Name: developing an experimental aneurysm model in a rabbit using an elastase-treated vessel pouch
Uploaded: 2025-04-28T12:15:06.000+00:00
Duration: 1 min 19 s
Description: Source: Wanderer, S., et al. Arterial Pouch Microsurgical Bifurcation Aneurysm Model in the Rabbit. J. Vis. Exp. (2020)This video demonstrates the ...

developing an experimental aneurysm model in a rabbit using an elastase-treated vessel pouch

Developing an Experimental Aneurysm Model in a Rabbit Using an Elastase-Treated Vessel Pouch

After tightening the 6-0 ligature, use a temporary vessel clip to clamp the right common carotid artery as far distally as possible to avoid endothelial damage to create a long vessel segment for irrigation to prevent thrombogenesis. To harvest the pouch, cut the distal vessel to the 4-0 non-absorbable ligature.Then cut the vessel distal to the 6-0 non-absorbable ligature. Meticulously clean the arterial pouch of all soft tissue and use a vessel clip to measure the length, width, and depth of the pouch. If a pouch degradation is needed, pre-incubate the cleaned pouch with 100 units of porcine elastase dissolved in 5 milliliters of Tris buffer at room temperature for 20 minutes.For further preparation of the common carotid artery, place two micro swabs directly beneath the left common carotid artery to allow the vessel to be moved superficially. And place an additional micro swab with a blue padding under the left artery at the distal third for better visualization of the artery. Change sides to access the left side of the animal, and use microscissors and forceps to make a 2-millimeter fishmouth incision on the proximal side of the right common carotid artery.Use a second temporary vessel clip to clamp the left distal common carotid artery, and clamp the proximal left common carotid artery with two additional temporary vessel clips. When all of the clamps have been placed, liberate the distal third of the left common carotid artery completely from the soft tissue and perform an arteriotomy.Now flush the recipient vessel with heparinized saline and liberate the complex from adventitia. Then suture the right common carotid artery to the left common carotid artery. Transfer the arterial pouch from the heparinized saline solution into the surgical field where the bifurcation is planned.While keeping all of the aspects of the vessel complex hydrated with a continuous saline irrigation, suture the pouch to the vessel and then remove all of the temporary vascular clamps in stepwise manner. When all of the clamps have been removed, then close the operative situs according to standard protocols.

developing-an-experimental-aneurysm-model-rabbit-using-an-elastase

Universidad de Cartagena UDEC

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JoVE Encyclopedia of Experiments

Neuroscience

Neuropathology

Cerebrovascular Diseases

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All procedures involving animal models have been reviewed by the local institutional animal care committee and the JoVE veterinary review board.&#160;&#160;&#160;&#160;NOTE: House all animals at a room temperature of 22&#8210;24 Celsius (&#176;C) and maintain a 12-hour (h) light/dark cycle. Provide free access to water, pellet, and ad libitum hay diet every time. Statistical analyses were performed using the non-parametric Wilcoxon-Mann-Whitney-U test. A probability value (p) of &#8804; 0.05 was considered significant.1. Presurgical phase<ol><li>Perform a detailed preoperative clinical examination of all rabbits planned for surgery immediately next to a quiet, aseptic operating room, maintaining a temperature of 23 &#177; 3 &#176;C.<ol><li>Record the weight of each animal macroscopically and evaluate the mucous membranes, capillary refill time, and pulse quality.</li><li>Further on, perform cardiac auscultation with a stethoscope and abdominal palpation.</li><li>Based on the clinical findings, attribute an American Society of Anesthesiologists (ASA) classification to each rabbit19. Include only animals with an ASA I score in the study.</li><li>Shave both outer ears with an electric shaver and apply prilocaine-lidocaine cream on both auricular arteries and veins.</li></ol></li><li>Sedate the rabbit with a combination of 20 milligrams (mg)/kilogram (kg) of ketamine, 100 mg/kg of dexmedetomidine, and 0.3 mg/kg of methadone injected subcutaneously (SC) via a syringe.</li><li>Leave each animal undisturbed for at least 15 min.</li><li>After that, under supplementary oxygenation with 3 liters (l) /minute (min) through a loose face mask and steady monitoring through a pulse oximeter, place a 22 G cannula in the left auricular central artery and another 22 G cannula in the auricular vein of the contralateral ear.</li><li>Shave the surgical field (neck) and inject 0.75% peri-incisional ropivacaine intradermally. Next, shave the forehead and prepare to place pediatric electroencephalographic (EEG) sensors.</li><li>Induce general anesthesia with propofol 1-2 mg/kg intravenously (IV) to effect. Then, immediately intubate the trachea of all rabbits with a silicone tube (3 millimeters (mm) internal diameter) under capnographic control. Afterward, transport all rabbits to the operating room, place them in dorsal recumbency, and connect the tube to a pediatric circle system.</li><li>Achieve anesthesia deepening and maintenance through isoflurane in oxygen, targeting a maximal end-tidal isoflurane concentration of 1.3%.</li><li>Ensure clinical and instrumental monitoring (pulse oximetry, doppler, and invasive blood pressure, 3-lead electrocardiogram, EEG, rectal temperature monitoring, and inhaled and exhaled gases) until tracheal extubation.</li><li>To maintain hydration, Ringer&#8217;s lactate is provided at a continuous rate infusion (CRI) of 5 ml/kg/h through venous access. Always confirm proper anesthesia using toe pinches at an interval of 10 min.</li><li>Disinfect the surgical field using povidone-iodine from the manubrium sterni to both jaw angles. Now, perform sterile draping of the surgical field.</li><li>During surgery, provide analgesia with lidocaine at a CRI of 50 microgram (&#181;g)/kg/min and fentanyl at 3&#8210;10 &#181;g/kg/h. Apply spontaneous or assisted ventilation as well as permissive hypercapnia. Perform arterial blood gas analysis at least one time during surgery.</li><li>Treat relevant hypotension (mean arterial pressure &lt; 60 mmHg) with noradrenaline. Prevent hypothermia (rectal temperature &#8804; 38 &#176;C) using a heating pad or a heating forced-air warming system.</li></ol>2. Surgical phase &#8211; Step I<ol><li>Start the surgery with a median skin incision from the manubrium sterni to the level of the jaw angles/larynx. Sharply dissect the skin and soft tissue with a scalpel, surgical scissors, and forceps. Separate the subcutis and the fat pad medially by blunt dissection.</li><li>Enter the anterior upper ridge of the sternocleidomastoid muscle medially on the left side by blunt dissection using micro forceps and surgical scissors.</li><li>Macroscopically, perform blunt preparation and carefully separate the left CCA from the vagal nerve distally to avoid laryngeal paresis by further using micro forceps and surgical scissors (Figure 1). Note that the bifurcation of the left CCA serves as an intraoperative landmark (Figure 2 and&#160;Figure 3A). For all the following steps, use a soft tissue spreader to improve surgical visualization.</li><li>After successful preparation and liberation of the left distal CCA from the vagal nerve, administer papaverine (40 mg/ml, 1:1 diluted in 0.9% isotonic sodium chloride solution) locally. Continuously protect all vessel segments with micro swabs followed by further papaverine administration externally. Place the papaverine-soaked left CCA below the autologous muscle tissue to protect the vessel from drying under the light of the operation microscope.</li><li>Switch sides while maximizing the surgeon&#8217;s comfort during the operative procedure. Repeat the same surgical procedure on the right side. Dissect the CCA distally and proximally up to the predefined landmarks (carotid bifurcation at the level of the jaw angles/larynx and internal jugular vein;&#160;Figure 3A,B). Reinsert a spreader and administer micro swabs and papaverine as described previously.</li><li>Before the ligation of the right proximal CCA, inject heparin (500 international units (IU)/kg) systemically via a venous ear catheter.</li><li>Use a surgical microscope from now on. First, ligate the right proximal CCA with a 4-0 non-absorbable suture directly at the end of the macroscopically visible proximal landmark to avoid any tension on the arterial vessel.<ol><li>Secondly, apply a 6-0 non-absorbable ligature exactly 4&#8210;5 mm distally by using a vessel clip for measurement, considering that after cutting distally from the first 4-0 ligature, the resulting arterial pouch will be of standardized length of about 3&#8210;4 mm in every animal (Figure 4A,C).</li></ol></li><li>After tightening the 6-0 ligature, clamp the right CCA as far distally as possible with a temporary vessel clip (as normally used in cerebral aneurysm surgery) to avoid any endothelial damage and to create a long vessel segment for irrigation in order to prevent thrombogenesis (Figure 4B).</li><li>Now perform a cut distally to the 4-0 non-absorbable ligature. To harvest the arterial pouch (Figure 4C), perform a second cut distally to the 6-0 non-absorbable ligature.</li><li>Clean the arterial pouch meticulously from all soft tissue and measure its length, width, and depth (Figure 4C) with a vessel clip. If no further modification is needed, keep the autologous arterial graft in a heparinized solution (500 IU/100 ml in 0.9% isotonic sodium chloride) at room temperature until further use.</li></ol>3. Arterial pouch degradation<ol><li>If an arterial pouch degradation is needed, clean it meticulously of soft tissue and preincubate it with 100 IU of porcine elastase dissolved in 5 ml of Tris-buffer at room temperature on the day of experiment for 20 min. Do not use a brush technique. Incubate the arterial pouch intra- and extra-luminally by using a shaker.</li><li>Before putting the pouch in a heparinized solution of 0.9% isotonic sodium chloride, gently swipe it three times for 3 min with anatomical forceps in 0.9% isotonic sodium chloride solution to wash out the remaining porcine elastase.</li><li>If needed, keep the lumen of the arterial pouch opened up with a microtube made of silicone; meticulously protect the left and right CCA during the whole surgical procedure with wet micro paddings.</li></ol>4. Surgical phase &#8211; Step II<ol><li>For further preparation of the CCA, place two round micro swabs directly beneath it to move the artery more superficially. Now, put one micro swab with purple padding under the left CCA at the distal third for better visualization of the artery.</li><li>Flush the right proximal CCA with a solution of 0.9% isotonic sodium chloride combined with 500 IU of heparin dissolved in 100 ml of 0.9% isotonic sodium chloride. In order to create a tension-free anastomosis, place the right CCA under the fat pad/peritracheal musculature by using surgical scissors to tunnel it to the left side. Remove the soft tissue of the artery.<ol><li>Now perform a 2 mm fish mouth incision on the proximal side of the right CCA using a micro scissor and forceps.</li></ol></li><li>Change the side on the operating table. Clip the left distal CCA with another temporary vessel clip followed by the proximal left CCA with two temporary vessel clips. Protect all exposed vessel segments from drying out under the surgical light using wet micro swabs.</li><li>Liberate the distal third of the left CCA completely from soft tissue and perform an arteriotomy. Use surgical microforceps and gently grab some soft tissue. Now elevate the artery and incise the left distal CCA slowly with a surgical microscissor. Flush the vessel segments with heparin (500 IU dissolved in 100 ml of 0.9% isotonic sodium chloride solution).</li><li>After performing the arteriotomy with curved micro forceps and micro scissors, enlarge the arteriotomy located at the distal third of the left CCA distally, measuring about 2-fold of the diameter of the right blunt of the carotid artery and the autologous graft. This allows sufficient blood flow into the arterial pouch.</li><li>Take the arterial pouch out of the heparinized saline solution. Place the pouch in the surgical field, where the bifurcation is planned. Start suturing the rear of the right carotid blunt caudally-located with a non-absorbable 9-0 suture, followed by a suture on the cranially-located rear side at the level of the fish mouth incision. Finish sewing the rear from distal to proximal by single stitches.</li><li>While suturing, keep all elastase preincubated pouches moist with continuous irrigation. While suturing the vessel wall of the pouch, use curved surgical micro forceps to gently open up the lumen with its tip. Whenever suturing parts of the left or proximal right CCA, use straight surgical micro forceps. Afterwards, suture the horizontal back side.</li><li>Next suture the horizontal front side, starting at the dome of the aneurysm moving to its base. Afterwards, start with single stitches distally on the front side moving caudally.<ol style='list-style-type:decimal;'><li>For all steps 4.5&#8210;4.8 while suturing the anastomosis pay attention just to grab the part of the vessel close to the arteriotomy to avoid iatrogenic stenosis. Also, continuously moisten all vessel segments during the whole surgical procedure extraluminally with a syringe filled with heparinized sodium chloride solution (500 IU dissolved in 100 ml of 0.9% isotonic sodium chloride) and protect them with wet micro swabs.</li><li>Before finishing the anastomosis, irrigate the whole complex with a heparinized 0.9% isotonic sodium chloride solution intraluminal (500 IU dissolved in 100 ml of 0.9% isotonic sodium chloride). Beware that elastase-modified arterial pouches have to be sewn on as quickly as possible because of their strong tendency to dry out and to thrombose. Because of the aggressive behavior of the residual elastase concentration in the pouch regarding digesting circumferential vessels, proceed fast with the surgery to re-perfuse the vessel complex quickly.</li></ol></li><li>Remove all temporary vascular clamps stepwise.<ol style='list-style-type:decimal;'><li>Remove the distal clamp from the left CCA. Accept minor bleeding and staunch it by gently imprinting micro swabs on the anastomosis. Afterwards, remove the clamp of the right CCA, press gently with micro swab and forceps to avoid thrombus formation.</li><li>If needed, replace the temporary vascular clips to provide enough coagulation. Afterward, relieve both vessel clips from the left side proximally. If needed in any step, replace clips to allow coagulation or to perform re-stitching.</li></ol></li><li>At this stage perform fluorescence angiography of the vessel complex (Figure 5) NOTE: Fluorescence angiography is performed by administering 1 ml of fluorescein IV, using 2 bandpass filters, a smartphone with video camera, and a bicycle spotlight. This procedure has been already described elsewhere20,21,22.</li><li>Lastly, close the operative situs. Readapt and gently suture the fat pad with a 3-0 resorbable suture with single nodes to protect the anastomosis. Close subcutis and skin in the same fashion.</li></ol>5. Postsurgical phase<ol><li>Discontinue the isoflurane and systemic analgesia administration at the end of the surgery and provide tracheal extubation as soon as the swallowing reflex has returned.</li><li>Administer 0.5 mg/kg of meloxicam IV, 10 mg/kg aspirin (ASS) IV, 100 &#181;g of vitamin B12 SC and 20 mg/kg of clamoxyl IV.</li><li>Provide supplementary oxygenation and active warming until the rabbits have spontaneously regained sternal recumbency.</li><li>Perform postoperative follow-up and animal care four times a day for the first three days in accordance with the guidelines for the assessment and management of pain in rodents and rabbits23,24.</li><li>Administer post-operative analgesia via a fentanyl patch (12 &#181;g/h) applied on the outer ear, meloxicam once a day SC for three days, and methadone as rescue therapy SC, according to the score sheet for pain evaluation. Administer 250 IU/kg low-molecular heparin (LMH) subcutaneously for three days in all rabbits.</li></ol>

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<a href='https://appjove.unicartagenaproxy.elogim.com/v/61157/arterial-pouch-microsurgical-bifurcation-aneurysm-model-in-the-rabbit'>Source: Wanderer, S., et al. Arterial Pouch Microsurgical Bifurcation Aneurysm Model in the Rabbit. J. Vis. Exp. (2020)</a>This video demonstrates the creation of an experimental aneurysm model in a rabbit using an elastase-treated vessel pouch. After excising a segment of the right CCA, the pouch is treated with elastase, then sutured to the left CCA to restore blood flow. The resulting stress on the weakened pouch walls induces aneurysm formation.

<img src='https://cloudfront.jove.com/files/ftp_upload/23290/23290_figure_1_editor_23290.jpg' alt='23290_figure_1.jpg' />Figure 1: Initial operative step.Initial operative step, depicting the left carotid artery (white arrow), vagal nerve (black arrow) (A) and the careful separation of the left carotid artery from the vagal nerve distally to avoid laryngeal paresis.<i...

Source: Wanderer, S., et al. Arterial Pouch Microsurgical Bifurcation Aneurysm Model in the Rabbit. J. Vis. Exp. (2020)This video demonstrates the ...

Begin with an anesthetized rabbit with surgically exposed carotid arteries or CCAs supported by a blue pad for clear visualization.Tie off the right CCA with sutures and clamp it distally to restrict blood flow.Cut the section of the right CCA containing the tight knot to create a vessel pouch and clean it in heparinized saline to remove soft tissue.Treat the pouch with a buffer containing elastase to degrade elastin fibers, weakening the vessel.Support the left CCA and clip it to restrict blood flow.Remove the attached soft tissues and pierce the left CCA to release trapped blood.&#160;Inject saline containing heparin to prevent blood clotting.&#160;Suture the cut right CCA to the left CCA. Later, ligate the elastase-treated pouch.Now, remove all clamps to restore blood flow and suture the incision.Blood flow in the artificial carotid bifurcation induces stress on the weakened vessel pouch walls, causing it to bulge and form an aneurysm.&#160;

6 vues. Developing an Experimental Aneurysm Model in a Rabbit Using an Elastase-Treated Vessel Pouch

Vidéo: Developing an Experimental Aneurysm Model in a Rabbit Using an Elastase-Treated Vessel Pouch - Expérience

Porcine Model of Infrarenal Abdominal Aortic Aneurysm

Large animal models to study abdominal aortic aneurysms are sparse. The purpose of this model is to create reproducible, clinically significant infrarenal abdominal aortic aneurysms (AAA) in swine. To achieve this, we use a combination of balloon angioplasty, elastase and collagenase, and a lysyl oxidase inhibitor, called &#946;-aminopropionitrile (BAPN), to create clinically significant infrarenal aortic aneurysms, analogous to human disease.
Noncastrated male swine are fed BAPN for 7 days prior to surgery to achieve a steady state in the blood. A midline laparotomy is performed and the infrarenal aorta is circumferentially dissected. An initial measurement is recorded prior to aneurysm induction with a combination of balloon angioplasty, elastase (500 units)/collagenase (8000 units) perfusion, and topical elastase application. Swine are fed BAPN daily until terminal procedure on either postoperative day 7, 14, or 28, at which time the aneurysm is measured, and tissue procured. BAPN + surgery pigs are compared to pigs that underwent surgery alone.
Swine treated with BAPN and surgery had a mean aortic dilation of 89.9% &#177; 47.4% at day 7, 105.4% &#177; 58.1% at day 14, and 113.5% &#177; 30.2% at day 28. Pigs treated with surgery alone had significantly smaller aneurysms compared to BAPN + surgery animals at day 28 (p &#60; 0.0003). The BAPN + surgery group had macroscopic and immunohistochemical evidence of end stage aneurysmal disease.
Clinically significant infrarenal AAA can be induced using balloon angioplasty, elastase/collagenase perfusion and topical application, supplemented with oral BAPN. This model creates large, clinically significant AAA with hallmarks of human disease. This has important implications for the elucidation of AAA pathogenesis and testing of novel therapies and devices for the treatment of AAA. Limitations of the model include variation in BAPN ingested by swine, quality of elastase perfusion, and cost of BAPN.&#160;

This novel model creates robust infrarenal abdominal aortic aneurysms in swine using a combination of balloon angioplasty, elastase/collagenase perfusion, topical elastase application, and oral compound &#946;-aminopropionitrile administration, which interferes with collagen cross-linking.

Modèle porcin de l'anévrisme aortique abdominal infrarenal

Large animal models to study abdominal aortic aneurysms are sparse. The purpose of this model is to create reproducible, clinically significant infrarenal ...

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JoVE Journal

Médecine

Microsurgical Creation of Giant Bifurcation Aneurysms in Rabbits for the Evaluation of Endovascular Devices

Giant aneurysms are dangerous lesions requiring endovascular treatment, with high rates of aneurysm recanalization and re-rupture. Reliable in vivo models are rare but are required for testing new endovascular devices.&#160;We demonstrate the technical aspects of the creation of giant bifurcation aneurysms in New Zealand white rabbits (2.5-5.5 kg). A 25-30 mm long venous pouch is taken from the external jugular vein, and a bifurcation between both carotid arteries is created microsurgically. The pouch is sutured in the bifurcation to mimic a giant aneurysm. This protocol summarizes our previously published standard technique for venous pouch true arterial bifurcation aneurysms and highlights its essential modification steps for giant aneurysms. Using this modified technique, we were able to create an animal model for giant aneurysms with high comparability to humans regarding the hemodynamics and coagulation systems. Furthermore, low morbidity and high aneurysm patency rates were achieved. The proposed giant aneurysm model offers an excellent possibility for testing new endovascular devices.

Here, we describe the technique for the microsurgical creation of giant bifurcation aneurysms in rabbits for the evaluation of endovascular devices.

Création microchirurgicale d’anévrismes de bifurcation géants chez le lapin pour l’évaluation de dispositifs endovasculaires

Giant aneurysms are dangerous lesions requiring endovascular treatment, with high rates of aneurysm recanalization and re-rupture. Reliable in vivo models ...

Neurosciences

Mouse Abdominal Aortic Aneurysm Model Induced by Perivascular Application of Elastase

Abdominal aortic aneurysm (AAA), although primarily asymptomatic, is potentially life-threatening as the rupture of AAA usually has a devastating outcome. Currently, there are several distinct experimental models of AAA, each emphasizing a different aspect in the pathogenesis of AAA. The elastase-induced AAA model is the second most used rodent AAA model. This model involves direct infusion or application of porcine pancreatic elastase (PPE) to the infrarenal segment of the aorta. Due to technical challenges, most elastase-induced AAA model nowadays is performed with the external application rather than an intraluminal infusion of PPE. The infiltration of elastase will cause degradation of elastic lamellae in the medial layers, resulting in the loss of aortic wall integrity and subsequent dilation of the abdominal aorta. However, one disadvantage of the elastase-induced AAA model is the inevitable variation of how the surgery is performed. Specifically, the surgical technique of isolating the infrarenal segment of the aorta, the material used for aorta wrapping and PPE incubation, the enzymatic activity of PPE, and the time duration of PPE application can all be important determinants that affect the eventual AAA formation rate and aneurysm diameter. Notably, the difference in these factors from different studies on AAA can lead to reproducibility issues. This article describes a detailed surgical process of the elastase-induced AAA model through direct application of PPE to the adventitia of the infrarenal abdominal aorta in the mouse. Following this procedure, a stable AAA formation rate of around 80% in male and female mice is achievable. The consistency and reproducibility of AAA studies using an elastase-induced AAA model can be significantly enhanced by establishing a standard surgical procedure.

The present protocol describes a standardized surgical method for the elastase-induced AAA model through the direct application of elastase to the adventitia of infrarenal abdominal aorta in mice.

Modèle d’anévrisme de l’aorte abdominale de souris induit par l’application périvasculaire d’élastase

Abdominal aortic aneurysm (AAA), although primarily asymptomatic, is potentially life-threatening as the rupture of AAA usually has a devastating outcome. ...

Developing an Experimental Aneurysm Model in a Rabbit Using an Elastase-Treated Vessel Pouch

Transcription

Developing an Experimental Aneurysm Model in a Rabbit Using an Elastase-Treated Vessel Pouch