Name: model of ischemia and reperfusion injury in rabbits
Uploaded: 2023-11-03T13:40:00
Description: Watch this Scientific Journal Video about Model of Ischemia and Reperfusion Injury in Rabbits at JoVE.com

The original study in which this protocol was used was supported by National Heart, Lung, and Blood Institute Grants HL-103642 and HL-088206

This investigation was conducted according to the National Institutes of Health&#39;s guidelines on animal care and use and was approved by the Boston Children&#39;s Hospital&#39;s Animal Care and Use Committee (Protocol 20-08-4247R). All the animals received humane care in compliance with the Guide for the Care and Use of Laboratory Animals.
1. Animal species, anesthetic, and analgesic agents
<ol>
	<li>Animal species: Use New Zealand White rabbits (wild type strain; female ...

<ol>
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Heart and Circulatory Physiology. 287 (5), H1967-H1976 (2004).</li><li>Rao, V., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Insulin+cardioplegia+for+elective+coronary+bypass+surgery.">Insulin cardioplegia for elective coronary bypass surgery.</a> The Journal of Thoracic and Cardiovascular Surgery. 119 (6), 1176-1184 (2000).</li><li>Vinten-Johansen, J., Zhao, Z. Q., Jiang, R., Zatta, A. J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Myocardial+protection+in+reperfusion+with+postconditioning.">Myocardial protection in reperfusion with postconditioning.</a> Expert Review of Cardiovascular Therapy. 3 (6), 1035-1045 (2005).</li><li>Wakiyama, H., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Selective+opening+of+mitochondrial+ATP-sensitive+potassium+channels+during+surgically+induced+myocardial+ischemia+decreases+necrosis+and+apoptosis.">Selective opening of mitochondrial ATP-sensitive potassium channels during surgically induced myocardial ischemia decreases necrosis and apoptosis.</a> European Journal of Cardio-Thoracic Surgery. 21 (3), 424-433 (2002).</li><li>Chen, Q., Moghaddas, S., Hoppel, C. L., Lesnefsky, E. J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Reversible+blockade+of+electron+transport+during+ischemia+protects+mitochondria+and+decreases+myocardial+injury+following+reperfusion.">Reversible blockade of electron transport during ischemia protects mitochondria and decreases myocardial injury following reperfusion.</a> Journal of Pharmacology and Experimental Therapeutics. 319 (3), 1405-1412 (2006).</li><li>Lesnefsky, E. J., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=rather+than+reperfusion,+inhibits+respiration+through+cytochrome+oxidase+in+the+isolated,+perfused+rabbit+heart:+Role+of+cardiolipin.">rather than reperfusion, inhibits respiration through cytochrome oxidase in the isolated, perfused rabbit heart: Role of cardiolipin.</a> American Journal of Physiology. Heart and Circulatory Physiology. 287 (1), H258-H267 (2004).</li><li>McCully, J. D., Rousou, A. J., Parker, R. A., Levitsky, S. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Age-+and+gender-related+differences+in+mitochondrial+oxygen+consumption+and+calcium+with+cardioplegia+and+diazoxide.">Age- and gender-related differences in mitochondrial oxygen consumption and calcium with cardioplegia and diazoxide.</a> The Annals of Thoracic Surgery. 83 (3), 1102-1109 (2007).</li><li>Mandel, I. 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A., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Remote+ischemic+preconditioning+reduces+myocardial+and+renal+injury+after+elective+abdominal+aortic+aneurysm+repair:+A+randomized+controlled+trial.">Remote ischemic preconditioning reduces myocardial and renal injury after elective abdominal aortic aneurysm repair: A randomized controlled trial.</a> Circulation. 116, 98-105 (2007).</li><li>Pogwizd, S. M., Bers, D. M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Rabbit+models+of+heart+disease.">Rabbit models of heart disease.</a> Drug Discovery Today: Disease Models. 5 (3), 185-193 (2008).</li><li>Tanaka, K., Hearse, D. J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Reperfusion-induced+arrhythmias+in+the+isolated+rabbit+heart:+characterization+of+the+influence+of+the+duration+of+regional+ischemia+and+the+extracellular+potassium+concentration.">Reperfusion-induced arrhythmias in the isolated rabbit heart: characterization of the influence of the duration of regional ischemia and the extracellular potassium concentration.</a> Journal of Molecular and Cellular Cardiology. 20 (3), 201-211 (1988).</li><li>Milani-Nejad, N., Janssen, P. M. L. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Small+and+large+animal+models+in+cardiac+contraction+research:+advantages+and+disadvantages.">Small and large animal models in cardiac contraction research: advantages and disadvantages.</a> Pharmacology &amp; Therapeutics. 141 (3), 235-249 (2014).</li><li>Gupta, M. P. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Factors+controlling+cardiac+myosin-isoform+shift+during+hypertrophy+and+heart+failure.">Factors controlling cardiac myosin-isoform shift during hypertrophy and heart failure.</a> Journal of Molecular and Cellular Cardiology. 43 (4), 388-403 (2007).</li><li>Lapierre, H., Chan, V., Sohmer, B., Mesana, T. G., Ruel, M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Minimally+invasive+coronary+artery+bypass+grafting+via+a+small+thoracotomy+versus+off-pump:+A+case-matched+study.">Minimally invasive coronary artery bypass grafting via a small thoracotomy versus off-pump: A case-matched study.</a> European Journal of Cardio-Thoracic Surgery. 40 (4), 804-810 (2011).</li><li>Aubin, H., Akhyari, P., Lichtenberg, A., Albert, A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Additional+right-sided+upper+&amp;#34;half-mini-thoracotomy&amp;#34;+for+aortocoronary+bypass+grafting+during+minimally+invasive+multivessel+revascularization.">Additional right-sided upper &amp;#34;half-mini-thoracotomy&amp;#34; for aortocoronary bypass grafting during minimally invasive multivessel revascularization.</a> Journal of Cardiothoracic Surgery. 10, 130 (2015).</li><li>Hu, N., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Ligation+of+the+left+circumflex+coronary+artery+with+subsequent+MRI+and+histopathology+in+rabbits.">Ligation of the left circumflex coronary artery with subsequent MRI and histopathology in rabbits.</a> Journal of the American Association for Laboratory Animal Science. 49 (6), 838-844 (2010).</li><li>Sievers, R. E., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=A+model+of+acute+regional+myocardial+ischemia+and+reperfusion+in+the+rat.">A model of acute regional myocardial ischemia and reperfusion in the rat.</a> Magnetic Resonance in Medicine. 10 (2), 172-181 (1989).</li><li>Rodr&#237;guez, B., Trayanova, N., Noble, D. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Modeling+cardiac+ischemia.">Modeling cardiac ischemia.</a> Annals of the New York Academy of Sciences. 1080, 395-414 (2006).</li><li>Sinusas, A. J., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Quantification+of+area+at+risk+during+coronary+occlusion+and+degree+of+myocardial+salvage+after+reperfusion+with+technetium-99m+methoxyisobutyl+isonitrile.">Quantification of area at risk during coronary occlusion and degree of myocardial salvage after reperfusion with technetium-99m methoxyisobutyl isonitrile.</a> Circulation. 82 (4), 1424-1437 (1990).</li><li>Masuzawa, A., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Transplantation+of+autologously+derived+mitochondria+protects+the+heart+from+ischemia-reperfusion+injury.">Transplantation of autologously derived mitochondria protects the heart from ischemia-reperfusion injury.</a> American Journal of Physiology. Heart and Circulatory Physiology. 304 (7), H966-H982 (2013).</li><li>Pombo, J. F., Troy, B. L., Russell, R. O. J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Left+ventricular+volumes+and+ejection+fraction+by+echocardiography.">Left ventricular volumes and ejection fraction by echocardiography.</a> Circulation. 43 (4), 480-490 (1971).</li><li>McCully, J. D., Wakiyama, H., Hsieh, Y. J., Jones, M., Levitsky, S. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Differential+contribution+of+necrosis+and+apoptosis+in+myocardial+ischemia-reperfusion+injury.">Differential contribution of necrosis and apoptosis in myocardial ischemia-reperfusion injury.</a> American Journal of Physiology. 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Our protocol demonstrates a reliable methodology for performing acute regional myocardial ischemia in the rabbit. The left mini-thoracotomy approach is ideal for survival cases, for which the incision and associated pain must be minimized. Importantly, diuretic therapy was not necessary prior to extubation, and there was no mortality intraoperatively in the non-survival group or at 4 weeks postoperatively in the survival group. When the design of the protocol requires a non-survival case, or when more detailed monitoring...

Cardiovascular diseases are the leading cause of death in the world and contribute to over 18 million deaths each year1,2,3. Acute myocardial infarction (MI) is a common medical emergency that develops when a blood clot or a piece of atheromatous plaque blocks the blood flow of a coronary artery. This causes regional myocardial ischemia in the territory that the artery perfuses.
The present study describes a protocol that utilizes a simple and reliable methodology to create in situ acute regional myocardial ischemia in a rabbit model for non-survival and survival experiments. The initial goal of this method was to evaluate the effects of mitochondrial transplantation on modulating myocardial necrosis and increasing the post-ischemic heart function following an ischemic event. Previous research has demonstrated the occurrence of mitochondrial alterations and a rapid decline in high-energy phosphate levels following the onset of ischemia and a reduction in the oxygen supply, resulting in a drastic decrease in the cardiac energy stores4. Investigators have attempted to improve post-ischemic function and lessen myocardial tissue necrosis using pharmacological interventions and/or procedural techniques, but these techniques provide limited cardioprotection and have minimal impact on mitochondrial damage and dysfunction5,6,7. Our team and others have previously shown that mitochondrial damage primarily occurs during ischemia and that contractile recovery can be enhanced and the myocardial infarct size decreased with the preservation of mitochondrial respiratory function during reperfusion8,9,10. Thus, we hypothesized that mitochondrial transplantation from tissues unaffected by ischemia to the area of ischemia prior to reperfusion would provide an alternative approach to reduce myocardial necrosis and enhance myocardial function. Herein, we detail the protocol used to test this theory and the representative results obtained from our initial study analysis.
Furthermore, several investigators have focused on other topics integral to defining the impact of myocardial ischemia-reperfusion injury and establishing appropriate therapeutic interventions. One such area of research is that of preconditioning. Myocardial ischemic preconditioning is a cardioprotective mechanism activated by brief ischemic stress that results in a reduction in the rate of cardiac cell necrosis during subsequent episodes of prolonged ischemia. These mechanisms can be activated by either hypoxia or coronary occlusion. Mandel et al. demonstrated that hypoxic-hyperoxic preconditioning helped to maintain the balance of nitric oxide metabolites, reduced endothelin-1 hyperproduction, and supported organ protection11. Moreover, the concept of remote ischemic preconditioning, a phenomenon whereby single-organ preconditioning provides systemic protection, has been explored. Ali et al. found that, in patients undergoing elective open abdominal aortic aneurysm repair, remote preconditioning, performed by intermittently cross-clamping the common iliac artery to serve as a stimulus, reduced the incidence of postoperative myocardial injury, myocardial infarction, and renal impairment12.
Rabbit models offer potential advantages over models with other species and have been used in multiple different scenarios for decades, including the induction of arrhythmias, global and regional ischemic models, and cardiac contraction research, amongst others13,14,15. Although the rabbit heart is smaller than that of a dog or pig, it is large enough to easily perform surgical procedures at a much lower cost13. The rabbit heart is often used as it closely parallels the human heart; indeed, it has a similar metabolic rate, expresses &#946;-myosin heavy chain, andlacks significant myocardial xanthine oxidase16. The technique herein described to induce regional myocardial ischemia is simple, repeatable, and cost-effective. This method allows for both non-survival and survival cases, as only regional ischemia is induced rather than global ischemia, and the materials needed are non-specialized. Two different surgical approaches (i.e., sternotomy and mini-thoracotomy) can be utilized, thus providing the operator and experimental protocols more freedom in terms of the study design. Additionally, the procedure does not require the use of a cardiopulmonary bypass. In this context, minimally invasive approaches to coronary artery bypass grafting have become valuable alternatives for patients in need of multi-vessel revascularizaiton17,18. This model could be used to study the differences between these approaches and provide an animal-based learning tool for surgical trainees. Additionally, performing cardiac catheterization utilizing this model may be useful for physiological research and/or surgical training.
Our model provides a methodology for applications in which inducing regional myocardial ischemia and subsequently measuring the infarct size, myocardial function, and cellular changes are of importance. With this protocol, we have been able to evaluate several markers of cellular function and adaptation to ischemia and the proposed therapeutic intervention (i.e., mitochondrial transplantation) by examining the internalization of organelles, oxygen consumption, high-energy phosphate synthesis, and the induction of cytokine mediators and proteomic pathways. These outcomes are important in preserving the myocardial energetics, cell viability, and cardiac function and allow for the objective evaluation of cardioprotective techniques following ischemia-reperfusion injury. This model could be used to study similar biologic pathways and alternatives in the field of post-ischemic myocardial pathology and recovery.
The goal of this protocol is to provide a highly reproducible methodology to induce in situ acute regional myocardial ischemia in the rabbit for non-survival and survival experiments. This model provides a methodology with high survival, low intraoperative mortality, and minimal morbidity19. Other models for acute regional myocardial ischemia have been described using radiolabeled materials, contrast agents, magnetic resonance imaging, or computer simulations20,21,22. Our protocol provides a reliable and simple methodology that is cost-effective, consistently reproducible, and has a low technical demand and, thus, can be performed by investigators without surgical expertise. This protocol accommodates either a survival project using a left mini-thoracotomy or a non-survival model using a midline sternotomy.

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			<td>World Precision Instruments</td>
			<td>14119</td>
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			<td>Integra</td>
			<td>P6280</td>
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			<td>Echocardiography machine</td>
			<td>Philips</td>
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			<td>Electrocardiography machine</td>
			<td>Meditech</td>
			<td>MD908B</td>
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			<td>Endotracheal tube</td>
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			<td>1&#8211;4 &#181;g/kg transdermal patch</td>
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			<td>Glass plates</td>
			<td>&#160;United Scientific</td>
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			<td>Heparin Sodium</td>
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			<td>NDC 69-0058-02</td>
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			<td>Hot water blanket</td>
			<td>3M</td>
			<td>55577</td>
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			<td>Isoflurane</td>
			<td>Penn Veterinary Supply, INC</td>
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			<td>Ketamine</td>
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			<td>NDC 42023-138-10</td>
			<td>10 mg/kg IV</td>
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			<td>Lab Chart 7 Acquisition Software</td>
			<td>Adinstruments</td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>Lactated Ringer&#39;s solution</td>
			<td>ICUmedical</td>
			<td>NDC 0990-7953-09</td>
			<td>10 mL/kg/h</td>
		</tr>
		<tr>
			<td>Laryngoscope</td>
			<td>Welch Allyn</td>
			<td>68044</td>
			<td></td>
		</tr>
		<tr>
			<td>Left ventricule lumen catheter&#160;3Fr</td>
			<td>McKesson</td>
			<td>385764-EA</td>
			<td></td>
		</tr>
		<tr>
			<td>Lidocaine (1%)</td>
			<td>Pfizer</td>
			<td>4276-01</td>
			<td>1&#8211;1.5 mL/kg IV</td>
		</tr>
		<tr>
			<td>LVDP transducer</td>
			<td>Edward</td>
			<td>PDP-ED</td>
			<td></td>
		</tr>
		<tr>
			<td>Marking pen</td>
			<td>Viscot</td>
			<td>1451SR-100 Unsterile</td>
			<td></td>
		</tr>
		<tr>
			<td>Mayo scissors</td>
			<td>Mayo</td>
			<td>S7-1098</td>
			<td></td>
		</tr>
		<tr>
			<td>Medetomidine</td>
			<td>Entireoly Pets Pharmacy</td>
			<td>NDC 015914-005-01</td>
			<td>0.25 mg/kg IM</td>
		</tr>
		<tr>
			<td>Metzenbaum scissors</td>
			<td>Cole-Parmer</td>
			<td>UX-10821-05</td>
			<td></td>
		</tr>
		<tr>
			<td>Monastra. Blue pigment 98%</td>
			<td>Chemsavers</td>
			<td>MBTR1100G</td>
			<td></td>
		</tr>
		<tr>
			<td>Monocryl 5-0</td>
			<td>Ethicon</td>
			<td>Y463G</td>
			<td></td>
		</tr>
		<tr>
			<td>Mosquito clamp</td>
			<td>Shioda</td>
			<td>802N</td>
			<td></td>
		</tr>
		<tr>
			<td>PDS 3-0</td>
			<td>Ethicon</td>
			<td>42312201</td>
			<td></td>
		</tr>
		<tr>
			<td>Piezoelectric sonomicrometry crystals</td>
			<td>Sonometrics</td>
			<td>Small 2mm round</td>
			<td></td>
		</tr>
		<tr>
			<td>Plegets</td>
			<td>DeRoyal</td>
			<td>32-363</td>
			<td></td>
		</tr>
		<tr>
			<td>Povuine Iodine Prep Solutions</td>
			<td>Medline</td>
			<td>MDS093940</td>
			<td></td>
		</tr>
		<tr>
			<td>Precision vaporized system face mask</td>
			<td>Yuwell</td>
			<td>B07PNH69BF</td>
			<td></td>
		</tr>
		<tr>
			<td>Prolene 3-0</td>
			<td>Ethicon</td>
			<td>8665G</td>
			<td></td>
		</tr>
		<tr>
			<td>Proline 5-0</td>
			<td>Ethicon</td>
			<td>8661G</td>
			<td></td>
		</tr>
		<tr>
			<td>Pulse oximetry probe</td>
			<td>Masimo</td>
			<td>9216-U</td>
			<td></td>
		</tr>
		<tr>
			<td>Rib spreader</td>
			<td>Medline</td>
			<td>MDS5621025</td>
			<td></td>
		</tr>
		<tr>
			<td>S12 Pediatric Sector Probe</td>
			<td>Phillips</td>
			<td>21380A</td>
			<td></td>
		</tr>
		<tr>
			<td>Sonomicrometer</td>
			<td>Sonometrics</td>
			<td>BZ10123724</td>
			<td></td>
		</tr>
		<tr>
			<td>Sterile gauze</td>
			<td>Medline</td>
			<td>3.00802E+13</td>
			<td></td>
		</tr>
		<tr>
			<td>Sterile towels</td>
			<td>McKesson</td>
			<td>MON 277860EA</td>
			<td></td>
		</tr>
		<tr>
			<td>Sternal retractor</td>
			<td>Medline</td>
			<td>MDS5610321</td>
			<td></td>
		</tr>
		<tr>
			<td>Sutures for closure</td>
			<td>J&#38;J Dental</td>
			<td>8698G</td>
			<td></td>
		</tr>
		<tr>
			<td>Telemetriy monitor</td>
			<td>Meditech</td>
			<td>MD908B</td>
			<td></td>
		</tr>
		<tr>
			<td>Temperature probe</td>
			<td>Omega</td>
			<td>KHSS-116G-RSC-12</td>
			<td></td>
		</tr>
		<tr>
			<td>Triphenyl tetrazolium chloride (1%)</td>
			<td>Millipore</td>
			<td>MFCD00011963</td>
			<td></td>
		</tr>
		<tr>
			<td>Ventilator</td>
			<td>MedGroup</td>
			<td>MSLGA 11</td>
			<td></td>
		</tr>
		<tr>
			<td>Vicryl 2-0</td>
			<td>Ethicon</td>
			<td>V635H</td>
			<td></td>
		</tr>
		<tr>
			<td>Vinyl tubing</td>
			<td>ABE</td>
			<td>DISW 3001</td>
			<td></td>
		</tr>
	</tbody>
</table>

model of ischemia and reperfusion injury in rabbits

The protocol here provides a simple, highly replicable methodology to induce in situ acute regional myocardial ischemia in the rabbit for non-survival and survival experiments. New Zealand White adult rabbit is sedated with atropine, acepromazine, butorphanol, and isoflurane. The animal is intubated and placed on mechanical ventilation. An intravenous catheter is inserted into the marginal ear vein for the infusion of medications. The animal is pre-medicated with heparin, lidocaine, and lactated Ringer&#39;s solution. A carotid cut-down is performed to obtain arterial line access for blood pressure monitoring. Select physiologic and mechanical parameters are monitored and recorded by continuous real-time analysis.
With the animal sedated and fully anesthetized, either a fourth intercostal space small left thoracotomy (survival) or midline sternotomy (non-survival) is performed. The pericardium is opened, and the left anterior descending (LAD) artery is located.
A polypropylene suture is passed around the second or third diagonal branch of the LAD artery, and the polypropylene filament is threaded through a small vinyl tube, forming a snare. The animal is subjected to 30 min of regional ischemia, achieved by occluding the LAD by tightening the snare. Myocardial ischemia is confirmed visually by regional cyanosis of the epicardium. Following regional ischemia, the ligature is loosened, and the heart is allowed to re-perfuse.
For both survival and non-survival experiments, the myocardial function can be assessed via an echocardiography (ECHO) measurement of the fractional shortening. For non-survival studies, data from sonomicrometry collected using three digital piezoelectric ultrasonic probes implanted within the ischemic area and the left ventricle developed pressure (LVDP) using an apically inserted left ventricle (LV) catheter can be continuously acquired for evaluating the regional and global myocardial function, respectively.
For survival studies, the incision is closed, a left needle thoracentesis is performed for pleural air evacuation, and postoperative pain control is achieved.

Following the protocol (Figure 1), myocardial ischemia was confirmed immediately by the direct visualization of cyanosis of the epicardium.
Standard ECGs (three limb leads: I, II, and III, and three computed augmented leads: aVL, aVR, and aVF) were recorded continuously pre-ischemia, during ischemia, and at reperfusion (Figure 2). The ECGs demonstrate tachycardia, arrhythmias (i.e., ventricular fibrillation), conduction system defects...

Watch this Scientific Journal Video about Model of Ischemia and Reperfusion Injury in Rabbits at JoVE.com

Model of Ischemia and Reperfusion Injury in Rabbits

The present study demonstrates a highly reproducible animal model of acute regional myocardial ischemia and reperfusion injury in rabbits using a left mini-thoracotomy for survival cases or a midline sternotomy for non-survival cases.

The protocol here provides a simple, highly replicable methodology to induce in situ acute regional myocardial ischemia in the rabbit for non-survival and ...

This protocol provides a simple, reliable, and reproducible methodology to induce in situ acute regional myocardial ischemia and reperfusion injury in a rabbit model for non-survival and survival experiments. This technique has minimal mortality and morbidity via two different surgical approaches. The methodology is cost-effective and has low technical demand and thus can be performed by investigators without surgical expertise.Exposing the LAD through a mini-thoracotomy can be challenging. We recommend making a fourth intercostal space anterior parasternal incision extending five to six centimeters laterally and practicing such exposure and rabbit necropsy prior. To perform a left mini-thoracotomy for survival studies, elevate the left side of the anesthetized rabbit approximately 30 degrees using a pillow.Palpate and outline the bony landmarks with a felt-tipped marking pen. Using a number 10 blade, incise the skin overlying the fifth rib, extending from adjacent to the lateral border of the sternum to five to six centimeters laterally. Using electrocautery, divide the pectoralis major muscle medially, followed by the serratus anterior muscle laterally.Then divide the intercostal muscles above the fifth rib to preserve the neurovascular bundle. Using sharp dissection, incise the parietal pleura with Metzenbaum scissors, carefully enter the pleural space through the fourth intercostal space, and extend the initial pleural incision in both directions parallel to the rib until a rib spreader or sternal retractor can be inserted. Place a rib spreader or sternal retractor within the rib space and widen it to visualize the heart and pericardial sac.Use DeBakey forceps to lift the pericardium. Open it with Metzenbaum scissors and proceed with LAD artery isolation. This will provide optimal visualization of the anterolateral surface of the heart with adequate exposure to the LAD and its branches.To isolate the LAD artery, encircle its third diagonal branch with a 3-0 polypropylene suture on a taper needle, then remove the needle. In survival cases, trim the three 3-0 polypropylene thread used to isolate the LAD and loosely tie the ends together. The three 3-0 polypropylene thread is used to identify the area at risk and the infarct zone upon harvesting the heart.Post-surgery, tie two 2-0 Polyglactin 910 figure-of-eight stitches around the ribs. Close the muscular and subcutaneous layers with a 3-0 polydioxanone suture in a running fashion. Then close the skin in a subcuticular fashion using a 5-0 monofilament suture.Finally, perform a needle thoracentesis to evacuate the pleural error. For non-survival studies, immediately proceed with midline sternotomy using curved Mayo scissors. Using a sternal retractor to visualize the heart and pericardial sac, open the pericardium as previously demonstrated.Visualize the 3-0 polypropylene thread loop placed during the previously performed thoracotomy portion of the procedure. To isolate the LAD artery, encircle its third diagonal branch with a 3-0 polypropylene suture on a taper needle. Then remove the needle and thread both ends of the polypropylene filament through a small vinyl tube to form a snare.Using DeBakey forceps, place a rectangular PTFE pledget between the two polypropylene filaments, sandwiching it between the isolated LAD artery and the vinyl tube. Tighten this snare by pressing down on the vinyl tube and pulling up on the polypropylene suture filaments to occlude the coronal artery. Clamp the tube using a mosquito clamp to maintain the desired tightness.Confirm myocardial ischemia by observing regional cyanosis of the epicardium. Remove the snare after 30 minutes of ischemia induction. At the end of the experiment, harvest the heart for biochemical and tissue analysis.The recorded ECGs at pre-ischemia, during ischemia, and reperfusion demonstrated tachycardia, arrhythmias, conduction system defects, the development of infarct-related Q waves, and ST segment deviation. The 2D echo readings showed that the fractional shortening decreased during ischemia and post-ischemia compared to pre-ischemia. After 30 minutes of induced regional myocardial ischemia, evidence of myocardial necrosis was observed.The most critical protocol steps are carefully encircling the LAD without damaging the artery or causing venous bleeding, appropriately placing the PTFE pledget to prevent vasospasm, and including the LAD to create a consistent area at risk. This methodology is useful in vascular injury, chronic myocardial ischemia, and acute myocardial stunning models to unveil cardiovascular molecular mechanics, pathophysiological mechanisms, and therapeutic targets, demonstrating usability and developing diagnostic and treatment algorithms.

model-of-ischemia-and-reperfusion-injury-in-rabbits

Research

JoVE Journal

Medicine

Normothermic Cardiac Arrest and Cardiopulmonary Resuscitation: A Mouse Model of Ischemia-Reperfusion Injury

Acute Kidney Injury (AKI) is a common, highly lethal, complication of critical illness which has a high mortality1-4 and which is most 
frequently caused by whole-body hypoperfusion.5,6 Successful reproduction of whole-body hypoperfusion in rodent models has been fraught with 
difficulty.7-9,9,10 Models which employ focal ischemia have repeatedly demonstrated results which do not translate to the clinical setting, and larger 
animal models which allow for whole body hypoperfusion lack access to the full toolset of genetic manipulation possible in the mouse.11,12 However, in recent 
years a mouse model of cardiac arrest and cardiopulmonary resuscitation has emerged which can be adapted to model AKI.13 This model reliably reproduces 
physiologic, functional, anatomic, and histologic outcomes seen in clinical AKI, is rapidly repeatable, and offers all of the significant advantages of a murine surgical 
model, including access to genetic manipulative techniques, low cost relative to large animals, and ease of use. Our group has developed extensive experience 
with use of this model to assess a number of organ-specific outcomes in AKI.14,15

A powerful model for perioperative and critical care related acute kidney injury is presented. Using whole body hypoperfusion induced by cardiac arrest it is possible to nearly replicate the histologic and functional changes of clinical AKI.

Acute Kidney Injury (AKI) is a common, highly lethal, complication of critical illness which has a high mortality1-4 and which is most 
frequently caused ...

Ischemia-reperfusion Model of Acute Kidney Injury and Post Injury Fibrosis in Mice

Ischemia-reperfusion induced acute kidney injury (IR-AKI) is widely used as a model of AKI in mice, but results are often quite variable with high, often unreported mortality rates that may confound analyses. Bilateral renal pedicle clamping is commonly used to induce IR-AKI, but differences between effective clamp pressures and/or renal responses to ischemia between kidneys often lead to more variable results. In addition, shorter clamp times are known to induce more variable tubular injury, and while mice undergoing bilateral injury with longer clamp times develop more consistent tubular injury, they often die within the first 3 days after injury due to severe renal insufficiency. To improve post-injury survival and obtain more consistent and predictable results, we have developed two models of unilateral ischemia-reperfusion injury followed by contralateral nephrectomy. Both surgeries are performed using a dorsal approach, reducing surgical stress resulting from ventral laparotomy, commonly used for mouse IR-AKI surgeries. For induction of moderate injury BALB/c mice undergo unilateral clamping of the renal pedicle for 26 min and also undergo simultaneous contralateral nephrectomy. Using this approach, 50-60% of mice develop moderate AKI 24 hr after injury but 90-100% of mice survive. To induce more severe AKI, BALB/c mice undergo renal pedicle clamping for 30 min followed by contralateral nephrectomy 8 days after injury. This allows functional assessment of renal recovery after injury with 90-100% survival. Early post-injury tubular damage as well as post injury fibrosis are highly consistent using this model.

We describe models of moderate and severe ischemia-reperfusion-induced kidney injury in which the mice undergo unilateral renal pedicle clamping followed by simultaneous or delayed contralateral nephrectomy, respectively. These models consistently give rise to renal dysfunction and post-injury fibrosis, but injury severity and survival are dependent on mouse background, age and surgical equipment.

Ischemia-reperfusion induced acute kidney injury (IR-AKI) is widely used as a model of AKI in mice, but results are often quite variable with high, often ...

Murine Model of Intestinal Ischemia-reperfusion Injury

Intestinal ischemia is a life-threatening condition associated with a broad range of clinical conditions including atherosclerosis, thrombosis, hypotension, necrotizing enterocolitis, bowel transplantation, trauma and chronic inflammation. Intestinal ischemia-reperfusion (IR) injury is a consequence of acute mesenteric ischemia, caused by inadequate blood flow through the mesenteric vessels, resulting in intestinal damage. Reperfusion following ischemia can further exacerbate damage of the intestine. The mechanisms of IR injury are complex and poorly understood. Therefore, experimental small animal models are critical for understanding the pathophysiology of IR injury and the development of novel therapies.
Here we describe a mouse model of acute intestinal IR injury that provides reproducible injury of the small intestine without mortality. This is achieved by inducing ischemia in the region of the distal ileum by temporally occluding the peripheral and terminal collateral branches of the superior mesenteric artery for 60 min using microvascular clips. Reperfusion for 1 hr, or 2 hr after injury results in reproducible injury of the intestine examined by histological analysis. Proper position of the microvascular clips is critical for the procedure. Therefore the video clip provides a detailed visual step-by-step description of this technique. This model of intestinal IR injury can be utilized to study the cellular and molecular mechanisms of injury and regeneration.

Here we describe the detailed procedure of intestinal ischemia-reperfusion in mice which results in reproducible injury without mortality to encourage the standardization of this technique across the field. This model of intestinal ischemia-reperfusion injury can be utilized to study the cellular and molecular mechanisms of injury and regeneration.

Intestinal ischemia is a life-threatening condition associated with a broad range of clinical conditions including atherosclerosis, thrombosis, ...

A Mouse Model of Retinal Ischemia-Reperfusion Injury Through Elevation of Intraocular Pressure

Retinal ischemia-reperfusion (I/R) is a pathophysiological process contributing to cellular damage in multiple ocular conditions, including glaucoma, diabetic retinopathy, and retinal vascular occlusions. Rodent models of I/R injury are providing significant insights into mechanisms and treatment strategies for human I/R injury, especially with regard to neurodegenerative damage in the retinal neurovascular unit. Presented here is a protocol for inducing retinal I/R injury in mice through elevation of intraocular pressure (IOP). In this protocol, the ocular anterior chamber is cannulated with a needle, through which flows the drip of an elevated saline reservoir. Using this drip to raise IOP above systolic arterial blood pressure, a practitioner temporarily halts inner retinal blood flow (ischemia). When circulation is reinstated (reperfusion) by removal of the cannula, severe cellular damage ensues, resulting ultimately in retinal neurodegeneration. Recent studies demonstrate inflammation, vascular permeability, and capillary degeneration as additional elements of this model. Compared to alternative retinal I/R methodologies, such as retinal arterial ligation, retinal I/R injury by elevated IOP offers advantages in its&#160;anatomical specificity, experimental tractability, and technical accessibility, presenting itself as a valuable tool for examining neuronal pathogenesis and therapy in the retinal neurovascular unit.

This article describes a procedure for inducing retinal ischemia-reperfusion injury by elevated intraocular pressure in mice. Retinal ischemia-reperfusion injury by elevated intraocular pressure serves to model human pathologies characterized by compromised oxygen and nutrient delivery in the retina, enabling researchers to examine potential cellular mechanisms and treatments for human diseases of the retinal neurovascular unit.

Retinal ischemia-reperfusion (I/R) is a pathophysiological process contributing to cellular damage in multiple ocular conditions, including glaucoma, ...

Preclinical Model of Hind Limb Ischemia in Diabetic Rabbits

Peripheral vascular disease is a widespread clinical problem that affects millions of patients worldwide. A major consequence of peripheral vascular disease is the development of ischemia. In severe cases, patients can develop critical limb ischemia in which they experience constant pain and an increased risk of limb amputation. Current therapies for peripheral ischemia include bypass surgery or percutaneous interventions such as angioplasty with stenting or atherectomy to restore blood flow. However, these treatments often fail to the continued progression of vascular disease or restenosis or are contraindicated due to the overall poor health of the patient. A promising potential approach to treat peripheral ischemia involves the induction of therapeutic neovascularization to allow the patient to develop collateral vasculature. This newly formed network alleviates peripheral ischemia by restoring perfusion to the affected area. The most frequently employed preclinical model for peripheral ischemia utilizes the creation of hind limb ischemia in healthy rabbits through femoral artery ligation. In the past, however, there has been a strong disconnect between the success of preclinical studies and the failure of clinical trials regarding treatments for peripheral ischemia. Healthy animals typically have robust vascular regeneration in response to surgically induced ischemia, in contrast to the reduced vascularity and regeneration in patients with chronic peripheral ischemia. Here, we describe an optimized animal model for peripheral ischemia in rabbits that includes hyperlipidemia and diabetes. This model has reduced collateral formation and blood pressure recovery in comparison to a model with a higher cholesterol diet. Thus, the model may provide better correlation with human patients with compromised angiogenesis from the common co-morbidities that accompany peripheral vascular disease.

We describe a surgical procedure used to induce peripheral ischemia in rabbits with hyperlipidemia and diabetes. This surgery acts as a preclinical model for conditions experienced in peripheral artery disease in patients. Angiography is also described as a means to measure the extent of introduced ischemia and recovery of perfusion.

Peripheral vascular disease is a widespread clinical problem that affects millions of patients worldwide. A major consequence of peripheral vascular ...

Evaluation of Coronary Flow Reserve After Myocardial Ischemia Reperfusion in Rats

Coronary artery disease is the leading cause of death worldwide. After an acute myocardial infarction, early and successful myocardial intervention via recanalization of the coronary artery is the most effective strategy for reducing the size of ischemic myocardium. The coronary microvasculature cannot be visualized and imaged&#160;in vivo, but there are several invasive and noninvasive techniques that can be used to assess parameters which depend directly on coronary microvascular function. The endothelial function after ischemia reperfusion can be assessed also at the level of the coronary circulation via the coronary flow reserve (CFR).&#160;In this study, peak velocity of left anterior descending (LAD) coronary arteries was measured in rats in vivo via Transthoracic Doppler Echocardiography during resting and stress challenge (induced by Dobutamine). A normal heart can increase its coronary blood flow up to four times above the resting values during stress induction. Following ischemia reperfusion, we found a significantly diminished CFR, which can be used as a marker of coronary microvascular dysfunction. CFR has opened a window on the importance of microvascular dysfunction and has been shown to predict cardiovascular risk independent of whether the severe obstructive disease is present.

Coronary flow reserve (CFR), is defined as the ratio of maximal coronary blood flow to the resting coronary blood flow. We present a protocol for evaluating CFR in rats via ultrasound, which offers the opportunity to predict cardiovascular risk factors in the absence of obstructive coronary disease.

Coronary artery disease is the leading cause of death worldwide. After an acute myocardial infarction, early and successful myocardial intervention via ...

A Pre-clinical Rat Model for the Study of Ischemia-reperfusion Injury in Reconstructive Microsurgery

Ischemia-reperfusion injury is the main cause of flap failure in reconstructive microsurgery. The rat is the preferred preclinical animal model in many areas of biomedical research due to its cost-effectiveness and its translation to humans. This protocol describes a method to create a preclinical free skin flap model in rats with ischemia-reperfusion injury. The described 3 cm x 6 cm rat free skin flap model is easily obtained after the placement of several vascular ligatures and the section of the vascular pedicle. Then, 8 h after the ischemic insult and completion of the microsurgical anastomosis, the free skin flap develops the tissue damage. These ischemia-reperfusion injury-related damages can be studied in this model, making it a suitable model for evaluating therapeutic agents to address this pathophysiological process. Furthermore, two main monitoring techniques are described in the protocol for the assessment of this animal model: transit-time ultrasound technology and laser speckle contrast analysis.

Here, we describe a pre-clinical animal model for studying the pathophysiology of ischemia-reperfusion injury in reconstructive microsurgery. This free skin flap model based on the superficial caudal epigastric vessels in the rat may also allow for the evaluation of different therapies and compounds to counteract ischemia-reperfusion injury-related damage.

Ischemia-reperfusion injury is the main cause of flap failure in reconstructive microsurgery. The rat is the preferred preclinical animal model in many ...

Delayed Intramyocardial Delivery of Stem Cells after Ischemia Reperfusion Injury in a Murine Model

There is significant interest in the use of stem cells (SCs) for the recovery of cardiac function in individuals with myocardial injuries. Most commonly, cardiac stem cell therapy is studied by delivering SCs concurrently with the induction of myocardial injury. However, this approach presents two significant limitations: the early hostile pro-inflammatory ischemic environment may affect the survival of transplanted SCs, and it does not represent the subacute infarction scenario where SCs will likely be used. Here we describe a two-part series of surgical procedures for the induction of ischemia-reperfusion injury and delivery of mesenchymal stem cells (MSCs). This method of stem cell administration may allow for the longer viability and retention around damaged tissue by circumventing the initial immune response. A model of ischemia reperfusion injury was induced in mice accompanied by the delivery of mesenchymal stem cells (3.0 x 105), stably expressing the reporter gene firefly luciferase under the constitutively expressed CMV promoter, intramyocardially 7 days later. The animals were imaged via ultrasound and bioluminescent imaging for confirmation of injury and injection of cells, respectively. Importantly, there was no added complication rate when performing this two-procedure approach for SC delivery. This method of stem cell administration, collectively with the utilization of state-of-the-art reporter genes, may allow for the in vivo study of viability and retention of transplanted SCs in a situation of chronic ischemia commonly seen clinically, while also circumventing the initial pro-inflammatory response. In summary, we established a protocol for the delayed delivery of stem cells into the myocardium, which can be used as a potential new approach in promoting regeneration of the damaged tissue.

Stems cells are continuously investigated as potential treatments for individuals with myocardial damage, however, their decreased viability and retention within injured tissue can impact their long-term efficacy. In this manuscript we describe an alternative method for stem cell delivery in a murine model of ischemia reperfusion injury.

There is significant interest in the use of stem cells (SCs) for the recovery of cardiac function in individuals with myocardial injuries. Most commonly, ...

Organ Ischemia-Reperfusion Injury by Simulating Hemodynamic Changes in Rat Liver Transplant Model

Orthotopic liver transplantation (OLT) in rats is a tried and proven animal model used for preoperative, intraoperative, and postoperative studies, including ischemia-reperfusion injury (IRI) of extrahepatic organs. This model requires numerous experiments and devices. The duration of anhepatic phase is closely related to the time to develop IRI after transplantation. In this experiment, we used hemodynamic changes to induce extrahepatic organ damage in rats and determined the maximum tolerance time. The time until the most severe organ injury varied for different organs. This method can easily be replicated and can also be used to study IRI of the extrahepatic organs after liver transplantation.

This paper provides a detailed description of how to build an animal model of the anhepatic phase (liver ischemia) in rats to facilitate basic research into ischemia-reperfusion injury after liver transplantation.

Orthotopic liver transplantation (OLT) in rats is a tried and proven animal model used for preoperative, intraoperative, and postoperative studies, ...

A Rat Lung Transplantation Model of Warm Ischemia/Reperfusion Injury: Optimizations to Improve Outcomes

From our experience with rat lung transplantation, we have found several areas for improvement. Information in the existing literature regarding methods for choosing appropriate cuff sizes for the pulmonary vein (PV), pulmonary artery (PA), or bronchus (Br) are varied, thus making the determination of proper cuff size during rat lung transplantation an exercise of trial and error. By standardizing the cuffing technique to use the smallest effective cuff appropriate for the size of the vessel or bronchus, one can make the transplantation procedure safer, faster, and more successful. Since diameters of the PV, PA, and Br are related to the body weight of the rat, we present a strategy to choosing an appropriate size using a weight-based guide. Since lung volume is also related to body weight, we recommend that this relationship should also be considered when choosing the proper volume of air for donor lung inflation during warm ischemia as well as for the proper volume of PBS to be instilled during bronchoalveolar lavage (BAL) fluid collection. We also describe methods for 4th intercostal space dissection, wound closure, and sample collection from both the native and transplanted lobes.

Here, we present optimizations to a rat lung transplantation model that serve to improve outcomes. We provide a size guide for cuffs based on body weight, a measurement strategy to ascertain the 4th intercostal space, and methods of wound closure and BAL (bronchoalveolar lavage) fluid and tissue collection.

From our experience with rat lung transplantation, we have found several areas for improvement. Information in the existing literature regarding methods ...