• Wrong document? Swap it for free
  • Written by students who passed
  • Immediately available after payment
  • Read online or as PDF
Sell
Where do you study
Your language
Document preview thumbnail
Preview 4 out of 109 pages
Class notes

NUR 2221 Ortho Exam 1 Notes | Complete Solutions | Broward College

Document preview thumbnail
Preview 4 out of 109 pages

NUR 2221 Ortho Exam 1 Notes | Complete Solutions | Broward College

Content preview

EXAM 1 NOTES:



CHAPTER 56: A&P AND ASSESSMENT OF THE NERVOUS SYSTEM

CENTRAL NERVOUS SYSTEM (CNS): consists of the brain, spinal cord, and cranial nerves I and II

PERIPHERAL NERVOUS SYSTEM (PNS): consists of cranial nerves III to XII, spinal nerves, and the
peripheral components of the autonomic nervous system (ANS)

NEURONS: primary functional unit of the nervous system

 Consists of a cell body
 Multiple dendrites (receivers)
 An axon (transmitter)

3 characteristics of neurons:

 EXCITABILITY: The ability to generate a nerve impulse
 CONDUCTIVITY: the ability to transmit an impulse
 INFLUENCE: the ability to influence other neurons, muscle cells, or glandular cells by transmitting
nerve impulses to them

GLIAL CELLS (glia or neuroglia): provide support, nourishment and protection to the neurons

 Constitute almost half of the brain and spinal cord mass
 5 to 10 times more numerous than neurons
 Most primary CNS tumors involve glial cells – primary malignancies involving neurons are rare
 Are mitotic and can replicate
 Divided into MICROGLIA and MACROGLIA
o MICROGLIA: specialized macrophages capable of phagocytosis
 Protect the neurons
 Mobile within the brain
 Multiply when the brain is damaged
o MACROGLIA:
 Include ASTROCYTES (most abundant)
 Found primarily in gray matter
 Provide structural support to neurons
 Their processes form the blood-brain barrier
 Play a major role in synaptic transmission
 When brain is injured, they act as phagocytes for neuronal debris
 Proliferation of astrocytes contributes to the formation of scar tissues
(GLIOSIS) in the CNS
 OLIGODENDROCYTES
o Specialized cell that produce the myelin sheath of nerve fibers in the CNS
o Primarily found in white matter of the CNS

, o SCHWANN CELLS myelinate the nerve fibers in the periphery
 EPENDYMAL CELLS
o line the brain ventricles
o aid in the secretion of cerebrospinal fluid

NERVE REGENERATION

 If the axon is damaged, the cell attempts to repair itself
 Try to grow back to their original destinations by sprouting many branches from the damaged
ends of the axons
 Generally less successful in the CNS than in the PNS

NERVE IMPULSE

 Initiation of a nerve impulse involves the generation of an action potential
o Once an action potential is initiated, a series of action potentials travels along the axon
o When the impulse reaches the end of the nerve fiber, it is transmitted across the
synapse (junction) by a chemical interaction involving neurotransmitters
o This chemical interaction generates another set of action potentials in the next neurons
o Process repeats until the impulse reaches its destination
 Many peripheral nerve axons have NODES OF RANVIER( gaps in the myelin sheath)
o Allow an action potential to travel much faster by jumping from node to node without
traversing the insulated membrane segment
 This process is called SATLATORY (hopping) CONDUCTION
o In an unmyelinated fiber, the wave of depolarization travels the entire length of the
axon, with each portion of the membrane becoming depolarized in turn
 SYNAPSE: the structural and functional junction between two neurons
 NEUROTRANSMITTERS: chemicals that affect the transmission of impulses across the synaptic
clef
o Excitatory neurotransmitters activate postsynaptic receptors that increase the likelihood
that an action potential will be generated
o Inhibitory neurotransmitters activate postsynaptic receptors that inhibit the likelihood
that an action potential will be generated
o ACETYLCHOLINE
 A decrease in acetylcholine-secreting neurons is seen in Alzheimer’s disease
 Myasthenia gravis results from a reduction in acetylcholine receptors
 A weakness and rapid fatigue of muscles under voluntary control
 Symptoms: droopy eyelid and mouth, difficulty swallowing, double
vision, unsteady walk

o AMINES
 EPINEPHRINE (ADRENALIN)
 Both a hormone and neurotransmitter
 Produced in neurons of CNS and neurosecretory cells of adrenal medulla

,  Critical component of the fight-or-flight response of the SNS
(sympathetic nervous system)
 NOREPINEPHRINE
 Both a hormone and neurotransmitter
 Has important role as neurotransmitter released from SNS affecting the
heart
 Along with epinephrine, has important role in fight-or-flight response,
increasing heart rate, triggering the release of glucose from energy
stores, and increasing blood flow to skeletal muscle
 SEROTONIN
 Primarily found in GI tract, platelets and CNS
 Involved in moods, emotions, and sleep
 DOPAMINE
 Produced in several areas of the brain
 Involved in emotions and moods and regulating motor control
 Parkinson’s disease results from destruction of dopamine-secreting
neurons
o AMINO ACIDS
 GABA (GAMMA-AMINOBUTYRIC ACID)
 Chief inhibitory neurotransmitter in CNS
 Regulated neuronal excitability throughout the nervous system
 Drugs that increase GABA function have been used to treat seizure
disorders
 GLUTMATE and ASPARTATE
 Play key role in learning and memory
 Sustained release of glutamate and prolonged excitation is toxic to nerve
cells
 Glutamate is a destruction factor in amyotrophic lateral sclerosis
o NEUROPEPTIDES
 ENDORPHINS and ENKEPHALINS
 Endogenous opioids that function as neurotransmitters
 Produced in pituitary gland and hypothalamus
 Produce analgesia and a feeling of well being
 The opioids morphine and heroin bind to endorphin and enkephaline
receptors and produce same effect as the endogenous opioids
 SUBSTANCE P
 Neurotransmitter in pain transmission pathways
 Morphine blocks its release
 Neurotransmitters continue to combine with the receptor sites at the postsynaptic membrane
until they are inactivated by enzymes, are taken up by the presynaptic endings, or diffuse away
from the synaptic regions

CENTRAL NERVOUS SYSTEM

 SPINAL CORD

, o Continuous with the brainstem
o Exits from the cranial cavity through the foramen magnum
o Cross section reveals gray matter centrally located in an H shape and is surrounded by
white matter
o Gray matter contains:
 the cell bodies of voluntary motor neurons
 preganglionic autonomic motor neurons
 association neurons (interneurons)
o white matter contains the axons of the ascending sensory and the descending
(suprasegmental) motor fibers)
 the myelin surrounding these fibers gives them their white appearance
o ASCENDING TRACTS
 In general, carry specific sensory information to higher levels of the CNS
 Info comes from special sensory receptors in the skin, muscles and joints,
viscera, and blood vessels
 Enters the spinal cord by way of the dorsal roots of the spinal nerves
 The FASCICULUS GRACILIS and the FASCICULUS CUNEATUS (commonly called the
dorsal or posterior columns) carry information and transmit impulses concerned
with touch, deep pressure, vibrations, position sense, and kinesthesia
(appreciation of movement, weight and body parts)
 SPINOCEREBELLAR TRACTS: carry information about muscle tension and body
position to the cerebellum for coordination of movement
 SPINOTHALAMIC TRACTS carry pain and temperature sensations
o DESCENDING TRACTS
 Carry impulses that are responsible for muscle movement
 Among the most important are the CORTICOBULBAR and CORTICOSPINAL
TRACTS collectively termed the PYRAMIDAL TRACT
 These tracts carry volitional (voluntary) impulses from the cerebral cortex to the
cranial and peripheral nerves
 Another group of descending motor tracts carries impulses from the
extrapyramidal system (all motor systems except the pyramidal) concerned with
voluntary movement
o LOWER AND UPPER MOTOR NEURONS
 Lower motor neurons are the final common pathway through which descending
motor tracts influence skeletal muscle
 The cell bodies of the LMNs (lower motor neurons), which send axons to
innervate the skeletal muscles of the arms, trunk, and legs, are located
in the anterior horn of the corresponding segments of the spinal cord
(e.g., cervical segments contain LMNs for the arms)
 LMN lesions generally cause weakness or paralysis, denervation atrophy,
hyporeflexia or areflexia and decreased muscle tone
 Upper motor neurons originate in the cerebral cortex and project downward
 The corticobulbar tract ends in the brainstem
 The corticospinal tract descends into the spinal cord

Document information

Uploaded on
September 21, 2026
Number of pages
109
Written in
2026/2027
Type
Class notes
Professor(s)
Unknown
Contains
All classes
$25.99

Wrong document? Swap it for free Within 14 days of purchase and before downloading, you can choose a different document. You can simply spend the amount again.
Written by students who passed
Immediately available after payment
Read online or as PDF

Seller avatar
Reputation scores are based on the amount of documents a seller has sold for a fee and the reviews they have received for those documents. There are three levels: Bronze, Silver and Gold. The better the reputation, the more your can rely on the quality of the sellers work.
NurseHenny
4.4
(31)
Sold
175
Followers
75
Items
2113
Last sold
15 hours ago



Why students choose Stuvia

Created by fellow students, verified by reviews

Quality you can trust: written by students who passed their tests and reviewed by others who've used these notes.

Didn't get what you expected? Choose another document

No worries! You can instantly pick a different document that better fits what you're looking for.

Pay as you like, start learning right away

No subscription, no commitments. Pay the way you're used to via credit card and download your PDF document instantly.

Student with book image

“Bought, downloaded, and aced it. It really can be that simple.”

Alisha Student

Working on your references?

Create accurate citations in APA, MLA and Harvard with our free citation generator.

Working on your references?

Frequently asked questions