Renal Disease Techniques and Protocols Edited by Michael S. Goligorsky, MD, PhD M E T H O D S I N M O L E C U L A R M E D I C I N E TM Renal Disease Techniques and Protocols Edited by Michael S. Goligorsky, MD, PhD Animal Care in Biological Experiments 3 3 1 Standards of Animal Care in Biological Experiments Ellen M. Levee 1. Introduction The use of animals is a necessary component of experimentation. The utiliza- tion of animals is a privilege not a right. Therefore, certain guidelines must be maintained in order to ensure their humane care and use. This chapter includes the basic principles of animal care and use, and reviews various procedures that are specific to renal experimentation. Our goal is also to provide guidance to the knowledgeable neophyte and serve as a refresher for the seasoned researcher. Individuals who are conducting research that involves animal use should enlist the help and guidance of the laboratory animal professional(s) at their respective institutions. Guidance may be provided by an institutional program or individual mentoring, but is a regulatory requirement that must be fulfilled. Proper care and use of animals will provide the investigator with the best scientific results. Unwanted variables in experimental procedures may result from improper care and use, and may confound results. Rodents are the most commonly used animal for experimental procedures. In light of the evolving transgenic technology, this trend will most likely continue. The use of animals in research is closely regulated by various government and granting agencies. Standards of appropriate animal care and use are set forth in the Guide for the Care and Use of Laboratory Animals, commonly known as the Guide, and the Animal Welfare Act. The Institutional Animal Care and Use Committee (IACUC) must approve any work involving the use of animals. The IACUC is the oversight committee mandated by law to ensure the humane care and use of animals at each institution (see Note 1). 2. Materials 2.1. Rodent Survival Surgery Sterile surgical instruments (depending on the surgery) and suture and hemostatic materials. From: Methods in Molecular Medicine, vol. 86: Renal Disease: Techniques and Protocols Edited by: M. S. Goligorsky © Humana Press Inc., Totowa, NJ 01/Leve/001-012/F5.5.03 5/5/03, 10:52 AM3 4 Levee 2.2. Anesthetics 2.2.1. Preemptive and Postoperative Analgesics Available for Rodents 1. Morphine: 10 mg/kg SQ q 6–12 h. 2. Buprenorphine: 1 mg/kg SQ q 12 h. 3. Meperidine: 20 mg/kg SQ or im q 8–12 h. 4. Acetaminophen: 100–300 mg/kg PO q 4 h. 2.2.2. Commonly Used and Approved Anesthetics for Rodents 1. Pentobarbital sodium: 35–45 mg/kg intraperitoneal (ip) or intravenous (iv) for rats and guinea pigs; 60–90 mg/kg ip or iv for mice, gerbils and hamsters. 2. Ketamine HCL: 60–90 mg/kg im in all rodents but requires the addition of xylazine (4–8 mg/kg im) or acepromazine (1–2.5 mg/kg im) for anesthetic plane. 3. Inhalant anesthetic agents (isoflurane, halothane) may be used to effect in a properly vented hood. 3. Methods 3.1. Housing The proper housing of laboratory animals is important in order to eliminate the effects of unwanted variables and to maintain animals in a disease-free state. In today’s animal research environment, the quality of laboratory ani- mals is such that most rodent pathogens and genetic manipulation cause little overt clinical signs but may have profound or unexpected effects on research outcome. The Guide addresses the appropriate standards of animal care for many of the species used in research. Cage size, bedding material, cage sani- tation, temperature, relative humidity, and photoperiod are all parameters that must be controlled in order to produce sound scientific results. All animal room lights should be on a timer. Light:Dark cycles may be either 12:12 or 14:10, depending upon the type of animal work being done. Reversed light cycles are indicated at times. Species-specific metabolism caging may be used for the collection of urine and feces. The principle of the metabolism cage is to house the animal in a cage with a wire grid floor. The cage is set on a funnel device so that the urine falls onto the sides of the funnel and is chan- neled into a collection container. The feces drop into a collecting jar. Feeding and watering compartments are constructed in a way that prevents the food and water from significantly contaminating the urine or feces. For collection of small amounts of urine in rodents, it may suffice to rapidly remove the rodent and place the urethral opening over a collecting tube. Rodents fre- quently urinate upon being handled. Gentle manual expression of the bladder may also be employed. 01/Leve/001-012/F5.5.03 5/5/03, 10:52 AM4 Animal Care in Biological Experiments 5 3.2. Fasting and Water Restriction The practices of fasting or water restriction may be required for some experimental protocols. These states must be scientifically justified in the ani- mal use proposal. All animals that undergo water restriction or fasting must be closely monitored by the investigator. Behavioral and physiological parameters that will be recorded must be established by the research team before the onset of the experiment. Hydration levels and weight loss should be closely followed (see Note 2). 3.3. Blood Collection Blood collection in the rodent may be performed from various sites. The volume of blood in all animals is 60–80 mL/kg. Ten percent of the total vol- ume can be removed from the animal without causing any detrimental effects. As a general rule, the smallest volume possible should be removed. The fre- quency of the removal of blood is another consideration that should be addressed in the experimental design. Sterile technique and proper training of the animal handler are essential for a successful outcome. Light anesthesia must be employed in the collection of blood from all sites except the tail vein. The method of cardiac puncture should be reserved for terminal bleeds. Indwelling catheters may be used for serial blood withdrawals. The following are acceptable sites for blood withdrawal in the lightly anesthetized rodent: retro-orbital sinus (mouse) or ophthalmic venous plexus (rat), the jugular vein (rat), and nail clipping. 3.4. Protocols Because the majority of animal models in research are rodents, the remain- der of this chapter focuses on procedures that utilize rodents in general, as well as renal-based investigations. 3.4.1. Rodent Survival Surgery This should be carefully planned in order to ensure adequate time for both the procedure and postoperative recovery time. All materials should be pre- pared in advance. Rodents should undergo an acclimation period upon arrival to the facilities before any manipulations are performed. Animals should be acquired from approved sources and should be free of disease. The personnel performing the surgical procedures should be well-trained in the technique as well as proper handling of the animal in general. A balanced anesthetic regi- men should allow for an appropriate surgical plan, yet should not interfere with the experiment being carried out. Preemptive and postoperative analgesia should be considered as part of the surgical plan and IACUC review process, 01/Leve/001-012/F5.5.03 5/5/03, 10:52 AM5 6 Levee and should be tailored to the procedure involved. It is imperative to maintain sufficient animal records, including anesthetic doses, intra-operative notes, and postoperative care. It is generally unnecessary to withhold food and water pre- operatively from rodents. A model protocol for survival rodent surgery, which is consistent with inter- pretation of the guidelines and which provides satisfactory aseptic conditions, is indicated here: 1. Surgery should be conducted on a clean, uncluttered lab bench or table surface. The surface should be wiped with a disinfectant before and after use, and/or cov- ered with a clean drape. 2. Hair should be removed from the surgical site with clippers or a depilatory. The surgical site should be treated first with an antiseptic scrub and then with an antiseptic solution (chlorhexidine or povidone iodine scrub and solution). 3. All instruments should be sterilized, but the surgical instruments or devices being used may determine the method of choice. Fine-gauge catheters may be steril- ized with ethylene oxide. Acceptable techniques for cold sterilization include soaking in 2% glutaraldehyde for 10 h, in 8% formaldehyde and 70% alcohol for 18 h, or in 6% stabilized hydrogen peroxide for 6 h (2). Glass bead sterilizers may be used to maintain instrument sterility in multiple rodent surgery or after cold sterilization. 4. The surgeon should wash his hands with an antiseptic surgical scrub preparation and then aseptically put on gloves. If working alone, the surgeon should have the animal anesthetized and positioned, and have the first layer of the double-wrapped instrument pack opened before putting on sterile gloves. 5. The surgeon should wear a face mask. A cap and sterile gown are recommended, but not required. 6. Multiple surgeries present special problems. After the first surgery, the sterilized instruments may be kept in a sterile tray containing cold sterilizing agent or in an ultrasonic sterilizer or a bead sterilizer (the preferred method). The sterilizing agent should be replaced when contaminated with blood or other body fluids. Sterile gloves should be changed between surgeries. 7. The abdominal or thoracic body wall should be closed with absorbable suture material. The skin should be closed with staples, a nonabsorbable suture mate- rial, or the newer absorbable skin sutures in a simple interrupted pattern. Skin sutures or staples should be removed 7–10 d after surgery. 8. Rodents should be recovered from anesthesia in a warmed environment. Anti- biotics should not be given routinely after surgery unless justified by the spe- cific procedure. 3.5. Specific Survival Surgical Procedures 3.5.1. Chronic Catheterization of Blood Vessels Chronic catheterization of blood vessels is often necessary in order to administer test materials or obtain serial blood samples. The jugular vein, 01/Leve/001-012/F5.5.03 5/5/03, 10:52 AM6 Animal Care in Biological Experiments 7 carotid artery, tail vein, and femoral artery all lend themselves to chronic cath- eterization (see Note 3). 3.5.1.1. JUGULAR VEIN CATHETERIZATION 1. The rat is anesthetized and placed on its back with its head toward the surgeon. The surgical site is prepared as previously described. 2. An incision is made parallel to and on one side of the midline in the neck of the rat. 3. The jugular vein is located (right external jugular vein) and is gently cleaned of fat and tissue using blunt dissection. The vein should be cleared of extraneous tissue of a length of at least 1.5 cm leading to the point where it passes under- neath the pectoral muscle. Care must be taken not to handle the vein in order to prevent tearing and spasms from occurring. 4. A pair of small or jeweler’s forceps is passed under the vein, and a doubled piece of suture is passed beneath the vein and cut into two pieces. 5. The anterior tie is gently moved cranially as far as possible along the “cleaned” vessel. The suture is then tied to occlude the vessel. 6. The posterior tie is moved gently toward the pectoral muscle, allowing several millimeters between it and the anterior ligature. The first throw of the posterior ligature is done, but it is left loosely around the vein. 7. Next, the jugular vein is lightly lifted by using an opened small or jeweler’s for- ceps under it, or gently lifting the ends of the posterior ligature vertically. 8. A small incision is made in the vein to allow introduction of the catheter (i.d. ~0.5 mm and o.d. ~0.6–1 mm) toward the heart. The opening may be enlarged with a forceps, or a catheter introducer may be employed. If blood is to be withdrawn or blood pressure measured via the catheter, then the tip of the cath- eter should be advanced until it lies within the superior vena cava or right atrium. If test materials are to be injected, then only a few millimeters of cath- eter are needed to lie within the vein. 9. The catheter is tested for patency by withdrawing a small amount of blood via a syringe filled with saline. If the catheter is patent, the blood is flushed back into the catheter and the catheter is filled with the heparin/saline lock solution (20 U heparin/1 mL saline). A stainless steel pin is placed in the end of the catheter. Care must be taken to avoid introducing air into the catheter or vein. The poste- rior ligature is then tied around the vein and catheter. 10. The catheter is fixed to the fascia with a suture. A tension or stress loop should be placed, allowing slack in order to compensate for the animal’s movements. This loop helps avoid the catheter from being displaced. 11. The rat is then placed in lateral recumbency, and the dorsal nape of the neck is aseptically prepared. 12. A small incision is made in the nape of the neck. A 16 gauge trocar or a straight forceps is passed through the incision which travels subcutaneously down the side of the neck and exits anterior to the site of entry of the catheter into the jugular vein. The end of the catheter is then grasped by the forceps or passed through the trocar, and passed subcutaneously to the incision at the nape of the neck. 01/Leve/001-012/F5.5.03 5/5/03, 10:52 AM7 8 Levee 13. The catheter exits outside the incision at the nape of the neck, and is either stop- pered or attached outside the cage to an infusion pump. The two skin incisions are then closed using interrupted sutures. 14. Proper catheter maintenance requires daily flushing with fresh heparin/saline solution. 3.5.1.2. CAROTID ARTERY CATHETERIZATION 1. The rat is anesthetized and placed on its back with its head toward the surgeon. The surgical site is prepared as previously described. 2. An incision is made parallel to and on one side of the midline in the neck of the rat. 3. The carotid artery is located medial to and below the jugular vein. The carotid artery (left carotid artery) is gently cleaned of fat and tissue using blunt dissec- tion between the omohyoid, sternomastoid, and sternohyoid muscles. Care should be taken to avoid damaging the vagus nerve. The artery should be cleared of extraneous tissue of a length of at least 1.5 cm. 4. A pair of small or jeweler’s forceps is passed under the artery, and a doubled piece of suture is passed beneath the vessel and cut into two pieces. 5. The anterior tie is gently moved cranially as far as possible along the “cleaned” vessel. The suture is then tied to occlude the vessel. 6. The posterior tie is moved gently several millimeters from the anterior ligature. The first throw of the posterior ligature is done, but it is left loosely around the artery. 7. The vessel is then lightly lifted, either by using an opened small or jeweler’s forceps under it or gently lifting the ends of the posterior ligature vertically. An aneurysm clamp is used to occlude the carotid at the most distal point. 8. A small stab incision is made in the artery to allow the catheter to be gently forced through it. 9. The posterior ligature is then tied around the carotid artery and catheter. The cath- eter is advanced toward the heart after removing the aneurysm clamp. The tip of the catheter should lie in the aortic arch. 10. The catheter is then fixed to the fascia via suture. A tension or stress loop should be placed, allowing slack in order to compensate for the animal’s movements. This loop helps avoid displacement of the catheter. 11. The catheter is exteriorized through the dorsal nape of the neck as described for the jugular vein catheterization prepared. 3.5.1.3. FEMORAL ARTERY CATHETERIZATION 1. The rat is anesthetized and placed on its back with its head toward the surgeon. The surgical site is prepared as previously described. 2. An incision is made on the proximal medial surface of the hind limb, extending into the groin area. 3. The femoral artery is located in the groin region. The femoral artery is gently separated from the femoral vein and nerve by blunt dissection. The artery should be cleared of extraneous tissue for several millimeters. 01/Leve/001-012/F5.5.03 5/5/03, 10:52 AM8 Animal Care in Biological Experiments 9 4. A pair of small or jeweler’s forceps is passed under the artery, and a doubled piece of suture is passed beneath the vessel and cut into two pieces. 5. The posterior tie is gently moved distally as far as possible along the “cleaned” vessel. The suture is then tied to occlude the vessel. 6. The anterior tie is moved gently several millimeters from the anterior ligature. The first throw of the anterior ligature is done, but it is left loosely around the artery. 7. An aneurysm clamp is used to occluded the artery anterior to the ligature. 8. A small stab incision is made in the artery to allow the catheter to be gently forced through it. 9. The anterior ligature is then tied around the artery and catheter. The catheter is advanced toward the body after removing the aneurysm clamp. The tip of the catheter should lie in the dorsal aorta. 10. The catheter is then fixed to the fascia via suture. A tension or stress loop should be placed, allowing slack in order to compensate for the animal’s movements. This loop helps to avoid the catheter from being displaced. 11. The catheter is passed subcutaneously along the body and exteriorized through the dorsal nape of the neck as described for the jugular-vein catheterization. 3.5.2. Nephrectomy 3.5.2.1. UNILATERAL NEPHRECTOMY Nephrectomized rats normally do well with one kidney. The remaining kid- ney undergoes hypertrophy. 1. The rat is anesthetized and placed in ventral recumbency. The surgical site is prepared as previously described. 2. A dorsoventral incision is made posterior to the costal border of the thorax. This incision should penetrate the abdominal cavity. 3. Using the perirenal fat in order to grasp the kidney, it is freed of its connective tissue and exteriorized from the abdominal cavity. 4. The adrenal gland is located at the anterior pole of the kidney, is detached from the kidney by blunt dissection of its attachments, and is replaced in the abdomi- nal cavity. 5. A suture is placed around the renal vessels and ureter as far as possible toward the midline without occluding any collateral vessels. The suture is securely tied around the vessels and the ureter. 6. The vessels and ureter are transected next to the kidney. The kidney is removed and discarded. 7. The incision is closed in layers, using a simple interrupted suture pattern. 3.5.2.2. 5/6 NEPHRECTOMY This technique is used to induce a model of chronic renal failure. 1. The rat is anesthetized and placed in ventral recumbency. The surgical site is prepared as previously described. 01/Leve/001-012/F5.5.03 5/5/03, 10:52 AM9 10 Levee 2. A dorsoventral incision is made posterior to the costal border of the thorax. This incision should penetrate the abdominal cavity. 3. Using the perirenal fat in order to grasp the kidney, it is freed of its connective tissue and exteriorized from the abdominal cavity. 4. The adrenal gland is located at the anterior pole of the kidney, is detached from the kidney by blunt dissection of its attachments, and is replaced in the abdomi- nal cavity. 5. The anterior and posterior poles, along with much of the cortical tissue, are removed using a scalpel. 6. The remaining renal tissue is wrapped in hemostatic gauze and returned to the abdominal cavity. The remaining kidney tissue hypertrophies. 7. The incision is closed in layers, using a simple interrupted suture pattern. 8. Two weeks following the initial surgery, the contralateral kidney is removed following the procedure described for the unilateral nephrectomy. 4. Notes 1. The CEO or Institutional Official following membership guidelines promulgated by regulations appoints the IACUC members. The IACUC reviews, approves, requests modifications, or denies approval of all proposals for laboratory use of animals. The IACUC also reviews the institution’s program of care and use on a semi-annual basis and inspects the animal facilities. The animal use proposal must address specific concerns including rationale for the use of animals, as well as the chosen species; justification of the proposed number of animals to be used; a detailed description of the all procedures to be performed; the qualifica- tions and training of personnel; a literature search for alternatives to procedures that may potentially cause pain or distress; the method of euthanasia, and the use of appropriate anesthetics and analgesics when indicated. A program of Animal Care and Use must involve a veterinarian with specific training and experience in the use of animals for research purposes. The investigator should solicit the help of the attending veterinarian in developing an accurate, thorough animal use pro- posal. The role of the laboratory animal facility staff and the IACUC is that of facilitator, and their collective knowledge should be drawn upon. 2. In water restriction studies, states of dehydration may lead to decreased con- sumption of food and should be considered in the experimental design. 3. Consideration regarding the choice of catheter should include thromboresistant construction, readily sterilized to reduce the chance of infection, easily inserted, stable longevity, and expediency factors. Bonding techniques to impregnate the catheter with anticoagulants and/or antibiotics may be employed. A heparin/ saline lock will further diminish the chance of a thrombus block of the catheter. Acknowledgment Special thanks to Mark M. Klinger, DVM, DipACLAM, for his review and suggestions to this chapter. 01/Leve/001-012/F5.5.03 5/5/03, 10:52 AM10 Animal Care in Biological Experiments 11 References 1. Guide for the Care and Use of Laboratory Animals, U.S. Dept. of Health and Human Services, Public Health Service, National Institutes of Health, Publication No. 85–23, Revised 1996. 2. Simmons, B. P. (1983) CDC guidelines for the prevention and control of nosoco- mial infections. Am J. Infect. Control 11(13). 3. Wyatt, J. (1989) An institutional protocol for aseptic technique on survival sur- gery of rodents. Synapse 22(1), 10–14. 4. Waynforth, H. B. and Flecknell, P. A. (1992) Experimental and Surgical Tech- niques in the Rat, 2nd ed., Academic Press Limited, San Diego, CA, pp. 212–233. 01/Leve/001-012/F5.5.03 5/5/03, 10:52 AM11 [...]... the thymus and spleen underwent massive apoptotic involution The early mortality of the mutants was caused by renal failure resulting from a severe PKD The presence of dilated proximal and distal tubular segments and hyperproliferation of epithelium and interstitium characterized the renal cystic disease (32) Cystic kidneys from bcl-2–/– mice displayed nuclear localization of β-catenin and a loss of... of hypertension, insulin resistance, and hyperlipidemia (1), and is often accompanied by obesity (2,3) We selected the metabolic syndrome because: i) the metabolic syndrome is a prototypical web-of-causality disease; ii) the metabolic syndrome is a leading cause of morbidity and mortality in From: Methods in Molecular Medicine, vol 86: Renal Disease: Techniques and Protocols Edited by: M S Goligorsky... and fed state, plasma glucose and insulin levels are higher in 38-wk-old male obese, compared with lean ZSF1 rats (Fig 3) Moreover, male obese ZSF1 rats are more glucosuric compared with male lean ZSF1 rats (Fig 4) and more polyuric compared with age-matched male WKY, SHR, and lean and obese SHHF/Mcc-facp (Table 2) 03/Jack/029-046/F 35 4/21/03, 10:00 AM 36 Tofovic and Jackson Fig 2 Plasma glucose and. .. renal cilia and their relationship to cystic disease (30) 3.2 SBM Mouse The SBM transgenic mice carry a fusion gene that includes the SV40 enhancer, the β-globin promoter, and the c-myc coding region, which is expressed at high levels in the renal tubular epithelium These transgenic mice develop markedly enlarged kidneys, runting, and muscular atrophy The cysts are scattered throughout the cortex and. .. both adult and pediatric patients PKD can be either inherited as a dominant (ADPKD) or a recessive trait (ARPKD) or acquired The disease is characterized by massive renal enlargement associated with the growth of fluid-filled intrarenal cysts ADPKD, the most common cystic disease, is caused by mutations at three distinct loci: PKD1, PKD2, and PKD3 The PKD1 locus was mapped to human Chr 16p13.3, and the... demonstrated a reduced activity, expression, and altered distribution of SHP-2 and PTP 1B The altered regulation of PTP 1B and SHP-2 in kidneys from bcl-2–/– mice correlated with sustained phosphorylation of FAK and paxillin Taken together, the renal cyst formation in the bcl-2–/– mice is believed to be a result of improper cell–cell interactions that interferes with renal maturation by continued activation... of renal cilium Am J Physiol Renal Physiol 282, F541–F552 31 Trudel, M., Barisoni, L., Lanoix, J., and D’Agati, V (1998) Polycystic kidney disease in SBM transgenic mice: role of c-myc in disease induction and progression Am J Pathol 152, 219–229 32 Veis, D J., Sorenson, C M., Shutter, J R., and Korsmeyer, S J (1993) Bcl-2deficiency mice demonstrate fulminant lymphoid apoptosis, polycystic kidneys, and. .. 33 Sorenson, C M and Sheibani, N (2002) Altered regulation of SHP-2 and PTP 1B tyrosine phosphatases in cystic kidneys from bcl-2 -/- mice Am J Physiol Renal Physiol 282, F442–F450 34 Somlo, S and Markowitz, G S (2002) The pathogenesis of autosomal dominant polycystic kidney disease: an update Curr Opin Nephrol Hypertens 4, 385–394 35 Calvet, J P and Grantham, J J (2001) The genetics and physiology of... ADPKD develop renal, hepatic, and pancreatic cysts, abdominal and inguinal hernias, heart-valve defects, and aortic and cerebral aneurysms (1) ARPKD is encountered less frequently PKHD1, a locus on human Chr 6p21-cen that predisposes individuals to develop ARPKD, has been reported ARPKD patients primarily develop cysts in the collecting ducts, with hepatic fibrosis as an associated extrarenal manifestation... 03/Jack/029-046/F 29 4/21/03, 10:00 AM 30 Tofovic and Jackson modern societies (3,4); iii); the metabolic syndrome carries a high risk for renal disease (5,6) and iv) rat models of the metabolic syndrome are now readily available and reasonably well-described 2 A Brief History of the Development of Rat Models of the Metabolic Syndrome 2.1 Obese and Lean Zucker Rat In 1961, Zucker and Zucker (7) at the Laboratory of . Renal Disease Techniques and Protocols Edited by Michael S. Goligorsky, MD, PhD M E T H O D S I N M O L E C U L A R M E D I C I N E TM Renal Disease Techniques and Protocols Edited. instruments (depending on the surgery) and suture and hemostatic materials. From: Methods in Molecular Medicine, vol. 86: Renal Disease: Techniques and Protocols Edited by: M. S. Goligorsky ©. government and granting agencies. Standards of appropriate animal care and use are set forth in the Guide for the Care and Use of Laboratory Animals, commonly known as the Guide, and the Animal