different proteins from the cytokeratin family. Neurofilaments are about 10 nm in diameter, too small to be seen under the light microscope, but they aggregate in response to certain chemical fixatives. When silver stains are applied, such aggregates can be visualized as neurofibrils

80
Q

microfilaments

A

A twisted pair of actin filaments, forming the thinnest of the 3 major types of cytoskeletal elements.

microfilaments, (7 nm), are twisted pairs of actin filaments. All 3 kinds of cytoskeletal elements contribute to maintaining the shape of the neuron. Microtubules also serve as the substrate along which organelles are transported through neuronal processes. Microfilaments are important for anchoring membrane molecules in place (e.g., receptor molecules at synapses), for shuttling things to and from the cell membrane, and for movement of the advancing tip of growing axons.

81
Q

dendritic tree

A

the total array of dendrites,

it can have an elaborate structure

82
Q

axon hillock

A

The axon arises abruptly from an axon hillock on one side of the neuronal cell body or one of its proximal dendrites. Bundles of microtubules, accompanied by neurofilaments and mitochondria, funnel through the axon hillock into the initial segment of the axon

83
Q

initial segment

A

typically the most electrically excitable part of the neuron

part of the axon

84
Q

axonal transport

A

active process needed for normal function.

A variety of substances ranging from “used” organelles to intracellular chemical messengers need to be transported from synaptic endings back to the soma.

Microtubules serve as the “railroad tracks” for fast transport.

Some things move preferentially in the anterograde direction, others in the retrograde direction. This is made possible by the longitudinal polarity of microtubules: tubulin is a structurally polarized molecule and can be added only in one orientation to one end (called the plus end) of an existing microtubule. Axonal microtubules are oriented with their plus ends pointing away from the soma. 2 ATPases associated with microtubules serve as the motors for fast transport. Kinesin & Dynein moves some components in the retrograde direction (Fig. 1-17).

85
Q

anterograde

A

Transport away from the soma

86
Q

retrograde

A

transport toward the soma

87
Q

Slow axonal transport

A

moves soluble proteins—such as cytoskeletal proteins and cytoplasmic enzymes—in the anterograde direction at rates of a few millimeters a day; the mechanism of this movement is still not understood.

88
Q

Fast axonal transport

A

moves membrane-associated substances—mitochondria, lysosomes, vesicles of neurotransmitter precursors, and membrane components—at rates up to 400 mm a day.

Microtubules serve as the “railroad tracks” for fast transport.

89
Q

Kinesin

A

One of 2 ATPases associated with microtubules that serves as the motors for fast transport.

Kinesin bridges between microtubules and some membrane-associated cell components and moves them toward the plus end of the microtubule (i.e., in the anterograde direction).

90
Q

Dynein

A

One of 2 ATPases associated with microtubules that serves as the motors for fast transport.

Dynein moves some components in the retrograde direction

91
Q

tracer use

A

Neuroanatomical techniques take advantage of axonal transport to map out the connections between neurons .

Appropriate tracer substances injected into/near known neuronal cell bodies are transported anterogradely, revealing the locations of the neurons’ synaptic terminals.

Conversely, tracers injected near synaptic endings are taken up by the endings and transported retrogradely to the cell bodies (a method used covertly by some viruses, such as herpes, to gain access to the nervous system).

92
Q

Degeneration techniques

A

introduced in the 1800’s and are based on the reactions of neurons to injury. If an axon is severed, its formerly attached cell body undergoes a characteristic series of cytological changes (chromatolysis). Therefore, examining brain sections for chromatolytic cells can reveal the locations of the cell bodies of origin of the severed axons. While the cell body undergoes chromatolysis, the portion of the axon distal to the cut degenerates (Wallerian degeneration). The same distal changes occur if the damage is inflicted at the ultimate proximal location (i.e., if the cell body is destroyed). Special staining methods can be used to selectively stain degenerating axons or their synaptic terminals. Therefore, if a particular nucleus is destroyed, the path of axons originating there and the sites of their termination can be determined.

Although a great deal of information was gained over the years with the aid of degeneration techniques, their use is not without pitfalls. It is technically difficult, and sometimes impossible, to completely destroy a particular structure without also damaging nearby structures. In addition, because the segregation of gray and white matter is not absolute, axons passing through a given nucleus can be destroyed along with the cell bodies forming the nucleus. For these and other reasons, techniques that take advantage of axonal transport proved to be a great advance. Early methods of this type used radioactive substances (usually tritiated amino acids) that were introduced into an area of gray matter, taken up by the resident neurons, incorporated into macromolecules, and transported down the axons of these neurons. Eventually the synaptic terminals of these axons become radioactive. Subsequent methods have used the introduction of a marker substance (often a protein) into selected areas of gray matter, where it encounters synaptic terminals. The terminals take up the protein and transport it back to the parent neurons. A protein commonly used in such experiments is an enzyme called horseradish peroxidase, which can be detected with great sensitivity and resolution by appropriate histochemical procedures. Although this technique is typically used for retrograde transport studies, it can be used simultaneously for anterograde transport studies, labeling not only the neurons that project to a given area of gray matter but also the targets of axons that leave it. Certain fluorescent dyes can also be used in retrograde transport studies. By injecting two different dyes at two different sites in the nervous system, it is possible to determine whether any neurons have branching axons that project to both sites.

93
Q

Wallerian degeneration

A

Degeneration and removal of an axon and any associated myelin distal to a point of transection.

94
Q

chromatolysis

A

Swelling and apparent loss of Nissl substance of a neuronal cell body in response to axonal damage.

95
Q

Synaptic Contacts Mediate Information Transfer between Neurons

A

An enlargement (the presynaptic element) of a distal axonal branch abuts part of another neuron (the postsynaptic element), separated from it by a synaptic cleft 10-20 nm across. The presynaptic ending contains membrane-bound packets (synaptic vesicles) of neurotransmitter molecules; some vesicles release their contents into the synaptic cleft in response to electrical activity. The neurotransmitter diffuses across the synaptic cleft, binds to receptor molecules in the postsynaptic membrane, and causes an electrical signal in the postsynaptic neuron.

Most synapses have an axonal ending as the presynaptic element and part of a dendrite as the postsynaptic element, but in fact, any part of a neuron can be presynaptic to any part of another neuron (or sometimes even to itself).

96
Q

internode

A

The myelin between 2 nodes, formed by a single Schwann cell.

Adjacent internodes form the projections that cover the node between them. Internodes range in length from 0.2 - 2 mm, with larger-diameter axons having longer internodes and thicker myelin sheaths. This arrangement is part of what allows larger axons to conduct electrical signals more rapidly.

97
Q

unmyelinated axons

A

simply embedded in individual Schwann cells.

Most of the smaller axons in peripheral nerves do not acquire myelin sheaths. This lack of myelin, together with their small diameter, leads to relatively slow conduction of electrical signals by unmyelinated axons.

98
Q

Glia

A

Greek for “glue”

In contrast to the PNS, there are multiple kinds of glial cells in the CNS.

99
Q

Neurons, dendrites, synapses

A

Collect, integrate, transmit information; synthesize macromolecules

Located Gray matter

100
Q

Axons

A

Conduct information

Located in White matter

101
Q

Oligodendrocytes

A

Form myelin sheaths

Found in White (and gray) matter

102
Q

Protoplasmic astrocytes

A

Provide mechanical and metabolic support, response to injury

Found in Gray matter

103
Q

Fibrous astrocytes

A

Provide mechanical and metabolic support, response to injury

Located in White matter

104
Q

Microglia

A

Phagocytosis, response to injury

Found in Gray (and white) matter

105
Q

Ependymal cells

A

Line ventricles and choroid plexus, secrete cerebrospinal fluid

Walls of ventricles

106
Q

oligodendrocytes

A

Many CNS axons are wrapped in myelin sheaths that are fundamentally similar to those of PNS axons, except that in the CNS the sheaths are formed by a different population of glial cells called oligodendrocytes. As in the periphery, larger axons have thicker myelin and longer internodes. However, as the name implies (oligodendro- is Greek for “tree with a few branches”), individual oligodendrocytes produce internodes on multiple axons. A single oligodendrocyte may have dozens of branches, each ending as an internode. Unlike Schwann cells, oligodendrocyte processes do not envelop unmyelinated CNS axons, which can be directly exposed to the extracellular environment. Given their role as myelin-producing cells, oligodendrocytes are most prominent in white matter, but they are also found in gray matter. There they provide myelin sheaths for axons traversing the gray matter and also participate (along with other glial cell types) in surrounding neurons and their processes in a manner analogous to satellite cells in the PNS.

107
Q

radial glia

A

A third type of astrocyte that is present during development and forms a scaffolding that helps guide growing axons.

108
Q

Ependymal Cells

A

The CNS develops embryologically from a neuroepithelial tube. The cavity of the tube persists in the adult CNS as a system of ventricles with an epithelial lining of ependymal cells. In some locations the ependymal cells are specialized as a secretory epithelium that produces the cerebrospinal fluid (CSF) that fills the ventricles and bathes the CNS.

109
Q

Microglial Cells

A

Microglial cells, as their name implies, are smaller than oligodendrocytes and astrocytes (which together are sometimes called macroglia). Microglia seem not to be involved in the minute-to-minute metabolism and electrical signaling of the nervous system. Instead, they play the other major role in the nervous system’s response to injury. In the normal, healthy nervous system they use their numerous processes to sweep through extracellular spaces looking for damage or disease. When they find something, they proliferate, migrate to the affected site, transform into macrophages,* and devour pathogens and neuronal debris.