Pv loop experiments

Pressure Volume loops are widely used in basic and preclinical research. Left ventricular PV loops are considered to be the gold standard for hemodynamic assessment and are widely used in research to evaluate cardiac performance. While it has long been possible to measure pressure in real time from the left ventricle, measuring the volume was technically more difficult.

The use of ultrasonic sonomicrometry and the development of the conductance catheter triggered renewed interest in PV loops studies. In sonomicrometry, small ultrasonic transducers (usually referred to as "crystals") transmit signals to each other, and the distance between them is accurately determined based on the transit-time of the signals. By knowing the long and short axis lengths of the ventrical, ventricular volume is easily and accurately determined. Conductance cathethers measure instantaneous conductance in the left ventricle, which is then converted to blood volume using complex formulas and usually after determining and applying various correction factors. Typically only one method is used to perform PV studies in research settings.

The miniaturization of sonomicrometer crystals and pressure catheters have made mice PV loop studies feasible and more common.

Contents 1 Sonomicrometer method 2 Conductance catheter technique 3 Theory 4 Calibration and correction 5 Parameters 6 See also 7 References 8 External links

Sonomicrometer method

A sonomicrometer system is composed of an electronic signal-processing unit that is connected to small ultrasonic transducers (crystals). A computer acting as a data acquisition and display device obtains data in real time from the signal processor unit, while the crystals are implanted in or on the left ventrical. As few as 2 or as many as 6 crystals can be used to perform 1-axis, 2-axis, or 3-axis length measurements of the axial planes of the heart, usually at a rate of 200 to 2000 times per second. A typical sonomicrometer system has a resolution of 12 micrometres, enabling high-resolution measurements of the axial lengths.

Ventricular volume is computed directly (either in micro-liters or milli-liters) by combining the axial length measurements in standard spherical or ellipsoidal volume equations:

(for a single-axis measurement)

(for a two-axis measurement, where L1 is the length of the long axis)

(for a three-axis measurement)

When the axial measurements are acquired in terms of millimeters, then the volume units in these equations will be in terms of milliliters.

Conductance catheter technique

A conductance catheter contains two or more ring-shaped electrodes along its length. When a high-frequency low-amplitude constant current is passed through the outer electrodes to generate an electric field, the potential difference between any pair of inner electrodes is inversely proportional to the amount of conductive material at that site.

Conductance is defined as the applied current divided by the voltage measured between two adjacent electrodes.

The conductance catheter technique has no major drawbacks but requires careful calibration of conductance signals. Other techniques exist but this article focuses on the well-established conductance catheter technique.

(NOTE: For typical catheter configurations the linear relationship of the inverse potential difference to the amount of material is only an approximation. It is only valid for volumes where the diameter of that volume is less than the distance between the measuring electrodes.)

Theory

The formula by Baan et al. (1984) for obtaining ventricular volume is as follows:

where

• V is volume
• α is the alpha factor. The value is between 0 and 1 but closer to 1. As can be inferred from the above formula, if the alpha factor is not taken into account, the calculated volume is an underestimate.
• ρ specific resistance of blood
• L distance between pair of electrodes
• G measured conductance
• G^P parallel conductance

The conductance measured by the catheter is actually the conductance of the blood and of the surrounding myocardial tissue. This latter conductance is called the parallel conductance (G^P).

Calibration and correction

From the above equation, it can be seen that the volume measurement requires the knowledge of α, ρ, L, and G^P.

The equation may be considered to be a straight line of the form y = mx + b, where m (the gain) is a combination of the three terms 1/α, ρ, and L² and b (the offset) is G^P.

L is available from catheter data sheets, while ρ can be measured directly using appropriate equipment.

Ideally, gain should be determined in every experiment. While L is known and ρ can be measured, the α factor poses more difficulties. Indeed, the only way to obtain a reliable gain (encompassing α) involves directly measuring cardiac output. Therefore, for most purposes, an educated estimate is used based on values found in the literature.

To take into account the parallel conductance, G^P, the most common method involves injection of hypertonic saline into the subject—enough to temporarily reduce blood resistance, and therefore increase preload, but not so much as to alter haemodynamics. The minimum and maximum volumes (V_max and V_min) from each loop in the series of loops are plotted on a graph. V_max and V_min lines are extrapolated and at their point of intersection, where V_max is equal to V_min, must be zero—conductance is parallel conductance only. The volume at this point is the correction volume.

Admittance techniques offer an alternative to the saline bolus as a means of determining G^P.

Parameters

Several parameters can be calculated for each loop (e.g. end-diastolic pressure, end-systolic pressure, ejection and filling intervals, contractility index, stroke volume, and ejection fraction).

More importantly, other interesting parameters are derived from series of loops obtained under changing conditions. For example, the end-diastolic pressure-volume relationship (EDPVR) and end-systolic pressure-volume relationship (ESPVR) are derived from series of loops obtained by slowly inflating a balloon to occlude the inferior vena cava, a procedure that reduces cardiac preload.

EDPVR and ESPVR are valuable because they are load-independent indices of left ventricular function.

Other parameters derived from series of loops are:

• Time-varying elastance
• End-systolic elastance also called maximal elastance
• Preload recruitable stroke work
• Preload adjusted
• vs end-diastolic volume

See also

• Signal processing
• Iox acquisition software

References

Esposito G, Santana AL, Dilly K, Santos Cruz JD, Mao L, Lederer WJ, Rockman HA (2000) Cellular and functional defects in a mouse model of heart failure. Am J Physiol Heart Circ Physiol 279: H3101–H3112.

Sodums MT, Badke FR, Starling MR, Little WC, O'Rourke RA (1984) Evaluation of Left Ventricular Contratile Performance Utilizing End-Systolic Pressure-Volume Relationships in Conscious Dogs. Circulation Research. 54(6): 731-739.

Baan J et al. (1984). Continuous measurement of left ventricular volume in animals and humans by conductance catheter. Circulation 70: 812-823

Pacher P, Nagayama T, Mukhopadhyay P, Bátkai S, Kass DA (2008). Measurement of cardiac function using pressure–volume conductance catheter technique in mice and rats. Nature Protocols 3(9): 1422-34.

External links

• Sonometrics Corporation (Instrumentation, transducers and software for life science research labs)

• ADInstruments, Inc (Scientific instrumentation and PV Loop Software Module for life science research labs)
• Video on Vimeo Video of pv-loops acquisition and analysis

Cardiovascular system, physiology: cardiovascular physiology Heart Volumes Stroke volume = End-diastolic volume – End-systolic volume Cardiac output = Heart rate × Stroke volume Afterload · Preload Frank–Starling law of the heart · Cardiac function curve · Venous return curve Aortic valve area calculation · Ejection fraction · Cardiac index Dimensions Fractional shortening = (End-diastolic dimension – End-systolic dimension) / End-diastolic dimension Interaction diagrams Cardiac cycle · Wiggers diagram · Pressure volume diagram Tropism Chronotropic (Heart rate) · Dromotropic (Conduction velocity) · Inotropic (Contractility) · Bathmotropic (Excitability) · Lusitropic (Relaxation) Conduction system / Cardiac electrophysiology Cardiac action potential (Atrial action potential, Ventricular action potential) · Effective refractory period · Pacemaker potential · EKG (P wave, PR interval, QRS complex, QT interval, ST segment, T wave, U wave) · Hexaxial reference system Chamber pressure Central venous pressure/right atrial pressure → Right ventricular pressure → Pulmonary artery pressure → Pulmonary wedge pressure/left atrial pressure → Left ventricular pressure → Aortic pressure Other Ventricular remodeling Vascular system/ Hemodynamics Blood flow Compliance · Vascular resistance (Total peripheral resistance) · Pulse · Perfusion Blood pressure Pulse pressure (Systolic - Diastolic) · Mean arterial pressure Jugular venous pressure Portal venous pressure Regulation of BP Baroreflex · Kinin-kallikrein system · Renin-angiotensin system · Vasoconstrictors/Vasodilators · Autoregulation (Myogenic mechanism, Tubuloglomerular feedback) · Paraganglia (Aortic body, Carotid body, Glomus cell) M: HRT anat/phys/devp noco/cong/tumr, sysi/epon, injr proc, drug (C1A/1B/1C/1D), blte M: VAS anat(a:h/u/t/a/l,v:h/u/t/a/l)/phys/devp/cell/prot noco/syva/cong/lyvd/tumr, sysi/epon, injr proc, drug(C2s+n/3/4/5/7/8/9)