This work is funded by the National Natural Science Foundation of China (NSFC 81822002). We thank all the members who took part in this work.

The current protocol is approved by the ethics committee of Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China. This procedure is performed on male adult C57/BL6 mice (&#62;10 weeks of age). All surgical instruments were sterilized by autoclaving before the operation.
1. Preparation of surgical instrument
<ol>
	<li>Prepare a 5 mL syringe and pinch off the tip of the needle with a needle holder to blunt it.&#160;</li>
	<li>Prepare a 27 G needle and blunt it with a needle holder. Cutting the tip of the needle with ophthalmic scissors is an alternative way to blunt the needle.</li>
	<li>Bend the tip of the 27 G needle 90&#176;. 
	NOTE: This needle will be used as a spacer to tie with the aorta for vessel constriction.</li>
	<li>Use a commercially obtained iron wire (medical grade, 0.5 mm in diameter, see Table of Materials) and twine around the needle (Figure 1A). Form a small snare or loop at the blunted tip of the needle (Figure 1B). 
	NOTE: This reusable instrument acts as a special self-made retractor and allows one to pass silk suture under the aorta in the latter steps.</li>
	<li>Autoclave&#160;all the surgical tools before surgery (including the special retractor made above) to sterilize them.&#160;</li>
</ol>
2. Animal preparation
<ol>
	<li>Anesthetize the mouse via intraperitoneal injection of pentobarbital sodium solution (50 mg/kg, see Table of Materials) according to the body weight.&#160;Subcutaneously inject 100 &#956;L of 0.5% lidocaine locally into the surgical area.</li>
	<li>Confirm that the mouse is fully anesthetized by pinching the mouse&#39;s toe&#160;with the tip of the forceps.</li>
	<li>Apply ophthalmic ointment to both the eyes to prevent dryness while under anesthesia.&#160;</li>
	<li>Remove the hair from the throat and upper chest with depilatory cream or a clipper.</li>
	<li>Disinfect the unhaired area with three alternating scrubs of iodine and 70% ethanol in concentric circles moving outward.</li>
	<li>Place the mouse in the supine position on a heating pad covered with a sterile drape with its head pointing to the operator. Fix the extremities with adhesive tape and incisors with a 4-0 suture (Figure 2A).</li>
	<li>Insert a rectal probe (see Table of Materials) to monitor body temperature during the operation. Maintain the body temperature at 37 &#176;C during the whole operation.</li>
	<li>Put on a pair of sterile gloves. 
	NOTE: Once the sterile gloves are put on, do not touch other unsterilized areas or objects.</li>
	<li>Cut a hole (1-1.5 cm in diameter) in a new disposable sterile drape with sterilized ophthalmic scissors. Place the sterile drape over the mouse and ensure the unhaired operating field is visible through the hole. 
	&#8203;NOTE: This step allows the operator to avoid touching other unsterilized areas, which helps maintain sterile conditions during surgery.</li>
</ol>
3. Constriction of transverse aorta
<ol>
	<li>Make a 1.5 cm vertical skin incision at the level of the suprasternal notch (Figure 2B) with scalpel blade. Expand the skin incision down to the level of the sternal angle. 
	NOTE: The suprasternal notch is a notch located on the upper edge of the manubrium sterni. It is a surface symbol that can be detected when mouse hair is removed (Figure 2B). The sternal angle is the joint between manubrium sterni and corpora sterni. When the sternum is exposed, it presents as a horizontal white line on the sternum at the same level of costa secunda (Figure 2C).</li>
	<li>Carefully separate the skin and superficial fascia and expose the trachea and proximal sternal. Carefully make a 3-4 mm longitudinal midline incision to the sternum starting from the upper edge to the sternal angle (Figure 2D). 
	NOTE: The cut must not exceed the sternal angle, for there is a risk of causing acute pneumothorax in the mouse.</li>
	<li>Gently lift the sternum with forceps and the thymus and arcus aortae beneath it. Carefully use straight forceps and bluntly dissect the target vessel and tissues around it.</li>
	<li>Hold the previously self-made retractor (step 1.4) that contained a wire snare on the end of the user&#39;s right hand.</li>
	<li>Carefully pass the snare of the self-made retractor under the aorta between the left common carotid artery and the origin of the right innominate artery (Figure 2E).</li>
	<li>Pass the self-made retractor to the left hand to spare the right hand for other instruments.</li>
	<li>With microscopic tweezers in the right hand, pass a 7-0 silk suture through the loop of the snare at the end and pull out the retractor. This will allow to leave the silk suture around the artery for further ligation (Figure 2F). 
	NOTE: Be gentle and do not drag the aortic arch too much from its original position.</li>
	<li>Place a 27 G needle parallel to the aorta and tie the suture around the needle and the aorta (Figure 2G,H). 
	NOTE: The sham procedure should be the same, except that there is no aorta ligation.</li>
	<li>Hold on to the 27 G needle with ophthalmic forceps and another forceps holding the knot tied to the 27 G needle and aorta. Quickly but gently pull out the 27 G needle from the ligation (Figure 2H). 
	&#8203;NOTE: The knot must not be too tight, or it won&#39;t be easy to pull out the needle. Be careful when pulling out the needle in case of rupturing the aorta.</li>
	<li>Suture the skin with 4-0 synthetic monofilament&#160;suture in an interrupted suture pattern (Figure 2I).&#160;</li>
</ol>
4. Postoperative care
<ol>
	<li>Place the mouse on a warm pad (see Table of Materials) and wait for it to revive. Generally, the mouse revives in about 60 min. 
	NOTE: The animal must not be left unattended until it regains sufficient consciousness to the main sternal recumbency.</li>
	<li>Subcutaneously inject 0.5 mL of warm saline and monitor the animals&#39; fluid homeostasis. 
	NOTE: This step prevents animals from dehydration and hypovolemic circulation status.</li>
	<li>Apply erythromycin ointment to the wound surface every day for 3 days.</li>
	<li>For post-surgical pain treatment, administer 1 mg/L of buprenorphine local anesthetic&#160;parenterally to the incision site&#160;(see Table of Materials).</li>
	<li>Postoperatively, monitor the mouse for signs of infection and impairment (malnourishment, hunched posture, and ruffled fur). 
	&#8203;NOTE: Animals that underwent surgery are not returned to the company of other animals until fully recovered.</li>
</ol>
5. Ultrasound imaging
<ol>
	<li>Confirm successful ligation of the transverse aorta by calculating blood flow velocity via an ultra-sound imaging system12,13 (24 MHz, see Table of Materials) 28 days after surgery.
	<ol>
		<li>Anesthetize the animal with 4.5% isoflurane in 20% oxygen-enriched air and maintain with 0.5% isoflurane in 20% oxygen-enriched air.</li>
		<li>Place the mouse in a supine position and fix its extremities to the electrode with adhesive tape.</li>
		<li>Using depilatory cream, remove the chest hair and apply an ultrasonic coupling agent to the chest.</li>
		<li>Tilt the platform to the left as far as possible. While keeping the probe in the vertical position, gradually lower it along the right parasternal line on the chest with the notch pointing to the animal&#39;s chin.</li>
		<li>Under the B mode of the instrument, adjust the X and Y-axis until the aortic arch and constriction site are clearly visible.</li>
		<li>Click on the Pulse Wave Doppler button to switch to pulse wave mode.</li>
		<li>Adjust the dashed cursor sample volume box distal to the constricted site and find the stenotic jet with the highest velocity.</li>
		<li>Click on the Pulse Wave Doppler button again to get the waveform of aortic flow and measure the peak velocity. Calculate the blood flow velocity according to the peak of the wave patterns (Figure 3A,B).</li>
		<li>Set the imager to B mode. Rest the platform in the horizontal position. Rotate the probe 30&#176; to the left parasternal line.</li>
		<li>Adjust X and Y-axis to obtain a short axis view. Press M mode to show the indicator line and click on Cine Store to save the image for later measurement of cardiac wall thickness, chamber dimension, and ejection fraction. 
		NOTE: The formula for calculating ejection fraction: 100% * ((LV Vol;d - LV Vol;s) / LV Vol;d). The formula for calculating cardiac output: Stroke Volume * Heart rate (at the first frame drawn) / 1000. Most indexes such as ejection fraction and cardiac output can be measured automatically via the ultrasonic imaging system&#39;s software. LV Vol;d: diastolic volume of the left ventricle. LV Vol;s: systolic volume of the left ventricle.</li>
	</ol>
	</li>
</ol>

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The authors declared that there are no conflicts of interest.

The induction of sustained pressure overload can gradually cause cardiac hypertrophy and heart failure. This model has been used in numerous laboratories around the world14,15,16. The protocol provided an improved TAC method that does not need microsurgical skills or mechanical ventilation.
The most important step in this protocol is passing silk suture under the aortic arch. When the snare has hooked...

Heart failure is a complex clinical symptom that results from impaired structure and function of ventricular filling or ejecting blood1. The disease stage is mainly defined via the New York Heart Association function classification based on the severity of symptoms and physical activity2. For those patients with an ejection fraction of over 50%, structural and/or functional abnormalities raised natriuretic peptides to support the diagnosis of heart failure with preserved ejection fraction (HFpEF)2. Ischemic heart disease is a leading cause among multiple etiologies of heart failure. Thus, the myocardial infarction model (such as permanent coronary ligation) is often used to study pathophysiology after cardiac hypoperfusion or ischemia-reperfusion injury3,4. Besides acute myocardial injury, other risk factors such as hypertension, diabetes, obesity, and a family history of cardiomyopathy also contribute to the development of heart failure. After patients pass Stage A (at risk for heart failure) and enter Stage B (pre-heart failure), structural modification occurs1. For example, hypertensive patients first go through adaptive left ventricle hypertrophy, and then gradually develop into maladaptive cardiac hypertrophy and transit to heart failure through pathological remodeling5.
As the terminal stage of various cardiovascular diseases, chronic heart failure has been studied for decades6. Multiple mouse models have been widely used in heart failure research, including drug infusion (angiotensin II), metabolic disorders (diabetes or high caloric diet), and aortic constriction7. Among these models, angiotensin II perfusion is accompanied by various organ side effects, such as kidney7. Inducing metabolic disorders usually require a rather long period of time. Ascending aortic constriction has been considered to have limited relevance to human disease7.
TAC is a reliable model that increases afterload and induces cardiac hypertrophy as well as heart failure8. Open-chest TAC model was first described by Rockman et al. and was used in numerous laboratories around the world9. However, this classical TAC procedure causes a rather large trauma to mice and changes their normal behavior, which may take a long recovery time and disturb further treatment10. Other modified closed-chest TAC procedures did reduce some invasive steps but required microsurgical skills or mechanical ventilation10,11.
The present protocol details a step-by-step method with a minimally invasive approach to the aortic arch using a self-made retractor via a 3 mm midline incision of the upper edge of the sternum. This model does not need microsurgical skill, mechanical ventilation, or cutting through the ribs, thereby providing a rapid, surgical trauma-limited, uncomplicated, inexpensive way to perform TAC surgery.

<table><tbody><tr><td>4-0 nonabsorbable suture</td><td>Jinhuan</td><td>HM403</td><td>Used for suturing the skin</td></tr><tr><td>5 mL syringe</td><td>Haifuda Technology Co., Ltd.</td><td>BD-309628</td><td>Used for making snare containing retractor</td></tr><tr><td>7-0 nonabsorbable suture</td><td>Jinhuan</td><td>HM701</td><td>Used for aorta ligation</td></tr><tr><td>Animal temperature monitor</td><td>Kaerwen</td><td>FT3400</td><td>Used for monitoring body temperature</td></tr><tr><td>Buprenorphine&amp;nbsp;</td><td>Sigma</td><td>B-044</td><td>Used for post-surgical pain treatment</td></tr><tr><td>Depilatory cream&amp;nbsp;</td><td>Veet</td><td>N/A</td><td>Used for remove body hair from the surgical area</td></tr><tr><td>Heating Pad</td><td>Xiaochuangxin</td><td>N/A</td><td>Used for maintaining body temperature</td></tr><tr><td>Ibuprofen</td><td>MCE</td><td>HY-78131</td><td>Used for post-surgical pain treatment</td></tr><tr><td>Iron wire (0.5 mm)</td><td>Qing Yuan</td><td>Iron wire #26</td><td>Used for making snare containing retractor</td></tr><tr><td>Microscopic tweezers</td><td>RWD</td><td>F12006-10</td><td>Used for penetrating and separating the tissue to open operation space</td></tr><tr><td>Needle holder</td><td>RWD</td><td>F12005-10</td><td>Used for pinching off the tip of gauge needle and blunting it</td></tr><tr><td>Ophthalmic forceps</td><td>RWD</td><td>F14012-10&amp;nbsp;</td><td>Used for holding skin and other tissues</td></tr><tr><td>Ophthalmic scissors</td><td>RWD</td><td>S11001-08</td><td>Used for making sking incision of mouse</td></tr><tr><td>Pentobarbital sodium</td><td>Sigma</td><td>P3761</td><td>Used for mouse anesthesia</td></tr><tr><td>Sterile operating mat</td><td>Hale &amp;amp; hearty</td><td>211002</td><td>Used for placing animal during surgery</td></tr><tr><td>Ultra-sound imaging system</td><td>Fujifilm visualsonics</td><td>vevo1100</td><td>Used for measure the blood flow velocity, left ventricular wall thickness and ejection fraction, https://www.visualsonics.com/product/imaging-systems/vevo-1100</td></tr></tbody></table>

a modified technique for transverse aortic constriction in mice

Transverse aortic constriction (TAC) is a frequently used surgery in research regarding heart failure and cardiac hypertrophy based on the formation of pressure overload in mouse models. The main challenge of this procedure is to clearly visualize the transverse aortic arch and precisely band the target vessel. Classical approaches perform a partial thoracotomy to expose the transverse aortic arch. However, it is an open-chest model that causes a rather large surgical trauma and requires a ventilator during the surgery. To prevent unnecessary trauma and simplify the operating procedure, the aortic arch is approached via the proximal proportion of the sternum, reaching and binding the target vessel using a small self-made retractor that contains a snare. This procedure can be conducted without entering the pleura cavity and does not need a ventilator or microsurgical operation, which leaves the mice with physiological breathing patterns, simplifies the procedure, and significantly reduces operation time. Due to the less invasive approach and less operation time, mice can undergo fewer stress reactions and recover rapidly.

After successful TAC surgery, pressure overload was detected using an ultrasound imaging system. Four weeks after surgery, mice develop decreased heart function. In the present study, the efficacy of TAC surgery was validated via ejection fraction (EF), fractional shortening (FS), left ventricular mass (LV mass) and left ventricular internal diameter (LVID) of mice who underwent TAC surgery after 4 weeks. EF was significantly reduced in TAC mice after 4 weeks compared to sham mice (47% &#177; 10% vs. 78% &#177; ...

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A Modified Technique for Transverse Aortic Constriction in Mice

The present protocol describes a modified and simplified technique with a minimally invasive transverse aortic constriction (TAC) procedure using a self-made retractor. This procedure can be conducted without a ventilator or microscope and introduces pressure overload, eventually leading to cardiac hypertrophy or heart failure.

Transverse aortic constriction (TAC) is a frequently used surgery in research regarding heart failure and cardiac hypertrophy based on the formation of ...

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4.3K Views.  Huazhong University of Science and Technology. Dit protocol biedt een snelle chirurgische traumabeperking, ongecompliceerde en goedkope massa's om TAC-chirurgie uit te voeren. Dit model benadert de aortaboog met behulp van een zelfgemaakt retractor en heeft geen microchirurgische schaal of mechanische beademing nodig, waardoor chirurgisch trauma aanzienlijk wordt beperkt. Bereid om te beginnen een spuit van vijf milliliter voor.Maak de naald vervolgens bot door de punt af te knijpen met een naaldhouder. Maak een naald van 27 gauge ...

Video: A Modified Technique for Transverse Aortic Constriction in Mice

Pyrosequencing: A Simple Method for Accurate Genotyping

Pharmacogenetic research benefits first-hand from the abundance of information provided by the completion of the Human Genome Project. With such a tremendous amount of data available comes an explosion of genotyping methods. Pyrosequencing(R) is one of the most thorough yet simple methods to date used to analyze polymorphisms. It also has the ability to identify tri-allelic, indels, short-repeat polymorphisms, along with determining allele percentages for methylation or pooled sample assessment. In addition, there is a standardized control sequence that provides internal quality control. This method has led to rapid and efficient single-nucleotide polymorphism evaluation including many clinically relevant polymorphisms. The technique and methodology of Pyrosequencing is explained.


Pyrosequencing(R) is one of the most thorough yet simple methods to date used to analyze polymorphisms. This method has led to rapid and efficient single-nucleotide polymorphism evaluation including many clinically relevant polymorphisms. The technique and methodology of Pyrosequencing is explained.

Pharmacogenetic research benefits first-hand from the abundance of information provided by the completion of the Human Genome Project. With such a ...

Transverse Aortic Constriction in Mice

Transverse aortic constriction (TAC) in the mouse is a commonly used experimental model for pressure overload-induced cardiac hypertrophy and heart failure.1 TAC initially leads to compensated hypertrophy of the heart, which often is associated with a temporary enhancement of cardiac contractility. Over time, however, the response to the chronic hemodynamic overload becomes maladaptive, resulting in cardiac dilatation and heart failure.2 The murine TAC model was first validated by Rockman et al.1, and has since been extensively used as a valuable tool to mimic human cardiovascular diseases and elucidate fundamental signaling processes involved in the cardiac hypertrophic response and heart failure development. When compared to other experimental models of heart failure, such as complete occlusion of the left anterior descending (LAD) coronary artery, TAC provides a more reproducible model of cardiac hypertrophy and a more gradual time course in the development of heart failure. Here, we describe a step-by-step procedure to perform surgical TAC in mice. To determine the level of pressure overload produced by the aortic ligation, a high frequency Doppler probe is used to measure the ratio between blood flow velocities in the right and left carotid arteries.3, 4 With surgical survival rates of 80-90%, transverse aortic banding is an effective technique of inducing left ventricular hypertrophy and heart failure in mice.

Transverse aortic constriction (TAC) in the mouse is a commonly used experimental model to study mechanisms underlying cardiac hypertrophy and heart failure development. Here, we describe procedures to constrict the aorta to create a reproducible degree of cardiac hypertrophy in mice.

Transverse aortic constriction (TAC) in the mouse is a commonly used experimental model for pressure overload-induced cardiac hypertrophy and heart ...

Assessment of Cardiac Morphological and Functional Changes in Mouse Model of Transverse Aortic Constriction by Echocardiographic Imaging

Transverse aortic constriction (TAC) in mice has been used as a valuable model to study mechanisms of cardiac hypertrophy and heart failure1. A reliable noninvasive method is essential to assess real-time cardiac morphological and functional changes in animal models of heart disease. Transthoracic echocardiography represents an important tool for noninvasive assessment of cardiac structure and function2. Here we used a high-resolution ultrasound imaging system to monitor myocardial remodeling and heart failure progression over time in a mouse model of TAC. B-mode, M-mode, and Doppler imaging were used to precisely assess cardiac hypertrophy, ventricular dilatation, and functional deterioration in mice following TAC. Color and pulse wave (PW) Doppler imaging was used to noninvasively measure pressure gradient across the aortic constriction created by TAC and to assess transmitral blood flow in mice. Thus transthoracic echocardiographic imaging provides comprehensive noninvasive measurements of cardiac dimensions and function in mouse models of heart disease.

The goal of this protocol is to noninvasively assess cardiac structural and functional changes in a mouse model of heart disease created by transverse aortic constriction, using B- and M-mode echocardiography and color/pulse wave Doppler imaging.

Transverse aortic constriction (TAC) in mice has been used as a valuable model to study mechanisms of cardiac hypertrophy and heart failure1. A reliable ...

Medicine

Minimally Invasive Transverse Aortic Constriction in Mice

Minimally invasive transverse aortic constriction (MTAC) is a more desirable method for the constriction of the transverse aorta in mice than standard open-chest transverse aortic constriction (TAC). Although transverse aortic constriction is a highly functional method for the induction of high pressure in the left ventricle, it is a more difficult and lengthy procedure due to its use of artificial ventilation with tracheal intubation. TAC is oftentimes also less survivable, as the newer method, MTAC, neither requires the cutting of the ribs and intercostal muscles nor tracheal intubation with a ventilation setup. In MTAC, as opposed to a thoracotomy to access to the chest cavity, the aortic arch is reached through a midline incision in the anterior neck. The thyroid is pulled back to reveal the sternal notch. The sternum is subsequently cut down to the second rib level, and the aortic arch is reached simply by separating the connective tissues and thymus. From there, a suture can be wrapped around the arch and tied with a spacer, and then the sternal cut and skin can be closed. MTAC is a much faster and less invasive way to induce left ventricular hypertension and enables the possibility for high-throughput studies. The success of the constriction can be verified using high-frequency trans-thoracic echocardiography, particularly color Doppler and pulsed-wave Doppler, to determine the flow velocities of the aortic arch and left and right carotid arteries, the dimension of the blood vessels, and the left ventricular function and morphology. A successful constriction will also trigger significant histopathological changes, such as cardiac muscle cell hypertrophy with interstitial and perivascular fibrosis. Here, the procedure of MTAC is described, demonstrating how the resulting flow changes in the carotid arteries can be examined with echocardiography, gross morphology, and histopathological changes in the heart.

Minimally invasive transverse aortic constriction (MTAC) conserves the essentials of regular transverse aortic constriction (TAC) while eliminating the use of a ventilator with tracheal intubation. It proves to be a highly desirable method for high-throughput studies on left ventricular overload, particularly in translational studies.

Minimally invasive transverse aortic constriction (MTAC) is a more desirable method for the constriction of the transverse aorta in mice than standard ...

Technique of Minimally Invasive Transverse Aortic Constriction in Mice for Induction of Left Ventricular Hypertrophy

Transverse aortic constriction (TAC) in mice is one of the most commonly used surgical techniques for experimental investigation of pressure overload-induced left ventricular hypertrophy (LVH) and its progression to heart failure. In the majority of the reported investigations, this procedure is performed with intubation and ventilation of the animal which renders it demanding and time-consuming and adds to the surgical burden to the animal. The aim of this protocol is to describe a simplified technique of minimally invasive TAC without intubation and ventilation of mice. Critical steps of the technique are emphasized in order to achieve low mortality and high efficiency in inducing LVH.
Male C57BL/6 mice (10-week-old, 25-30 g, n=60) were anesthetized with a single intraperitoneal injection of a mixture of ketamine and xylazine. In a spontaneously breathing animal following a 3-4 mm upper partial sternotomy, a segment of 6/0 silk suture threaded through the eye of a ligation aid was passed under the aortic arch and tied over a blunted 27-gauge needle. Sham-operated animals underwent the same surgical preparation but without aortic constriction. The efficacy of the procedure in inducing LVH is attested by a significant increase in the heart/body weight ratio. This ratio is obtained at days 3, 7, 14 and 28 after surgery (n = 6 - 10 in each group and each time point). Using our technique, LVH is observed in TAC compared to sham animals from day 7 through day 28. Operative and late (over 28 days) mortalities are both very low at 1.7%.
In conclusion, our cost-effective technique of minimally invasive TAC in mice carries very low operative and post-operative mortalities and is highly efficient in inducing LVH. It simplifies the operative procedure and reduces the strain put on the animal. It can be easily performed by following the critical steps described in this protocol.

The aim of this protocol is to describe step-by-step the technique of minimally invasive transverse aortic constriction (TAC) in mice. By elimination of intubation and ventilation which are mandatory for the commonly used standard procedure, minimally invasive TAC simplifies the operative procedure and reduces the strain put on the animal.

Transverse aortic constriction (TAC) in mice is one of the most commonly used surgical techniques for experimental investigation of pressure ...

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

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 2nd 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.

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.

Research on cardiac hypertrophy and heart failure is frequently based on pressure overload mouse models induced by TAC. The standard procedure is to ...

Studying Left Ventricular Reverse Remodeling by Aortic Debanding in Rodents

To better understand the left ventricular (LV) reverse remodeling (RR), we describe a rodent model wherein, after aortic banding-induced LV remodeling, mice undergo RR upon removal of the aortic constriction. In this paper, we describe a step-by-step procedure to perform a minimally invasive surgical aortic debanding in mice. Echocardiography was subsequently used to assess the degree of cardiac hypertrophy and dysfunction during LV remodeling and RR and to determine the best timing for aortic debanding. At the end of the protocol, terminal hemodynamic evaluation of the cardiac function was conducted, and samples were collected for histological studies. We showed that debanding is associated with surgical survival rates of 70-80%. Moreover, two weeks after debanding, the significant reduction of ventricular afterload triggers the regression of ventricular hypertrophy (~20%) and fibrosis (~26%), recovery of diastolic dysfunction as assessed by the normalization of left ventricular filling and end-diastolic pressures (E/e&#39;&#160;and LVEDP). Aortic debanding is a useful experimental model to study LV RR in rodents. The extent of myocardial recovery is variable between subjects, therefore, mimicking the diversity of RR that occurs in the clinical context, such as aortic valve replacement. We conclude that the aortic banding/debanding model represents a valuable tool to unravel novel insights into the mechanisms of RR, namely the regression of cardiac hypertrophy and the recovery of diastolic dysfunction.

Here we describe a step-by-step protocol of surgical aorta debanding in the well-established mice model of aortic-constriction. This procedure not only allows studying the mechanisms underlying the left ventricular reverse remodeling and regression of hypertrophy but also to test novel therapeutic options that might accelerate myocardial recovery.

To better understand the left ventricular (LV) reverse remodeling (RR), we describe a rodent model wherein, after aortic banding-induced LV remodeling, ...

Operating Transverse Aortic Constriction with Absorbable Suture to Obtain Transient Myocardial Hypertrophy

Based on twice transverse aortic constrictions (TACs) in mice, it is proved that myocardial hypertrophic preconditioning (MHP) could attenuate cardiomyocyte hypertrophy and slow down progression to heart failure. For novices, however, the MHP model is usually quite difficult to establish because of the technical obstacles in ventilator operation, opening the chest repeatedly, and bleeding caused by debanding. To facilitate this model, to increase the surgical success rate and to reduce the incidence of bleeding, we switched to absorbable sutures for the first TAC combing with a ventilator-free technique. Using a 2-week absorbable suture, we demonstrated that this procedure could cause significant myocardial hypertrophy in 2 weeks; and 4 weeks after surgery, myocardial hypertrophy was almost completely regressed to the baseline. Using this protocol, the operators could master the MHP model easily with a lower operation mortality.

This protocol presents an improved method to obtain transient myocardial hypertrophy with absorbable suture, simulating left ventricular hypertrophy decrease after removing pressure overload. It could be valuable for the studies on myocardial hypertrophic preconditioning.

Based on twice transverse aortic constrictions (TACs) in mice, it is proved that myocardial hypertrophic preconditioning (MHP) could attenuate ...

Transverse Aortic Arch Banding in Mouse Model: A Minimally Invasive Technique in Mice for Induction of High Pressure in the Left Ventricle

Source: Zaw, A. M. et al. <a href="https://www.jove.com/video/55293" target="_blank">Minimally Invasive Transverse Aortic Constriction in Mice</a>. J. Vis. Exp. (2017)
In this video, we demonstrate an experimental protocol for minimally invasive transverse aortic constriction in mice to examine pressure overload-induced heart failure.

Source: Zaw, A. M. et al. Minimally Invasive Transverse Aortic Constriction in Mice. J. Vis. Exp. (2017)
In this video, we demonstrate an experimental ...

JoVE Encyclopedia of Experiments

Rodent Models

Adult

Surgical Aortic Debanding: A Procedure to Study Left Ventricular Reverse Remodeling in Murine Model of Aortic Constriction

Source: Goncalves-Rodrigues, P. et al. <a href="https://www.jove.com/video/60036" target="_blank">Studying Left Ventricular Reverse Remodeling by Aortic Debanding in Rodents</a>. J. Vis. Exp. (2021)
This video demonstrates the technique of aortic debanding, which can lead to reverse remodeling to limit the progression towards heart failure in a murine model. Post debanding, a significant reduction of ventricular afterload triggers regression of ventricular hypertrophy and fibrosis, causing a recovery in cardiac function.

A Modified Technique for Transverse Aortic Constriction in Mice

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