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In This Article

  • Summary
  • Abstract
  • Introduction
  • Protocol
  • Results
  • Discussion
  • Disclosures
  • Acknowledgements
  • Materials
  • References
  • Reprints and Permissions

Summary

This protocol describes a common and feasible method of inducing acute liver injury (ALI) via CCl4 exposure through an orogastric tube. CCl4 exposure induces ALI through the formation of reactive oxygen species during its biotransformation in the liver. This method is used to analyze the pathophysiology of ALI and examine different hepatoprotective strategies.

Abstract

Acute liver injury (ALI) plays a crucial role in the development of hepatic failure, which is characterized by severe liver dysfunction including complications such as hepatic encephalopathy and impaired protein synthesis. Appropriate animal models are vital to test the mechanism and pathophysiology of ALI and investigate different hepatoprotective strategies. Due to its ability to perform chemical transformations, carbon tetrachloride (CCl4) is widely used in the liver to induce ALI through the formation of reactive oxygen species. CCl4 exposure can be performed intraperitoneally, by inhalation, or through a nasogastric or orogastric tube. Here, we describe a rodent model, in which ALI is induced by CCl4 exposure through an orogastric tube. This method is inexpensive, easily performed, and has minimal hazard risk. The model is highly reproducible and can be widely used to determine the efficacy of potential hepatoprotective strategies and assess markers of liver injury.

Introduction

The frequency of toxic insults to the liver, especially due to alcohol and drug abuse, is increasing. Acute liver injury (ALI) is associated with high mortality rates and has caused clinical concerns1,2. Toxic injury leads to death signaling pathways in the liver, resulting in hepatocyte apoptosis, necrosis, or pyroptosis. ALI plays a crucial role in the development of hepatic failure, which is characterized by severe liver dysfunction including complications such as hepatic encephalopathy and impaired protein synthesis3,4. Although recent research has increased our knowledge about the physiological and pathological changes accompanying hepatic failure, it has not completely explained the pathomolecular features that affect the mechanisms of cell death. Furthermore, no medications are currently available to reverse the progressive deterioration in ALI patients. Currently, the only significantly effective treatment is liver transplantation5,6.

In order to investigate the mechanism and pathophysiology of ALI and to test different hepatoprotective strategies, different animal models are used to induce ALI. A preferable animal model of ALI should mimic the pathological process of the disease via a reliable, validated, inexpensive and easy to apply method. Examples of experimental models include hepatotoxic agents, surgical procedures such as total or partial hepatectomy, complete or transient devascularization, and infective procedures7,8,9. Known hepatotoxic substances include galactosamine, acetaminophen, thioacetamide, azoxymethane and CCl4. Of these, CCl4 is widely used although it has not yet been well characterized10,11,12,13.

CCl4 is an organic colorless liquid compound with a sweet smell and almost no flammability at lower temperatures. Exposure to high concentrations of CCl4 can cause damage to the central nervous system, including deterioration of the liver and kidneys. CCl4 induces ALI through its biotransformation in the liver, which forms reactive oxygen species. This occurs via the P450 cytochrome enzyme 2E1, forming an active metabolite and resulting in cell damage by macromolecule binding, enhancement of lipid peroxidation and disturbance of intracellular calcium homeostasis14. In addition, the CCl4 model can be used to stimulate the astrocytes at the level of RNA synthesis15. This hepatotoxin has been administered by the intraperitoneal, intraportal, oral, and intragastric routes16.

In this protocol, we describe in detail CCl4-induced ALI in rats via an orogastric tube. This method induces robust and reproducible ALI that can be used to investigate the pathogenesis of ALI. Determination of liver disease severity is monitored by measurement of serum glutamate-pyruvate transaminase (GPT), glutamic oxaloacetic transaminase (GOT) enzymes and total bilirubin (TB) as well as definitive histological diagnosis by hematoxylin and eosin (H&E) stained liver tissues. Exposure to CCl4 through an intragastric access allows for a practical, inexpensive, minimally invasive method with minimal hazard risk.

Protocol

The experiments were conducted according to the recommendations of the Declarations of Helsinki and Tokyo and to the Guidelines for the Use of Experimental Animals of the European Community. The experiments were approved by the Animal Care Committee of Ben-Gurion University of the Negev.

NOTE: The CCl4 model has been generated and used in a previous study17. The protocol timeline is demonstrated in Table 1.

1. Preparing rats for the experimental procedure

NOTE: Select adult male Sprague Dawley rats weighing 300−350 g.

  1. Obtain approval for experiments from Institutional Animal Care and Use Committee (IACUC).
  2. Maintain rats at room temperature (22 °C ± 1 °C), with 12 h light and 12 h dark cycles. Provide rat chow and water ad libitum.
  3. Perform all experiments between 6:00 a.m. and 12:00 p.m.
  4. Shave the rat and disinfect the skin with alcohol.

2. Determination of serum GOT, GPT, and TB baseline levels

  1. Anesthesia
    1. Prepare a continuous isoflurane administration system to induce anesthesia. Make sure the vaporizer system is filled with isoflurane.
    2. Anesthetize the rat with 2% isoflurane. Confirm that the rat is fully anesthetized by observing the movement and pedal reflex in response to external stimuli.
      NOTE: Use 1−5% isoflurane for anesthesia induction and maintenance.
  2. Cannulate the tail vein with a 22 G catheter.
  3. Collect a 0.5 mL blood sample at baseline. Ensure that the blood volume retrieved does not exceed IACUC guidelines.
  4. Perform blood biochemical analysis including the measurements of serum GOT, GPT and TB, as previously described18.
    NOTE: Examinations of liver enzymes and TB level were carried out in the biochemical laboratory of Soroka Medical Center. Blood samples were analyzed using a fluorescence method on a chemistry analyzer (Table of Materials).

3. Induction of acute liver injury in rats

CAUTION: Exposure to high concentrations of CCl4, including absorption through vapor or skin, can have negative effects on the central nervous system and cause degeneration of the liver and kidneys. Prolonged exposure can cause coma or death.

  1. Prepare a 50% solution of CCl4 (Table of Materials) by mixing CCl4 with olive oil as a vehicle in a 1:1 ratio.
    NOTE: The solution should be prepared according to IACUC guidelines for non-pharmaceutical grade compounds.
  2. Induce hepatotoxicity in vivo by CCl4 administration via an orogastric tube.
    1. Insert a 16 G orogastric tube (3 inches deep) through the oral cavity of the rat.
    2. Expose the rat to different doses of CCl4 by injecting a syringe with one of the following diluted solutions into the rat’s stomach: 1 mL/kg (mild ALI), 2.5 mL/kg (moderate ALI), or 5 mL/kg (severe ALI) of the 50% solution. For the sham-operated control group, expose the rat to 5 mL/kg olive oil only.

4. Determination of serum GOT, GPT, and TB levels after 24 h

  1. Anesthesia
    1. Prepare a continuous isoflurane administration system to induce anesthesia. Make sure the vaporizer system is filled with isoflurane.
    2. Anesthetize the rats with 2% isoflurane. Confirm that the rat is fully anesthetized by observing the movement and pedal reflex in response to external stimuli.
  2. Collect blood samples at 24 h from CCl4 exposure.
  3. Perform blood biochemical analysis including measurements of serum GOT, GPT and TB.

5. Liver collection for histological examination

  1. Euthanize the rat by replacing the inspired gas mixture with 20% O2/80% CO2. Ensure that CO2 is delivered at a predetermined rate in accordance with IACUC guidelines.
  2. Ensure death by checking for lack of heartbeat and confirm by a secondary method in accordance with IACUC guidelines.
  3. Place the rat on a dissecting board with its dorsal surface facing down and abdomen facing up. Shave the abdomen of the rat.
  4. With a scalpel, incise the full length of the ventrum skin from the anus to the chin. Separate the skin. Incise the abdominal wall with a scalpel from the anus to the xyphoid cartilage, exposing the abdominal viscera.
  5. Using scissors and forceps, isolate the liver by dissecting it from its ligaments and attachments. Starting at the liver hilum, carefully perform a hepatectomy by releasing all the liver lobes from attachments. Dissect and cut away all ligaments and blood vessels.
  6. Transfer the liver into a Petri dish. Fix the liver in a 4% buffered formaldehyde solution (Table of Materials) for at least 24 h.

6. Histological examination

  1. Sample preparation
    1. After fixation, cut the sample into 5 μm thick slice series by microtome sectioning.
    2. Gently place the slices on glass slides with a soft brush, 1 slice per slide.
    3. Perform H&E staining as previously described19.
  2. Examine the slices under a microscope at 200x magnification using a 20 mm objective lens (Table of Materials).
    NOTE: The liver sections should be graded by a specialized pathologist blinded to the treatment protocol. A score of 0 indicates no liver abnormalities, 1–2 indicates mild liver injury, 3–4 indicates moderate liver injury, and 5–6 indicates severe liver injury20,21,22.

Results

The TB, GOT, and GPT levels significantly increased 24 h after inducing ALI (more at higher CCl4 doses) compared to sham-operated controls (p < 0.001) (Figure 1). The levels of TB, GOT, and GPT at baseline were normal and were not significantly different than sham-operated controls. At 24 h, all three interventional groups, 1 mL/kg CCl4 (1, 1−2), 2.5 mL/kg CCl4 (3, 3−4), and 5 mL/kg CCl4 (4, 4−5.75), had a significantly higher...

Discussion

In this protocol, CCl4 is used as a liver toxin to induce ALI in rats. ALI is characterized by loss of hepatic parenchyma and subsequent dysregulation of the liver’s metabolic and synthetic functions. Drugs, viruses, toxins, autoimmune diseases, metabolic diseases, and vascular disorders all induce hepatocyte death, and the subsequent inflammatory response contributes to the pathogenesis of ALI.

The initial insult to the liver leads to cytokine production, chemokine release, a...

Disclosures

The authors have nothing to disclose.

Acknowledgements

The authors gratefully acknowledge Bertha Delgado, Department of Pathology, Soroka Medical Center, Faculty of Health Sciences, Ben-Gurion University of the Negev, for her help in the laboratory as well as in the histology analysis.

Materials

NameCompanyCatalog NumberComments
22 G catheter BD Neoflon TMBecton Dickinson Infusion Therapy AB
4% buffered formaldehyde solutionSigma - Aldrich lab materials technologies
BD Microtainer SST TM TubesBecton Dickinson and Company
Carbone tetrachlorideSigma - Aldrich lab materials technologiesCAS 56-23-5
Isofluran, USP 100%Piramamal Critical Care, Inc
Olympus AU2700 Chemistry-Immuno AnalyzerOlympus (MN, USA)Analysis of blood samples was done by the fluorescence method
Olympus BX 40 microscopeOlympus
RAT Feeding NeedlesORCHID SCIENTIFICS
SYRINGE SET 1 and 2 ml MEDI -PLUSShandong Zibo Shanchuan Medical Instruments Co., Ltd

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