Physiology of the

cardiovascular systemPart 1

Physiological properties of the cardiac muscle –

automacy and rhythmicity, conductivity, excitability,

contractility.

The cardiac cycle. Heart sounds. Arterial pulse.

Regulation of the cardiovascular system.

Practical tasks

•Physiological properties of the cardiac muscle

•Auscultation of the heart sounds

•Examination of the arterial pulse

•Experiments on an isolated heart

© Katarína Babinská MD, PhD, MSc, Institute of Physiology CU, Bratislava

What is the transmembrane potential?

• is the difference in electric potential between

the interior and the exterior of a biological cell.

• it exists across the membranes of almost all

cells in the body - also in the cardiac muscle

cells

• related to ion distribution across the membrane

and its changes

a cell

electrode

out

electrode

in

oscilloscope

– shows a potential difference

= transmembrane potential

action potential - after stimulation – record shows a curve with a typical shape

-90

Resting membrane potential, action potential

0

mV

t (ms)

resting membrane potential - unstimulated cell – record shows a straight line

-90

0

mV

Changes of the potential are due to ion flows

Physiological properties of the cardiac muscle

1. Automacy and rhythmicity (Chronotropy)

ability of the cardiac muscle cells (in sinus node) to generate spontaneously action

potentials at a regular pace (= self-excitation)

2. Conductivity (Dromotropy)

ability to transmit the excitation generated in the sinus node to all the heart muscle

fibres in a pre-defined pattern via a specialised conducting system

3. Excitability (Bathmotropy)

ability of the cardiac muscle cells to respond to the incoming excitation by AP -

when the stimulus arrives to the cardiac muscle cells it causes their depolarization

4. Contractility (Inotropy)

capability of the cardiac muscle to respond to a stimulus by contraction

Activity 1: List the physiological properties of the cardiac muscle (in both

English and Greek terminology) and define them in 1 sentence.

1. Automacy and rhythmicity (Chronotropy)

• ability of the cardiac muscle to generate

spontaneously action potentials

at a regular pace (= self-excitation)

Sino-atrial (SA) node (sinus node)

• generator of electric activity of the heart

• small strip of cardiac cells in

superior/postero/lateral wall of the right atrium

(close to the opening of vena cava superior)

• cells capable of self-excitation at regular intervals (normally 60-100/min)

• from SA node the excitation is spread to excite all cardiac muscle cells, therefore

SA node = the heart pacemaker (the only normal pacemaker)

Mechanism of the sinus nodal rhytmicity

Sinus node• „unquiet“ cells – instant changes in transmembrane potential

- no real resting membrane potential („straight line“)

- minimum value: -55 mV

Curve of transmembrane potential in sinus node

-55

-40

mV

0t (ms)

1 2 3

Activity 2: Draw and describe the curve of transmembrane potential in the

sinus node (names of the periods, ion changes, voltage, duration).

1 2 3

Phases of the transmembrane potential in the sinus node

1 2 3Curve of transmembrane potential in sinus node

A. at the beginning Na+ ions leak through the funny channels into the cardiac muscle

cells - membrane is untight for Na+ (cause slow depolarization)

B. later T-type of Ca2+ voltage gated channels are activated (at about -50 mV)

-due to higher concentration in ECF the Ca2+ ions move slowly in concentration

gradient inwards (slow depolarization proceeds)

- these channels are specific for the pacemakers !!!

1. Spontaneous diastolic depolarization (SDD, praepotential)

- a slow increase of the transmembrane potential (from -55 mV to a less negative value)

- without any external stimulus !!!

-

55

A

B

1 2 3 Curve of transmembrane potential in sinus node

2. Depolarization

• after the threshold -40 mV is reached a steep rise in transmembrane potential

occurs

• allowed by opening of the L-type Ca2+ voltage gated channels

• Ca++ ions move from extracellular space (in concentration gradient) into the

cells and cause depolarization of the sinoatrial cells

• overshoot to positive values (transpolarization)

-

55

1 2 3 Curve of transmembrane potential in sinus node

3. Repolarization

- Ca2+ channels get inactivated

- K+ channels open

- K+ moves outwards

- the transmembrane potential returns to its minimum value

-

55

Positive and negative chronotropic effect

Positive

Negative

Baseline

- positive – potentials in sinus node are generated with higher frequency

- negative – potentials in sinus node are generated with lower frequency

2. Conductivity (Dromotropy)

- excitation travels from the sinus node to all the heart muscle fibres in a pre-

defined pattern via a specialised conducting system

The cardiac muscle includes

- working myocardium

(main function: contraction/pumping)

- conduction system

(main function: fast transmission

of action potentials)

Activity 3: Draw a scheme of heart and indicate how the action potential

is spread to the atria and ventricles.

Cardiac muscle – syncytium

- cardiomyocytes cells connected by gap junctions

- allow the transport of ions, i.e. transmission of AP from one cardiac muscle cell to

another

- all the cells of working myocardium are activated (and contracted) as one unit

Conduction pathways include:

• excitation of the atria – from the SA node → to all muscle cells of atria

1. from a muscle cell to the neighbouring ones via gap junctions (0,3 m/s)

2. interatrial bundles – anterior, middle, posterior (1 m/s) – cardiomyocytes „specilized on

conductivity (from SA node to the AV node)

• excitation of the ventricles - AV node – the only pathway from atria to ventricles

(because atria and ventricles are separated by a non-conductive fibrous tissue)

− SA node to AV node (velocity 1 m/s) :

− through the A-V node (0,03 m/s)

− bundle of Hiss (2 m/s)

− right and left bundle branch (Tawara branches)

− Purkinje fibres (2 - 4 m/s)

− cardiac muscle cells (0,3 m/s)

Duration of the transmission of AP from SA node to myocardium

• first depolarization (and also

contraction) the of atria occurs

• depolarization (and also

contraction) of ventricles

occurs with a time delay

• delay is caused by a slow

transmission through the

AV-node

• the delay allows for efficient

function of the heart as a pump

– first contract the atria

– slightly later contract the ventricles

0,03 s0,16 s

0,22 s

0,17 s

0,18 s0,19 s

0,00 s

• not only the cells of SA node, also other parts of the conduction system are

capable of self excitation - however at slower pace:

atrio – ventricular node 40 – 60/ minute

Purkinje fibres 15 – 40/ minute

- these also begin their self-excitation

(at the same time as SA node)

- normally they do not get self-excited

because the action potential from SA node

arrives here faster and causes their excitation

- they produce potentials only in abnormal

cases

sino-atrial node

= heart pacemaker (the only normal)

ectopic (secondary) pacemakers

– other than S-A node - abnormal (e.g. junctional rhythm – generated in AV node)

Gradient of cardiac automacy

3. Excitability (Bathmotropy)

• phase 2 - plateau–opening of L type voltage gated Ca++

channels (inflow if ions)

– channels open slowly and remain open

for longer time than fast channels

– K channels remain open

• phase 3 - repolarization– K+ channels are open (K outflow)

• phase 4 - resting membrane

potential–ions are restored by pumps (Na/K –

pump, Ca - pump)

• phase 0 - depolarization

– opening of fast voltage gated Na+ channels, Na+ moves into the cardiac muscle cell

– transpolarization (upstroke) – transmembrane potential: 20 – 30 mV

• phase 1 - early repolarization – fast Na+ channels inactive, K channels open

Curve of transmembrane potential in working myocardium

ms

Activity 4: Draw and describe the curve of transmembrane potential in a cardio-

myocyte of working myocardium (periods, ion changes, voltage, duration).

Refractory periods in the cardiac muscle

• Extrasystole – abnormal premature stimulation resulting in systole

• Absolute refractory period (ARP)

– period of action potential when cardiac muscle cells do not react to next stimulation at all

– in myocardium it has a long duration – protection from:

a/ tetanic contraction of the myocardium

b/ premature depolarization (that would make the heart pump less effective – the heart

would have insufficient time to get filled with blood)

• Relative refractory period (RRP)

– follows the absolute refractory period - myocardium is more difficult to stimulate – responds

only to very strong excitatory signals

ARP RRP

ms

extrasystole compensatory pause

no no yes

yes no

The all or nothing principle

• the cardiac muscle operates according to the all or nothing principle

– insufficient stimulation (subthreshold stimulus) causes no contraction (no response) of

a cardiac muscle fibre

– sufficient stimulation (threshold and suprathreshold stimulus) causes maximum

contraction of a cardiac muscle fibre

• according to the all or nothing law operate both

1. individual cardiac muscle fibres - similarly to the skeletal muscle

2. the heart as a whole - in contrast to striated muscle – because myocardium

is a syncytium – action potential is quickly transmitted to all heart muscle

cells through gap junctions, thus they are activated in one time

subtheshold threshold suprathresholdstimulus stimulus stimulus

no response maximum maximumcontraction contraction

4. Contractility (inotropy) – excitation/contraction coupling

Automacy and rhythmicity (chronotropy)

- Positive chronotropic effect – increased automacy (faster generation of AP)

- Negative chronotropic effect – decreased automacy (slower generation of AP)

Conductivity (dromotropy)

- Positive dromotropic effect – faster conduction of the AP

- Negative dromotropic effect – slower conduction

Excitability (bathmotropy)

- Positive bathmotropic effect – higher excitability of the cardiac muscle

- Negative bathmotropic effect – lower excitability of the cardiac muscle

Contractility (inotropy)

- Positive inotropic effect – stronger contraction of the cardiac muscle

- Negative inotropic effect – weaker contraction of the cardiac muscle

Neurotransmitters and drugs with effects on the heart

The cardiac cycle

• The cardiac cycle is the series of events comprising a complete contraction and

relaxation of the heart's four chambers:

1. filling of the ventricles (diastole of the ventricles)

2. period of isovolumic (isometric) contraction of the ventricles

3. period of ejection

4. period of isovolumic relaxation of the ventricles

1. Filling of the ventricles (ventricular diastole)

• starts after previous systole – when ventricles relax

• intraventricular pressures fall below atrial pressures (= 0 in diastole)

• the AV valves open and ventricular filling begins

• the blood flow during ventricular filling generates the third heart sound (S3) -

by tensing of chordae tendineae and AV ring during ventricular filling

Filling of the ventricles has 3 periods:

1A. Rapid filling (great A-V pressure difference)

1B. Slow filling (smaller A-V pressure difference)

1C. Systole of the atria – generates the fourth heart sound (S4)

• at the very end of the ventricular filling, the ventricular

volumes are maximal = the end-diastolic volume (EDV)

•the left ventricular EDV is typically about 120 ml

• a rapid increase in myocyte tension

and intraventricular pressure

• as intraventricular pressure exceeds atrial pressure

- the AV valves close

• closure of the AV valves results in the first heart sound (S1)

(the 1st sound is caused by the closing of the AV valves + vibration of the myocardium)

• ventricular pressure rises rapidly without a change in ventricular blood volume (no

ejection occurs so far)

• ventricular blood volume does not change because all valves are closed during

this phase ("isovolumic" or "isovolumetric“)

2. Isovolumetric contraction

3. Ejection

• when the intraventricular pressures exceed the

pressures within the aorta and pulmonary artery, which

causes the aortic and pulmonary valves to open

• pressure gradient propels blood into the aorta and

pulmonary artery from their respective ventricles

• Pressures in the ventricles (systole)– left ventricle 125 mm Hg

– right ventricle 25 mm Hg

• about 70 ml of blood are ejected = stroke (systolic)

volume

• ejection fraction = systolic volume/ end-diastolic volume

(normal value in the rest: 60 %)

4. Isometric (isovolumetric) relaxation

• the ventricles relax

• the intraventricular pressures fall (below in aorta and pulmonary artery)

• pressure in aorta and pulmonary artery exceeds the pressurein the ventricles the aortic and pulmonary valves abruptly close causing the second heart sound (S2)

• In diastole the pressures in the ventricles fall to

– left ventricle 0 mm Hg

– right ventricle 0 mm Hg

• end-systolic volume - the volume of blood that remains in a ventricle (50 ml in the left ventricle)

• left atrial pressure continues to rise because of venous return from the lungs.

Task: Auscultation of the heart sounds

Heart sounds

heart sounds are the noises (sound) generated during the cardiac cycle (lub-dub)

sounds are examined by

- auscultation by a stethoscope

- phonocardiography – a curve is recorded

• the first sound (systolic) – „lub“

– the first of the paired heart sounds, following the longer diastolic period

– generated by closing of AV valves (bicuspid and tricuspid)

and vibrations of ventricular myocardium

• the second sound (diastolic) – „dub“

– generated by closing of semilunar valves

– shorter duration and higher frequency than the first heart sound

• the third sound

– generated by blood flow into ventricles during the period of rapid filling

• the fourth sound

– generated by the systole of atria

• usually first and second sound are audible, the third and fourth rarely

Task: Auscultation of the heart sounds

- examine in a quiet place

- the patient may lie or sit

1st sound (is examined on 2 spots)

A/ tricuspid valve – 5th intercostal space,

parasternally on the right (left)

B/ bicuspid valve – 5th intercostal space,

medioclavicular line, left

2nd sound (is examined on 2 spots)

A/ aortic valve – 2nd intercostal space, parasternally, right

B/ pulmonary valve – 2nd intercostal space, parasternally, left

- evaluate rhythm/accent (regular)

- synchronisation (normally closing of 2 valves generates 1 synchonized sound)

-the 3rd and 4th sounds are only sometimes audible – mainly in children, young adults -

examine when lying on the left side, slightly leaning to the front

Murmurs - abnormal heart sounds produced by abnormal patterns of blood flow in the

heart (e.g. due to defective heart valves)

Measurement of the arterial pulse

Arterial pulse

- systole - ejection of blood from left ventricle into aorta

- aorta and large arteries – elastic type of arteries

- rise in volume/pressure in aorta - distention of the aortic vessel wall

Pulse (wave) - a wave of vibration of the vessel wall caused by ejection of blood

during cardiac systole that is transmitted down the aorta and arteries

-it can be plapated over superficial arteries

- central pulse: carotid artery, a. femoralis (branches of aorta)

- peripheral pulse: radial a., popliteal a., etc.

diastole

systole

diastole

Arterial pulse – a pulse wave

- caused by closing of the aortic valve)

Velocity of the pulse wave

1. is higher than velocity of the blood flow !!!

2. inverse association with arterial elasticity – therefore increases with age

(elasticity drops down due to atherosclerosis)

3. decreases with the diameter of the vessel

more elastic

less elastic

Measurement of pulse

1. by palpation

- 2 (3) fingers are put over the artery

(usually a. radialis, a. carotis)

- can be determined by palpation of any artery

2. sphygmography – registration of a pulse curve by

an instrument

- pulse is mostly measured/determined per 1 minute

- if measured for 30 seconds - multiply by 2

- if measured for 15 seconds - multiply by 4

- most precise value is obtained by 1 min

measurement (due to heart rate oscilations)

Examination of pulse informs about:

- the cardiac function (heart rate)

- the function of vessels – not palpable pulse – probably no blood flow

http://1mhowto.com/wp-content/uploads/2015/05/How-to-examine-your-body.jpg

In previous times also other qualities of the pulse were evaluated

3. amplitude large/small (magnus/parvus)

4. velocity of the pulse wave increase (celer/ tardus)

5. suppressibility (mollis – easily suppressive, durus – hardly suppressive)

Task:

a/ find the pulse over different arteries (carotid, radial, popliteal, dors. pedis, etc.)

b/ measure the a pulse rate / min in a volunteer

c/ evaluate if the pulse rate is: normal/abnormal, reular/irregular

Evaluation of the pulse examination

1. frequency

• normal 60-100/ min

• bradycardia <60/ min

(normal in sleep, trained people, abnormal causes: e.g. hypothyrosis, heart disease)

• tachycardia (pulsus frequens) >100/ min

(normal in physical activity, stress, abnormal causes e.g. hyperthyrosis, heart disease)

2. rhythm – regular / irregular

Regulation of the cardiac function

Autoregulation: Frank - Starling mechanism (law)

Autonomic nervous system

Norepinephrine (symp. neurotransmitter)Sympathetic mimetics (adrenergic effect)

Stimulation of frequency conductivity contractility excitability

Acetylcholine (neurotransmitter) Inhibition of: frequency conductivity

Parasympatethic mimetics Inhibitory effect (parasympathetic–like)

Parasympathetic lytics Simulation (delete parasymp. inhibition)

Sympatethic mimetics Stimulation (sympathetic-like effect)

Sympathetic lytics Inhibition (delete sympathetic effect)

Humoral regulation

Epinephrine (hormone) stimulatory effect – all physiological properties

Ions - calcium (Ca2+)- potassium (K+)

↑ contractility (the heart may stop in systole)

↓ automacy, batmotropy (heart may stop in diastole)

Thyroxine - stimulates automacy (+ increases sensitivity to catecholamines,

therefore other physiological properties are stimulated, too)

Glucagon Increased heart rate and force

Effect of the temperature

- higher body temperature – stimulation (higher permeability of cell membranes to ions)

- lower body temperature – inhibition (lower permeability of cell membranes to ions)

Protocol

- you will administer different cardioactive drugs to yor patient and monitor their

effect

- the cardiac action will be shown by a curve determined by its frequency and

amplitude

Task: Sim Heart

- Sim Heart is a simulation program that monitors the cardiac activity and the

effects of cardio-active drugs

Evaluate (for each substance given) the effect of your treatment

• chages in frequency (heart rate – chronotropy)

• changes in amplitude (strength) of the cardiac contraction - inotropy

substance A substance B

Your patient need the following substances include

A/ Neurotransmitters

1. sympathetic:

– epinephrine (adrenaline, Adr) – stimulatory effect on the cardiac muscle

(the cardiac muscle has mainly beta1 receptors)

2. parasympathetic: acetylcholine (ACh) – generates inhibitory effect on the

cardiac muscle

B/ Calcium blockers - cardio-active drugs

- calcium - decisive role in the electromechanical coupling of cardiac contraction

- due to limited intracellular calcium storage the heart is dependent on the

calcium flowing in from the extracellular space

- calcium blockers like verapamil block the calcium channels

C/ Substances with competitive effect (antagonists, inhibition)

• the action of neurotransmitters can be suppressed by specific blockade of their

receptors with appropriate receptor antagonists (competitive inhibition).

– atropine competes for the muscarinic a receptors and it is inhibitor of the ACh

– propranolol blocks the epinephrine action by binding to beta receptors,

phentolamine binds to adrenergic alpha receptors

D/ Cardiac glycosides (digitalis glycosides) - cardio-active drugs

• increase the force of heart contraction

• tendency to (e.g. strophantin) trigger arrythmias

3. Select a substance

1. Switch on

4. Choose the appropriate

concentration: always 10-4

5. Transfer the selected tube

into the apparatus and

preset the dose (100)

2. Change the settings

Speed 1 cm/s

Resolution 5mV/Div

– the curve of basal activity of

the heart will appear

6. Start testing the effects of a substance by

pressing the arrow down and arrow left

- to stop testing press the STOP button

- Indicate if the effect was positive (+), negative (-) or no change was observed (0)

- Draw a curve of the change

Protocol / Results

Substance Chrono-

tropy

Inotropy Curve

Epinephrine

Acetylcholine

Verapamil

Atropine

Epinephrine, then add α

blocker phentolamine

Epinephrine, than add β

blocker propranolol

Strophantine

- Click PhysioEx 9.1

- Choose Exercise 6 – Cardiovascular Physiology

- Perform Activities 2, 3, 4 ,5

- You are not expected to perform the pre-lab or post-lab quiz

- In menu always choose the option Experiment

- Do the experiments according to the procedure on the left side

- Answer also the questions

- When ready, submit your data, go to Lab report and generate PDF (name it

with your names)

- send PDF to your e-mail, please complete it at home and bring next week to

the practicals – results/anwers to the questions will be discussed

Task: Physio Ex 9.1