A Reproducible Intensive Care Unit-Oriented Endotoxin Model in Rats

Summary

Here, we present a reproducible intensive care unit-oriented endotoxin model in rats.

Abstract

Sepsis and septic shock remain the leading cause of death in intensive care units. Despite significant improvements in sepsis management, mortality still ranges between 20 and 30%. Novel treatment approaches in order to reduce sepsis-related multiorgan failure and death are urgently needed. Robust animal models allow for one or multiple treatment approaches as well as for testing their effect on physiological and molecular parameters. In this article, a simple animal model is presented.

First, general anesthesia is induced in animals either with the use of volatile or by intraperitoneal anesthesia. After placement of an intravenous catheter (tail vein), tracheostomy, and insertion of an intraarterial catheter (tail artery), mechanical ventilation is started. Baseline values of mean arterial blood pressure, arterial blood oxygen saturation, and heart rate are recorded.

The injection of lipopolysaccharides (1 milligram/kilogram body weight) dissolved in phosphate-buffered saline induces a strong and reproducible inflammatory response via the toll-like receptor 4. Fluid corrections as well as the application of norepinephrine are performed based on well-established protocols.

The animal model presented in this article is easy to learn and strongly oriented towards clinical sepsis treatment in an intensive care unit with sedation, mechanical ventilation, continuous blood pressure monitoring, and repetitive blood sampling. Also, the model is reliable, allowing for reproducible data with a limited number of animals in accordance with the 3R (reduce, replace, refine) principles of animal research. While animal experiments in sepsis research cannot easily replaced, repetitive measurements allow for a reduction of animals and keeping septic animals anesthetized diminishes suffering.

Introduction

Sepsis and its more severe form, septic shock, are syndromes on the ground of an infection, resulting in an overshooting inflammatory reaction with the release of cytokines, leading to physiological and biochemical changes with a suppressed immune defense and fatal results^1,2. This unbalanced inflammatory reaction results in organ dysfunction and organ failure in various vital organs such as lung, kidney, and liver. With 37%³, sepsis is one of the most common reasons for a patient to be admitted to an intensive care unit (ICU). Mortality of sepsis currently ranges around 20-30%⁴. Early and effective antibiotic treatment is of utmost importance⁵. Fluid and vasopressor resuscitation need to be installed early, other than that, treatment is purely supportive⁶.

Sepsis is defined as a proven or suspected infection with bacteria, fungi, viruses, or parasites, which is accompanied by organ dysfunction. Septic shock criteria are met when a further cardiovascular collapse irresponsive to fluid treatment alone, and a lactate level of more than 2 millimole/liter is present². Sepsis related organ failure may occur in any organ, but is very common in the cardiovascular system, the brain, the kidney, the liver, and the lung. Most patients suffering from sepsis require endotracheal intubation to secure the patient's airway, to protect from aspiration, and to apply positive end expiratory ventilation with a high fraction of inspired oxygen to prevent or overcome hypoxia. In order to tolerate a tracheal tube and mechanical ventilation, patients usually require sedation.

Endotoxins, such as lipopolysaccharides (LPS) as a component of the membrane of gram negative bacteria induce a strong inflammatory reaction via the toll-like receptor (TLR) 4⁷. Activation of a defined pathway ensures a stable inflammatory reaction. Cytokines like cytokine induced neutrophil chemoattractant protein 1 (CINC-1), monocyte chemoattractant protein 1 (MCP-1), and interleukin 6 (IL-6) are known as prognostic factors for severity and outcome in this model⁸. Intravenous LPS application has been successfully used to study various aspects of sepsis in rats^8,9.

Treatment of sepsis is still a challenge, particularly due to the lack of predictive animal models. If endotoxemia with activation of systemic inflammation is an adequate model for the development of pharmacological therapies is debatable. However, with the well-known LPS-induced TLR 4 pathway important knowledge can be gained.

Protocol

All experiments presented in this protocol were approved by the Veterinary Authorities of the Canton Zurich, Switzerland (approval numbers 134/2014 and ZH088/19). Moreover, all steps performed in this experiment were in accordance with the Guidelines on Experiments with Animals by the Swiss Academy of Medial Sciences (SAMS) and Guidelines of the Federation of European Laboratory Animal Science Associations (FELASA).

1. Anesthesia induction and animal monitoring

1. Keep male Wistar rats with a weight of 250-300 gram (g) in ventilated cages under pathogen-free conditions. Provide a 12-12-hour light/dark cycle at an ambient temperature of 22 ± 1 °C, and free access to food and water.
2. Induce general anesthesia either by volatile induction with isoflurane (concentration of 3-5%) in an anesthesia induction box for 30 seconds (Figure 1A) or alternatively, induce anesthesia with a single-shot injection of ketamine/xylazine (10/1 milligram (mg) per 100 g body weight).
3. Transfer the animal to a working place and lay the animal on a heating-mat throughout the entire experiment. Keep the body-temperature between 36.5 and 37 °C.
4. Use a nosecone to provide oxygen (600 mL/minute). Add isoflurane 2-3% if volatile anesthesia was chosen for anesthesia maintenance. Make sure that the animal is spontaneously breathing.
5. Confirm the level of anesthesia by the absence of the toe-pinch reflex prior to the installation of tracheostomy and arterial and venous catheters.
6. Verify a sufficient oxygenation by peripheral oxygen saturation monitoring (normal oxygen saturation 98 - 100%).
7. Use an ointment (Vitamin A ointment) to protect the eyes.
8. Prepare sterile surgical instruments and catheters on a side table as displayed in Figure 1B.
9. Additionally, prepare pressure and oxygen saturation monitoring as displayed in Figure 1C.

2. Intravenous access

1. Apply a tourniquet at the rat's proximal tail to facilitate venous access (Figure 2A).
2. Disinfect the tail 3 times with alcohol.
3. Induce a G26 intravenous catheter into one of the two lateral tail veins.
   NOTE: From our experience it is easier to place the intravenous access at the distal part of the rat's tail, because the vein here is located closer to the skin. In addition, in case of a failed cannulation, there is enough space to move proximally.
4. Strictly avoid air injection.
5. Untie the tourniquet after placing the intravenous catheter.
6. Fix the intravenous catheter in place with adhesive tape (Figure 2B).
7. Connect syringe-pumps to the intravenous access for continuous fluid and drug application.
8. Use 3-way stopcocks for bolus fluid, drug application, and venous blood sampling.

3. Tracheostomy

1. Shave the animal's anterior neck-area.
2. Disinfect the shaved skin 3 times with providone-iodine solution.
3. Perform a circa 2 cm longitudinal incision using a scalpel (with a blade number 10).
4. Retract the skin with 2-0 silk sutures.
5. Bluntly prepare the larynx and the trachea with surgical scissors (Figure 3A).
6. Make sure to open the trachea with surgical micro scissors at the 3-5^th tracheal clasp.
7. Insert a sterile tracheal cannula into the trachea. Be careful, do not insert the cannula too deeply in order to avoid unilateral ventilation.
8. Fix the cannula in place using a 2-0 silk suture.
9. Connect the cannula to a ventilator for pressure or volume-controlled ventilation (Figure 3B).

4. Arterial access

1. Disinfect the rat tail 3 times with povidone-iodine solution.
2. Cut the skin using a scalpel (with a blade number 10) circa 1 cm longitudinally at the ventral side.
3. Take care, do not cut too deeply to avoid an injury of the tail artery.
4. Use a surgical microscope to expose the artery carefully. Cut the fascia surrounding the artery with surgical micro scissors.
5. Ligate the distal part of the artery using a 6-0 silk suture.
6. Prepare a proximal 6-0 silk suture but do not tighten the silk (Figure 4A).
7. Introduce a G-26 catheter into the artery between the distal and proximal silk suture.
8. Once the catheter is in the artery, tighten the proximal silk suture and fix the catheter in place (Figure 4B).
9. Connect the catheter to a pressure transducer to provide continuous arterial pressure measurement (normal mean arterial pressure: 60 - 100 mmHg) (Figure 4C).
10. Additionally, place a 3-way stopcock between the catheter connected to the pressure transducer and the G-26 catheter for arterial blood sampling.

5. Baseline measurement, sepsis induction and follow-up measurements

1. After the animal reached a steady state, inject the LPS.
2. Collect blood samples when a steady state is reached (usually after 15-30 minutes).
3. Replace fluid loss from blood samples by Ringer's solution in a ratio of 1:4.
4. To induce sepsis, inject the LPS as a bolus or as a continuous LPS application.
5. For the bolus application, inject 1 mg of LPS/kilogram body weight (kg) dissolved in phosphate buffered saline (PBS) at a concentration of 1 mg/mL.
6. For continuous application, inject 300 µg of LPS/kg/hour throughout the entire experiment using a syringe pump (stock solution of LPS: 1 mg/mL in PBS).
7. Avoid air-injection at all times in order to prevent air embolism.
8. Define fluid replacement protocols, vasoconstrictor application protocols, and abortion criteria (for example hypotension defined as a mean arterial blood pressure below 50 mmHg for more than 30 minutes despite fluid replacement) before setting up the experiment.
   NOTE: We suggest a continuous infusion of Ringer's solution at a rate of 10 mL/kg/hour.
9. Subtract any continuous administration of fluids (e.g., for continuous LPS application) from the amount infused so that the results are comparable with those of the control groups.
   NOTE: At the end of the experiment, and prior to harvesting any organs such as liver, kidney or spleen for further analyses such as histological or biochemical examination animals can be euthanized by an incision of the inferior cava vein. The recommended method of euthanasia is to bring the animals to a surgical plane of anesthesia prior to incision of the inferior vena cava and injection of ice-cold saline into the left heart, especially if inflammatory markers in organs are to be assessed. Ensure to comply with the legal requirements and local guidelines. To verify sepsis-related organ failure, pro-apoptosis marker like caspase-3 may be analyzed as well as α1-microglobuline to verify tubular damage in the kidneys. The organ specific analysis of markers like CINC-1, MCP-1 and IL-6 may also provide information about the organ specific inflammatory response.

Results

The system presented allows for endotoxemia with hemodynamically stable animals as reported previously⁹. While the mean arterial pressure remains stable in animals with, and without LPS stimulation LPS treated animal develop characteristics of sepsis such as a negative base excess and a strong inflammatory reaction measured by plasma cytokines (6 hours after application) such as CINC-1 (867 ng/mL), MCP-1 (5027 ng/mL), and IL-6 (867 ng/mL)⁸, Figure 5

Discussion

The protocol described here allows for a highly reproducible, yet simple to learn sepsis model, which can be adapted according the research question. Essential in vivo data referring to organ function such as heart rate, blood pressure, and peripheral arterial oxygen saturation may be collected continuously, and blood sampling may be performed repetitively throughout the experiment. In addition, modifications with regard to fluid replacement protocols and vasopressor support can be installed. Given the hemodynamic stabil...

Materials

Name	Company	Catalog Number	Comments
2-0 silk sutures	Ethicon, Sommerville, NJ	K833	Standard surgical
26 intravenous catheter	Becton Dickinson, Franklin Lakes, NJ	391349	Standard anesthesia equipment
6-0 LOOK black braided silk	Surgical Specalities Corporation, Wyomissing, PA	SP114	Standard surgical
Alaris Syringe Pump	Bencton Dickinson
Betadine	Mundipharma, Basel, Switzerland	7.68034E+12	GTIN-number
Curved fine tips microforceps	World precision instruments (WPI), Sarasota, FL	504513	Facilitates vascular preparation
Fine tips microforceps	World precision instruments (WPI), Sarasota, FL	501976	Tips need to be polished regularly
Infinity Delta XL Anesthesia monitoring	Draeger, Lübeck, Germany
Isoflurane, 250 mL bottles	Attane, Piramal, Mumbai, India	LDNI 22098	Standard vet. equipment
Ketamine (Ketalar)	Pfitzer, New York, NY
Lipopolysaccharide (LPS) from Escherichia coli, serotype 055:B5	Sigma, Buchs, Switzerland
Q-tips small	Carl Roth GmbH, Karlsruhe, Germany	EH11.1	Standard surgical
Ringerfundin	Bbraun, Melsungen, Germany
Tec-3 Isofluorane Vaporizer	Ohmeda, GE-Healthcare, Chicago, IL	not available anymore	Standard vet. equipment
Xylazine (Xylazin Streuli)	Streuli AG, Uznach, Switzerland