A Recovery Cardiopulmonary Bypass Model Without Transfusion or Inotropic Agents in Rats

Summary

Here, we present a protocol to describe a simple recovery cardiopulmonary bypass model without transfusion or inotropic agents in a rat. This model allows the study of the long-term multiple organ sequelae of cardiopulmonary bypass.

Abstract

Cardiopulmonary bypass (CPB) is indispensable in cardiovascular surgery. Despite the dramatic refinement of CPB technique and devices, multi-organ complications related to prolonged CPB still compromise the outcome of cardiovascular surgeries, and may worsen postoperative morbidity and mortality. Animal models recapitulating the clinical usage of CPB enable the clarification of the pathophysiological processes that occur during CPB, and facilitate pre-clinical studies to develop strategies protecting against these complications. Rat CPB models are advantageous because of their greater cost-effectiveness, convenient experimental processes, abundant testing methods at the genetic or protein levels, and genetic consistency. They can be used for investigating the immune system activation and synthesis of proinflammatory cytokines, compliment activation, and production of oxygen free radicals. The rat models have been refined and have gradually taken the place of large-animal models. Here, we describe a simple CPB model without transfusion and/or inotropic agents in a rat. This recovery model allows the study of the long-term multiple organ sequelae of CPB.

Introduction

In 1953, Dr. John H. Gibbon Jr. successfully performed the first cardiac surgery using CPB¹, and it subsequently became an essential modality in cardiovascular surgery. While the techniques and devices have been dramatically refined, multi-organ complications related to CPB still compromise the outcome of cardiovascular surgeries, and may affect postoperative morbidity and mortality². CPB-related organ damage is caused by immune system activation and synthesis of proinflammatory cytokines, compliment activation, and production of oxygen free radicals². Its pathophysiology, however, has not been fully elucidated.

Animal models recapitulating the clinical usage of CPB enable the clarification of the pathophysiological processes during and after CPB; this can facilitate pre-clinical studies in developing strategies to avoid these complications. Since Popovic et al. first reported a rat CPB model in 1967³, rat CPB models have been refined, and have gradually taken the place of large-animal models due to greater cost-effectiveness, convenient experimental processes, and a plethora of testing methods in genetic and protein levels. Additionally, inbred rats can be genetically identical, reducing possible biological biases.

Fabre et al. first established a recovery model that allowed the study of the long-term multiple organ sequelae of CPB⁴. The advantages of this simple survival model are the flexibility (CPB flow and duration), stable vital condition, and reproducibility in systemic inflammation. Rat CPB models have become crucial for the investigation of therapeutic strategies that aim to prevent multi-organ injury during CPB⁵, and various models for simulating the clinical situations during CPB have recently been developed. De Lange et al. developed a cardiac arrest model, which can be used to characterize the enzymatic, genetic, and histological responses related to myocardial injury⁷. Peters et al. arranged myocardial infarction and controlled reperfusion using a miniaturized CPB model to analyze heart disfunction through the focal ischemia and reperfusion injury⁸. Jungwirth et al. first established a deep hypothermic circulatory arrest (DHCA) model, which can elucidate the global ischemia and reperfusion injury by DHCA and supports potential neuroprotective strategies⁶. Studies using DHCA investigate the influence of hypothermia, reperfusion, and/or hemolysis-triggered signaling events⁹. Deep hypothermia may affect the activation and inactivation of various enzymes and pathways and the mechanisms remain unknown¹⁰. On the other hand, cardiac arrest models or heart ischemia models must be used to investigate ischemia and reperfusion heart injury. These various rat CPB models that highly recapitulate human CPB may reveal pathological processes related to CPB and help mitigate CPB-related complications.

This protocol demonstrates a simple CPB model without transfusion or inotropic agents in a rat. This model allows for the study of long-term multiple organ sequelae of CPB.

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Protocol

Prior to experiment, all rats should be given one week to acclimate. All surgical procedures on animals should be carried out in accordance with the Guide for the Care and Use of Laboratory Animals (www.nap.edu/catalog/5140.html) or other appropriate ethical guidelines. Protocols should be approved by the animal welfare committee at the appropriate institution before proceeding. All subsequent procedures must be performed under aseptic conditions. 

1. Preparing CPB Circuit

Note: Wear personal protective equipment including gloves, eyewear, and a clean coat or disposable gown.

1. Set-up of CPB circuit
   1. Connect polyvinyl chloride tubes with a venous reservoir, predesigned for CPB circuit, and a modified neonatal membrane oxygenator as shown in Figure 1. Ensure all connections are tight and do not leak water.
   2. Set a CPB circuit to the roller pump device according to the manufacturer's protocols.
   3. Keep the roller pump on a height-adjustable table and adjust the table's height to 10 cm below the experimental desk.
2. Priming of CPB circuit
   1. Mix 12 mL of hydroxyethyl starch solution with 0.1 mL of heparin and 0.5 mL of 7% sodium bicarbonate solution for priming CPB circuit.
   2. Prime the circuit with 11 mL of the priming solution, with the pump roller gently rotating. Put an 18-gauge venting needle into the reservoir for venting air.
   3. Hit the membrane oxygenator several times to deair, with tilting the oxygenator. Air must be obscured completely to avoid air embolism and insufficient oxygenation. During the circuit priming, heat the circuit by an electric heat lamp set on the reservoir.

2. Procedure Before CPB

NOTE: The surgical field and devices should be disinfected by 70% alcohol or a quaternary ammonium compound before use.

1. Anesthesia and animal setting
   1. Anesthetize a rat with 3.0% isoflurane-mixed air inhalation in a vaporizer. Set the rat on a work-stand and intubate a 16-gauge cannula into the trachea. Follow your local animal care guidelines regarding analgesia dosage and frequency (e.g.
      buprenorphine 0.005 mg/kg s.c.)
      ​NOTE: Rats must be at deep anesthesia and lose reflexes. The respiration should be rhythmic but not be arrested.
   2. Transfer the rat to an operating table equipped with an electric heating pad. Start the mechanical ventilation with 8 mL/kg of tidal volume, a respiratory rate of 70 cycles/min, and 30% of inspired oxygen fraction monitored by the oxygen sensor.
   3. Maintain the anesthesia with 1.5-2.0% isoflurane, and with an additional administration of ketamine/xylazine at CPB initiation.
   4. Monitor the rectal temperature by using the rectal probe. Maintain normothermic body temperature of 37 °C by adjusting the temperature of the heat pad and placing the circuit over the heat lamp.
   5. Set the rat in supine position and stretch the four limbs by fixing with needles. Monitor the heart rate by setting the ECG electrode needle to the bilateral shoulder and left abdomen. Place a moist gauze or apply ophthalmic ointment to the eyes to prevent dryness.
2. Cannulation
   1. After disinfecting the surface of the whole body by sprayingby spraying 70 % ethanol or another antiseptic solution, shave the hair by a razor on the bilateral inguinal region and right cervical region. Local anesthetics (such as lidocaine) should be used before making the skin incision. NOTE: As an alternative, a surgical scrub of the incision site can be used instead of the whole body spray of 70% ethanol to avoid a drop in body temperature.
   2. Incise the skin (approximately 5 mm) at the bilateral inguinal regions and right cervical region by scissors and bluntly dissect the tissues to expose the right main femoral artery. Separate the artery carefully from the vein and nerve nearby. Ligate at the end of common femoral artery by 4-0 silk and exposure by tension.
   3. Cut the arterial wall (approximately 1 mm) of right common femoral artery by micro scissors in perpendicular direction to the artery, and carefully cannulate a 24-gauge intravenous catheter from the incision to a depth of 1 cm for monitoring systemic arterial pressure and analyzing gas partial pressure in arterial blood.
   4. Administrate heparin sodium (500 IU/kg) from the catheter.
   5. Follow steps 2.2.2 and 2.2.3 to cannulate a 24-gauge intravenous catheter into the left common femoral artery as an arterial infusion line for the CPB circuit.
   6. Insert a 17-gauge multi-orifice angiocatheter into the right internal jugular vein and advance it into the right atrium and inferior vena cava (IVC). Do not push the catheter roughly as the vessel can easily break. Connect the catheter to the CPB circuit for venous drainage.
   7. Cover each cannulated region with a moist gauze to avoid contamination.

3. Procedure During CPB

1. Deliver 100% oxygen gas to the oxygenator at 0.8 L/min during CPB and decrease the respiratory rate to 30 cycles/min. The arterial oxygen partial pressure is required from 200 to 400 mmHg.
2. At the beginning of CPB, increase the temperature setting of the heat pad to the maximum, 42 °C, to mitigate the immediate drop of the body temperature after CPB initiation. Adjust the setting temperature to 37 °C when the body temperature returns to 36 °C.
3. Carefully start the CPB flow and keep an eye on the volume of the blood in the reservoir. An empty reservoir may cause air embolism. If the volume of the blood in the reservoir decreases, lower the pump flow by adjusting the table height, or changing the position of the drainage catheter. Do not re-position the venous drainage catheter, which might easily cause perforation of the right atrium and/or arrhythmia.
4. Increase and keep the pump flow at 100 mL/kg/min, while the mean blood pressure is maintained at 70 mmHg. When the appropriate blood pressure is maintained, a small volume of at least 1 mL in the reservoir is acceptable. If there is less than 1 mL of the blood in the reservoir, it may cause an air embolism in organs.
5. If the blood pressure is unstable, add 2-3 mL of the priming solution to the circuit (it may cause anemia after the CPB).

4. Procedure After CPB

1. Clamp the venous drainage tube and remove it from the circuit. Infuse the remaining blood in the circuit gradually to the artery to maintain the blood pressure.
2. Increase the respiratory rate to 70 cycles/min.
3. Remove the venous drainage catheter and the left arterial catheter, then ligate the vessel in the proximal and distal site.
4. Remove the arterial line from the right femoral artery 60 min after the end of CPB.
5. Clean each wound with saline and close the wound with sutures.
6. End the anesthesia and extubate the intratracheal tube after checking the spontaneous breathing of the animal.
7. Administer warmed sterile isotonic fluids, and use a heat mat and electrical heat lamp to keep the animals warm. Check the conditions of the animal frequently until recovery from anesthesia. Provide respiratory support when required. NOTE: Once the animal begins moving around, the heat source should be removed from part of the cage to allow the animal to choose the warm or cool side.
8. Keep the animal apart from the company of other animals until the respiration fully regains. Do not return the animal to the company until full recovery.
9. Check the food and water intake after the recovery from anesthesia and provide appropriate nutritional support. Administer analgesics and check for signs of discomfort or pain.

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Results

Figure 1 shows the entire CPB circuit. The physiological variables in this model are shown in Figure 2, and include rectal temperature, mean arterial blood pressure, and heart rate. Figure 3 shows the arterial blood gas analyses during CPB, including partial pressure of arterial oxygen, partial pressure of arterial carbon dioxide, hematocrit, base excess, serum expression of potassium, and poten...

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Discussion

In this rat CPB model, the serum and lung expression levels of inflammatory cytokines and HMGB-1, a key transcription factor regulating the inflammatory responses, dramatically increased after CPB. Previous clinical studies showed that the serum secretion of HMGB-1 level is elevated in patients undergoing cardiovascular surgery¹¹, and the peak serum HMGB-1 level during CPB was associated with more severe systemic inflammatory response syndrome and lung oxygenation impairment after CPB

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Materials

Name	Company	Catalog Number	Comments
Rodent Ventilator 7025	Ugo Basile	7025	Ventilator
OxiQuant B	ENVITEC	46-00-0023	Oxygen Sensor
CMA 450 Temperature Controller	CMA	8003759	Temperature Controller
CMA 450 Heating Pad	CMA	8003763
CMA 450 Rectal Probe	CMA	8003761
DIN(8) to Disposable BP Transducer	ADInstruments	MLAC06
Disposable BP Transducer	ADInstruments	MLT0670
IX-214 Data Recorder	iWorx Systems	IWX-214	amplifier
LabScribe software	iWorx Systems		software
Roller pump	Furue Science	Model RP-VT	pump
Happy Cath	Medikit	EB 19G 4HCLs PP	17-gauge multiorifice angiocatheter
SURFLO ETFE I.V. Catheter	Terumo	SR-OX2419CA	24-gauge angiocatheter
Oxygenator	Mera	HPO-002
CPB circuit	Mera	custom-made
Hespander fluid solution	Fresenius Kabi	3319547A4035	Hydroxyethyl starch