The cardiovascular system the heart
1 / 40

The Cardiovascular System: The Heart - PowerPoint PPT Presentation

  • Uploaded on

The Cardiovascular System: The Heart. Heart pumps over 1 million gallons per year Over 60,000 miles of blood vessels. Heart Location. Apex - directed anteriorly, inferiorly and to the left Base - directed posteriorly, superiorly and to the right

I am the owner, or an agent authorized to act on behalf of the owner, of the copyrighted work described.
Download Presentation

PowerPoint Slideshow about ' The Cardiovascular System: The Heart' - zia-mcfadden

An Image/Link below is provided (as is) to download presentation

Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author.While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server.

- - - - - - - - - - - - - - - - - - - - - - - - - - E N D - - - - - - - - - - - - - - - - - - - - - - - - - -
Presentation Transcript
The cardiovascular system the heart
The Cardiovascular System: The Heart

  • Heart pumps over 1 million gallons per year

  • Over 60,000 miles of blood vessels

Heart location
Heart Location

  • Apex - directed anteriorly, inferiorly and to the left

  • Base - directed posteriorly, superiorly and to the right

  • Anterior surface - deep to the sternum and ribs

  • Inferior surface - rests on the diaphragm

  • Right border - faces right lung

  • Left border (pulmonary border) - faces left lung

  • Heart is located in the mediastinum

    • area from the sternum to the vertebral column and between the lungs


  • Fibrous pericardium

    • dense irregular CT

    • protects and anchors the heart, prevents overstretching

  • Serous pericardium

    • thin delicate membrane

    • contains

      • parietal layer-outer layer

      • pericardial cavity with pericardial fluid

      • visceral layer (epicardium)

  • Epicardium

    • visceral layer of serous pericardium

  • Myocardium

    • cardiac muscle layer is the bulk of the heart

  • Endocardium

    • chamber lining & valves

Myocardium cardiac muscle
Myocardium – cardiac muscle

  • shares structural and functional characteristics with both skeletal and smooth muscle

    • skeletal & cardiac – striated

      • thin filaments contain troponin and tropomyosin – regulates cross-bridge formation

      • possess a definitive tension-length relationship

      • plentiful mitochondria and myoglobin

      • well-developed T-tubule structure

    • smooth & cardiac – calcium enters the cytosol of the muscle cell from the SR and the ECF during excitation

      • through voltage-gated calcium channels in the PM and the T-tubule membrane – dihydropyridine receptors

      • calcium entry from the ECF triggers its release from the SR

      • displays pace-makes activity – initiates its own APs without external influence

      • interconnected by gap junctions (intercalated discs) – enhance the spread of APs

      • innervated by the ANS

  • unique – 1. cardiac muscle fibers are joined in a branching network

    • 2. action potentials last longer than skeletal before repolarization

Right atrium

Right Ventricle

Right Atrium

  • Receives blood from 3 sources

    • superior vena cava, inferior vena cava and coronary sinus

  • Interatrial septum partitions the atria

  • Fossa ovalis is a remnant of the fetal foramen ovale

  • Tricuspid valve

    • Blood flows through into right ventricle

    • has three cusps composed of dense CT covered by endocardium

  • Forms most of anterior surface of heart

  • Papillary muscles are cone shaped trabeculae carneae (raised bundles of cardiac muscle)

  • Chordae tendineae: cords between valve cusps and papillary muscles

  • Interventricular septum: partitions ventricles

  • Pulmonary semilunar valve: blood flows into pulmonary trunk

Left atrium

Left Ventricle

Left Atrium

  • Forms the apex of heart

  • Chordae tendineae anchor bicuspid valve to papillary muscles (also has trabeculae carneae like right ventricle)

  • Aortic semilunar valve:

    • blood passes through valve into the ascending aorta

    • just above valve are the openings to the coronary arteries

  • Forms most of the base of the heart

  • Receives blood from lungs - 4 pulmonary veins (2 right + 2 left)

  • Bicuspid valve: blood passes through into left ventricle

    • has two cusps

    • to remember names of this valve, try the pneumonic LAMB

      • Left Atrioventricular, Mitral, or Bicuspid valve

Atrioventricular valves
Atrioventricular Valves

  • A-V valves open and allow blood to flow from atria into ventricles when ventricular pressure is lower than atrial pressure

    • occurs when ventricles are relaxed, chordae tendineae are slack and papillary muscles are relaxed

  • A-V valves close preventing backflow of blood into atria

    • occurs when ventricles contract, pushing valve cusps closed, chordae tendinae are pulled taut and papillary muscles contract to pull cords and prevent cusps from everting

Semilunar Valves

  • SL valves open with ventricular contraction

    • allow blood to flow into pulmonary trunk and aorta

  • SL valves close with ventricular relaxation

    • prevents blood from returning to ventricles, blood fills valve cusps, tightly closing the SL valves

Blood circulation
Blood Circulation

  • Systemic circulation

    • left side of heart pumps blood through body

    • left ventricle pumps oxygenated blood into aorta

    • aorta branches into many arteries that travel to organs

    • arteries branch into many arterioles in tissue

    • arterioles branch into thin-walled capillaries for exchange

      of gases and nutrients

    • deoxygenated blood begins its return in venules

    • venules merge into veins and return to right atrium

  • Pulmonary circulation

    • right side of heart pumps deoxygenated blood to lungs

    • right ventricle pumps blood to pulmonary trunk

    • pulmonary trunk branches into pulmonary arteries

    • pulmonary arteries carry blood to lungs for exchange of gases

    • oxygenated blood returns to heart in pulmonary veins

The cardiovascular system the heart

SVC/IVCRight Atrium(tricuspid valve)Right Ventricle

Passage of Blood through the Heart


(pulmonary semilunar valve)

Pulmonary Arteries


Pulmonary Vein

Left Atrium

bicuspid (mitral) valve


Left Ventricle


(aortic semilunar valve)

Conduction system of heart
Conduction System of Heart

  • two types of cardiac muscle cells

    • 1. contractile cells

      • 99% of cardiac muscle cells

      • Do mechanical work of pumping

      • Normally do not initiate own action potentials

    • 2. autorhythmic cells

      • Do not contract

      • Specialized for initiating and conducting action potentials responsible for contraction of working cells

The cardiovascular system the heart

  • intercalated discs – join cardiac cells

    • two types of membrane junctions

      • a. desmosomes – abundant in tissues under considerable stress

        • formation of a proteinaceous plaque on each PM surface (desmoglein, desmocollin)

        • plaques are joined to each other by adhesion proteins – cadherins (require calcium for interaction)

        • cadherins link to the underlying cytoskeleton (intermediate filaments)

      • b. gap junctions – two PMs are connected by a “channel” made of specific proteins = connexons

        • connexons are 6 protein subunits that form a hollow tube-like structure

        • two connexons join end to end to connect the cells

        • allow a free flow of materials from cell to cell

        • allow for the spread of electricity within each atrium and ventricle

        • no gap junctions connect the atrial and ventricular contractile cells – block to electrical conduction from atria to ventricle!!!

        • also a fibrous skeleton the supports the valves – nonconductive

        • therefore a specialized conduction system must exist to allow the spread of electricity from atria to ventricles

The cardiovascular system the heart

  • atrial conduction system/interatrial pathway – spread of electricity from right to left atrium ending in the LA

    • through gap junctions of the contractile cells

  • internodal pathway – spread of electricity to the AV node via autorhythmic cells

    • SA to AV node – 30msec

    • BUT spreads relatively slowly through the AV node

    • this allows for complete filling of the ventricles before they are induced to contract = AV nodal delay

  • ventricular conduction system (Purkinje system) – Bundles of His and Purkinje fibers

    • travel time = 30 msec

    • PFs conduct impulse 6 times faster than the ventricular muscle cells would on their own

    • the PFs do not connect with every ventricular contractile cell

    • so the impulse spreads via gap junctions through the ventricle muscle – similar to the atrial system

    • diffusion through the PFs allow for simultaneous contraction of all ventricular cells

Rhythm of conduction system
Rhythm of Conduction System

  • SA node fires spontaneously 90-100 times per minute

  • AV node fires at 40-50 times per minute

  • If both nodes are suppressed fibers in ventricles by themselves fire only 20-40 times per minute

  • Artificial pacemaker needed if pace is too slow

  • Extra beats forming at other sites are called ectopic pacemakers

    • caffeine & nicotine increase activity

Normal pacemaker activity

failure of SA node

blockage of transmission from SA through the AV node

Normal pacemaker activity

  • various autorhythmic cells have different rates of depolarization to threshold – so the rate of generating an AP differs

  • AP propagated through gap junctions or through the conduction system of the heart

  • contraction rate is driven by the SA node – fastest autorhythmic tissue

  • in some cases – the normally slowest Purkinje fibers can become overexcited = ectopic focus

    • premature APs

    • premature ventricular contraction (PVC)

    • occurs upon excess caffeine, alcohol, lack of sleep, anxiety and stress

    • some organic conditions can also lead to this

Cardiac excitation
Cardiac excitation

  • efficient cardiac function requires three criteria

  • 1. atrial excitation and contraction should be complete before ventricular excitation and contraction

    • opening and closing of valves within the heart depend upon pressure – which is generated by muscle contraction

    • so simultaneous contractions of atria and ventricles would lead to permanent closure of the AV valves – myocardium of the ventricles is larger and stronger

    • normally – atrial excitation and contraction occurs about 160 msec before ventricular

  • 2. cardiac fiber excitation should be coordinated to ensure each chamber contracts as a unit

    • muscle fibers cannot become excited randomly

    • role of the gap junctions

  • 3. atria and ventricles should be functionally coordinated

    • atria contract together, ventricles contract together

    • permits efficient pumping of blood into the pulmonary and systemic circuits

    • uncontrolled excitation and contraction of ventricular cells – fibrillation

    • correction by:

      • 1. electrical defibrillation

      • 2. mechanical defibrillation

Cardiac muscle action potentials
Cardiac muscle action potentials

  • pacemaker potential of the autorhythmic cells

  • provided by the SA node

    • interactions by several different ionic mechanisms

    • cells do NOT have voltage- gated Na+ channels

    • 1. decreased outward K+ current

      • “Normal” leak of Na in coupled to a decreased leak in K+ out

      • so the Na+ inflow doesn’t change but the K+ flow decreases – membrane constantly drifts toward threshold

    • 2. increased inward Ca+ current

      • T-type Ca+ channels (voltage-gated) open as the membrane drifts toward threshold – open before threshold is reached

      • brief and extra influx of Ca increases the depolarization to threshold

      • at threshold – L-type Ca channels open – longer lasting voltage-gated channel

      • greater influx of calcium – so the influx of calcium (rather than Na) is what drives the depolarization phase of the action potential

      • repolarization through the closing of these Ca channels and the opening of voltage-gated K+ channels

Cardiac muscle action potentials1
Cardiac muscle action potentials

  • AP in the contractile cells of the myocardium are initiated by the autorhythmic cells and spread via gap junctions

  • but the mechanism differs from that of the autorhythmic cells

    • 1. AP from autorhythmic cells activates “fast” voltage-gated Na+ channels (similar to neurons) = Na+ entry

    • 2. Na+ permeability will then plummet to its resting level due to the action of Na+ pumps

    • 3. BUT the MP potential is held a positive for an extended period of time due to the opening of L-type voltage-gated Ca+ channels PLUS the delay in the opening of voltage-gated K+ channels for repolarization

      • prolongs the positivity inside the cell

      • Produces a plateau phase

    • 4. inactivation of these Ca+ channels and delayed opening of voltage-gated K+ channels

      • results in a sudden opening of K+ channels and a rapid repolarization

Ap and contraction
AP and contraction

  • the “slow” L-type Ca+ channels are found within the T-tubules

  • triggers the opening of Ca+ channels within the adjacent lateral sacs of the SR (foot proteins) –

  • this “Ca-induced Ca release” triggers a very large release of Ca+ from the SR

  • burst of Ca+ = Ca+ sparks

  • SR supplies 90% of the Ca+ required for contraction

  • together with the slow removal of Ca+ - results in a long sustained contraction of heart muscle

Ap and contraction1
AP and contraction

  • Ca+ triggers the same series of events as seen in skeletal muscle

    • BUT – the amount of Ca+ release can directly affect the number of cross-brides formed in cardiac muscle and can directly affect the strength of the contraction!

    • so cardiac muscle must ensure adequate release of Ca+

    • elevated ECF Ca+ can increase the strength of contraction

      • e.g. digitalis – alters the activity of the Na/K transporter = increases Ca transport into the cell

        • elevates intracellular contraction, increases the plateau phase which increases the strength of contraction and the duration of the contraction

      • e.g. verapamil – Ca+ channel blocker – blocks inflow of Ca from the ECF – decreases contraction

  • refractory period of cardiac muscle is longer than skeletal muscle (250msec)

    • cannot be restimulated until the contraction is almost over

    • prevents the development of tetanus

    • allows for the emptying of the chambers

Electrocardiogram ecg or ekg
Electrocardiogram---ECG or EKG

  • electrical currents generated by the heart are also transmitted through the body fluids

  • can be measured on the surface of the chest

  • therefore it is not a direct measurement of the actual electrical conductivity of the heart itself

  • represents the overall spread of activity through the heart during depolarization – sum of all electrical activity

  • measured through the placement of 6 leads on the chest wall (V1 – V6) PLUS 6 limb leads (I, II, III, aVR, aVL and aVF)

  • it's usual to group the leads according to which part of the left ventricle (LV) they look at.

    • AVL and I, as well as V5 and V6 are lateral, while II, III and AVF are inferior.

    • V1 through V4 tend to look at the anterior aspect of the LV

  • see EKG lab handouts

  • ECG paper is traditionally divided into 1mm squares. Vertically, ten blocks usually correspond to 1 mV, and on the horizontal axis, the paper speed is usually 25mm/s, so one block is 0.04s (or 40ms).

    • Note that we also have "big blocks" which are 5mm on their side.

Electrocardiogram ecg or ekg1
Electrocardiogram---ECG or EKG

  • P wave

    • atrial depolarization

    • SA depolarization is too weak to measure

    • smaller than the QRS complex due to the smaller size of the atrial muscle mass

    • will be affected by abnormalities in the pacemaker activity of the SA node

  • PR segment/PQ interval – AV nodal delay

    • P to Q interval

    • conduction time from atrial to ventricular excitation

    • no net current flow within the heart musculature & the flow through the AV node is too small to measure– baseline

    • if activity in the AV node is abnormal – this interval ill be affected

  • QRS complex

    • ventricular depolarization

    • will be affected by the appearance of an ectopic focus (region of hyperactive ventricular contraction)

  • ST segment – time during which ventricles are contracting and emptying

    • ventricles are completely depolarized and the cells are in their plateau phase

  • T wave

    • ventricular repolarization

  • TP interval

    • time during which ventricles are relaxing and filling

The cardiovascular system the heart

each heartbeat = cardiac cycle

-SL valves close “dup”

-AV valves open

-filling of atria & ventricles begins

-contraction of atria

-AV valves open

-filling of ventricles = “Ventricular

Filling stage”

-contraction of ventricles

-AV valves close “lub”

-SL valves open

-blood to lungs and body

**Heart Murmur**

Cardiac cycle
Cardiac cycle

  • A. Midventricular diastole

    • during most of the ventricular diastole, the atrium is also in diastole = TP interval on the EKG

    • as the atrium fills during its diastole, atrial pressure rises and exceeds ventricular pressure (1)

    • the AV valve opens in response to this difference and blood flows into the right ventricle

    • the increase in ventricular volume rises even before the onset of atrial contraction (2)

Cardiac cycle1
Cardiac cycle

  • B. Late ventricular diastole

    • SA node reaches threshold and fires its impulse to the AV node = P wave (3)

    • atrial depolarization results in contraction – increases the atrial pressure curve (4 – green line)

    • corresponding rise in ventricular pressure (5 – red line) occurs as the ventricle fills & ventricular volume increases (6)

    • the impulse travels through the AV node

    • the atria continue to contract filling the ventricles

  • C. End of ventricular diastole

    • once filled the ventricle will start to contract and enter its systole phase

    • ventricular diastole ends at the onset of ventricular contraction

    • atrial contraction has also ended

    • ventricular filling has completed

    • ventricle is at its maximum volume (7) = end-diastolic volume (EDV), 135ml

Cardiac cycle2
Cardiac cycle

  • D. Start of ventricular systole

    • at the end of this contraction is the onset of ventricular excitation (8) = QRS complex

    • the electrical impulse has left the AV node and enters the ventricular musculature

    • this induces ventricular contraction

    • ventricular pressure will begin to rise rapidly after the QRS complex (red line)

    • this increase signals the onset of ventricular systole (9)

    • atrial pressure is at its lowest point as its contraction has ended and the chamber is empty (green line)

    • the ventricular pressure now exceeds atrial – AV valve closes

Cardiac cycle3
Cardiac cycle

  • E. isovolumetric ventricular contraction

    • ventricular pressure also opens the semilunar valves

    • however, just after the closing of the AV and opening of the SL is a brief moment where the ventricle is a closed chamber (10) = isovolumetric contraction

    • ventricular pressure continues to rise (red line) but the volume within the ventricle does not change (11)

  • F. Ventricular ejection

    • ventricular pressure will now exceed aortic pressure as the ventricle continues is contraction (12)

    • aortic SL is forced open and the ventricle empties

    • this volume of blood – stroke volume (SV)

    • the ejection of blood into the aorta increases its pressure (aortic pressure) and the aortic pressure curve rises (13 – purple line)

    • ventricular volume now decreases (14 – blue line)

  • F. End of ventricular systole

    • as the ventricular volume drops

    • BUT ventricular pressure continues to rise as the contraction increases its force (red line) – then starts to decrease as blood begins to be ejected

    • at the end of the systole there is a small volume of blood that remains in the ventricle – end-systole volume (ESV), 65ml (15)

    • EDV-ESV = SV (point 7 – point 15)

  • G. Ventricular repolarization

    • T wave – point 16

    • as the ventricle relaxes – ventricular pressure falls below aortic and the aortic SL closes (17)

    • this closure produces a small disturbance in the aortic pressure curve – dicrotic notch (18)

Cardiac cycle4
Cardiac cycle

  • H. Isovolumetric ventricular relaxation – Start of Ventricular Diastole

    • all valves are closed because ventricular pressure still exceeds atrial pressure – isovolumetric relaxation (19)

    • chamber volume remains constant (20)

  • I. Ventricular filling/MidVentricular Diastole

    • as VP falls below AP – the AV valve opens again (21) and ventricular filling starts again increasing ventricular volume (blue line)

    • as the atria fills from blood from the pulmonary veins (lungs) it increases AP

    • with the AV valve open this blood fills the ventricle rapidly (23)

    • then slows down (24) as the blood drains the atrium

    • during this period of reduced filling, blood continues to come in from the pulmonary veins – goes directly into the ventricle

    • cycle starts again with a new SA depolarization

The cardiovascular system the heart


  • Stethoscope

  • Sounds of heartbeat are from turbulence in blood flow caused by valve closure

    • first heart sound (lubb) is created with the closing of the atrioventricular valves

    • second heart sound (dupp) is created with the closing of semilunar valves

  • Heart sounds

Cardiac output
Cardiac Output

  • Amount of blood pushed into aorta or pulmonary trunk by a ventricle

  • Determined by stroke volume and heart rate

  • CO = SV x HR

    • at 70ml stroke volume & 75 beat/min----5 and 1/4 liters/min

    • entire blood supply passes through circulatory system every minute – each half of the heart pumps half the total volume of blood

    • at rest the heart pumps 2.5 million liters of blood per year!

    • during exercise – rise to 20 to 25 liters per minute

  • Cardiac reserve is the ratio of the maximum output to normal cardiac output at rest

    • average is 4-5 while athlete is 7-8

Stroke volume
Stroke volume

  • end-diastolic volume (amount of blood in a ventricle after filling) - end-systolic volume (amount of blood left in a ventricle after systole)

  • SV = EDV- ESV

    • ESV – measured by EKG – end of the T wave

    • EDV – measured using MRI, CT scan or a ventriculography (catheter in the ventricle and injection of an X-ray visible dye)

  • two components influence SV

  • 1. intrinsic control

    • heart’s inherent ability to vary SV

    • depends on the direct correlation between end-diastolic volume (EDV) and stroke volume

    • as more blood returns to the heart, the heart pumps out more blood

    • BUT the heart does not eject all the blood it contains

    • this control depends on the length-tension relationship of cardiac muscle – similar to skeletal muscle

    • for cardiac muscle – resting cardiac muscle length is less than lo

      • muscle length is determined by the extent of ventricular filling – increased EDV, increased ventricular volume

      • filling the ventricle with more blood stretches the cardiac muscle

      • as the cardiac cell is stretched – the spacing between thick and thin microfilaments is reduced

      • the myofilaments are pulled closer together

      • allows more cross-bridge formation

  • 2. extrinsic control

    • sympathetic and parasympathetic control

Regulation of heart rate
Regulation of Heart Rate

  • Nervous control from the cardiovascular center in the medulla

    • OUTPUT: 1. Sympathetic impulses increase heart rate and force of contraction

    • 2. Parasympathetic impulses decrease heart rate through the vagus

    • INPUT : 1. Chemoreceptors detect changes in blood chemistry

    • 2. Proprioceptors monitor changes in body activity

    • 3. Baroreceptors (pressure receptors) detect changes in BP

    • Heart rate is also affected by hormones and ions

    • epinephrine & norepinephrine from adrenal medulla, thyroid hormones

    • ions (Na+, K+, Ca2+)

    • age, gender, physical fitness, and temperature

Regulation of heart rate1
Regulation of Heart Rate

  • Sympathetic impulses increase heart rate and force of contraction

    • supplies the atrial and ventricular musculature (including the SA and AV nodes)

    • speeds up contraction rate by speeding up the rate of depolarization of the autorhythmic cells of the SA node

      • decreases K+ permeability by inactivating K+ channels

      • with fewer K+ ions leaving the cell – the inside becomes less negative – depolarizing effect

      • swifter drift towards threshold

    • also reduces the AV delay by enhancing the L-type Ca+ channels

    • speeds the rate of conduction through the Bundles and Purkinje fibers

  • parasympathetic impulses decrease heart rate through the vagus nerve

    • primarily supplies the SA and AV nodes

    • little effect on ventricular conduction system or ventricular contractile cells

    • decreases the excitability of the AV node – increases AV delay (hyperpolarizes the AV node)

    • in contractile cells of the atria – shortens the AP and reduces the inward Ca+ flow shortening the plateau phase – weakened atrial contraction

Risk factors for heart disease
Risk Factors for Heart Disease

  • Risk factors in heart disease:

    • high blood cholesterol level

    • high blood pressure

    • cigarette smoking

    • obesity & lack of regular exercise.

  • Other factors include:

    • diabetes mellitus

    • genetic predisposition

    • male gender

    • high blood levels of fibrinogen

    • left ventricular hypertrophy

Plasma lipids and heart disease
Plasma Lipids and Heart Disease

  • Risk factor for developing heart disease is high blood cholesterol level.

    • promotes growth of fatty plaques

    • Most lipids/cholesterol are transported as lipoproteins

    • cholesterol is unable to travel freely in the blood – combined with a protein (apolipoproteins) made in the liver = lipoprotein

      • low-density lipoproteins (LDLs)

      • high-density lipoproteins (HDLs)

      • very low-density lipoproteins (VLDLs)

    • HDLs remove excess cholesterol from circulation – travels to the liver where it is degraded

    • LDLs are associated with the formation of fatty plaques – LDLs are oxidized by the liver

      • oxidized LDL can damage endothelial linings – inflammatory response

      • inflammatory response leads to the accumulation of a fatty plaque at the area of damage

      • this plaque becomes covered with smooth muscle cells and fibroblasts

      • the fibroblasts can become calcified into a bone-like material

    • VLDLs contribute to increased fatty plaque formation

    • mutations in apolipoprotein genes may contribute to plaque formation also

  • There are two sources of cholesterol in the body:

    • in foods we ingest & formed by liver