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In This Article

  • Summary
  • Abstract
  • Protocol
  • Results
  • Discussion
  • Disclosures
  • Acknowledgements
  • Materials
  • References
  • Reprints and Permissions

Summary

We describe the protocol to perform a cardiac stress test induced by dobutamine and monitored by cardiac catheterization in normal mice. Also we show its application to unmask subclinical cardiac disease in high fat diet-induced obese mice.

Abstract

Dobutamine is a β-adrenergic agonist with an affinity higher for receptor expressed in the heart (β1) than for receptors expressed in the arteries (β2). When systemically administered, it increases cardiac demand. Thus, dobutamine unmasks abnormal rhythm or ischemic areas potentially at risk of infarction.

Monitoring of heart function during a cardiac stress test can be performed by either ecocardiography or cardiac catheterization. The latter is an invasive but more accurate and informative technique that the former.

Cardiac stress test induced by dobutamine and monitored by cardiac catheterization accomplished as described here allows, in a single experiment, the measurement of the following hemodynamic parameters: heart rate (HR), systolic pressure, diastolic pressure, end-diastolic pressure, maximal positive pressure development (dP/dtmax) and maximal negative pressure development (dP/dtmin), at baseline conditions and under increasing doses of dobutamine.

As expected, in normal mice we observed a dobutamine dose-related increase in HR, dP/dtmax and dP/dtmin. Moreover, at the highest dose tested (12 ng/g/min) the cardiac decompensation of high fat diet-induced obese mice was unmasked.

Protocol

Protocol was approved by the Ethic Committee of Facultad de Medicina Clinica Alemana-Universidad del Desarrollo.

I. Preparing Dobutamine Infusion

  1. Dissolve 10 mg of dobutamine in 20 ml of sterile distillated water, in order to obtain a stock solution of 500 μg/ml dobutamine. Aliquot and store at -20 °C. This solution can be used at least for 3 months.
  2. Thaw an aliquot of dobutamine stock solution at room temperature.
  3. Dilute dobutamine stock solution in sterile 0.9% NaCl, in order to obtain dobutamine working solution, which concentration is calculated using the formula: dobutamine (μg/ml) = body weight x 0.2.
  4. Fill a 1 ml syringe 29Gx1/2" with dobutamine working solution.
  5. Insert the needle of the syringe into a 20 cm PE-10 tube.
  6. Adjust the syringe in the infusion pump following manufacturer instructions.
  7. Set up the ramp infusion in a step-to-step format with an increase of 10 μl/min for each step, for 6 steps.

II. Preparing Pressure Sensor

  1. To minimize signal drift, submerge pressure sensor in sterile water at 37 °C for at least 15 min. Do not soak the catheter more than 0.5 cm deep, in order to prevent that hydrostatic pressure affects the pressure sensor.
  2. Electronically calibrate the pressure sensor at 25 and 100 mmHg. Electric input (Volt) is converted to pressure signal (mmHg).
  3. Set the sampling rate of 2 k/s and use the filter low pass with a cut off at 100 Hz. Set pressure signal to zero mmHg.
  4. Mark the catheter 15 mm from the tip. Distant to reach the heart from the introduction point was estimated by echocardiography, detecting the presence of the catheter into the left ventricule.

III. Preparing Mouse for Catheterization

  1. Weight C57BL/6 male mice, 30-32 week-old.
  2. Inject intraperitoneally 60 μg/kg ketamine and 4 μg/kg xylazine1. Note: Other anesthetics might be used, for example: 350 - 450 μg/kg avertin, 50 μg/kg pentobarbital or 1.5 - 2% isoflurane2-3.
  3. Shave the neck with an electric razor.
  4. Place the anesthetized mouse in supine position on a warmed isothermal heating plate. Secure its limbs with paper tape.
  5. Perform a toe pinch to confirm complete sedation.
  6. Gently insert a rectal probe to monitor body temperature. Using vaselinized probe is recommended.
  7. If body temperature differs from 37 °C ± 0.5 °C, adjust it via the heating plate.
  8. Put mouse snout near the oxygen supply.
  9. Place the mouse neck region under the stereomicroscope.

IV. Data Acquisition

  1. In the LabChartPro 7 software, select one channel for pressure registration and one channel for heart rate (HR) registration. For the latter, select the option "Cyclic Measurements" and setup measurement as rate.
  2. For the pressure channel set the scale range: 0 to 150 mmHg.
  3. For HR channel set scale range: 200 to 600 bpm.
  4. Press the start key to begin the registration.
  5. Insert comments indicating procedures performed, for example: anesthesia administration, start of dobutamine infusion, dobutamine concentration, breathing changes.

V. Cardiac Catheterization4,5

  1. Perform a small incision on the right side near the jaw. With scissors separate the skin-muscular connective tissue.
  2. Perform a longitudinal dissection (1.5 - 2 cm) on the right side of the trachea. Separate the connective tissue, fat and muscle with curved forceps, in order to expose the right carotid artery near the trachea.
  3. Place an expander in the animal right side to expose the carotid artery. Pulsatile pressure generated by the heart facilitates the identification of the artery. The jugular vein, which is dark red, is on the right.
  4. Separate the artery from adjacent tissues with curved forceps. The vagus nerve, which resembles a white thread, lies along the artery.
  5. Cut a 20 cm piece of 6/0 silk thread and "double" it.
  6. Pass the "double" thread under the artery from left to right. Cut the thread, in order to obtain separate ends.
  7. Pass a third thread (10 cm) below the artery.
  8. Tie a tight knot in the thread positioned near to the head, and a loose one in the more distal thread.
  9. Tie a loose knot in the middle thread, and fix the right end of the middle thread to the heating pad with a paper tape.
  10. Keep carotid artery moist by dropping sterile 0.9% NaCl. Dry off excess of liquid with cotton buds.
  11. Stretch the lower thread with a hemostat clamp.
  12. Fix the position of the hemostat scissor by pinching the skin of the abdomen, stretching the upper thread, in order to occlude blood flow. Verify that connective tissue around the artery has been removed. The artery should be full of blood and deprived of pulse. Prevent threads from producing a torque force on the artery.
  13. Make a cross section nick near the bottom of the artery with a Vannas micro-scissor. Blood drops will be spilled.
  14. Insert the catheter into the carotid artery. Be sure to introduce the entire pressure sensor. Verify that there is no blood loss.
  15. Gently adjust the middle thread knot, in order to hold the catheter in place. Do not compress too much, the pressure sensor is very fragile.
  16. Release the hemostat scissors from the animal abdomen.
  17. Hold the catheter with the hand and push the middle thread, in order to avoid blood loss. Note: artery should be full of blood.
  18. Start recording pressure signals.
  19. When the catheter is inside, the arterial pressure signal fluctuates from 60-70 to 100-120 mmHg. The shape of the pressure signal is shown in Figure 1.A. Note: if you are interested on, at this time point you can record arterial pressure if signal is stable for at least 5 min. HR values were obtained from the pressure waveforms considering an interval of 30 sec of record signal. It is possible to use also an ECG method for direct measurement of HR, according with the investigation goals.
  20. Gently push the catheter up to observe a change in the shape of the pressure signal (Figure 1.B). Once the catheter is inside the left ventricle, the pressure signal fluctuates from 0 to 100-120 mmHg. If it is difficult to slide the catheter, pinch animal chest with two fingers.
  21. Continuously control breath rate, body temperature, anesthesia level and pressure signal. All of them should remain stable.

VI. Infusion of Dobutamine

  1. For jugular vein cannulation be sure to peel back the adipose tissue around the vein, in order to prevent its perforation. The surgical procedure for vein occlusion is similar to the procedure shown for carotid artery.
  2. Introduce a PE-10 tube into the vein. Confirm that blood flow is not blocked moving backward the syringe plunger.
  3. Dobutamine infusion starts with 10 μl/min and finish with 60 μl/min. In every step, the infusion rate is maintained for 2 min6.
  4. After the last dobutamine dose, euthanize the animal with an overdose of anesthesia.

VII. Data Analysis

  1. For data analysis, choose the section of the recorded data of your interest. Be sure to consider a time interval where pressure signal is stable.
  2. Select the Setup icon in the Blood Pressure module. Indicate the selected type of pressure signal.
  3. Automatically the LabChartPro 7 software displays mean, maximum and minimum values for HR, systolic pressure (Pmax), diastolic pressure (Pmin), end-diastolic pressure (EDP), maximal positive pressure development (dP/dtmax) and maximal negative pressure development (dP/dtmin). In addition, cardiac parameters can be depicted on the pressure trace.

Results

The arterial pressure signal is defined by systolic and diastolic pressure. When the pressure sensor is inside the left ventricle, its pressure (LVP) waveform is characterized by a drop to zero of the diastolic pressure and the appearance of the left atrial contraction before ventricle contraction (Figure 1). At baseline condition, ketamine-xylazine anesthetized normal mice had HR of 280 ± 24, Pmax of 107 ± 8, Pmin of 5 ± 1, EDP of 14 ± 2, dP/dtmax

Discussion

Cardiac stress test induced by dobutamine and monitored by cardiac catheterization is laborious. Nonetheless, following the protocol here describe and with a short time of training, it is possible to assess six hemodynamic parameters in a single experiment that last approximately one hour.

The critical steps of the protocol here presented are the cannulations of blood vessels. Regarding the cannulation of carotid artery, the incision performed should be deep enough to break the three tissue la...

Disclosures

No conflicts of interest declared.

Acknowledgements

We thank Dr. Helio Salgado, Renata Lataro and Mauro de Oliveira, School of Medicine of Ribeirão Preto, University of Sao Paulo and Dr. Ben Janssen, Cardiovascular Research Institute Maastricht, Maastricht University, for generous assistance during the set up process.

This work was supported by FONDECYT grant N° 11090114 to S.D.C.

Materials

NameCompanyCatalog NumberComments
Reagents
PE-50/10Warner Instruments64-0752
Silk thread 6/0 HR17TagumSN0713K
Xylacin 20 mg/mlLaboratorio Centrovet
Ketamine 100 mg/mlDrag Pharma
Sodium chloride 0.9%Lab Sanderson S.A.
Dobutamine hydrochlorideSigma-AldrichD0676
Syringe U-100 Insulin 29G x ½"Terumo Medical Co.
Forceps Dissecting Micro 11.5 cm Style 7Lawton Medizintechnik09-0959
Graefe Forceps Cvd 0.7mm 7cmLawton Medizintechnik62-0263
Clamps Dieffenbach bulldog Cl Str 38 mm Lawton Medizintechnik60-010
Vannas Scissors 8 cm Str FhLawton Medizintechnik63-1400
Equipment
SPR-671 MiKro-Tip Pressure catheterMillar instruments840-6719
PCU-2000 Pressure Control UnitMillar instruments880-0129
PowerLab 4/30ADinstruments Pty Ltd.ML866
LabChartPro 7 ADinstruments Pty Ltd.MLU260/7
Legato200 Infusion PumpKdScientificKD-KDS210P
TCAT-2LV Temperature controller and isothermal heating platePhysiTemp instruments Inc.
Medical Oxygen supplyIndura
Rectal probe ADinstruments Pty Ltd.MLT1404
Trinocular microscope, axial illuminationLW ScientificZ2B-TRI-ETNE, ILP-1502-LTS1, ILP-1502-DGGF

References

  1. Hart, C. Y., Burnett, J. C., Redfield, M. M. Effects of avertin versus xylazine-ketamine anesthesia on cardiac function in normal mice. Am. J. Physiol. Heart Circ. Physiol. 281, H1938-H1945 (2001).
  2. Janssen, B. J., et al. Effects of anesthetics on systemic hemodynamics in mice. Am. J. Physiol. Heart Circ. Physiol. 287, H1618-H1624 (2004).
  3. Lorenz, J. N. A practical guide to evaluating cardiovascular, renal, and pulmonary function in mice. Am. J. Physiol. Regul. Integr. Comp. Physiol. 282, R1565-R1582 (2002).
  4. Lorenz, J. N., Robbins, J. Measurement of intraventricular pressure and cardiac performance in the intact closed-chest anesthetized mouse. Am. J. Physiol. 272, H1137-H1146 (1997).
  5. Nemoto, S., DeFreitas, G., Carabello, B. A. Cardiac catheterization technique in a closed-chest murine model. Contemp. Top. Lab Anim. Sci. 42, 34-38 (2003).
  6. Daniels, A., et al. Impaired cardiac functional reserve in type 2 diabetic db/db mice is associated with metabolic, but not structural, remodelling. Acta Physiol. (Oxf). 200, 11-22 (2010).
  7. De Celle, T., et al. Long-term structural and functional consequences of cardiac ischaemia-reperfusion injury in vivo in mice. Exp. Physiol. 89, 605-615 (2004).
  8. Huntgeburth, M., et al. Transforming growth factor beta oppositely regulates the hypertrophic and contractile response to beta-adrenergic stimulation in the heart. PLoS One. 6, e26628 (2011).
  9. Reddy, A. K., et al. Cardiac function in young and old Little mice. J. Gerontol. A. Biol. Sci. Med. Sci. 62, 1319-1325 (2007).
  10. Christoffersen, C., et al. Cardiac lipid accumulation associated with diastolic dysfunction in obese mice. Endocrinology. 144, 3483-3490 (2003).

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Keywords Cardiac Stress TestDobutamineCardiac CatheterizationHemodynamic ParametersHeart RateSystolic PressureDiastolic PressureEnd diastolic PressureDP dtmaxDP dtminObesityHigh fat Diet

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