Test 2
Lecture 8 central nervous system(CNS)- part 2
Autonomic Motor System responsible for involuntary movement
- Neural pathways: a series of neurons connected by synapses that form a line of communication for a specific task
Automatic patterned response = reflex
Neural pathways for reflexes = reflex arc
Components of reflex arc - stimulus hits
1 sensory receptor → 2 afferent neuron → 3 Integrating center → 4 efferent neurons → 5 effector (organ muscle,gland)
Response occurs
4 classes of Reflexes
1. Spinal - Muscle spindle stretch reflex
Cranial - pupillary reflex
2. Somatic (voluntary) - Muscle spindle stretch reflex
Autonomic (involuntary) -baroreceptor to control blood pressure
3. Innate - Muscle spindle stretch reflex
Conditioned - salivation reflex of Pavlov’s dogs
4. Monosynaptic - Muscle spindle stretch reflex
Polysynaptic - all other reflexes
Muscle spindle stretch reflex
Spinal reflex
Only known monosynaptic reflex in the body
For leg extension, the stretch reflex triggers contraction of the quadriceps and inhibition of the hamstring
Withdrawal reflex - automatic reflex to painful stimulus
nociceptors
Crossed-extensor reflex - initiated simultaneously with the withdrawal reflex
eflexes can sometimes be overridden
– Brain activates inhibitory neurons in spinal
cord to suppress reflex
– PSPs sum so if inhibitory influence from brain
> excitatory influence from nociceptor →
withdrawal reflex inhibited
pupillary light reflex
autonomic, cranial reflex
• Innate reflex
• Polysynaptic reflex
• Reflex arc:– photoreceptors → afferent neurons
→ midbrain nuclei → efferent neurons → pupils
Somatic Motor System
Responsible for voluntary movement
Voluntary Motor control
4 components
idea, program, execution, feedback Involves
Idea
Limbic system
Association areas
Supplementary motor area
Program
Supplementary motor area
premotor area
Primary motor cortex
Execution
Pyramidal tract axons originate in primary
motor cortex and terminate in
ventral horn of spinal cord
• Called upper motor neurons
– Most cross to contralateral side in
medullary pyramids
– Also have collaterals that travel to
other motor areas
– Fine control of voluntary movement
of the distal extremities (especially
forearms, hands and fingers)
Extrapyramidal tract-All motor pathways outside
pyramidal tracts
– Support voluntary movement of
the proximal extremities
– Indirect input to motor neurons
– Several pathways
Motor neuron
Feedback
sensory system
cerebellum - critical for motor coordination, provides feedback control of motor function, contributes to muscle tone, stores programs for remembered activities
thalamus
Basal nuclei
Basal Nuclei in Motor control
Functions similar to cerebellum
• Feedback control of voluntary movements
• Select purposeful over unwanted movements
• Damage can result in
– Huntington's chorea fast movement
• Genetic disorder of basal nuclei
• Pathway from basal nuclei to thalamus is lost
– Parkinson's disease mid brain dopamine often associated with slow movement
• Disease of basal nuclei -
• Lack of dopamine in substantia nigra (inhibitory area of midbrain)
Brainstem
ALL lead to muscle contraction and movement
Language sleep learning and memory
wernicke’s area
Language comprehension
• Wernicke's aphasia
– Difficulty understanding both
written and spoken language
– Can speak words but they make
no sense
Broca’s area
Language expression
• Broca's aphasia
– Can comprehend and know what want
to say but cannot make correct sounds
or write the words
Sleep- study of sleep
Active process
• Theories on purpose of sleep
– Lets body rest
– Lets brain rest
– Enhances memory
– Enhances learning
– Supports adequate immune system function
– A time delay of about 3 hours after learning before sleeping improves
declarative memory consolidation
– May prevent the buildup of abnormal proteins found in Alzheimer’s
Disease.
Electroencephalogram (EEG): Electrodes on the
scalp detect synaptic potentials produced by cell
bodies and dendrites in the cerebral cortex. Four
patterns for adults are usually seen:
1. Alpha waves: awake, relaxed brain with eyes closed;
most in parietal and occipital lobes
2. Beta waves: produced with visual stimulation and mental
activity; seen most in frontal lobe; evoked activity
3. Theta waves: found in sleeping adults and newborns;
increase when awake doing tasks that require attention
and memory, during sleep deprivation and severe
emotional stress; most from occipital and temporal lobes
4. Delta waves: seen in sleep and an awake infant, from all
over the cerebrum; indicates brain damage if seen from
an awake adult
May be genetically controlled, although sleep is affected by environmental
factors
• Neurotransmitters involved
1) Histamine and other NTs – wakefulness
2) Adenosine & GABA – sleep
Two recognized categories:
1) REM: rapid eye movement; state when dreams occur; EEG shows theta
waves
2) Non-REM: also called resting sleep; divided into four stages, determined
by EEG waves seen. Stages 3 and 4 are often called slow-wave sleep,
characterized by delta waves.
Sleep-Wake Cycles
• Ascending reticular activating system (ARAS)
– Critical in maintaining alert wakefulness
– Part of reticular formation
– Projections to thalamus, hypothalamus, and
forebrain
• Forebrain: induces slow-wave sleep (SWS)
leep-Wake Neurotransmitters
Awake state
– Acetylcholine
• ARAS
• Mimicked by nicotine
– Norepinephrine and
dopamine
• ARAS
• Mimicked by
amphetamines and
cocaine
Sleep state
– Adenosine
• SWS induced by forebrain
• Blocked by caffeine
– Acetylcholine
• REM sleep
• Pons
Sleep – EEG Waves
• Awake (alert) – beta waves
– Generated by many neurons at different times
• Awake (resting) – alpha waves
– More synchronization of electrical activity
• Stage 1 Sleep
– Lightest sleep i.e. lowest arousal threshold
• Stage 2 Sleep
– light sleep
• Stage 3 Sleep
– moderate sleep
• Stage 4 Sleep
– deep sleep i.e. highest arousal threshold
• REM Sleep
Learning and Memory
Learning
– Acquisition of new information
– Hippocampus is important
Associative learning
– making connections between two (or more) stimuli
Non-associative learning
– Habituation
– Sensitization
Whether you become habituated or sensitized to a stimulus depends on circumstance – if
perceive stimulus to be important become sensitized, if unimportant, habituated
Memory
– Retention of information, skills, or thoughts
Memory Processes
Procedural memory = implicit
– Learned motor skills and behaviors
– Automatic response: does not require a conscious effort
– Cerebellum is involved
Declarative memory = explicit
– Learned facts, events, and experiences
– Requires conscious effort for recall
– Hippocampus is involved
Short-Term and Long-Term Memory
• Information is first stored as short-term (working)
memory
– Lasts seconds to hours
– Information is lost unless consolidated
– Frontal lobe is critical for short-term memory
• Consolidation from short-term memory to long-term
memory
– Mechanism unknown
• Long-term memory
– Lasts years to lifetime
– Temporal lobe and hippocampus important
Plasticity in the Nervous System
• Learning and memory involve plasticity= limited ability to
alter anatomy and function in response to changes in
activity patterns
– Development of new synapses
– Long-term modulation of existing synapses
– Recently shown new neurons develop
– One example of plasticity = long term potentiation (LTP)
• LTP = repetitive stimulation of a particular synapse leads to increase in strength of the synaptic connection i.e. increases likelihood that AP will be triggered in postsynaptic cell
• Increases in synaptic strength occur because of increase
in size of EPSPs generated in post synaptic cell
Plasticity in the Nervous System
Increase in sensitivity of
postsynaptic cell can be due
to increased sensitivity to NT
released at that synapse,
increase in amount of NT
released or both
Glutamate
receptors AMPA
and NMDA are
agonist
Exercise and the Brain
• Research indicates
that exercise enhances brain
activity
– Aerobic exercise in the elderly can improve cognitive
function and slow dementia in Alzheimer’s patients
– Can also improve mood disorders at any age
– How?
• Possibly exercises enhances metabolic activity of brain
• Increased blood flow to brain which may enhance brain
activity and decrease brain deterioration
Lecture 11: immune system
Immunity
Immune response - recognition and elimination of pathogenic agents
Disposal - Aging cells, cellular debris from diseased tissue, sometimes mutant cells
wound healing
Anatomy of the immune system
Physical barriers -
skin - tightly packed cell arranged in layers
mucous membranes - form a continuous barrier with skin. Produce viscous mucus or acid (GI tract)
Leukocytes- white blood cells, wide range of immune response
Granulocytes-With cytoplasmic granules containing secretory products- release via degranulation
Agranulocytes - no granules
Phagocytes - engulf foreign particles and microorganisms and remove them from blood or tissue; neutrophils, eosinophils, and monocytes being in blood and neutrophils being most abundant, while macrophages were in tissue as well dendritic cells
Lymphocytes - 3 major types
Lymphoid tissues - Central, Peripheral
Central lymphoid tissue → Bone marrow, thymus, fetal liver
Peripheral lymphoid tissue → spleen, lymph nodes, tonsils, adenoids, lymph nodules of GI tract
B lymphocytes - When they contact antigens (foreign particle or abnormal molecule) and tag foreign entities for destruction , contacts antigen plasma cells secrete antibodies ( or immunoglobulins)
T lymphocytes- Do direct damage to foreign or abnormal cells (infected, mutant or transplanted cells) contact infectecell and days later cytotoxic t cell secretes and creates pores in target cell’s membrane causing the cell to fill ith fluid and cell lysis
Natural Killer- important in fighting viral infections make up a small amount of lymphocytes; similar mechanism to T cells but recognize cells differently, show immediate readiness-→ fast response compared to B and T cells, operate early and nonspecifically perforins are secreted causing cell lysis part of innate and also specific response
Can undergo clonal expansion and display increased cytotoxicity to
repeat antigens
Inflammation -Interferons
– Prevents spread of viruses in body
• Interferes with viral replication
– Proteins secreted by leukocytes and virus-infected cells =
interferon-α and interferon-β
Virus infected cell
accumulates viral
nucleic acid
Healthy
cell
Healthy
cell
Healthy
cell
Interferon synthesized and
secreted
Host cell usually
dies
Healthy cells resistant
How?
• RNA degrading
enzymes
• Protein synthesis
inhibitors
• Block production of
new viruses
Nonspecific Defenses- Activation of innate
immunity
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Interferons (Cont’d)
– Interferon-γ
• Secreted from active T cells and NK cells
• Inhibits viral replication
• Enhances phagocytosis by macrophages
• Boosts antibody production in B cells
• Helps activate NK cells and cytotoxic T cells
• Inhibits cell division—defense against cancer
Nonspecific Defenses- Activation of innate
immunity
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Complement system
– Can act specifically or non-specifically depending on
whether antibodies are present
• Completes actions of specific antibodies
– Consists of 30 plasma proteins that destroy invading
microorganisms especially bacteria
– Complement cascade can be activated in three ways…
Nonspecific Defenses- Activation of innate
immunity
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Complement system (Cont’d)
Antibody binding
Binding of serum protein (Lectin)
to bacteria
Direct binding of
complement
protein to carbs
on surface of
bacterial cells
Nonspecific Defenses- Activation of innate
immunity
Figure 23.7 (Pearson) | Complement activation and actions
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• Depends on
presence of
antibodies
• Proteins: C1 – C9
• Non-specific, fast compared to classical
pathway; does not rely on production of
antibodies
• Lectins bind specific carbs
• MBL = mannose binding lectin
• Non-specific, fast
compared to classical
pathway; does not
rely on production of
antibodies
• Activates at point
further along than
classical i.e. at C3
Complement system (Cont’d)
Nonspecific Defenses- Activation of innate
immunity
Figure 23.8 (Pearson) | Complement pathways
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Details of MAC (Membrane Attack Complex
Layers of Defense
Physical – skin, mucous membranes, mucus and other secretions
Chemical – enzymes, antibodies, pH
Non-specific (innate) Immune Response
Rapid, non-specific, no memory
Cells – macrophages*, neutrophils, NK cells, dendritic cells*, eosinophils, basophils
Chemical – complement system, interferons
Specific (adaptive) Immune Response
Slow, specific, memory
Humoral immunity and Cell-mediated responses – B cells (plasma cells), T cells
(cytotoxic T, Helper, Regulatory T cells)
Antibody-mediated responses – antibodies
Pathogen destruction/suppression
Defense Mechanisms - 2 types: innate, adaptive
Innate (nonspecific) immunity – inherited; includes
physical barriers, phagocytosis, and more; trained
immunity – cells that show increased effectiveness
during a second exposure to a pathogen that may be
due to epigenetic cell changes
Adaptive (specific) immunity – learned from exposure
to specific pathogens (immunological memory); function
of lymphocytes and antigens
Virus,bacterium parasite and fungi activate immune system
Nonspecific Defenses- Activation of innate
immunity
• Fast protection, recognition of pathogen but non-specific
• Cells distinguish “self” from “non-self” via pathogen-associated molecular
patterns (PAMPs) unique to the pathogens
– Pattern recognition receptors (PRRs) on immune cells bind to PAMPs to initiate the
innate immune response
– Examples of PAMPs include:
1) Includes lipopolysaccharides (LPS) found in the envelop of Gram-negative bacteria
2) Peptidoglycan from the cell walls of Gram-positive bacteria
• Non-specific defenses include:
1. Physical barriers (previously covered, slide 6)
2. Inflammation
3. Interferons
4. Complement system
Lecture 9 Muscle Physiology
Muscles
There are 3 muscle types smooth cardiac a skeletal
Muscles like neurons are excitable tissues
Action potentials induce contractions to generate force→movement occurs
Skeletal muscle
Tendons -connective tissue that transmit
force from the muscle to the bone.
Muscles are connected to bone via
tendons
Fascicles -bundles of individual
muscle cells. Each fascicle
contains thousands of muscle
cells, called muscle fibers
perimysium - connective
tissue. Divides the body into
numerous bundles of
individual muscle cells
(fascicles)
endomysium thin connective
tissue covering each muscle fiber
Epimysium - connective
tissue surrounding the
muscle tissue
Structure at the Cellular Level
muscle fiber or fascicles components
multiucleated
sarcolemma - plasma membrane
sarcoplam - cytoplam
mitochondria Myofibrils
arcoplasmic reticulum (SR)
• Surrounds each myofibril
• Associates with T-Tubules
• Near the T-tubules, the SR has regions
called, Lateral sacs/terminal cisternae
= store calcium
– Transverse tubules (T-tubules) – run
continuous with the sarcolemma and
plays a role in muscle contraction
components of a muscle fiber (Cont’d)
– Note relationship between sarcolemma and T-tubule
– Note relationship between SR and terminal cisternae
– Triad = one T-
tubule and two
terminal cisternae
(lateral sacs)
Functions:
– Sarcoplasmic reticulum (SR) and transverse tubules (T-
tubules) are important in activation of muscle contractions
• Transmit signals from sarcolemma to myofibrils
– Sarcoplasmic reticulum and terminal cisternae
• Store Ca2+
• SR membrane has calcium pumps
– Active transport of calcium ions into SR
– Cytoplasmic levels of calcium normally low due to pumps
Motor units & Somatic neurons
• A motor unit = one somatic motor neuron +
all the muscle fibers it innervates
• Functional Principle:
• When a motor neuron is activated, all
muscle fibers in its motor unit
contract simultaneously
• The cell body of a somatic motor
neuron is located in the ventral
horn of the spinal cord gray matter.
• A single axon exits via the ventral
root of a spinal nerve.
• The axon branches into multiple
collateral fibers, each innervating
a different muscle fiber.
Neuromuscular Junction & Muscle Fiber Activation
Each muscle fiber is
innervated by a single somatic
motor neuron via a synaptic
bouton.
• The neuron releases
acetylcholine (ACh) at
the neuromuscular
junction (NMJ).
• ACh binds to receptors
on the motor end plate
(specialized region of the
sarcolemma).
Motor End Plate Structure:
• Deep folds increase surface area
• Crests: high density of ACh
receptors
• Troughs: rich in voltage-gated Na⁺
channel
Structure at the molecular level
Myofibrils
– Contain protein fibers
• Thick filaments -myosin
• Thin filaments - actin
9
2(thin):1(thick) ratio
Orderly arrangement
of thick and thin
filaments give skeletal
and cardiac muscle
striated appearance
Structure of Sarcomere at the
Molecular Level