Name: demonstration of the rat ischemic skin wound model
Uploaded: 2015-04-01T15:00:00
Description: Watch this Scientific Journal Video about Demonstration of the Rat Ischemic Skin Wound Model at JoVE.com

The authors would like to acknowledge funding support from the University of South Florida, Department of Surgery (Mack Wu, MD, PhD).

הערה: אישור לכל נהלים בבעלי החיים המוצגים להלן התקבל מאוניברסיטת הדרום פלורידה הוועדה של טיפול בבעלי חיים (IACUC) ולציית לכל הדרישות של צער בעלי החיים החוק והמדריך לטיפול ושימוש בחי מעבדה. 1. הכנת גיליונות סיליקון ומכשירי ניתוח <ol st...

<ol>
	<li>Ansell, D. M., Holden, K. A., Hardman, M. J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Animal+models+of+wound+repair:+Are+they+cutting+it.">Animal models of wound repair: Are they cutting it.</a> Experimental dermatology. 21 (8), 581-585 (2012).</li><li>Dorsett-Martin, W. A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Rat+models+of+skin+wound+healing:+a+review.">Rat models of skin wound healing: a review.</a> Wound repair and regeneration : official publication of the Wound Healing Society [and] the European Tissue Repair Society. 12 (6), 591-599 (2003).</li><li>Davidson, J. M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Animal+models+for+wound+repair.">Animal models for wound repair.</a> Arch Dermatol Res. 290 (S1-11), (1998).</li><li>Finn, G., Magnus, S. A., Tonny, K. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Models+for+use+in+wound+healing+research:+A+survey+focusing+on+in+vitro+and+in+vivo+adult+soft+tissue).">Models for use in wound healing research: A survey focusing on in vitro and in vivo adult soft tissue).</a> Wound Repair and Regeneration. 8, (2000).</li><li>Gould, L. J., Leong, M., Sonstein, J., Wilson, S. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Optimization+and+validation+of+an+ischemic+wound+model.">Optimization and validation of an ischemic wound model.</a> Wound repair and regeneration : official publication of the Wound Healing Society [and] the European Tissue Repair Society. 13 (6), 576-582 (2004).</li><li>Loots, M. 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=Differences+in+cellular+infiltrate+and+extracellular+matrix+of+chronic+diabetic+and+venous+ulcers+versus+acute+wounds.">Differences in cellular infiltrate and extracellular matrix of chronic diabetic and venous ulcers versus acute wounds.</a> The Journal of investigative dermatology. 111 (5), 850-857 (1998).</li><li>Schwartz, D. A., Lindblad, W. J., Rees, R. R. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Altered+collagen+metabolism+and+delayed+healing+in+a+novel+model+of+ischemic+wounds.">Altered collagen metabolism and delayed healing in a novel model of ischemic wounds.</a> Wound Repair Regen. 3 (2), 204-212 (1995).</li><li>Chen, C., 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=Molecular+and+mechanistic+validation+of+delayed+healing+rat+wounds+as+a+model+for+human+chronic+wounds.">Molecular and mechanistic validation of delayed healing rat wounds as a model for human chronic wounds.</a> Wound Repair and Regeneration. 7, (1999).</li><li>Zhang, Q., Chang, Q., Cox, R. A., Gong, X., Gould, L. J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Hyperbaric+oxygen+attenuates+apoptosis+and+decreases+inflammation+in+an+ischemic+wound+model.">Hyperbaric oxygen attenuates apoptosis and decreases inflammation in an ischemic wound model.</a> The Journal of investigative dermatology. 128 (8), 2102-2112 (2008).</li><li>Zhang, Q., Gould, L. J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Hyperbaric+oxygen+reduces+matrix+metalloproteinases+in+ischemic+wounds+through+a+redox-dependent+mechanism.">Hyperbaric oxygen reduces matrix metalloproteinases in ischemic wounds through a redox-dependent mechanism.</a> The Journal of investigative dermatology. 134 (1), 237-246 (2013).</li><li>Moor, A. 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=Consequences+of+age+on+ischemic+wound+healing+in+rats:+altered+antioxidant+activity+and+delayed+wound+closure.">Consequences of age on ischemic wound healing in rats: altered antioxidant activity and delayed wound closure.</a> Age (Dordrecht, Netherlands). 36 (2), 733-748 (2014).</li><li>Roy, S., 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=Characterization+of+a+preclinical+model+of+chronic+ischemic+wound).">Characterization of a preclinical model of chronic ischemic wound).</a> Physiological genomics. 37 (3), 211-224 (2009).</li><li>Biswas, S., 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=Hypoxia+inducible+microRNA+210+attenuates+keratinocyte+proliferation+and+impairs+closure+in+a+murine+model+of+ischemic+wounds.">Hypoxia inducible microRNA 210 attenuates keratinocyte proliferation and impairs closure in a murine model of ischemic wounds.</a> Proceedings of the National Academy of Sciences of the United States of America. 107 (15), 6976-6981 (2010).</li><li>Winocour, S., Vorstenbosch, J., Trzeciak, A., Lessard, L., Philip, A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=CD109,+a+novel+TGF-beta+antagonist,+decreases+fibrotic+responses+in+a+hypoxic+wound+model.">CD109, a novel TGF-beta antagonist, decreases fibrotic responses in a hypoxic wound model.</a> Exp Dermatol. 23 (7), 475-479 (2014).</li></ol>

<html> ריפוי פצעים בחולדות היה לעתים קרובות הנושא לוויכוח בשל יכולתם לרפא את הפצעים נגועים ושיעור גבוה של שונות interanimal 5. אחת מהמטרות המקוריות של המודל במהלך פיתוחו היה כדי להקטין וריאציה זו. שינויים ברוחב של הדש, צמצום מספר הפצעים במיקום ספציפי (התמקד בדש עם מיקום ?...

פיתוח תרופות יעיל ותרופות ריפוי פצע אחרות דורשים מתאימים בדגמי vivo, למרות בעיות ידועות בתרגום ממצאים במודלים של בעלי חיים לטיפולים אנושיים 1. להלן תיאור של פרוטוקול מפורט לשימוש במודל עכברים של ריפוי עור איסכמי פצע לחקור מנגנונים שעוד יותר את ההבנה של ריפוי פצע פתולוגי. מיני החולדה, לעתים קרובות מועסק בשל הזמינות רחבה, גודלה והטבע הצייתן משמש לפצע לימודי ריפוי כפי שהוא גדול מספיק כדי לספק שטח עור מתאים לפציעת incisional וexcisional, הדמיה ורקמות אוסף 2. עם זאת יש לקחת בחשבון זהיר שהעור של עכברים ובני אדם הוא שונים מבחינה אנטומית, עם חולדות שהופנו לבעלי חיים רופפים עור כ. מאפיין מובהק זה מאפשר להתכווצות פצע, ולא epithelialization לתרום באופן משמעותי לסגירת העור של העכברים wounds 2. בנוסף, הנוכחות של שריר carnosus מִרפָּד תת-עורי בחולדות, תורמת לריפוי על ידי שתי היווצרות ההתכווצות וקולגן 3,4. הבחנות אנטומיים חשובות מאוד אלה נחשבו בפיתוח מודל פצע עור איסכמי חולדה ושינויים ספציפיים יושמו כדי להקטין התכווצות פצע ולהפחית את ההשפעה של השריר carnosus מִרפָּד 5. בכיבי רגל סוכרתיים, כיבים ברגלי ורידים, וכיבי לחץ, ריפוי מתעכב ופצעים אלה נחשבים כרוניים. הפצעים מתאפיינים בדלקת מופרזת, המונעת את הפצע מהתקדמות לשלבים הבאים של תיקון פצע 6. אחד הגורמים העיקריים בהתפתחות של פצע כרוני הוא איסכמיה המקומית רקמה (זרימת דם מופחתת) 5 תורמת לחוסר היכולת לנקות את הדלקת. בזמן שבמהלכו מודל זה היה מפותח ותקף (ב2003-4), לא היו מודלים של בעלי חיים סטנדרטיים שיכול לספק מספיק רקמה לבדיקת אינדוקציה של אנגיוגנזה במיטת הפצע, שלב מפתח בריפוי פצע נורמלי והמוטיבציה לפיתוח מודל זה 5. שאמרו, המודל שהוצג כאן הוא שינוי של מודל פצע איסכמי המתואר במקור על ידי שוורץ et al. 7 ולאחר מכן השתמש בצורה שונה על ידי et al חן. 8 במודל פצע איסכמי שונה, שינויים נעשו כדי לעקוף את המאפיינים אנטומיים שהוזכרו לעיל של העכברוש שיובילו לריפוי על ידי התכווצות ולא epithelialization: (1) שני פצעי excisional עובי מלאים נוצרים בתוך דש עור הגב וbipedicled שריר carnosus מִרפָּד מוסר מהפצע למיטה על ידי לנתח בדיוק מעל fascia השריר. (2) יש הדש עצמו ממדים צרים יותר, על מנת להבטיח שאספקת דם היא אקראית ופצעים הממוקמים בנקודת האמצע של tהוא הדש הוא איסכמי. (3) גיליון סיליקון מוחדר מתחת לדש, מניעת readherence וreperfusion של הדש מהרקמה בסיסית. התכווצות פצע מוגבלת (לא בוטל) על ידי עיגון או תפירת הדש לגיליון סיליקון 5. לאחרונה המודל נעשה שימוש במחקרים שנעו בין השפעות לחץ חמצן על פצע איסכמי ריפוי 9,10 לריפוי פצע איסכמי בצעיר לעומת חולדות בגילי 11 והוכיח להיות מודל אמין של איסכמיה רקמות הממושכת. הממדים של הדש bipedicled גם הותאמו לזני עכברוש שונים, כוללים ספראג Dawley (ארוך 11 סנטימטרים על ידי 2 סנטימטרים רוחב) וחולדות F344 (ארוך 10.5 סנטימטר על 3.0-3.5 סנטימטרים רוחב) ומינים אחרים, ובכלל זה חזירים 12 ועכברים 13,14. סרט הווידאו הזה מנצל את מתח החולדה טהור F344 בהפגנה של מודל פצע עור איסכמי. אישור לכל נהלים בבעלי החיים המוצגים להלן היה להשיגed מאוניברסיטת הדרום פלורידה הוועדה של טיפול בבעלי חיים (IACUC) ולציית לכל הדרישות של צער בעלי החיים החוק והמדריך לטיפול ושימוש בחי מעבדה.

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demonstration of the rat ischemic skin wound model

הנטייה לפצעים כרוניים בבני אדם עולה עם הזדקנות, תנאי מחלה כמו סוכרת ותפקוד לב וכלי דם פגום, ולחץ תמידי עקב חוסר תנועה. מודלים של בעלי החיים פותחו ניסיון שכדי לחקות את התנאים האלה לצורך קידום ההבנה של המורכבות של פצעים כרוניים שלנו. המודל המתואר כאן הוא מודל דש עור איסכמי חולדה המאפשר הפחתה ממושכת של זרימת דם וכתוצאה מכך פצעים שהפכו איסכמי ודומה פנוטיפ כרוני פצע (כלי דם מופחתים, דלקת מוגברת וסגירת פצעים מתעכבת). הוא מורכב מדש גב bipedicled עם 2 פצעים איסכמיים ממוקמים במרכז ו -2 פצעים אינם איסכמי לרוחב הדש כפקדים. בנוסף רומן למודל דש עור איסכמי זה הוא המיקום של גיליון סיליקון מתחת לדש שמתפקד כמחסום וסד למניעת revascularization ולהפחית התכווצות כלרפא את הפצעים. למרותדיון של שימוש בחולדות לריפוי פצע לימודים בשל ההבדלים אנטומיים ופיסיולוגיים שונים לגמרי שלהם בהשוואה לבני אדם (כלומר, הנוכחות של שריר carnosus מִרפָּד, תוחלת חיים קצרה, מספר הגדל של זקיקי שיער, וביכולתם לרפא את הפצעים נגועים) השינויים מועסקים במודל זה הופכים אותו לאלטרנטיבה יקרה לדגמי דש עור איסכמי שפותחו בעבר.

פרוטוקול מודל ריפוי עכברוש איסכמי פצע צריך לקחת כ 20 דקות לכל בעל חיים אם ביצע ביעילות. לפני היישום של הלבשת המודל אמור להופיע כפי שהוא מיוצג באיור 1G. זה יהיה חשוב כדי לוודא שהדש ופצעי bipedicled בי הם איסכמי. מתח חמצן תת עורי (PscO 2) ברמה של הפצעים כבר נמדד במהלך...

Watch this Scientific Journal Video about Demonstration of the Rat Ischemic Skin Wound Model at JoVE.com

Demonstration of the Rat Ischemic Skin Wound Model

החולדה, בשל הגודל, הזמינות, וההתנהגות לא הצייתנית שלה, נוצלה כמודל מחקר במשך שנים רבות. המטרה של פרוטוקול זה היא לנצל את החולדה כמודל ריפוי עור פצע איסכמי לספק תובנה חשובה הפתופיזיולוגיה של פצעים כרוניים.

הפגנה של דגם פצע עור העכברוש איסכמי

The propensity for chronic wounds in humans increases with ageing, disease conditions such as diabetes and impaired cardiovascular function, and ...

demonstration-of-the-rat-ischemic-skin-wound-model

Research

JoVE Journal

Medicine

Accurate and Simple Measurement of the Pro-inflammatory Cytokine IL-1&beta; using a Whole Blood Stimulation Assay

Inflammatory processes resulting from the secretion of soluble mediators by immune cells, lead to various manifestations in skin, joints and other tissues as well as altered cytokine homeostasis. The innate immune system plays a crucial role in recognizing pathogens and other endogenous danger stimuli. One of the major cytokines released by innate immune cells is Interleukin (IL)-1. Therefore, we utilize a whole blood stimulation assay in order to measure the secretion of inflammatory cytokines and specifically of the pro-inflammatory cytokine IL-1&beta; 1, 2, 3.
Patients with genetic dysfunctions of the innate immune system causing autoinflammatory syndromes show an exaggerated release of mature IL-1&beta; upon stimulation with LPS alone. In order to evaluate the innate immune component of patients who present with inflammatory-associated pathologies, we use a specific immunoassay to detect cellular immune responses to pathogen-associated molecular patterns (PAMPs), such as the gram-negative bacterial endotoxin, lipopolysaccharide (LPS). These PAMPs are recognized by pathogen recognition receptors (PRRs), which are found on the cells of the innate immune system 4, 5, 6, 7. A primary signal, LPS, in conjunction with a secondary signal, ATP, is necessary for the activation of the inflammasome, a multiprotein complex that processes pro-IL-1&beta; to its mature, bioactive form 4, 5, 6, 8, 9, 10.
The whole blood assay requires minimal sample manipulation to assess cytokine production when compared to other methods that require labor intensive isolation and culturing of specific cell populations. This method differs from other whole blood stimulation assays; rather than diluting samples with a ratio of RPMI media, we perform a white blood cell count directly from diluted whole blood and therefore, stimulate a known number of white blood cells in culture 2. The results of this particular whole blood assay demonstrate a novel technique useful in elucidating patient cohorts presenting with autoinflammatory pathophysiologies.

Accurate and Simple Measurement of the Pro-inflammatory Cytokine IL-1&amp;#946; using a Whole Blood Stimulation Assay

We describe a simple immunoassay to measure the production of pro-inflammatory cytokines, such as IL-1 beta production, in patients presenting with autoinflammatory phenotypes. By activating cells in whole blood cultures with pathogen-associated molecular patterns, specifically with lipopolysaccharide, cytokine secretion can be conveniently evaluated in whole blood supernatants.

מדידה מדויקת ופשוטה 1β-IL Pro-ציטוקין דלקתי באמצעות גירוי Assay Whole Blood

Inflammatory processes resulting from the secretion of soluble mediators by immune cells, lead to various manifestations in skin, joints and other tissues ...

A Simplified Technique for Producing an Ischemic Wound Model

One major obstacle in current diabetic wound research is a lack of an ischemic wound model that can be safely used in diabetic animals. Drugs that work well in non-ischemic wounds may not work in human diabetic wounds because vasculopathy is one major factor that hinders healing of these wounds. We published an article in 2007 describing a rabbit ear ischemic wound model created by a minimally invasive surgical technique. Since then, we have further simplified the procedure for easier operation. On one ear, three small skin incisions were made on the vascular pedicles, 1-2 cm from the ear base. The central artery was ligated and cut along with the nerve. The whole cranial bundle was cut and ligated, leaving only the caudal branch intact. A circumferential subcutaneous tunnel was made through the incisions, to cut subcutaneous tissues, muscles, nerves, and small vessels. The other ear was used as a non-ischemic control. Four wounds were made on the ventral side of each ear. This technique produces 4 ischemic wounds and 4 non-ischemic wounds in one animal for paired comparisons. After surgery, the ischemic ear was cool and cyanotic, and showed reduced movement and a lack of pulse in the ear artery. Skin temperature of the ischemic ear was 1-10 &deg;C lower than that on the normal ear and this difference was maintained for more than one month. Ear tissue high-energy phosphate contents were lower in the ischemic ear than the control ear. Wound healing times were longer in the ischemic ear than in the non-ischemic ear when the same treatment was used. The technique has now been used on more than 80 rabbits in which 23 were diabetic (diabetes time ranging from 2 weeks to 2 years). No single rabbit has developed any surgical complications such as bleeding, infection, or rupture in the skin incisions. The model has many advantages, such as little skin disruption, longer ischemic time, and higher success rate, when compared to many other models. It can be safely used in animals with reduced resistance, and can also be modified to meet different testing requirements.

We have developed a minimally invasive technique to create a rabbit ischemic ear wound model by dividing the central artery and nerve and the cranial neurovascular bundle. A subcutaneous tunnel then cuts all subcutaneous tissues. This procedure causes minimal skin disruption and can be safely used in diabetic animals.

טכניקה פשוטה לייצור דגם פצע איסכמי

One major obstacle in current diabetic wound research is a lack of an ischemic wound model that can be safely used in diabetic animals. Drugs that work ...

Endothelin-1 Induced Middle Cerebral Artery Occlusion Model for Ischemic Stroke with Laser Doppler Flowmetry Guidance in Rat

Stroke is the number one cause of disability and third leading cause of death in the world, costing an estimated $70 billion in the United States in 20091, 2. Several models of cerebral ischemia have been developed to mimic the human condition of stroke. It has been suggested that up to 80% of all strokes result from ischemic damage in the middle cerebral artery (MCA) area3. In the early 1990s, endothelin-1 (ET-1) 4 was used to induce ischemia by applying it directly adjacent to the surface of the MCA after craniotomy. Later, this model was modified 5 by using a stereotaxic injection of ET-1 adjacent to the MCA to produce focal cerebral ischemia. The main advantages of this model include the ability to perform the procedure quickly, the ability to control artery constriction by altering the dose of ET-1 delivered, no need to manipulate the extracranial vessels supplying blood to the brain as well as gradual reperfusion rates that more closely mimics the reperfusion in humans5-7. On the other hand, the ET-1 model has disadvantages that include the need for a craniotomy, as well as higher variability in stroke volume8. This variability can be reduced with the use of laser Doppler flowmetry (LDF) to verify cerebral ischemia during ET-1 infusion. Factors that affect stroke variability include precision of infusion and the batch of the ET-1 used6. Another important consideration is that although reperfusion is a common occurrence in human stroke, the duration of occlusion for ET-1 induced MCAO may not closely mimic that of human stroke where many patients have partial reperfusion over a period of hours to days following occlusion9, 10. This protocol will describe in detail the ET-1 induced MCAO model for ischemic stroke in rats. It will also draw attention to special considerations and potential drawbacks throughout the procedure.

Several animal models of cerebral ischemia have been developed to simulate the human condition of stroke. This protocol describes the endothelin-1 (ET-1) induced middle cerebral artery occlusion (MCAO) model for ischemic stroke in rats. In addition, important considerations, advantages, and shortcomings of this model are discussed.

אנדותלין-1 דגם מושרה מזרח מוחות עורקים ספיגים לשבץ איסכמי עם הדרכת Flowmetry ליזר דופלר בעכברוש

Stroke is the number one cause of disability and third leading cause of death in the world, costing an estimated $70 billion in the United States in ...

Angiogenesis in the Ischemic Rat Lung

The adult lung is perfused by both the systemic bronchial artery and the entire venous return flowing through the pulmonary arteries. In most lung pathologies, it is the smaller systemic vasculature that responds to a need for enhanced lung perfusion and shows robust neovascularization. Pulmonary vascular ischemia induced by pulmonary artery obstruction has been shown to result in rapid systemic arterial angiogenesis in man as well as in several animal models. Although the histologic assessment of the time course of bronchial artery proliferation in rats was carefully described by Weibel 1, mechanisms responsible for this organized growth of new vessels are not clear. We provide surgical details of inducing left pulmonary artery ischemia in the rat that leads to bronchial neovascularization. Quantification of the extent of angiogenesis presents an additional challenge due to the presence of the two vascular beds within the lung. Methods to determine functional angiogenesis based on labeled microsphere injections are provided.

The lung is perfused by both the systemic bronchial artery and pulmonary arteries. In most lung pathologies, it is the smaller systemic vasculature that shows robust neovascularization. Cessation of pulmonary blood flow promotes brisk bronchial angiogenesis. We provide surgical details of inducing left pulmonary artery ischemia that promotes bronchial neovascularization.

באנגיוגנזה ריאות עכברוש איסכמי

The  adult lung is perfused by both the systemic bronchial artery and the entire  venous return flowing through the pulmonary arteries. In most lung ...

Murine Model of Wound Healing

Wound healing and repair are the most complex biological processes that occur in human life. After injury, multiple biological pathways become activated. Impaired wound healing, which occurs in diabetic patients for example, can lead to severe unfavorable outcomes such as amputation. There is, therefore, an increasing impetus to develop novel agents that promote wound repair. The testing of these has been limited to large animal models such as swine, which are often impractical. Mice represent the ideal preclinical model, as they are economical and amenable to genetic manipulation, which allows for mechanistic investigation. However, wound healing in a mouse is fundamentally different to that of humans as it primarily occurs via contraction. Our murine model overcomes this by incorporating a splint around the wound. By splinting the wound, the repair process is then dependent on epithelialization, cellular proliferation and angiogenesis, which closely mirror the biological processes of human wound healing. Whilst requiring consistency and care, this murine model does not involve complicated surgical techniques and allows for the robust testing of promising agents that may, for example, promote angiogenesis or inhibit inflammation. Furthermore, each mouse acts as its own control as two wounds are prepared, enabling the application of both the test compound and the vehicle control on the same animal. In conclusion, we demonstrate a practical, easy-to-learn, and robust model of wound healing, which is comparable to that of humans.

A murine model of cutaneous wound healing that can be used to assess therapeutic compounds in physiological and pathophysiological settings.

מודל עכברי של ריפוי פצע

Wound healing and repair are the most complex biological processes that occur in human life. After injury, multiple biological pathways become activated. ...

Ischemic Tissue Injury in the Dorsal Skinfold Chamber of the Mouse: A Skin Flap Model to Investigate Acute Persistent Ischemia

Despite profound expertise and advanced surgical techniques, ischemia-induced complications ranging from wound breakdown to extensive tissue necrosis are still occurring, particularly in reconstructive flap surgery. Multiple experimental flap models have been developed to analyze underlying causes and mechanisms and to investigate treatment strategies to prevent ischemic complications. The limiting factor of most models is the lacking possibility to directly and repetitively visualize microvascular architecture and hemodynamics. The goal of the protocol was to present a well-established mouse model affiliating these before mentioned lacking elements. Harder et al. have developed a model of a musculocutaneous flap with a random perfusion pattern that undergoes acute persistent ischemia and results in ~50% necrosis after 10 days if kept untreated. With the aid of intravital epi-fluorescence microscopy, this chamber model allows repetitive visualization of morphology and hemodynamics in different regions of interest over time. Associated processes such as apoptosis, inflammation, microvascular leakage and angiogenesis can be investigated and correlated to immunohistochemical and molecular protein assays. To date, the model has proven feasibility and reproducibility in several published experimental studies investigating the effect of pre-, peri- and postconditioning of ischemically challenged tissue.

The window of the murine dorsal skinfold chamber presented visualizes a zone of acute persistent ischemia of a musculocutaneous flap. Intravital epi-fluorescence microscopy permits for direct and repetitive assessment of the microvasculature and quantification of hemodynamics. Morphologic and hemodynamic results can further be correlated with histological and molecular analyses.

פגיעה ברקמות איסכמי בהגבו skinfold לשכת העכבר: דגם דש עור לחקור איסכמיה מתמיד חריפה

Despite profound expertise and advanced surgical techniques, ischemia-induced complications ranging from wound breakdown to extensive tissue necrosis are ...

A Mouse Fetal Skin Model of Scarless Wound Repair

Early in utero, but not in postnatal life, cutaneous wounds undergo regeneration and heal without formation of a scar. Scarless fetal wound healing occurs across species but is age dependent. The transition from a scarless to scarring phenotype occurs in the third trimester of pregnancy in humans and around embryonic day 18 (E18) in mice. However, this varies with the size of the wound with larger defects generating a scar at an earlier gestational age. The emergence of lineage tracing and other genetic tools in the mouse has opened promising new avenues for investigation of fetal scarless wound healing. However, given the inherently high rates of morbidity and premature uterine contraction associated with fetal surgery, investigations of fetal scarless wound healing in vivo require a precise and reproducible surgical model. Here we detail a reliable model of fetal scarless wound healing in the dorsum of E16.5 (scarless) and E18.5 (scarring) mouse embryos.

During mammalian development, early gestational skin wounds heal without a scar. Here we detail a reliable and reproducible model of fetal scarless wound healing in the cutaneous dorsum of E16.5 (scarless) and E18.5 (scarring) mouse embryos.

דגם עור עכבר עוברי של תיקון פצע צלקות

Early in utero, but not in postnatal life, cutaneous wounds undergo regeneration and heal without formation of a scar. Scarless fetal wound healing occurs ...

Rat Model of Photochemically-Induced Posterior Ischemic Optic Neuropathy

Posterior Ischemic optic neuropathy (PION) is a sight-devastating disease in clinical practice. However, its pathogenesis and natural history have&#160;remained poorly understood. Recently, we developed a reliable, reproducible animal model of PION and tested the treatment effect of some neurotrophic factors in this model1. The purpose of this video is to demonstrate our photochemically induced model of posterior ischemic optic neuropathy, and to evaluate its effects with retrograde labeling of retinal ganglion cells. Following surgical exposure of the posterior optic nerve, a photosensitizing dye, erythrosin B, is intravenously injected and a laser beam is focused onto the optic nerve surface. Photochemical interaction of erythrosin B and the laser during irradiation damages the vascular endothelium, prompting microvascular occlusion mediated by platelet thrombosis and edematous compression. The resulting ischemic injury yields a gradual but pronounced retinal ganglion cell dieback, owing to a loss of axonal input - a remote, injury-induced and clinically relevant outcome. Thus, this model provides a novel platform to study the pathophysiologic course of PION,&#160;and can be further optimized for testing therapeutic approaches for optic neuropathies as well as other CNS ischemic diseases.

The goal of this protocol is to photochemically induce ischemic injury to the posterior optic nerve in rat. This model is critical to studies of the pathophysiology of posterior ischemic optic neuropathy, and therapeutic approaches for this and other optic neuropathies, as well as of other CNS ischemic diseases.

מודל עכברוש של אחורי איסכמי אופטי נוירופתיה המושרית photochemically

Posterior Ischemic optic neuropathy (PION) is a sight-devastating disease in clinical practice. However, its pathogenesis and natural history ...

A Piglet Model of Neonatal Hypoxic-Ischemic Encephalopathy

Birth asphyxia, which causes hypoxic-ischemic encephalopathy (HIE), accounts for 0.66 million deaths worldwide each year, about a quarter of the world&#8217;s 2.9 million neonatal deaths. Animal models of HIE have contributed to the understanding of the pathophysiology in HIE, and have highlighted the dynamic process that occur in brain injury due to perinatal asphyxia. Thus, animal studies have suggested a time-window for post-insult treatment strategies. Hypothermia has been tested as a treatment for HIE in pdiglet models and subsequently proven effective in clinical trials. Variations of the model have been applied in the study of adjunctive neuroprotective methods and piglet studies of xenon and melatonin have led to clinical phase I and II trials1,2. The piglet HIE model is further used for neonatal resuscitation- and hemodynamic studies as well as in investigations of cerebral hypoxia on a cellular level. However, it is a technically challenging model and variations in the protocol may result in either too mild or too severe brain injury. In this article, we demonstrate the technical procedures necessary for establishing a stable piglet model of neonatal HIE. First, the newborn piglet (&#60; 24 hr old, median weight 1500 g) is anesthetized, intubated, and monitored in a setup comparable to that found in a neonatal intensive care unit. Global hypoxia-ischemia is induced by lowering the inspiratory oxygen fraction to achieve global hypoxia, ischemia through hypotension and a flat trace amplitude integrated EEG (aEEG) indicative of cerebral hypoxia. Survival is promoted by adjusting oxygenation according to the aEEG response and blood pressure. Brain injury is quantified by histopathology and magnetic resonance imaging after 72 hr.

Hypoxic-ischemic encephalopathy following perinatal asphyxia can be studied using animal models. We demonstrate the procedures necessary for establishing a piglet model of neonatal hypoxic-ischemic encephalopathy.

דגם חזרזיר של ילודים חוסר חמצן-איסכמי אנצפלופתיה

Birth asphyxia, which causes hypoxic-ischemic encephalopathy (HIE), accounts for 0.66 million deaths worldwide each year, about a quarter of the ...

The Rodent Model of Nonarteritic Anterior Ischemic Optic Neuropathy (rNAION)

Nonarteritic anterior ischemic optic neuropathy (NAION) is a focal ischemic lesion of the optic nerve that affects 1/700 individuals throughout their lifetime. NAION results in optic nerve edema, selective loss of the retinal ganglion cell neurons (RGCs) and atrophy of the optic nerve. A rodent model of NAION that expresses most NAION features and sequelae has been developed, which is applicable to both rats and mice. This model utilizes a focal laser application of 532 nm wavelength to illuminate a photoactive dye, Rose Bengal (RB), to cause capillary damage and leakage at the targeted anterior optic nerve (the laminar region). After rNAION induction, there is an early optic nerve ischemia, optic nerve edema, and intraneural inflammation, followed by selective RGC and axonal loss. Since the optic nerve is a CNS white matter tract, the rNAION model is applicable to mechanistic studies of selective white matter ischemia, as well as neuroprotective analyses and short and long-term mechanisms of glial and neuronal response to ischemia.

The Rodent Model of Nonarteritic Anterior Ischemic Optic Neuropathy rNAION

The following report describes how to replicate the rodent model of nonarteritic anterior ischemic optic neuropathy (rNAION), using the appropriate dye, contact lens and laser parameters. We also reveal the appropriate steps for evaluating the rNAION lesion in vivo.

המודל המכרסם של Nonarteritic Anterior Ischemic Optic נוירופתיה (rNAION)

Nonarteritic anterior ischemic optic neuropathy (NAION) is a focal ischemic lesion of the optic nerve that affects 1/700 individuals throughout their ...