A Rodent Model of The Ross Operation: Syngeneic Pulmonary Artery Graft Implantation in A Systemic Position

Summary

We demonstrate how to establish a murine model of pulmonary root implantation into the descending aorta to simulate the Ross procedure. This model enables the medium/long-term evaluation of pulmonary autograft remodeling in a systemic position, representing the basis of developing therapeutic strategies to promote its adaptation.

Abstract

The Ross operation for aortic valve disease has regained new interest due to its outstanding long-term results. Nonetheless, when employed as freestanding root replacement, the possible dilation of the pulmonary autograft and subsequent aortic regurgitation is described. Several animal models have been proposed. However, these are usually limited to ex-vivo models or in-vivo experiments with relatively expensive large animal models. In this study, we sought to establish a rodent model of pulmonary artery graft (PAG) implantation in a systemic position. A total of 39 adult Lewis rats were included. Immediately after euthanasia, the pulmonary root was harvested from a donor animal (n=17). Syngeneic recipient (n=17) and sham-operated (n=5) rats were sedated and ventilated. In the recipient group, the PAG was implanted with an end-to-end anastomosis in infra-renal abdominal aortic position. Sham-operated rats underwent only transection and re-anastomosis of the aorta. Animals were followed with serial ultrasound studies for two months and post-mortem histological analysis. The median PAG diameter in the native position was 3.20 mm (IQR=3.18-3.23). At follow-up, the median diameter of the PAG was 4.03 mm (IQR=3.74-4.13) at 1 week, 4.07 mm (IQR=3.80-4.28) at 1 month, and 4.27 mm (IQR=3.90-4.35) at 2 months (p<0.01). Peak systolic velocity was 220.07 mm/s (IQR=210.43-246.41) at 1 week, 430.88 mm/s (IQR=375.28-495.56) at 1 month, and 373.68 mm/s (IQR=305.78-429.81) at 2 months (p=0.02) and did not differ from the sham-operated group at the end of the experiment (p=0.5). Histological analysis did not show any sign of endothelial thrombosis. This study showed that rodent models may allow for the evaluation of the long-term adaptation of the pulmonary root to a high-pressure system. A systemically placed syngeneic PAG implantation represents a simple and feasible platform for the development and evaluation of novel surgical techniques and drug therapies to further improve the outcomes of the Ross operation.

Introduction

Congenital aortic valve stenosis is a subgroup of congenital heart disease characterized by an obstruction of the left ventricular tract in which the lesion is located at the valvular level. The malformation affects approximately 0.04-0.38 per 1000 live births¹.

The available options for the correction are many, each with its own advantages and disadvantages. For patients suitable for a biventricular correction², the approach may be aimed at valve repair (percutaneous or surgical valvulotomy) or its replacement³. The latter is preferred when the aortic valve is considered unsalvageable; however, the available options are limited for pediatric patients. Indeed, bioprosthetic valves are not indicated for aortic replacement in the young population due to their early calcification⁴. On the other hand, degeneration in mechanical valves is considerably slower, but these require lifelong anticoagulant therapy⁵. In addition, the major limitation of these prostheses is represented by the lack of growth potential, which predisposes the patients to additional reinterventions.

An interesting therapeutic option in the pediatric population is the transfer of the pulmonary autograft to the aortic position named "Ross operation". In this case, the pulmonary valve is then replaced with a homograft (Figure 1)⁶. This procedure can possibly represent the best surgical choice for children because the pulmonary autograft preserves its growth potential and does not carry the risks of lifelong anticoagulant therapy. Furthermore, the Ross procedure can be of great value also in young adults to avoid a mechanical or biological valve, having the potential to become the best surgical solution.

Results after aortic valve replacement with pulmonary autograft are excellent, with survival greater than 98% and good long-term outcomes⁷. Literature studies report 93% and 90% freedom from replacing the pulmonary homograft at 4 and 12 years, respectively⁸.

The major limitation of this procedure is the tendency of the autograft to dilate in the long term, especially when employed as a freestanding root replacement. This can cause valvular incompetence which may require a reintervention. Indeed, the longest follow-up study performed so far reports freedom from reoperation for autograft replacement of 88% at 10 years and 75% at 20 years⁹.

The possibility of recreating a Ross operation in an experimental setting represents a fundamental prerequisite to investigate the underlying mechanism of the pulmonary autograft adaption to systemic pressures. Several models have been proposed in the past. However, these are usually limited to ex-vivo experiments or in-vivo animal models with a relatively expensive large animals. In this study, we sought to establish a rodent model of pulmonary artery graft (PAG) implantation in a systemic position, as freestanding root.

Protocol

All procedures have been approved by the University of Padova Animal Care Committee (OPBA, protocol number n° 55/2017) and authorized by the Italian Ministry of Health (Authorization n° 700/2018-PR), in compliance with the European Union Directive 2010/63/UE and the Italian Law 26/2014 for the Care and Use of Laboratory Animals.

1. Animal care and experimental model

1. Ensure all Lewis rats are obtained from a single company (Table of materials). Maintain the rats in conventional facilities with free access to food and water.
2. Ensure that the weight of the rats ranges from 320-400 g for the recipient group and 200-250 g for the donor group.

2. Preoperative protocol

NOTE: All operations must be performed under clean conditions. Use male and female adult Lewis rats as recipients and donors as well in order to perform a syngeneic transplant.

1. Perform an intraperitoneal injection of tramadol (5 mg/kg) 15 min before surgery.
2. Administer a single dose of intramuscular Gentamicin (5 mg/kg) immediately before surgery.
3. For anesthesia induction, supply 4% sevoflurane in 1 L/min of oxygen to a poly(methyl methacrylate) chamber where the animal is placed. For anesthesia maintenance, use 2.0-2.5% sevoflurane in 1 L/min of oxygen throughout the procedure.
4. Shave the animal along the midline for 2 cm width from the sternum to 1 cm above the genital area with a razor. Then, sterilize the skin with iodine solution.
5. In order to prevent the animal from getting wet and to prevent heat dispersion during the surgery, cover the animal with a transparent plastic film.
6. Evaluate the level of anesthesia before performing the procedure by assessing the absence of response to a noxious stimulus.

3. Donor operation

1. Animal and heart preparation:
   1. Place the anesthetized animal on a cork tray with the caudal side facing the surgeon. Perform a xipho-pubic incision of about 5-6 cm, and retract the two musculocutaneous flaps laterally.
   2. Administer a volume of 1 mL of saline solution at 4 °C containing 500 IU of heparin through the abdominal vena cava.
   3. After 1 min, cut the diaphragm from left to right and perform an anterior thoracotomy to expose the heart.
   4. Cool the beating heart by dripping saline solution at 4 °C.
   5. Perform a pericardiectomy and a thymectomy in order to obtain a complete view of the aortic arch. Remove the remaining fatty tissues surrounding the aorta.
   6. Cut at the arch, just above the origin of the innominate artery; sever the latter one, too.
   7. Cut the thoracic inferior vena cava (IVC) and insert a 22 G cannula to infuse the heart with 20-25 mL of saline solution at 4 °C, exerting light pressure. Discontinue the perfusion when the heart stops beating and flow from the aorta became clear.
2. PAG explant:
   NOTE: An accurate harvesting and delicate handling of the PAG is mandatory for achieving optimal implantation in the recipient. Do not touch it directly with instruments, instead use cotton swabs.
   1. Perform an ultrasound study to assess the PA diameter in its native position.
   2. Insert a micro-plier under the posterior wall of the vessel and cut the latter using a micro-scissor as close as possible to its bifurcation to maximize the length of the PAG.
   3. Gently hold the PA with the ring-tipped micro-forceps and separate it from the right ventricle with the micro-spring scissors. Harvest the PAG, including some right ventricular muscle.
3. PAG preparation:
   1. Place the PAG on a gauze moistened with cold saline on the operating table and inspect the vessel under the operating microscope.
   2. Cut any abundant surrounding tissue, leaving only 1 mm of ventricular muscle. Set the length of the vessel at 5 mm.

4. Pulmonary artery graft (PAG) implantation

1. Preparation of the recipient animal:
   1. Place the anesthetized animal on a cork tray with the caudal side facing the surgeon.
   2. Perform a median longitudinal incision and use two mini retractors to keep the abdomen open.
   3. Extract the intestines with two cotton swabs and cover them with a gauze soaked with 39 °C saline allowing the visualization of the retroperitoneal area with exposure of the infra-renal abdominal aorta (AA).
      NOTE: During the surgery, it is important to occasionally moisten the intestines using a syringe containing 39 °C saline to prevent hypothermia, a critical condition common in rodents.
   4. Strip the posterior parietal peritoneum between the two renal arteries and the iliac bifurcation using two cotton swabs and remove the fatty tissue around the infrarenal AA. Leave only a small portion of fat above the AA, to facilitate handling on the vessel.
   5. Separate the AA from the IVC. To perform this procedure, first, pass a curved forceps behind the posterior aortic wall and use it to open a passage between the AA and IVC. Then, use a 2-0 silk suture to create a loop around the AA, in order to lift the vessel and separate the AA from IVC. Ligate any lumbar artery arising from the infrarenal AA with 6/0 silk suture and divide it.
   6. Rotate the animal 90° counterclockwise, placing the head on the operator's left side. The AA now lay horizontally in the microscopic field.
   7. Use two Yasargil clips to clamp the infrarenal AA and place them at a distance of 1.5 cm from each other. Transect the AA at the midpoint between the two clips.
   8. Irrigate the two ends of the vessels with heparin (1 UI/mL) in saline solution to remove any clots. Remove any adventitial debris from the vessels.
2. PAG implantation:
   1. Place the PAG between the two ends, with the ventricular end towards the cranial portion of the animal.
   2. Use a 10-0 polypropylene suture to perform two landmark single stitches connecting the PG to the AA. Perform the procedure on both ends of the PAG by placing the suture on opposite sides of the vessel circumference.
   3. Perform an end-to-end anastomosis between PAG and AA, beginning with the distal end. Use one of the two ends of the distal landmark suture for the posterior anastomosis using a recipient-to-graft out-in/in-out sequence to perform a running suture of about six stitches.
   4. Once the suture reaches the proximal landmark, perform a double half hitch completed by a square knot using the suture and one of the two ends of the proximal landmark suture. Apply rubber-shod mosquito forceps to the sutures to provide traction.
   5. Perform the same anastomosis on the anterior wall. Carry on the entire procedure on the proximal end of the PAG. Take particular attention when performing the proximal anastomosis to avoid including any leaflet in the suture line.
   6. Release the distal clip first to let the PAG be filled with retrograde blood (low-pressure flow) in order to check the anastomosis. Repair any blood leakage with a single suture. Once the distal anastomosis is evaluated, perform the same procedure on the proximal end.
3. Final stages of the operation on the recipient:
   1. Assess the patency of the PAG and apply two strips of gelatin sponge over the suture lines on both sides of the PAG (if necessary). Exert gentle pressure for a few seconds with two cotton swabs to help hemostasis.
   2. Relocate the intestines into the abdominal cavity and close the walls with a 4/0 polypropylene running suture.

5. Sham-operated procedure

1. Perform an identical preparation of the animal as previously illustrated for recipient rats.
2. Cut the infra-renal AA, midway between the renal and the iliac arteries' origin.
3. Reapproximate the two ends of the AA using an end-to-end anastomosis, as previously described. Remove the two clips and perform an accurate hemostasis procedure.
4. Reposition the intestines and close the abdominal wall in layers, as for the recipient animals.

6. Postoperative care and follow-up

1. Administer warm saline solution (5 mL) into the subcutaneous tissue of the animal's back for hydration. Place the rat under a heating lamp and visually monitor it until awakening, which usually takes up to 5 min after anesthesia is stopped. Place the animal in a cage at a room temperature of 22-24 °C, with immediate and unrestricted access to food and water.
2. Administer intramuscular tramadol (5 mg/kg) for postoperative analgesia twice daily for the first 48 h after surgery. Thereafter, monitor the recipient's health status and body weight daily, on a regular basis.
3. Follow-up: During the follow-up, perform seriate ultrasound studies at one week, one month, and two months to evaluate PAG function. During these studies, measure the vessel diameter, the peak systolic velocity (PSV), and the end-diastolic velocity. Measure these parameters inside the PAG and at the level of proximal and distal AA.
4. Euthanize the animals after two months of follow-up by application of CO₂ for a few minutes, and then explant the PAG, which will undergo histopathological analysis.

Results

A total of 39 adult Lewis rats were included in this study: 17 animals were used as PAG donors, 17 animals as recipients and 5 as sham-operated (control group) (Table 1). Male rats were 22 (56%) and female 17 (44%); the latter were used only in the donor group.

No fatal event occurred during the operation with 100% survival. During the follow-up, two animals of the transplant group had a fatal outcome, at 12 and 51 days, respectively; the survival rate at the end of the study ...

Discussion

Aortic valve replacement with the autologous pulmonary root (Ross operation) represents an attractive option for congenital aortic valve stenosis repair due to the favorable profile and potential growth of the autograft¹⁰. The major limitation to this procedure is the potential dilatation of the aortic neo-valve, which predisposes to the development of long-term regurgitation. The possibility of characterizing the modifications on the pulmonary artery after exposure to systemic pressures could rep...

Materials

List of materials used in this article

Name	Company	Catalog Number	Comments
0.9% Sodium Chloride	Monico SpA	AIC 030805105	Two bottles of 100 mL. The cold one (4°C) for flushing the harvesting organ; the warm one (39°C) for moistening, and rehydration of the recipient
7.5% Povidone-Iodine	B Braun	AIC 032151211
Barraquer	Aesculap	FD 232R	Straight micro needle holder for the vascular anastomoses
Castroviejo needle holder	Not available	J 4065	To close the animal
Clip applying forceps	Rudolf Medical	RU 3994-05	For clip application
Cotton swabs	Johnson & Johnson Medical SpA	N/A	Supermarket product. Sterilized
Curved micro jeweller forceps	Rudolf Medical	RU 4240-06	Used to pass sutures underneath the vases.
Depilatory cream	RB healthcare	N/A	Supermarket product
Electrocautery machine	LED SpA	Surton 200
Fine scissors	Rudolf Medical	RU 2422-11	For opening the abdomen (recipient)
Fine-tip curved Vannas micro scissors	Aesculap	OC 497R	Only for preparing the pulmonary root, cut the lumbar vases and the 10/0 Prolene
Fluovac Isoflurane/Halotane Scavanger unit	Harvard Apparatus Ltd	K 017041	Complete of anesthesia machine, anesthesia tubing, induction chamber and scavenger unit with absorbable filter
Gentamycin	MSD Italia Srl	AIC 020891014	Antibiotic. Single dose, 5 mg/kg intramuscular, administered during surgery
Heparin	Pharmatex Italia Srl	AIC 034692044	500 IU into the recipient abdominal vena cava
I.V. Catheter	Smiths Medical Ltd	4036	20G
Insulin Syringe, 1 mL	Fisher Scientific	14-841-33	To inject heparin in the harvesting animal and to flush the sectioned aorta in the recipient
Jeweler bipolar forceps	GIMA SpA	30665	0.25 mm tip. For electrocautery of very small vases
Lewis rats (LEW/HanHsd)	Envigo RMS SRL, San Pietro al Natisone, Udine, Italy	86104M	Male or female, weighing 200-250 g (pulmonary root harvesting animals) and 320-400 g (recipients)
Micro-Mosquito	Rudolf Medical	RU 3121-10	In number of four, with tips covered with silicon tubing. To keep in traction the Prolene suture during anastomosis
Operating microscope	Leica Microsystems	M 400-E	Used with 6x, 10x and 16x in-procedure interchangeable magnifications
Perma-Hand silk 2-0	Johnson & Johnson Medical SpA	C026D	To lift the aorta
Petrolatum ophthalmic ointment	Dechra	NDC 17033-211-38
Prolene 10-0	Johnson & Johnson Medical SpA	W2790	Very fine non-absorbable suture, with a BV75-3 round bodied needle, for the vascular anastomoses
Retractors	Not any	N/A	Two home-made retractors
Ring tip micro forceps	Rudolf Medical	RU 4079-14	For delicate manipulation
Sevoflurane	AbbVie Srl	AIC 031841036	Mixed with oxygen, for inhalatory anesthesia
Spring type micro scissors	Rudolf Medical	RU 2380-14	Straight; 14 cm long
Standard aneurysm clips	Rudolf Medical	RU 3980-12	Two clips (7.5 mm; 180 g; 1.77 N) to close the aorta
Sterile gauze of non-woven fabric material	Luigi Salvadori SpA	26161V	7.5x7.5 cm, four layers
Straight Doyen scissors	Rudolf Medical	RU/1428-16	For use to the donor
Straight micro jeweller forceps	Rudolf Medical	RU 4240-04	10.5 cm long. Used throughout the anastomosis
Syringes	Artsana SpA	N/A	20 mL (for the harvesting animal) and 5 mL (for the recipient). For saline flushing and dipping
TiCron 4-0	Covidien	CV-331	For closing muscles and skin
Tissue forceps V. Mueller	McKesson	CH 6950-009	Used for skin and muscles
Tramadol	SALF SpA	AIC 044718029	Analgesic. Single dose, 5 mg/kg intramuscular
Virgin silk 8-0	Johnson & Johnson Medical SpA	W818	For arterial branch ligation