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190 Cards in this Set

  • Front
  • Back
What situation could result in maternal antibodies attacking fetal blood cells during a second pregnancy?
Mom is Rh negative and fetus is Rh positive
(Hemolytic Disease of the Newborn - HDN)
Stercobilin and urobilin are both breakdown products of what component of blood?
Heme
The intrinsic and extrinsic pathways of blood clotting are identical after formation of ...
Prothrombinase
What are components of blood?
Blood plasma 55%
Formed elements
Platelets
White blood cells
Red Blood cells
Types of Bones
Long
Flat
Irregular
Short
Sesamoid
Long
Flat
Irregular
Short
Sesamoid
Long Bones
Long
Consist of a shaft and epiphysis
Slightly curved to absorb weight
Compact bone tissue & Spongy bone tissue
[e.g. femur, tibia, fibula, humerus, ulna, radius, phalanges]
Short Bones
Cube shaped
Spongy bone with a thin layer of compact bone tissue
[e.g. carpal and tarsal bones]
Flat Bones
Thin and composed of two nearly parallel plates of compact bone tissue enclosing a layer of spongy bone tissue
Afford protection and provide areas of attachment for muscles
[e.g. cranial bones, sternum, ribs, and scapulae]
Irregular Bones
Complex shapes
Vary in amount of spongy and compact bone
[e.g. vertebrae, hip bones, facial bones, and calcaneus]
Sesamoid Bones
Develop in certain tendons where there is considerable friction, tension and physical stress
Vary in number from person to person
Usually small
Protect tendons from excessive wear and tear
Often change the direction of pull of a tendon
[e.g. patellae, bones in palms and soles]
Axial Skeleton
The bones along a longitudinal axis of the body
[skull (cranium and face), hyoid, auditory ossicles, vertebral column, and thorax (sternum and ribs)]
80 Bones
The bones along a longitudinal axis of the body
[skull (cranium and face), hyoid, auditory ossicles, vertebral column, and thorax (sternum and ribs)]
80 Bones
Appendicular Skeleton
Whatever bones are added to the axial skeleton (appendages) 
[pectoral girdles (clavicle and scapula), upper limbs (humerus, ulna, radius, carpals, metacarpals, and phalanges), pelvic girdle, lower limbs (femur, patella, fibula, tibia, tarsals, m...
Whatever bones are added to the axial skeleton (appendages)
[pectoral girdles (clavicle and scapula), upper limbs (humerus, ulna, radius, carpals, metacarpals, and phalanges), pelvic girdle, lower limbs (femur, patella, fibula, tibia, tarsals, metatarsals, and phalanges)]
126 Bones
Fetal Vertebral Column
Single concave curve
Adult Vertebral Column
Four curves, two concave and two convex
Primary: Thoracic and Sacral curves that retain the concave shape
Secondary: Cervical and Lumbar curves that grow to be convex
Cranial Bones
Frontal
Parietal
Sphenoid 
Ethmoid
Lacrimal
Zygomatic
Vomer
Temporal
Nasal
Maxilla
Mandible
Occipital
Frontal
Parietal
Sphenoid
Ethmoid
Lacrimal
Zygomatic
Vomer
Temporal
Nasal
Maxilla
Mandible
Occipital
Scoliosis
Lateral bending of the vertebral column in the thoracic region
Kyphosis
Hunchback
Increase in the thoracic curve
Lordosis
Increase in the lumbar curve
"hollow back"
Atlas Vertebra
Large arch
No spinous process
Largest superior articulating process
First cervical vertebra
Axis Vertebra
Has an 8th process: Dens process (pivot)
Second cervical vertebra
Cervical Vertebrae
Have bifurcated spinous processes
Small bodies
Large vertebral arch
3 foramina: 1 vertebral foramen (largest in all the spinal column), 2 transverse foramina
Thoracic Vertebrae
Large and strong
Slanted spinous processes
Costal facets for articulation with the tubercles of the ribs
Superior articular facets for articulation with the heads of ribs
Demifacets on the sides
Lumbar Vertebrae
Largest and strongest
Largest bodies
Hatchet-shaped spinous processess
Quadrilateral in shape, thick and broad
Sacrum
Triangular bone formed by the union of 5 sacral vertebrae
8 sacral foramina
Top: Base; Bottom: Apex
Coccyx
Tailbone
Triangular in shape
Formed by the fusion on 4 coccygeal vertebrae
Points anteriorly
Sutures
Fxn: Immovable joints between bones of the skull that absorb shock and keep pressure from building up in the cranium
Coronal
Saggital
Lambdoid
Squamous
Fontanels
Fxn: "soft spots", membranous sections of the skull that allow the head to be flexible for birth and enable the brain the grow
Anterior
Posterior
Anterolateral (2)
Posterolateral (2)
Canal/Meatus
Tube-like passageway
Condyle
Rounded articular process
Foramen
Opening or hole through a bone
Fossa
Shallow depression
Ramus
Branch-like process
Fissure
Narrow slit or cleft in the bone
Spinal Process
Pointed posterior projection
Transverse Process
Extends laterally from each pedicle to the side
Sternoclavicular Joint
Where the clavicle articulates with the manubrium of the sternum
Acromioclavicular Joint
Where the scapula articulates with the clavical
Glenohumeral Joint
Where the scapula articulates with the humerus
The 3 hip bones
Ilium
Ischium
Pubis
Male Pelvis
Heavy
Rough
Large
Vertical
Narrow true pelvis
Tilted forward
Pelvic inlet is heart shaped
<90 degree pubic arch angle
Female Pelvis
Small
Light
Large true pelvis
Tilted forward
Flared
Pelvic inlet is round or oval
>90 degree pubic arch angle
Wide sciatic notch
True Pelvis
Portion of pelvis inferior to pelvic brim
Surrounds the pelvic cavity
False Pelvis
Portion of pelvis superior to pelvic brim
Wide area extending to top of the iliac crest
Directional Terms
Posterior
Anterior
Lateral
Medial
Superior
Inferior
Distal
Proximal
Contralateral
Ipsilateral
Number of Bones in the Upper Extremity
(And know where they are)
64
Clavicle - 2
Scapula - 2
Humerus - 2
Ulna - 2
Radius - 2
Carpals - 16
Metacarpals - 10
Phalanges - 28
Structural Joint Classification
Based on the presence or absence of a space between the articulating bones
Also based on the type of connective tissue that binds the bones together
Synovial
Cartilaginous
Fibrous
Synovial Joints
The bones forming the joint have a synovial cavity and are united by the dense irregular connective tissue of an articular capsule, and often by accessory ligaments
Cartilaginous Joints
No synovial cavity, and the bones are held together by cartilage
Fibrous Joints
No synovial cavity, and the bones are held together by dense irregular connective tissue that is rich in collagen fibres
Functional Joint Classification
Relates to the degree of movement the joint permits
Synarthrosis
Amphiarthrosis
Diarthrosis
Synarthrosis Joints
Immovable joint
Amphiarthrosis Joints
Slightly movable joint
Diarthrosis Joint
Freely movable joint
All are synovial joints
Hyaline Cartilage
The type of cartilage that covers the articular ends of bones
Synovial Fluid
The fluid that lubricates, reduces friction, and gives nutrition to a joint
Articular Cartilage
The tissue at the end of a bone that reduces friction in a joint
Bursae
The sac-like structure that is sometimes present to reduce friction
Synovial Membrane
Structure that secretes synovial fluid
Articular Capsule
Surrounds a synovial joint, encloses the synovial cavity, and unites the articulating bones
Fibrous Membrane
Consists of dense irregular connective tissue that attaches to the periosteum of the articulating bones
Synovial Cavity
A space between articulating bones
Factors affecting ROM in synovial joints
Articulating bones - shape or structure
Ligaments - tightness and strength
Muscles - Arrangement and tension
Body part contact
Hormones
Disuse
Aging in Joints
Decreased production of synovial fluid in joints
Articular cartilage thins
Ligaments shorten and lose flexibility
Rheumatism and Arthritis
Diseases of Joints
Rheumatoid Arthritis
Osteoarthritis
Gouty Arthritis
Rheumatoid Arthritis
Joints are swollen, stiff and painful
Body attacks its own tissues
Inflammation of the joints
Loss of function
Occurs bilaterally
Osteoarthritis
Due to wear and tear of the body
degenerative joint disorder
joint cartilage is gradually lost
ends of the bones are exposed
bones grow more and create spurs, which add to the discomfort
first the hips and the knees effected
mainly the articular cartilage
Gouty Arthritis
build up of uric acid in the blood
reacts with sodium and creates crystals that accumulate in the tissues of joints
kidneys and feet effected
associated with a lot of alcohol and red meat intake
Functions of Muscle Tissue
Movement
Stabilizing Body Positions
Storing and Moving Substances within the body
Heat production
Properties of Muscle Tissue
Electric Excitability
Contractibility
Extensibility
Elasticity
Electric Excitability
Ability to respond to a stimulus
Contractility
Develops tension and can shorten length (or vice versa)
Extensibility
Extend or stretch
Elasticity
Can return to original shape after contraction or extension
Skeletal muscle contraction will continue to occur as long as what chemicals are available in the cytosol of the muscle fibre?
Calcium Ions and ATP
Aerobic cellular respiration in skeletal muscles
Pyruvic acid generated by glycolysis enters the mitochondria
O2 is essential
CO2 is produced as a waste product
Can be used to generate ATP from fats, proteins or carbohydrates
After prolonged strenuous exercise has stopped, heavy breathing will often continue for several minutes in order to provide the oxygen needed to...
Convert the lactic acid produced during exercise back into glycogen
Resynthesize creatine phosphate
Replace oxygen displaced from muscle myoglobin
Myasthenia Gravis is an autoimmune disorder that targets the ACh receptors at the NMJ and ultimately reduces the number of available receptors. Predict what happens if you treat the patient with a drug that inhibits the activity of acetylcholinesterase?
Normal contraction
What region of a sarcomere contain thin filaments?
I band
The type of tendon formed when the connective tissue elements of a skeletal muscle extend as a broad flat layer
Aponeurosis
The sequence of structures that action potentials must move through to excite skeletal muscle contraction
Axon of neuron - Sarcolemma - T tubules
Myofibrils contain ...
Contractile proteins
Regulatory proteins
Structural proteins
Calcium ions are released from the sarcoplasmic reticulum into the cytosol ...
at the beginning of contraction
What energizes the myosin head?
ATP hydrolysis reaction
Epimysium
The outermost layer of dense, irregular connective tissue, encircling the entire muscle
Perimysium
A layer of dense, irregular connective tissue
Surrounds groups of 10-100 or more muscle fibres, separating them into bundles called fascicles
Endomysium
Penetrates the interior of each fascicle and separates individual muscle fibre from one another
Reticular fibres
Somatic Motor Neurons
Stimulate skeletal muscle fibres to contract
Joined with the muscle at the neuromuscular junction
Hypertrophy
The increase of the size of existing muscle fibres
Hyperplasia
The increase in the number of muscle cells
Sarcolemma
The plasma membrane of a muscle cell
Sarcoplasm
The cytoplasm of a muscle fibre
T Tubules
Tiny invaginations of the sarcolemma that tunnel in from the surface toward the centre of each muscle fibre
Myofilaments
Protein structures within myofibrils 
Thin filaments: composed mostly of protein actin
Thick filaments: composed mostly of the protein myosin
Both are directly involved in the contractile process
2 thin filaments for ever thick filament
Protein structures within myofibrils
Thin filaments: composed mostly of protein actin
Thick filaments: composed mostly of the protein myosin
Both are directly involved in the contractile process
2 thin filaments for ever thick filament
Sarcomere
The basic functional units of a myofibril
The filaments inside a myofibril are arranged in these compartments
Sarcomere Regions
Z disc
M line
I band
A band
H zone
Z disc
M line
I band
A band
H zone
Z disc
Narrow, plate-shaped region of dense protein material
Separate one sarcomere from the next
M line
The middle of the sarcomere
Formed by supporting proteins that hold the thick filaments together at the center
I band
A lighter, less dense area that contains the rest of the thin filaments but no thick filaments
A Z disc passes through the centre of each
A band
The darker middle part of the sarcomere
Extends the entire length of the thick filaments
H zone
Narrow
In the centre of each A band
Contains thick but no thin filaments
Location of the Heart
Mediastinum: from the sternum anteriorly to the vertebral column posteriorly, medially between the two lungs and the pleural membranes that cover them, sits on the diaphragm
Heart Layers
Pericardium - triple-layered sac that surrounds & protects the heart
Myocardium - middle layer; large thick muscle portion
Epicardium - thin, transparent outer layer of the heart wall
Endocardium - Inner layer
Contractile Proteins
Proteins that generate force during muscle contraction
-Myosin
-Actin
Regulatory Proteins
Proteins that help switch muscle contraction process on and off
-Tropomyosin
-Troponin
Structural Proteins
Proteins that keep thick and thin filaments of myofibrils in proper alignment, give myofibrils elasticity and extensibility, and link myofibrils to sarcolemma and extracellular matrix
-Titin
-Actinin
-Myomesin
-Nebulin
-Dystrophin
Myosin
Makes up thick filaments
A tail and two heads
Bind to myosin binding sites on actin molecules of thin filaments during muscle contraction
Actin
The main component of thin filaments
Tropomyosin
A component of thin filament
When the skeletal muscle is relaxed it covers myosin-binding sites on actin molecules to prevent myosin from binding to actin
Troponin
Component of thin filament
When Ca ions bind to it, it changes shape, which moves tropomyosin away from myosin-binding sites on actin molecules
Titin
Connects Z disc to M line of sarcomere
Stabilizes thick filament position
Can stretch and then spring back unharmed
Actinin
Protein of Z disc that attaches to actin molecules of thin filaments and to titin molecules
Myomesin
Forms M line of sarcomere
Binds to titin molecules and connects adjacent thick filaments to one another
Nebulin
Wraps around the entire length of each thin filament
Helps anchor thin filaments to Z discs
Regulates length of thin filaments during development
Dystrophin
Links thin filaments of sarcomere to integral membrane proteins in sarcolemma
Helps reinforce sarcolemma and help transmit tension generated by sarcomeres to tendons
4-Step Contraction
1.) Release of acetylcholine from synaptic vesicle 
2.) Activation of ACh receptors 
3.) Production of muscle action potential 
4.) Termination of ACh activity (ACh is broken down)
1.) Release of acetylcholine from synaptic vesicle
2.) Activation of ACh receptors
3.) Production of muscle action potential
4.) Termination of ACh activity (ACh is broken down)
Sliding Filament Theory
1.) ATP hydrolysis: myosin heads hydrolyze ATP and become reoriented and energized
2.) Attachment of myosin to actin to form cross-bridges
3.) Power stroke: Myosin cross-bridges rotate towards the centre of sarcomere
4.) Detachment of myosin from actin: as myosin heads bind to ATP, the cross-bridges detach from actin
Cross-bridges
When the myosin heads attach to actin during contraction
Role of Calcium in Contraction
An increase in Ca ion concentration in the sarcoplasm starts muscle contraction, and a decrease stops it
Stored inside the sarcoplasmic reticulum
Binds with troponin
Acetylcholine (ACh)
Neurotransmitter that's released because of the activation of a motor nueron
Acetylcholinesterase
Breaks down ACh after a short period of time (enzyme)
3 Sources of ATP
1.) Phosphagen System (stored ATP) 3 sec.
2.) Glycolysis (anaerobic respiration, no O2 available) 30-40 sec.
3.) Aerobic Respiration (krebs cycle, cellular respiration in the mitochondria, 36 mol. of ATP) min.-hours
Motor Unit
Consists of a somatic motor neuron plus all the skeletal muscle fibres it stimulates 
A single one makes contact with an average of 150 skeletal muscle fibres 
All of the muscle fibres in one unit contract in unison
Consists of a somatic motor neuron plus all the skeletal muscle fibres it stimulates
A single one makes contact with an average of 150 skeletal muscle fibres
All of the muscle fibres in one unit contract in unison
Twitch Contraction Periods
1.) Latent period: the delay (2 milliseconds)
2.) Contraction period: 10-100 milliseconds, Ca binds to troponin, myosin binding sites on actin are exposed, and cross-bridges form 
3.) Relaxation period: 10-100 milliseconds, Ca is actively transp...
1.) Latent period: the delay (2 milliseconds)
2.) Contraction period: 10-100 milliseconds, Ca binds to troponin, myosin binding sites on actin are exposed, and cross-bridges form
3.) Relaxation period: 10-100 milliseconds, Ca is actively transported back into the sarcoplasmic reticulum, myosin-binding sites are covered by tropomyosin, myosin heads detach from actin, and tension in the muscle fibre decreases
Unfused (incomplete) tetanus
A skeletal muscle fibre is stimulated at a rate of 20-30 times per second
Can only partially relax between stimuli
A skeletal muscle fibre is stimulated at a rate of 20-30 times per second
Can only partially relax between stimuli
Fused (complete) tetanus
Skeletal muscle fibre is stimulated at a higher rate of 80-100 times per second
Does not relax at all
Sustained contraction in which individual twitches cannot be detected
Skeletal muscle fibre is stimulated at a higher rate of 80-100 times per second
Does not relax at all
Sustained contraction in which individual twitches cannot be detected
Spasm
Sudden involuntary contraction of a single muscle within a large group of muscles
Cramps
Involuntary and often painful muscle contractions
Caused by inadequate blood flow to muscles, overuse and injury,or abnormal blood electrolyte levels
Tremor
Rhythmic
Oxygen Debt
The added oxygen over and above the resting oxygen consumption that is taken into the body after exercise
Used to "pay back" or restore metabolic conditions to the resting level
Functions of Blood
Transportation
Regulation
Protection
Plasma
91.5% water with dissolved solutes
Proteins: Albumins, globulins, fibrinogen
Albumins
Major clotting proteins
Antibodies and Enzymes
Synthesize in the liver
Give rise to blood's viscosity
Help maintain BP
Globulins
Make up antibodies (gamma)
Carry bilirubin and steroids (alpha)
Carry copper and iron (beta)
Control blood osmotic pressure
Act as carrier molecules
Fibrinogen
Involved in blood clot formation
Hematocrit
The percentage of the total blood volume occupied by RBCs
Erythropoiesis
Production of RBCs
Increased in low levels of O2
Production of RBCs
Increased in low levels of O2
Erythropoietin
Found in the kidneys and liver
Increases the number of RBC precursor cells to give rise to more RBCs
Fibrinolysis
Dissolves small inappropriate clots
Once the clot isn’t needed it dissolves those clots too
Development of Blood cells
Blood Types
A, B, AB, O
A, B, AB, O
Agglutination
The clumping of blood cells
Hemolysis
Getting the wrong type of blood
The rapid destruction of the donor red blood cells
Anemia
Low percentage of RBCs or hemoglobin
Most often the result of low iron intake, hemolysis, autoimmune disease, blood loss, or lack of production in the bone marrow
Polycythemia
The percentage of RBCs is abnormally high
The hematocrit may be 65% or higher
Sickle Cell Disease
The RBCs contain HB-S, an abnormal kind of hemoglobin
The RBCs are sickle-shaped and rupture easily
Leads to anemia
Contraction and Relaxation in a skeletal muscle fibre
How long are RBCs in circulation for?
120 days
Formation and Destruction of RBCs
1.) Macrophages in spleen, liver or red bone marrow phagocytize old RBCs
2.) Globin and Heme are split apart
3.) Globin broken down into amino acids
4.) Iron removed from the heme and associates with transferrin 
5.) Fe3+ detaches from transfe...
1.) Macrophages in spleen, liver or red bone marrow phagocytize old RBCs
2.) Globin and Heme are split apart
3.) Globin broken down into amino acids
4.) Iron removed from the heme and associates with transferrin
5.) Fe3+ detaches from transferrin and attaches to ferritin (iron-storage protein)
6.) Fe3+ reattaches to transferrin on release or absorption
7.) Fe3+ - transferrin complex is carried to red bone marrow where it is used for hemoglobin synthesis
8.) Erythropoiesis in red bone marrow results in the production of RBCs

9.) Non-iron portion of heme is converted to biliverdin and then into bilirubin
10.) Bilirubin enters the blood and is transported to the liver
11.) Bilirubin is released into bile and passes into the small and then large intestines
12.) In the large intestine bacteria convert bilirubin into urobilinogen
13.) Some urobilinogen is absorbed back into the blood and converted into a yellow pigment called urobilin and excreted in urine
14.) Most urobilinogen is eliminated in feces as a brown pigment called stercobilin
Granular vs. Agranular WBCs
If the cells appear granulated when stained
If the cells appear granulated when stained
Granular WBCs
Neutrophils (60-70%)
Eosinophils (2-4%)
Basophils (0.5-1%)
Agranular WBCs
Lymphocytes (20-25%)
Monocytes (3-8%)
Neutrophils
Phagocytosis
Most abundant
Nucleus has 2-5 lobes
Eosinophils
Combats effectiveness of histamines
Allergic reactions
Fights parasites
Nucleus has 2 lobes
Basophils
Inflammation response
Allergic reaction
Least numerous
Dark blue granules
Lymphocytes
"Immune Response"
Specific to different antigens int he body
Found in lymphoid tissues and lymph
T-cells: immune response, destroys bacteria
B-cells: develop into plasma cells to produce antibodies
NK Cells: defenders, attack microbes
Monocytes
Macrophages: wandering/fixed
Major histocompatibility antigens (MHC): proteins that protrude from the plasma membrane so the body can recognize them as foreign or not
Cell communication
Emigration
WBCs leaving the blood stream to collect where they’re needed
Chemotaxis
Signaling to bring phagocytes to the site where they’re needed
Platelet Formation
Thrombopoietin
Megakaryocyte growth and development hormone
Produced by the liver and kidneys
Megakaryocytes
Huge cells that splinter into 2000-3000 fragments, each fragment being a platelet
Megakaryoblasts
The precursor cells to megakaryocytic
Chambers of the Heart
Right atrium: received deoxygenated blood from the vena cava
Right ventricle: pumps blood out of the heart to the lungs through the pulmonary arteries 
Left atrium: receives newly oxygenated blood from the lungs through the pulmonary veins 
Lef...
Right atrium: received deoxygenated blood from the vena cava
Right ventricle: pumps blood out of the heart to the lungs through the pulmonary arteries
Left atrium: receives newly oxygenated blood from the lungs through the pulmonary veins
Left ventricle: pumps blood to the body through the aorta
Chordae Tendineae
Tendon-like cords connected to the valves
Papillary Muscles
Cone-shaped trabeculae carneae
Anchor the Chordae Tendineae
Septum
Either interventricular or interartriular
Separates the chambers (ventricles or atria)
The path of blood through the pulmonary and systemic circulations
Right atrium
Right atrium
Tricuspid valve
Right Ventricle
Pulmonary Valve
Pulmonary Trunk
Pulmonary Arteries
Pulmonary Capillaries
Pulmonary Veins
Left Atrium
Bicuspid Valve
Left Ventricle
Aortic Valve
Aorta
Systematic Arteries
Systematic Capillaries
Systematic Veins
Superior and Inferior Vena Cava
Coronary Sinus
Right atrium
Heart Valves and how they work
Atrioventricular and Semilunar
Blood always flows from an area of high pressure to an area of low pressure
The flow of blood operates the valves of the heart
Atrioventricular Valves
Bicuspid and Tricuspid
Semilunar Valves
Aortic and Pulmonary
Stenosis
The narrowing of a heart valve
Murmur
Abnormal sounds in the heartbeat cycle
Myocardium
Separates the different chambers of the heart
Coronary Arteries
Supply blood to the heart tissue
Coronary Circulation
Only the innermost tissues lining the chambers of the heart can derive oxygen from the blood flowing through those chambers
Only during the relaxation phase
Intercalated Discs
Connect the individual heart muscle cells
Thickening of the sarcomatic lining
Gap Junctions
Allow direct transmission of the depolarizing current from cell to cell, across the chambers of the heart, so that the cells contract in unison
Desmosomes
Hold the cardiac muscle cells together
Order of impulse conduction in the heart
SA (sinoatrial) Node
AV (atrioventricular) Node
AV Bundle
Bundle Branches
Purkinje fibres
Sinoatrial Node
The 'Natural Pacemaker'
Sets the pace for the rest of the conduction
Atrioventricular Node
Slows the signal down, allowing the atrium to mechanically move blood into the ventricles
Action Potential through the heart
step 1: Depolarization - threshold is reached and AP starts, opens Na+ gated channels (fast) and inflow into muscle fibre produced rapid depolarization
step 2: Plateau - maintains depolarization, Ca+2 gated channels (slow) open and inflow into cytosol through the sarcolemma into the cardiac fibre
step 3: Repolarization: Recovery of Resting Membrane Potential, K+ gated channels are opened and outflow closes Ca+2 and Na+ channels
Electrocardiogram (ECG)
Recording of the electrical current as APs pass through the heart
P wave
QRS Complex
T wave
Recording of the electrical current as APs pass through the heart
P wave
QRS Complex
T wave
P Wave
Atrial Depolarization
Small upwards deflection
Contraction
QRS Complex
Ventricular depolarization and atrial repolarization
Begins as a downward deflection, continues as a large upright triangular wave, and ends as a downward wave
T Wave
Ventricular repolarization
Dome-shaped upward deflection
Relaxation
Diastole
Relaxing
Systol
Contraction
Heart Sounds
'lub' - louder and longer
'dup' - shorter and quieter
Factors of Heart Rate
Hormones
Age
Gender
Fitness
Temperature