Circulatory System Flashcards

1
Q

describe the components of blood

A

main components are cells and plasma

cells - erythryocytes, leukocytes and thrombocytes

plasma - extracellular fluid, water, electrolytes, organic molecules, plasma proteins

plasma proteins are 60% albumin, 35% globulin, 4% fibrinogen and 1% regulatory proteins

plasma takes up 55% of blood volume, and cells take up 45% of blood volume.

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2
Q

describe red blood cells and how they are formed

A

morphology
- biconcave disc shape
- 6-8 microns

turnover
- average lifespan is 120 days, old are removed from circulation by mononuclear phagocyte system
- breakdown products of haemoglobin protein aspect is amino acids and haem is iron, biliverdin and bilirubin

formation
- made in red bone marrow, which is found at the epiphysis of long bones, hip, skull and sternum.
- regulated by erythropoietin, a glycoprotein cytokine, and rewuires folic acid and vitamin B12.
- iron is required for increasing the haemoglobin content of red blood cells
- day 1 is the proerythroblast
- day 2 is the basophilic erythroblast
- day 3 is the polychromatophilic erythroblast
- day 4 is the normoblast and this is when nucleus is ejected
- day 5-7 is the reticulocyte which enters the circulation

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3
Q

describe the structure and function of haemoglobin

A

structure
- 64,000 dalton weight
- globular protein
- 2 alpha and 2 beta chains
- each has four haeme groups, composed of a porphyrin ring and an iron atom
- porphyrin rings have 4 carbons and 1 nitrogen
- per red blood cell there are 200-300 haemoglobin molecules
- max saturation is 98%

function
- transport of oxygen via haemoglobin oxygen dissociation curve
- transport of carbon dioxide, carbon anhydrase produces bicarbonate and carbamino compounds

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4
Q

describe the features of the various leucocytes in the blood

A

neutrophils
- multilobed nucleus
- condensed chromatin
- 12-14 micrometers
- lifespan of a few days
- few organelles

eosinophils
- bilobed nucleus that segments with age
- 12-17 micrometers diameter

basophils
- 14-16 micrometers
- bilobed nucleus
- granules

monocyte
- largest, at 20 micrometers
- circulate for 3-4 days before migrating to tissues
- phagocytic
- large nucleus, does not stain as well because the chromatin is loosely packed

lymphocytes
- 6-9 micrometers
- 20-50% of leucocytes

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5
Q

describe the structure and function of platelets

A
  • derived from megakaryocytes in the bone marrow
  • cellular fragments of 2 micrometer diameter
  • involved in haemostasis
  • form platelet plugs by aggregating on damaged vessel walls and release of the vasoconstrictor thromboxane A2
  • source of platelet factor, which is a phospholipid important for coagulation.
  • normally there are 150-400x10>9 per litre
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6
Q

explain the different blood groups

A

erythrocytes carry antigens on their membrane, and these determine blood group

group A
- 42% of people in the UK
- has the A antigen
- AA and AO genotype
- anti B antibodies

group B
- 10% of people in the UK
- B antigen
- BB and BO genotype
- anti A antibodies

group AB
- 4% of people
- AB antigen
- AB genotype
- no natural antibodies

group O
- 44% of people in the UK
- no antigens
- OO genotype
- anti B and anti A antibodies

Rhesus factor positive
- 83% of people in the UK
- Rh antigen
- DD and DO genotype

Rhesus factor negative
- 17% of people
- no antigen
- OO genotype

Universal donor is O because they have no antigens

Universal recipient is AB because they have no antibodies

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7
Q

describe local control of blood flow

A

autoregulation
- maintenance of constant blood flow while arterial pressure changes

active hyperemia
- blood flow is proportional to metabolic activity
- increased blood flow when metabolic activity increases

reactive hyperemia
- increased blood flow in response to a prior period of decreased blood flow

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8
Q

explain the factors that determine resistance to blood flow and how it can be calculated

A

vessel diameter, length and blood viscosity

diameter
- change in diameter has a large change in resistance

viscosity
- increased viscosity can occur due to dehydration or immobility

length
- remains the same

poiseuilles equation
- flow is equal to radius to the power of 4 times change in pressure over viscosity times length of the vessel
- assumes flow is through a straight pipe, non pulsatile and smooth.
- flow equals change in pressure over change in resistance

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9
Q

describe the different kinds of circulations with specialised local control

A

coronary circulation
- perfusion of the myocardium
- maintains high basal rate of oxygen to cardiac muscle
- delivers 5% of cardiac output
- arteries originate at the foot of the aorta behind the cusps of the aortic valve
- left coronary divides into left circumflex (left atria and ventricle) and left anterior descending (septum, and parts of both ventricles)
- epicardial veins collect deoxygenated blood and transport it to the coronary sinus, emptying into the right atrium.
- thebesian veins drain blood directly from the ventricular wall to the cardiac chambers.
- at rest, 70-80ml per min per 100g. during exercise, 300-400ml per min per 100g.
- 80% of left coronary blood flow occurs during diastole

skeletal muscle circulation
- adapted to meet the metabolic demand of skeletal muscle during exercise
- at rest, blood flow is regulated by sympathetic innervation.
- during exercise, it is mediated by lactate, adenosine and potassium ions.
- adrenaline binds to beta 2 adrenergic to vasodilate, decreasing resistance and increasing blood flow
- alpha 1 induced adrenergic induces vasoconstriction to reduce blood flow

cerebral circulation
- maintains cerebral perfusion
- 50% of all vascular resistance occurs here
- basilar and internal carotid form the circle of willis, which preserves perfusion if the carotid artery is obstructed
- cerebral autoregulation when BP falls - vasodilation of cerebral resistance vessels. if falls below 60mmHg there is hypotension and confusion symptoms.
- cerebral resistance vessels are sensitive to local hypoxia. hypercapnia leads to vasodilation mediated by nitric oxide. hypocapnia leads to vasoconstriction.
- local hypoxia causes vasodilation.

pulmonary, renal and skin have special control as well

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10
Q

describe the local control mechanisms that alter arteriolar resistance and influence flow autoregulation

A

pulse pressure is force generated by the heart to overcome arterial resistance, afterload is the force the heart is pumping against.

mean arterial pressure can be determined from diastolic BP and pulse pressure, or from CO times TPR

local control is altering of the small arterioles in organs and tissues

hormonal local control
- adrenaline is released from the medulla to bind to beta 2 adrenergic and vasodilate
- if at high concentrations, adrenaline will bind to alpha 1 adrenoreceptors to vasoconstrict
- ANP is a vasodilator and influences blood volume in the kidneys
- angiotensin II constricts arterioles

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11
Q

describe the function of endothelial cells and relate to regulation of vascular compliance

A

vascular compliance is the ability of the blood vessel to passively expand and recoil in response to changes in pressure.

endothelium forms the tunica intima of blood vessel walls and can produce vasoactive substances that regulator vascular tone. also provides a friction free surface for blood flow by being arranged along the axis and will regulate permeability to form a barrier between blood and tissue. promotes angiogenesis, coagulation and fibrinolysis.

endothelium causes vasodilation by:

vasoactive substances produced from the endothelium include:
- nitric oxide, produced from nitrix oxide synthase from L arginine in vascular endothelial cells, in response to binding of Ach, ATP and bradykinin. induces relaxation and dilation.
- prostaglandin 12, eicosanoid, vasodilation via activation of protein kinase A.

endothelium causes vasoconstriction by:
- endothelin 1, due to stretch and stress, causes vasoconstriction by acting on ETa receptor
- thromboxane A2, eicosanoid activated by tissue injury and inflammation

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12
Q

describe the features of the different blood vessels

A

arteries
- blood from heart to tissue
- thick walls, lots of elastic
- pressure reservoir to maintain blood flow
- small volume at high pressure
- muscular arteries are coronary and renal

capillaries
- large cross sectional area
- low blood flow rate
- large surface area
- diameter of 5-10 micrometers
- flow depends on arteriolar supply
- no media or adventitia
- exchange between blood and tissue

veins
- blood from tissues to heart
- large diameter and large lumen
- thin, disorganised walls
- 70% of total blood volume
- valves to prevent backflow
- varicose veins if lost elasticity

vessel wall structure is the same for arteries and veins

tunica intima
- inner lining, separated from the media by the internal elastic lamina
- endothelial cells line it
- underlying layer of extracellular matric

tunica media
- elastin fibres and smooth muscle cells

tunica adventitia
- outer lining, thick connective tissue, nerve fibres and lymphatics

in larger vessels, vasa vesorum can perfuse the outer media - they are the vessels of vessels

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13
Q

describe the factors that influence transport of fluids across the capillary wall

A

capillaries have three classifications

continous
- muscle, skin, pulmonary system, CNS
- continous basement membrane
- tight intercellular clefts
- low permeability

fenestrated
- exocrine glands
- renal glomeruli
- perforations enable high permeability

discontinuous
- liver
- large intercellular clefts and gaps
- high permeability

hydrostatic pressure forces fluid out of the capillaries
osmotic pressure pulls fluid back into the capillaries

negative filtration pressure means the fluid will enter the capillaries.

as blood pressure drops, hydrostatic pressure drops.

colloid pressure is created by the proteins and remains the same becuase proteins stay in the blood

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14
Q

describe the clinical relevance of the lymphatic system and movement of insterstitial fluid

A

prevents oedema as it returns excess fluid to the circulation.

the amount of fluid filtering outward is almost equal to the amount being returned

controls the concentration of proteins in interstitial fluid, the volume of interstitial fluids and the interstitial fluid pressure

an increase in colloid osmotic pressure in interstitial fluid shifts the balance of forces at the membrane in favour of fluid filtration

increased interstitial fluid pressure increases rate of lymph flow

oedema can be caused by heart failure, lung damage, altitude sickness, and following major injury

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15
Q

describe the relationship between the structure and the function of the heart

A

left atria
- structure: thick myocardial wall, mitral valve links with ventrile
- function: receive blood from pulmonary vein, pump blood to left ventricle

right atria
- structure: tricuspid valve links with right ventricle
- function: receive blood from IVC and SVC

atrial septum
- fibromuscular wall separating the atria

left ventricle
- structure: thick muscular wall, posterior
- function: generate high pressure to eject blood through aortic valve to aorta to go to systemic circulation

right ventricle
- structure: thin muscular wall, pulmonary valve
- function: generate pressure to pump blood to pulmonary circulation

both ventricles contract at the same time and they pump the same volume of blood, but the pressures are different.

atrioventricular valves
- tricuspid, between right ventricle and atria, three cusps
- mitral, between left ventricle and atria, two cusps
- forced open by pressure differences and closed by pressure differences

papillary muscles
- fasten to atrioventricular valves
- muscular projections of ventricular walls connected to cusps via chordae tendinae
- prevent backflow of blood and limit valve cusp movements

semilunar valves
- pulmonary valve, right ventricle adn pulmonary artery. three valvules
- aortic valve, between left ventricle and aorta, three valvules
- open and close due to pressure differences

sound one
- lub
- av valves closing

second sound
- dub
- semilunar valves closing

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16
Q

explain the cardiac cycle and the control of heart rate

A

systole
- contraction of myocardium
- atrial and ventricular
- early ventricular systole: ventricles are contracting but semilunar valves are shut, tension and pressure are developing - this is called isovolumetric contraction
- rapid ventricular ejection occurs when pressure in ventricles exceeds the arterial pressure
- stroke volume is the volume of blood ejected from the ventricle during systole

diastole
- relaxation of the myocardium
- atrial diastole is masked by ventricular systole on ECGs
- facilitates refilling between contractions
- early diastole is when the ventricles are relaxing and the valves close
- isovolumetric relaxation, as there is no blood entering or leaving the ventricles
- ventricular filling occurs mid-late ventricular diastole and occurs via passive blood flow and atrial contraction

control of heart rate
- heart rate is determined by the rate of sino atrial node firing action potentials
- resting is 60-100 bpm
- autonomic nervous system determines rate of action potential firing

sympathetic control of heart rate
- alpha and beta adrenoreceptors
- mostly beta one adrenoreceptors that bind noradrenaline and adrenaline
- adrenaline is a hormone whereas noradrenaline is a neurotransmitter released from sympathetic nerves

noradrenaline binds to beta 1 adrenoreceptors
- stimulatory g protein
- adenylcyclase is activated
- cAMP is increased and activates protein kinase A
- protein kinase A phosphorylates and activates receptors and calcium ion channels
- positive chronotropy, ionotropy, lusitopy and dromotropy

parasympathetic control of heart rate
- rest and digest - reduce heart rate
- mediated by muscurinic receptors and binding of acetylcholine
- cholinergic nerves come from vagus

acetylcholine binds to muscarinic receptors
- at sino atrial and atrioventricular nodes
- inhibitory g protein activated
- cAMP is activated, potassium leaves cell
- negative chronotropy, ionotropy, demotropy and lusitropy

17
Q

describe the structure and function of cardiac myocytes

A

myocardium is specialised striated muscle that produces coordinated rhythmic contraction to pump blood around the body to meet the metabolic demands

cardiomyocytes are heart muscle cells

systolic calcium transient is the increase of calcium within the cardiac myocyte cytosol due to excitation contraction coupling

the size of the sytolic transient relates to the strength of myocardial contraction

cardiomyocyte contraction cycle

1 - calcium binds to troponin C, leading to a conformational change that displaces tropomyosin from the actin binding sites

2 - crossbridge formation occurs with ATP hydrolysation into ADP + P

3 - power stroke moves the actin filament toward the centre of the sarcomere, ADP + P heads are removed from the myosin heads

4 - actin is released with ATP binding to myosin. myosin heads are cocked back into firing position, ready to make crossbridges further downstream

5 - cycle continues until cellular calcium levels decrease allowing calcium to dissociate from troponin, tropomyosin returns to its original conformation so that is blocks actin binding sites

force of cardiac contraction is influenced by:
- systolic calcium concentration transient
- length of the heart muscle cell
- starlings law
( increased filling of heart chambers stretches the heart muscle. preload is the stretching of myocytes prior to contraction, indicated by ventricular end diastolic volume
- magnitude of stretch determines the strength of contraction

17
Q

explain the clinical importance of the electrocardiogram and examples of clinical scenarios relevant to dental practice

A

echocardiogram
- ultrasound scan
- assess structure and function
- 2D imaging - high temporal resolution

doppler echocardium
- erythrocytes reflect ultrasound waves
- sound waves measure blood flow through the heart

detects:
- impaired contractility, congenital heart disease
- myopathy - enlargemento f ventricular walls
- endocarditis - infection of endocardium that damages the valves
- heart failure - cannot pump to meet metabolic demands

electrocardiogram
- phasic change in potential difference between two electrodes
- electrodes are placed on limbs and the surface of the chest
- recorded on the computer
- diagnose arrythmia

phases of ECG
- P wave (atrial depolarisation)
- QRS complex (ventricular depolarisation
- T wave (ventricular repolarisation)
- P-R interval (delay through the atrioventricular node)
- S-T interval (plataeu phase of ventricular action potential)
- R-R interval (time between ventricular systole)

bradycardia is a slow heart rate
tachycardia is a fast heart rate

18
Q

describe the different terminology for excitation contraction coupling

A

the sarcolemma of living cells are electrically polarised

membrane potential
- potential difference between intracellular and extracellular sides of the cell membrane
- generated by ion gradients across the cell membrane
- ion channel proteins and transporters facilitate the transport of ions across the sarcolemma and they are selective for various ions

resting is -80mV for cardiomycocytes

depolarisation
- potential difference is less negative

repolarisation
- returns to normal following depolarisation, becomes more negative

action potential
- rapid rise and fall in voltage
- specific cell types have different patterns for action potential

intercalated discs
- located at longitudinal ends of cardiomyocytes
- facilitates electrical conduction from cell to cell

19
Q

explain the pathological conditions that can occur with heart valves

A

valve regurgitation
- blood leaks back into circulation
- occurs by a valve not closing tightly

valve stenosis
- thickening, or stiffening of the valve cusps
- prevents the heart valve from opening fully so not enough blood is flowing through

congenital heart defects
- often pulmonary and aortic valves do not form during developing
- can occur with av valves though

20
Q

describe the cardiovascular parameters

A

end diastolic volume
- volume of blood in the ventricle prior to contraction

end systolic volume
- volume of blood remaining in the ventricle after each ejection
- ventricles are not fully emptied during systole

stroke volume
- volume of blood ejected by the ventricle per contraction

ejection fraction
- volume of blood ejected as a fraction of end diastole volume
- measure of left ventricle efficiency
- normal is greater than 55%
- borderline low is 50-54%
- impaired is 36-49%
- severely impared is less than 35% of end diastolic volume

cardiac output
- volume of blood ejected in one minute
- stroke volume x heart rate

21
Q

describe the process of excitation contraction coupling in the myocardium

A
  • wave of electrical excitation travels from sino atrial node to myocytes of right atru and left atrium initiating atrial contraction
  • propagation of depolarisation by the action potential through the right atrium to the atrioventricular node
  • atrioventricular node acts as a delay point allowing the atria to completely empty blood
  • atrioventricular node is activated and facilitates action potential depolarisation along the interventricular septum via the bundle of his
  • bundle of his separates into the left and right bundle branches which innervate the ventricular walls of the myocardium
  • rapid propagation of the action potential along purkinje fibres initiates the coordianted simultaneous contraction of cardiac myocytes in the left and right ventricles
22
Q

describe the ventricular action potential

A

0 - 1 - 2 - 3 - 4
- resting membrane potential, 4 - sodium and calcium channels are closed, the potassium channels keep the MP at -90mV
- rapid depolarisation, 0 - sodium influx through open fast sodium channels
- early repolarisation, 1 - transient potassium channels open and potassium leaves which returns MP to 0mV
- plateau, 2 - influx of calcium ions through l type calcium channels, electrically balanced by potassium efflux
- repolarisation, 3 - calcium channels close by potassium channels remain open, return to -90mV
- return to 4

23
Q

describe sino atrial node action potential

A

0 - 3 - 4

  • 0, voltage gated calcium ions channels open and calcium ions enter the cell
  • 3 - voltage gated potassium channels open, potassium leaves cell, calcium channels close
  • 4 - voltage gated potassium channels close, sodium slowly enters through leaky sodium channels until the threshold of -40mV is met
24
Q

describe control and regulation of normal blood pressure

A

arterial blood pressure is maintained at around 120/80 mmHg

variations in blood flow to different organs must occur when demand arises to ensure there is adequate perfusion.

BP is greatest on waking and lowest during sleep, and increases in response to exercise, stress and sensory stimuli.
the pressure is the highest when blood enters the aorta on contraction of the left ventricle.

control and regulation occurs by two mechanisms: rapid and long term.

rapid regulation
- nerves

baroreceptors detect stretch and this monitors blood pressure. found in carotid sinus and aortic arch. carotid sinus baroreceptors are innervated by the sinus nerve of herring which combines with the glossopharyngeal nerve. aortic arch are innervated by the aortic nerve which combines with the vagus nerve.
baroreceptor sensitivity is reset during exercise and hypertension.
baroreceptors communicate with the medullary cardiovascular centre.

  • hormones
    to decrease arteriolar radius: sympathetic nerves, noradrenaline binds to alpha 1 adrenoreceptors to vasoconstrict.
    to increase the arteriolar radius: acetylcholine binds to muscarinic receptors, adrenaline binds to beta 2 adrenoreceptors, potassium and adenosine, and reduced PO2 lead to vasodilation.

long term regulation
- blood volume
influences venous pressure and return, end diastolic volume, stroke volume and cardiac output. increased volume increases pressure.
an increase in pressure will reduce volume due to an increase in renal excretion of water and salt.

25
Q

describe the relationship between the autonomic nervous system and blood pressure

A

sympathetic
- increased heart rate and contractility
- increased blood pressure
- fight or flight

parasympathetic
- rest and digest
- slow heart rate and contractility.

26
Q

describe the clinical assessment of blood pressure

A

measured using a sphygmomanometer to occlude the artery of an extremity with an inflatable cuff and by auscilation for detected of korotkoff sounds.

systolic blood pressure (pressure in arteries during contraction) over diastolic blood pressure (pressure in arteries during relaxation)

the mean arterial pressure is DBP over 1/3 pulse pressure (SDP-DBP)

27
Q

describe the clinical importance of blood pressure management

A

hypertension is when systolic is 140+ and diastolic is 90+.

secondary hypertension is when it results due to medication or underlying health conditions.

health conditions
- kidney conditions
- diabetes
- sleep apnea
- hormone issues like thyroid

medicines
- contraceptive pill
- non steroidal anti inflammatory drugs
- recreational drugs like cocaine and amphetamines.

damage caused from hypertension can lead to:
- cerebral aneurysms
- left ventricular hypertrophy
- thickening of arteries
- atherosclerosis

these effects can then lead to:
- renal disease
- heart failure
- angina
- stroke

HYPOTENSION
systolic 90 or less, diastolic 60 or less.

postural hypotension: abnormal drop in blood pressure when individuals stand up after sitting down

lead to dizziness and lightheadednes

more common in older people with underlying conditions affecting autonomic nervous system - parkinsons and diabetes

can be caused by dehydration or antihypertensives.

28
Q

describe local control of blood pressure

A

modified by changes in systemic vascular resistance and occurs in response to factors like metabolites, blood gas endothelium derived factors.

capillary fluid shift
- occurs due to venous dilators
- reduced proximal capillary hydrostatic pressure
- reduced hydrostatic means the intersitial fluid reenters capillaries

RAAS - change in blood volume

fluid regulation, endothelial factors, myogenic factors can impact blood pressure as well.

29
Q

describe the dental considerations for hypertension

A

many anti hypertensive drugs can interact with local anaesthetics and can lead to local anaesthetic toxicity.

stress can increase BP which can lead to acute complicatios like myocardial infarction or stroke

dental patients with CVD can have associated higher risk of complications due to release of endogenous catelochomines due to pain and stress

crucial that dental practitioners obtain an up to date medical history before commencing treatment.

30
Q
A