A Closed-chest Model to Induce Transverse Aortic Constriction in Mice

Summary

Here, we present a protocol of Transverse Aortic constriction (TAC) via a lateral thoracotomy. This technique is a minimally invasive, closed chest surgical procedure aiming to simulate pressure overload and heart failure in mice utilizing standard TAC laboratory settings.

Abstract

Research on cardiac hypertrophy and heart failure is frequently based on pressure overload mouse models induced by TAC. The standard procedure is to perform a partial thoracotomy to visualize the transverse aortic arch. However, the surgical trauma caused by the thoracotomy in open-chest models changes the respiratory physiology as the ribs are dissected and left unattached after chest closure. To prevent this, we established a minimally invasive, closed chest approach via lateral thoracotomy. Herein we approach the aortic arch via the 2^nd intercostal space without entering the chest cavities, leaving the mouse with a less traumatic injury to recover from. We perform this operation using standard laboratory settings for open chest TAC procedures with equal survival rates. Apart from maintaining physiological breathing patterns due to the closed chest approach, the mice seem to benefit by showing rapid recovery, as the less invasive technique appears to facilitate a fast healing process and to reduce immune response after trauma.

Introduction

Mouse models are often used to mimic human diseases¹. Transverse aortic constriction (TAC) is used to induce pressure overload and left ventricular hypertrophy². The open-chest TAC model in mice was validated by Rockman et al.³ and the surgical procedure is described in detail by DeAlmeida et al.⁴. Banding of the transverse aorta is more favorable in comparison to abdominal aortic constriction because a larger portion of the circulation can compensate negative effects of this latter procedure².

The banding of the transverse aorta leads to an increased arterial pressure in the ascending aorta and brachiocephalic artery but leaves sufficient perfusion of the organs via the distal vessels (i.e. the left common carotid artery, the left subclavian artery, and descending aorta). This leads to an increased cardiac afterload and an elevated cardiac wall stress. The wall stress subsequently decreases due to fiber thickening⁵. The chronic change in cardiac hemodynamics results in maladaptation and dilatation of the left ventricle. This way the TAC creates a reproducible model of cardiac hypertrophy eventually leading to heart failure.

The standard procedure for TAC as described by DeAlmeide et al.⁴ approaches the aortic arch via a partial upper thoracotomy via dissection of the ribs or the sternum and entering the mediastinum as well as the pleural cavity. This allows for a good view of the aortic arch and its side branches. Unfortunately, the dissected ribs cannot be reattached, which leaves them floating freely and thereby altering the breathing dynamics.

We, therefore, established a minimally invasive closed-chest approach to the aortic arch using a lateral surgical approach via the 2^nd intercostal space. The greatest advantage of this model is the ability to perform TAC without even cutting through the ribs. The surgical trauma is limited to the incision of the skin and the dissection of the intercostal muscles. This procedure minimizes the trauma itself and helps to maintain adequate chest stability.

Here we describe a detailed step-by-step procedure to perform TAC surgery in mice without performing the total or the upper thoracotomy. High frequency Doppler was used to ensure the success of TAC as previously described ^6,7.

Protocol

This protocol was approved by the Ethics Committee for Animal Experimentation LANUV Recklinghausen (#84-02.04.2016.A374). Generally, this procedure is performed on adult mice >10 weeks of age. However, it is possible to perform this surgery on younger animals as well. Surgical tools must be sterilized before use and all steps are to be performed under aseptic conditions.

1. Induction of Anesthesia and Intubation

1. Inject buprenorphine 0.1 µg/g body weight intraperitoneally for pain relief. Repeat the intraperitoneal injections of 0.1 mg/kg buprenorphine every 8 h for the next three days after surgery.
2. For induction, place the mouse into an anesthesia induction box which is connected to the vaporizer set to 3.0 Vol% of isoflurane with an oxygen flow of 1 L/min.
3. Ensure deep narcosis by inducing a tactile stimulus.
   NOTE: Increase Vol% of isoflurane up to 5%, if anesthesia induction fails or narcosis is not deep enough.
4. Pinch the tail of the mouse to ensure reflex absence. In case of complete absence of reflexes, weigh the mouse for optimal ventilator setup (see 1.12).
5. Move the mouse to a temperature-controlled operating table to maintain a body temperature of 37 °C throughout the procedure.
6. Place the nose of the mouse in a plastic cone which is connected to the anesthesia induction box to maintain narcosis.
7. Fix the upper incisors of the mouse with a nylon suture. Fixate the extremities with an adhesive tape.
8. Apply pressure on the hind paw with the tip of the forceps to ensure an adequate narcosis again. In the absence of a withdrawal reflex proceed with the following steps.
   NOTE: Increase volume % of isoflurane if anesthesia induction fails or narcosis is not deep enough and wait for the absence of the withdrawal reflex.
9. Place sterile ophthalmic lubricant on the corneas to prevent desiccation under anesthesia. 
10. Lubricate the rectal probe to avoid rectal trauma. Insert a rectal temperature probe to ensure a core temperature of 37 °C.
11. Depilate the throat and the upper chest with depilatory cream according to the manufacturer's instructions. Wipe off the cream after 1 min. If necessary, repeat this step until successful.
    NOTE: Use cotton-tipped swabs in case of bleeding.
12. Clean the depilated area with 70% ethanol. Then apply povidone-iodine for local skin disinfection 3 times and for at least 3 min.
13. Adjust ventilator settings to physiological parameters. Set the respiratory rate to 150/min and tidal volumes to 8-10 µL/g body weight (BW).
14. Put on a new pair of sterile gloves. Place the mouse under a surgical microscope and place a sterile fenestrated drape over the mouse.
15. Incise the skin at the midline about 3 mm under the mandibular down to the 2^nd rib. Identify midline and connective tissues of the submandibular gland. Then use angled intracapsular forceps to gently divide the gland at the midline bluntly with two forceps and explore the tracheal muscle.
16. Prepare the trachea gently by pulling the para-tracheal muscles apart bluntly with intracapsular forceps.
17. Pull on the tongue with forceps to straighten the throat for easier intubation conditions and gently insert an intubation cannula (OD 1.2 mm) inside the trachea. Confirm the intubation by direct visualization of the tube inside the trachea and by checking for proper chest movement.
18. Adjust the isoflurane concentration after intubation to 2% isoflurane with a flow of 1.0 L/min and 100% O₂.
    NOTE: If breathing movements do not stop or mice start moving, first increase the respiratory rate up to 180/min. If necessary, increase the isoflurane concentration up to 3.5% secondarily until the mouse stops breathing on its own. Evaluate leakages or inadequate filling of the vaporizer as the most common problems.
19. Alternatively, perform intubation as suggested in the following sub steps.
    1. Position the mouse on a table at a 60° angle.
    2. Fixate the extremities of the mouse with adhesive tape and recline the head.
    3. Place a cold-light source directly on the skin above the larynx.
    4. Pull the tongue gently with forceps to visualize the vocal chords.
    5. Insert a plastic tube of an IV-cannula (24 G) through the vocal chords and connect the plastic tube to the ventilator settings.
    6. Connect the ventilator to the cannula to confirm intubation by synchrone chest movements.
       NOTE: If breathing movements do not stop or mice start moving, first increase the respiratory rate up to 180 per min. If necessary, increase secondarily the isoflurane concentration up to 3.5% until the mouse stops breathing on its own. Evaluate leakages or inadequate filling of the vaporizer as the most likely problems.

2. Preoperative Doppler Measurement

1. Prepare both carotid arteries which lay adjunct to the trachea by gently pulling the connective tissue apart with forceps.
2. Place the tip of the 20 MHz Doppler probe with some sterile ultrasound gel on the right and the left carotid artery at an angle less than 45°.
3. Slowly rotate the probe to move it lateral and medial to find a Doppler signal and tilt the probe to optimize the signal.
4. Use a Doppler software to display and store flow velocities in the right and left common carotid arteries on a computer.

3. Thoracotomy

1. Use a set of sterile gloves for each individual mouse to prevent surgical site infections.
2. Expand the skin incision down to the 2^nd intercostal space with a scissor.
3. Identify the 2^nd intercostal space visually by counting the ribs and then bluntly penetrate this space with intracapsular forceps.
   NOTE: The 1^st rib is located under the clavicle and is therefore not visible because the 2^nd intercostal space is found between first visible rib (i.e. 2^nd rib) and the 3^rd rib.
4. Open the 2^nd intercostal space with the help of forceps tips and insert the retractors.
5. Adjust the retractors with a rubber band attached to the operating table to have a clear view of the thymus.
6. In case of bleeding use a cotton-tip and press on the superficial vessels for 2 min.

4. Banding of the Transverse Aorta

1. Adjust the magnification to 200% to identify midline and connective tissues. Then use angled forceps to gently divide the thymus. Remove fatty tissue until the aortic arch can be seen clearly.
2. Prepare a tunnel with angled tying forceps under the transverse aorta between the brachiocephalic artery and left common carotid artery (see Figure 1). Hold the end of a 6.0 suture with the help of fine forceps and pass the thread under the aortic arch.
3. Take the thread with the second forceps from the other side of the arch.
4. Cut off a 3-mm long piece length of a 27 G to use the needle as a the spacer for TAC-ligation for mice weighing between 19 - 25 g body weight and a 26 G needle as a spacer for mice >25 g BW.
5. Carefully place the spacer parallel to the transverse aorta.
6. Prepare a loose double knot on the spacer and ensure optimal placement of the spacer in parallel to the aorta. Then tie the first throw and quickly perform a second contrary throw. Remove the spacer promptly.
7. To perform sham mice for control, follow the same protocol omitting the ligation of the aorta.
8. Close the 2^nd intercostal space with a 6.0 polypropylene suture. Pay special attention to the subclavian vessels when ligating.
9. Suture the skin using a 6.0 polypropylene suture in a continuous suture pattern.

5. Confirmation of Successful Ligation of the Transverse Aorta

1. Place a 20 MHz Doppler probe on both sides of the neck at a 45° angle as in section 2.
2. Document the flow velocities on each side.
   NOTE: A successful TAC can be validated by Doppler flow velocity as shown in Figure 2. A flow velocity ratio of 4 - 10 between the right and left carotid artery usually guarantees adequate TAC (see Figure 2).

6. Heart harvest

1. Induce narcosis according to steps 1.2. and 1.3.
2. Place the mouse in an euthanasia chamber and adjust the carbon dioxide flow rate to displace 10 - 30% of the volume/minute.
3. Fixate the mouse on a surgery table. Open the abdomen with scissors and harvest blood from the inferior vena cava with a cannula for further analysis.
4. Cut the diaphragm and the sternal bone with strong scissors and remove the heart.
5. Remove all arterial and connective tissue before weighing the heart.
6. Separate the right ventricle and the septum from the left ventricle and weigh both samples.
7. Freeze both tissue samples in liquid nitrogen.

Results

A successful TAC guarantees the induction of pressure overload and left ventricular hypertrophy. An ad hoc validation of pressure overload can be achieved using Doppler flow velocity measurement as shown in Figure 2. While preoperative blood flow velocity is equal in both carotid arteries, TAC causes an augmented blood velocity in the right carotid artery due to elevated pressure in the left ventricle and aorta while causing post-stenotic attenuated blood flo...

Discussion

The rapid onset of hypertension due to TAC differs from clinically relevant hypertrophy caused by aortic stenosis or hypertension. Nevertheless, the use of small animal models to induce heart failure has many advantages and is, therefore, chosen by many investigators¹¹. This closed chest-model improves the already existing models of the surgical technique to induce transverse aortic constriction in mice⁴.

The most critical step is the passage und...

Materials

Name	Company	Catalog Number	Comments
Pressure-volume catheter	Millar Instruments, USA	SPR-839
Mouse ventilator	Harvard Apparatus GmbH, Germany	Minivent - TYPE 845
Mouse ventilator	Harvard Apparatus GmbH, Germany	Y-connection with intubation cannula OD 1.2mm 73-2844
Vaporizer	Dräger Medical AG&CO.KG, Germany	19.3 Isofluran-Vaporizer (a newer version is available under catalog number  D-877-2010)
Microscope	Leica Microsystems, Germany	MZ 7.5
Light source	Schott AG, Germany	KL 1500 LCD
6-0 Prolene	Ethicon, USA	Polypropylene suture BV-1 9.3 mm 3/8c	suture for surgery
Seraflex	Serag Wiessner, Germany	USP 5/0 schwarz;  IC108000	suture for constriction
Homoeothermic Controlled Operating Tables	Harvard Apparatus GmbH, Germany	Typ 872/3 HT with tripod stand and homoeothermic controller Type 874; 73-4233
Flexible Rectal Probe	Harvard Apparatus GmbH, Germany	1.6 mm OD; 55-7021
Doppler Signal Visualisation Instrument	Indus Instruments, USA	Doppler Signal Processing Workstation (DSWP) with 20MHz Pulsed Doppler Module
Arruga Intracapsular Forceps	Altomed, UK	A5400
Doppler Probe	Indus Instruments, USA	20MHz Tubing-mounted Probe
Jaffe Lid Retractor	Altomed, UK	A3513