group 4_baseline heart rate & ecg

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    Physiology of theCirculatory

    System: The baseline heart rate

    and ECG 

    DE LA PAZ | DUQUE | GALAROSA | GONZALESGroup 4

    4 Biology 6

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    SUMMARY 

    The frog heart is made of three chambers, one ventricle and two atria.

     Although it is similar to skeletal muscles, it is an involuntary muscle that

    does not need to be stimulated by nerves to contract. This is due to the

    action potentials that spontaneously begin in the pacemaker region inthe right atrium that spreads through the heart. An electrocardiogram

    (ECG) was used to test the electrical activity in the heart. An ECG

    translates the heart's electrical activity into line tracings. In this

    experiment, the baseline heart rate and ECG of the frog was observed.

    The baseline heart rate of the frog at room temperature is said to bearound 40 BPM, and it was found experimentally that the computed

    baseline heart rate is 31.7460 BPM, and the baseline heart rate from

    the data pad is 31.4273 BPM. The heart rate of the frog may be lower

    than normal due to the lower temperature in the laboratory. For the

    ECG, the tracing produced waves that consists of P waves, PRintervals, QRS complexes, ST segments, T waves, QT intervals, and,

    at times, U waves.

    Keywords: Circulatory system, heart, baseline heart rate,

    electrocardiogram

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    Introduction

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    Frog Heart

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    Frog Heart

    ▪ Ventricle: single chamber at the bottom of the heart

    ▪  Atria: two thin-walled chambers located above theventricle (darker red in color)

    ▪ Sinoatrial (SA) node

    – Pacemaker of the heart

    – Transmit electrical signals to make the heart contract ina rhythmic manner

    ▪  Aortic trunk

    –Right side of the ventricle

    – Less oxygenated blood: pulmocutaneous artery

    – More oxygenated blood: Carotid, aorta

    ▪ Sinus venosus:

    –Receives blood and delivers it to the right atria

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    Circulatory System

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    ECG

    ▪  An electrocardiogram (ECG) is a

    machine that can be used torecord and display the electricalactivity of the heart

    ▪ Different peaks shown in an ECG

    and each corresponds to voltagechanges in specific regions of theheart

    ▪ The ECG can be very helpful tothe lives of human beings

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    ECG

    ▪ P wave: atrial depolarization

    ▪ QRS complex: atrial repolarization and ventriculardepolarization

    ▪ T wave: ventricular repolarization

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    Methodology

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    Set-up and Calibration

    The Bridge Pod was plugged into the Pod Port onInput 1 of the PowerLab.

    PowerLab was turned on. LabChart waslaunched from the computer.

    “Frog heart settings” was opened and from theForce Channel Function pop-up menu, Bridge

    Pod was selected.

    The zeroing knob on the front of the Bridge Podwas turned until a reading of zero is seen in the

    dialog preview window.

    The mounting stand was set-up with theForce transducer mounted on the

    micropositioner.

    The force transducer cable was connected tothe back of the Bridge Pod.

     A piece of strong thread about 36cm in lengthwas tied to the force transducer. A small,

    barb-less hook was attached to the other endof the thread.

    The patient cable was attached to the Bio Amp pocket on the PowerLab.

    Three lead wires were attached to the Bio Amp Cable: Channel 1 positive and negative,

    and Earth.

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    Recording Baseline Heart Rate and ECG

     A heartbeat waveform in the Force Channeland an ECG signal in the ECG channel were

    seen.

    The tension on the heart was adjusted withthe micropositioner when a weak signal in the

    force channel was seen.

    “ Autoscale" button was clicked from the

    LabChart toolbox to scale all channels.

    The heart was gently lifted from the animal’sbody cavity, and the other end of the thread

    was tied to the force transducer.

    The slack in the thread was reduced byadjusting the micropositioner on the mounting

    stand.

    Lead wire alligator clips were attached to thefrog to record the ECG. Positive- left forelimb;Negative- Right forelimb; Earth- right hindlimb.

    In LabChart, the “Start” button was clicked andrecording was done for 30 seconds.

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    Results and Discussion

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    Determination of baseline heart rate

    ▪ asdf

    Number of beats  Time differential Calculated heart

    rate 

    Heart rate from

    data pad 

    32 beats 59.21 seconds 31.7460 BPM 31.4273 BPM

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    Baseline heart rate

    ▪ The baseline heart rate or resting heart rate is the

    number of contractions of the heart that occur in a singleminute while the body is at complete rest

    ▪ The baseline heart rate of a frog is said to be 40-50 BPM

    ▪  Amplitude and frequency of the heart beat varies

    according to the size of the animal, the bigger the animalthe lesser the frequency

    ▪ Temperature influences the heart rate of frogs

    – Frogs are ectotherms, animals that gains heat through

    the environment– The heart rate of the frogs reflect their metabolic rate

    which consequently increases with increasing bodytemperature and vice versa

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    Baseline heart rate

    ▪ Temperature influences the heart rate of frogs

    –In the experiment, the lower temperature in thelaboratory may have caused the baseline heart rate ofthe frogs to become lower than normal

    ▪ Changes in the environment influences the heart rate of

    the frog– Changes in the general metabolism induces

    bradycardia, or decreasing of the heart rate

    – Shortage of oxygen supply or an excess carbon

    dioxide also induces bradycardia– Exposure to nitrogen may cause an immediate

    tachycardia, or increasing heart rate

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    ECG

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    ECG

    Representation

    P wave Atrial depolarization

    PR

    interval

    Delay between atrial

    depolarization and ventricular

    activation

    PR

    segment

    Conduction from the

    atrioventricular (AV) node to

    Purkinje fibers

    QRS

    complexVentricular depolarization

    ST

    segment

    Electrical plateau of ventricular

    activation

    T wave Ventricular repolarization

    QT

    interval

    Time interval for ventricular

    depolarization and repolarization

    U wave Late ventricular repolarization

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    ECG

    ▪ Propagation of action potentials that causes the heart to

    contract

    ▪ The ECG trace repeats with every heart beat and showsthe compilation of electrical activity or action potential ofthe heart

    ▪ P wave

    – Represents atrial depolarization or atrial systole

    – A heart beat begins with an action potential signal fromthe SA node

    –The signal spreads to both atria causing the muscles ofthe atrium to depolarize and contract

    – Slow cell-to-cell atrial conduction spreads thedepolarization slower and gives the P wave a rounded

    deflection

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    ECG

    ▪ PR interval

    –Represents the time the impulse takes to reach theventricles from the SA node

    – Begins at the onset of the P wave and ends at theonset of the QRS complex

    Shows the delay between atrial depolarization andventricular activation

    ▪ PR segment

    – Represents when the signal leaves the atria and enter

    the ventricles though the AV node in the interatrialseptum, enters the bundle of His, and spreads throughthe bundle branches, and the Purkinje fibers that arefound along the ventricle walls

    – Follows atrial systole and preceding ventricular systole

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    ECG

    ▪ QRS complex

    –Represents the depolarization of the ventricles andconsequently ventricular systole

    – Immediately follows the P wave

    – The sharp deflection of the complex is due to the fast

    electrical impulse conduction done by ventricularconducting fibers, namely the bundle of His, bundlebranches, and the Purkinje fibers; and, the ventricularmuscle mass is greater than that of the atria

    – Q wave: is the downward deflection following the P

    wave– R wave: is the first upward deflection following the P

    wave

    – S wave: is the first downward deflection following the R

    wave

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    ECG

    ▪ QRS complex

    – Atrial repolarization is not visible because it coincideswith the onset of ventricular depolarization

    ▪ ST segment

    – Represents the electrical plateau of ventricular activity

    – At this phase the ventricles are uniformly depolarized

    – This segment is said to be isoelectric for there is no netelectric charge or difference in electrical potential

    ▪ T wave– Represents the ventricular repolarization, and

    consequently, ventricular diastole

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    ECG

    ▪ T wave

    –Ventricular muscles recover from the influx of ions andare returning to their resting state

    – At this point, more blood enters the ventricle inpreparation for its circulation into the arteries

    ▪ QT interval

    – Represents the time interval for the ventricle todepolarize and repolarize

    ▪ U wave

    – Represents the late repolarization of the Purkinje orventricular conducting fibers

    – Is usually not seen on the ECG

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    ECG

    ▪  An arrhythmia, also called dysrhythmia, is an irregular or

    abnormal heartbeat

    ▪ Types of arrhythmia:

    – Tachycardia: a fast heart rhythm

    Bradycardia: a slow heart rhythm– Supraventricular arrhythmias: arrhythmias that begin

    above the ventricles or in the atria

    – Ventricular arrhythmias: arrhythmias that begin in the

    ventricles– Bradyarrhythmias: slow heart rhythms that may be caused

    by disease in the heart’s conduction system, such as theSA node, atrioventricular AV node or HIS-Purkinje network

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    ECG

    ▪ Terms:

    – Action potential: the point at which a cell becomes electricallyactivated

    – Polarized: the resting electrical state of a cell

    – Depolarization: change in electrical state of a cell due to the inflow

    of positively charged ions– Repolarization: the return to the normal resting electrical state of a

    cell following an action potential

    – Isoelectric: the phase wherein the electrical charges through theheart are equal and there is no deflection that occurs on the ECGtrace

    – Systole: phase of the heartbeat when the heart muscle contractsand pumps blood

    – Diastole: phase of the heartbeat when the heart muscle relaxes

    and allows the chambers to fill with blood

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    Guide Questions

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    What do you call the first sound heard as pressure is being

    released from the cuff slowly? What does this sound

    indicate? 

    The first sound heard is the systolic pressure. This

    pressure indicates the pressure of the blood that is pumped

    out by the heart where the blood starts flowing again in the

    blood vessel after the flow has been disrupted by the

    pressure applied on the sphygmomanometer cuff.

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    Describe the basis for the delay between the arterial and

    ventricular contractions. 

    The delay between the arterial and ventricular contractions

    is due to the delay of the impulse conducted by the AV

    node to let the ventricle to be fully filled with blood and

    making sure that the atrium has already emptied its

    contents to the ventricle before ventricular contractionoccurs.

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    How did temperature affect heart rate? What do you

    suppose is a consequence being a poikilotherm? 

    Heart rate, controlled primarily by different chemical

    processes, increases as the temperature increases due to

    the fact that temperature supplies heat and heat is

    responsible for the atomic and molecular movement that

    speeds up the reactions in the body. Poikilotherms, beingunable to regulate their own body temperature and adapt

    only to their environment, cannot stabilize their metabolic

    activities efficiently because of their inability to regulate

    their own body temperature. Their heart rate can be veryactive on high environmental temperatures but their heart

    rate could also not be very active due to low temperature in

    the environment.

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    What is Starling’s Law of the Heart? Does your data

    support this law? 

    Starling’s  Law of the Heart states that the heart has the

    ability to change its force of contraction and therefore

    stroke volume in response to changes in venous return,

    simply put, as the heart wall increases in length more

    volume of blood could be accommodated thus increasingthe stroke volume. The length-tension applied to the

    ventricle stretches the cardiac sarcomere length thus

    increasing the ventricular chamber therefore increasing the

    stroke volume. Yes. The data obtained supports this law.

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    Describe the mechanisms by which the following drugs

    affect heart rate: 

     A. Acetylcholine 

     Acetylcholine (Ach) is a neurotransmitter that binds to

    muscarinic cholinergic receptors which in turn activates G

    proteins that results to hyperpolarization. Then,

    hyperpolarization allows the passage of K ions by opening

    K channels and thereby closing Na and Ca channels. Theclosing of the Na and Ca channels decreases the heart rate

    significantly.

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    Describe the mechanisms by which the following drugs

    affect heart rate: 

    B. Epinephrine 

    Epinephrine is a neurotransmitter that binds to adrenergic

    receptors such as β1 receptors which in turn activates

    cAMP where the depolarization frequency increases. Then,

    depolarization opens up Na and Ca channels permitting a

    spontaneous entrance of Na and Ca ions. The entry of Naand Ca ions generate an impulse that makes the heart rate

    faster.

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    Describe the mechanisms by which the following drugs

    affect heart rate: 

    C. Atropine & Acetylcholine 

     Atropine functions as cholinergic antagonist where it blocks

     Acetylcholine receptors. If the Ach receptors are blocked,

    the Ach neurotransmitter could not bind to muscarinic

    cholinergic receptors that the process is halted before it

    even began.

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    References

    1. ADInstruments. Physiology of the in situ amphibian heart. Retrieved on 6 April 2015,

    from

    http://jpkc.zju.edu.cn/k/554/preparation/experiment/pl/Frog%20Heart%20Protocol.doc.

    2. Electrocardiogram: MedlinePlus Medical Encyclopedia. (2015). Retrieved on 6 April

    2015, from http://www.nlm.nih.gov/medlineplus/ency/article/003868.htm.

    3. Frog Electrocardiogram. (2013). Retrieved on 6 April 2015, from

    http://www.iworx.com/documents/LabExercises/FrogECG.pdf.

    4. Herbert, T.J. (2011). Cardiac muscle and circulation. Retrieved on 6 April 2015, from

    http://www.bio.miami.edu/tom/courses/bil265/bil265goods/18_cardiac.html5. John, A.D. & Fleishr, L.A. (2006). Electrocardiography: The ECG. Anesthesiology

    Clinics, 24, 697-715.

    6. Kumar, S. (July 2007). ECG Tutorial for clinicians. Retrieved on 6 April 2015, from

    https://cardionotes.files.wordpress.com/2008/02/ecg-tutorial-by-dr-satish.pdf.

    7. Pal, G.K. & Pal, P. (2005). Textbook of practical physiology. (2nd ed.). Chennai, India:

    Orient Longman Private Ltd.

    8. Rastogi, S.C. (2005). Experimental physiology. Daryaganj, India: New Age

    International (P) Ltd.

    9. Sambo, J. (2012). Bio 22 Lab - Expt 19 (Group 4). Retrieved on 6 April 2015, from

    http://www.slideshare.net/JenSambo/bio-22-lab-expt-19-group-4

    10. Waitemata Cardiology. Electrocardiogram (ECG). Retrieved on 6 April 2015, from

    http://wcardio.co.nz/newsite/electrocardiogram-ecg/.

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    Physiology of theCirculatory

    System: The baseline heart rate

    and ECG 

    DE LA PAZ | DUQUE | GALAROSA | GONZALESGroup 4

    4 Biology 6