Name: inducing acute liver injury in rats via carbon tetrachloride (ccl4) exposure through an orogastric tube
Uploaded: 2020-04-28T13:30:00
Description: Watch this Scientific Journal Video about Inducing Acute Liver Injury in Rats via Carbon Tetrachloride CCl4 Exposure Through an Orogastric Tube at JoVE.com

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.

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. Prepar...

<ol>
	<li>Hoofnagle, J. H., Carithers, R. L., Shapiro, C., Ascher, N. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Fulminant+hepatic+failure:+Summary+of+a+workshop.">Fulminant hepatic failure: Summary of a workshop.</a> Hepatology. 21 (1), 240-252 (1995).</li><li>Rakela, J., Lange, S. M., Ludwig, J., Baldus, W. P. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Fulminant+hepatitis:+Mayo+clinic+experience+with+34+cases.">Fulminant hepatitis: Mayo clinic experience with 34 cases.</a> Mayo Clinic Proceedings. 60 (5), 289-292 (1985).</li><li>Riordan, S. M., Williams, R. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Treatment+of+hepatic+encephalopathy.">Treatment of hepatic encephalopathy.</a> New England Journal of Medicine. 337, 473-479 (1997).</li><li>Bernuau, J., Rueff, B., Benhamou, J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Fulminant+and+subfulminant+liver+failure:+Definitions+and+causes.">Fulminant and subfulminant liver failure: Definitions and causes.</a> Seminars in Liver Disease. 6 (2), 97-106 (1986).</li><li>Lidofsky, S. D. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Liver+transplantation+for+fulminant+hepatic+failure.">Liver transplantation for fulminant hepatic failure.</a> Gastroenterology Clinics of North America. 22 (2), 257-269 (1993).</li><li>Auzinger, G., Wendon, J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Intensive+care+management+of+acute+liver+failure.">Intensive care management of acute liver failure.</a> Current opinion in critical care. 14 (2), 179-188 (2008).</li><li>Wu, Q., 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=Protection+of+regenerating+liver+after+partial+hepatectomy+from+carbon+tetrachloride+hepatotoxicity+in+rats:+Roles+of+mitochondrial+uncoupling+protein+2+and+ATP+stores.">Protection of regenerating liver after partial hepatectomy from carbon tetrachloride hepatotoxicity in rats: Roles of mitochondrial uncoupling protein 2 and ATP stores.</a> Digestive Diseases and Sciences. 54 (9), 1918-1925 (2009).</li><li>Tu&#241;&#243;n, M. J., Alvarez, M., Culebras, J. M., Gonz&#225;lez-Gallego, J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=An+overview+of+animal+models+for+investigating+the+pathogenesis+and+therapeutic+strategies+in+acute+hepatic+failure.">An overview of animal models for investigating the pathogenesis and therapeutic strategies in acute hepatic failure.</a> World Journal of Gastroenterologyl. 15 (25), 3086-3098 (2009).</li><li>van de Kerkhove, M. P., Hoekstra, R., van Gulik, T. M., Chamuleau, R. A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Large+animal+models+of+fulminant+hepatic+failure+in+artificial+and+bioartificial+liver+support+research.">Large animal models of fulminant hepatic failure in artificial and bioartificial liver support research.</a> Biomaterials. 25 (9), 1613-1625 (2004).</li><li>Butterworth, R. F., 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=Experimental+models+of+hepatic+encephalopathy:+ISHEN+guidelines.">Experimental models of hepatic encephalopathy: ISHEN guidelines.</a> Liver International. 29 (6), 783-788 (2009).</li><li>Zhang, B., Gong, D., Mei, M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Protection+of+regenerating+liver+after+partial+hepatectomy+from+carbon+tetrachloride+hepatotoxicity+in+rats:+Role+of+hepatic+stimulator+substance.">Protection of regenerating liver after partial hepatectomy from carbon tetrachloride hepatotoxicity in rats: Role of hepatic stimulator substance.</a> Journal of Gastroenterology and Hepatology. 14 (10), 1010-1017 (1999).</li><li>Ugazio, G., Danni, O., Milillo, P., Burdino, E., Congiu, A. M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Mechanism+of+protection+against+carbon+tetrachloride+toxicity.+I.+prevention+of+lethal+effects+by+partial+surgical+hepatectomy.">Mechanism of protection against carbon tetrachloride toxicity. I. prevention of lethal effects by partial surgical hepatectomy.</a> Drug and Chemical Toxicology. 5 (2), 115-124 (1982).</li><li>Taniguchi, M., Takeuchi, T., Nakatsuka, R., Watanabe, T., Sato, K. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Molecular+process+in+acute+liver+injury+and+regeneration+induced+by+carbon+tetrachloride.">Molecular process in acute liver injury and regeneration induced by carbon tetrachloride.</a> Life Science. 75 (13), 1539-1549 (2004).</li><li>Gordis, E. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Lipid+metabolites+of+carbon+tetrachloride.">Lipid metabolites of carbon tetrachloride.</a> Journal of Clinical Investigation. 48 (1), 203-209 (1969).</li><li>Albrecht, J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Cerebral+RNA+synthesis+in+experimental+hepatogenic+encephalopathy.">Cerebral RNA synthesis in experimental hepatogenic encephalopathy.</a> Journal of Neuroscience Research. 6 (4), 553-558 (1981).</li><li>Terblanche, J., Hickman, R. <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+fulminant+hepatic+failure.">Animal models of fulminant hepatic failure.</a> Digestive Diseases and Sciences. 36 (6), 770-774 (1991).</li><li>Gruenbaum, B. F., 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=Cell-free+DNA+as+a+potential+marker+to+predict+carbon+tetrachloride-induced+acute+liver+injury+in+rats.">Cell-free DNA as a potential marker to predict carbon tetrachloride-induced acute liver injury in rats.</a> Hepatology International. 7 (2), 721-727 (2013).</li><li>Juricek, 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=Analytical+evaluation+of+the+clinical+chemistry+analyzer+Olympus+AU2700+plus.">Analytical evaluation of the clinical chemistry analyzer Olympus AU2700 plus.</a> Biochemia Medica. 20 (3), 334-340 (2010).</li><li>Feldman, A. T., Wolfe, D. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Tissue+processing+and+hematoxylin+and+eosin+staining.">Tissue processing and hematoxylin and eosin staining.</a> Methods in Molecular Biology. 1180, 31-43 (2014).</li><li>Wang, T., 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=Protective+effects+of+dehydrocavidine+on+carbon+tetrachloride-induced+acute+hepatotoxicity+in+rats.">Protective effects of dehydrocavidine on carbon tetrachloride-induced acute hepatotoxicity in rats.</a> Journal of Ethnopharmacology. 117 (2), 300-308 (2008).</li><li>Ye, X., 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=Hepatoprotective+effects+of+coptidis+rhizoma+aqueous+extract+on+carbon+tetrachloride-induced+acute+liver+hepatotoxicity+in+rats.">Hepatoprotective effects of coptidis rhizoma aqueous extract on carbon tetrachloride-induced acute liver hepatotoxicity in rats.</a> Journal of Ethnopharmacology. 124 (1), 130-136 (2009).</li><li>Wills, P. J., Asha, V. V. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Protective+effect+of+lygodium+flexuosum+(L.)+sw.+extract+against+carbon+tetrachloride-induced+acute+liver+injury+in+rats.">Protective effect of lygodium flexuosum (L.) sw. extract against carbon tetrachloride-induced acute liver injury in rats.</a> Journal of Ethnopharmacology. 108 (3), 320-326 (2006).</li><li>Senior, J. R. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Monitoring+for+hepatotoxicity:+What+is+the+predictive+value+of+liver+"function"+tests.">Monitoring for hepatotoxicity: What is the predictive value of liver "function" tests.</a> Clinical Pharmacology &amp; Therapeutics. 85 (3), 331-334 (2009).</li><li>Karmen, A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=A+note+on+the+spectrometric+assay+of+glutamic-oxalacetic+transaminase+in+human+blood+serum.">A note on the spectrometric assay of glutamic-oxalacetic transaminase in human blood serum.</a> Journal of Clinical Investigation. 34 (1), 131-133 (1955).</li><li>Hubner, G. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Ultrastructural+liver+damage+caused+by+direct+action+of+carbon+tetrachloride+in+vivo+and+in+vitro.">Ultrastructural liver damage caused by direct action of carbon tetrachloride in vivo and in vitro.</a> Virchows Archiv fur Pathologische Anatomie und Physiologie und fur Klinische Medizin. 339 (3), 187-197 (1965).</li><li>Newsome, P. N., Plevris, J. N., Nelson, L. J., Hayes, P. C. <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+fulminant+hepatic+failure:+A+critical+evaluation.">Animal models of fulminant hepatic failure: A critical evaluation.</a> Liver Transplantation. 6 (1), 21-31 (2000).</li></ol>

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&#8217;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...

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&#160;(GOT) enzymes and total bilirubin (TB) as well as definitive histological diagnosis by hematoxylin and eosin (H&#38;E) stained liver tissues. Exposure to CCl4 through an intragastric access allows for a practical, inexpensive, minimally invasive method with minimal hazard risk.

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			<td height="42" style="height:42px;width:212px;">22 G catheter BD Neoflon TM</td>
			<td style="width:153px;">Becton Dickinson Infusion Therapy AB</td>
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			<td height="63" style="height:63px;width:212px;">4% buffered formaldehyde solution</td>
			<td style="width:153px;">Sigma - Aldrich lab materials technologies</td>
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			<td></td>
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			<td height="42" style="height:42px;width:212px;">BD Microtainer SST TM Tubes</td>
			<td style="width:153px;">Becton Dickinson and Company</td>
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			<td height="63" style="height:63px;width:212px;">Carbone tetrachloride</td>
			<td style="width:153px;">Sigma - Aldrich lab materials technologies</td>
			<td style="width:116px;">CAS 56-23-5</td>
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			<td height="42" style="height:42px;width:212px;">Isofluran, USP 100%</td>
			<td style="width:153px;">Piramamal Critical Care, Inc</td>
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			<td height="42" style="height:42px;width:212px;">Olympus AU2700 Chemistry-Immuno Analyzer</td>
			<td style="width:153px;">Olympus (MN, USA)</td>
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			<td>Analysis of blood samples was done by the fluorescence method</td>
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			<td height="21" style="height:21px;width:212px;">Olympus BX 40 microscope</td>
			<td style="width:153px;">Olympus</td>
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			<td height="21" style="height:21px;width:212px;">RAT Feeding Needles</td>
			<td style="width:153px;">ORCHID SCIENTIFICS</td>
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			<td height="63" style="height:63px;width:212px;">SYRINGE SET 1 and 2 ml MEDI -PLUS</td>
			<td style="width:153px;">Shandong Zibo Shanchuan Medical Instruments Co., Ltd</td>
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inducing acute liver injury in rats via carbon tetrachloride (ccl4) exposure through an orogastric tube

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.

The TB, GOT, and GPT levels significantly increased 24 h after inducing ALI (more at higher CCl4 doses) compared to sham-operated controls (p &#60; 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&#8722;2), 2.5 mL/kg CCl4 (3, 3&#8722;4), and 5 mL/kg CCl4 (4, 4&#8722;5.75), had a significantly higher...

Watch this Scientific Journal Video about Inducing Acute Liver Injury in Rats via Carbon Tetrachloride CCl4 Exposure Through an Orogastric Tube at JoVE.com

Inducing Acute Liver Injury in Rats via Carbon Tetrachloride CCl4 Exposure Through an Orogastric Tube

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.

Inducing Acute Liver Injury in Rats via Carbon Tetrachloride (CCl4) Exposure Through an Orogastric Tube

Acute liver injury (ALI) plays a crucial role in the development of hepatic failure, which is characterized by severe liver dysfunction including ...

I would like to present our work about induced acute liver injury in rats via carbon tetrachloride exposure through orogastric tube. Select adult male Sprague-Dawley rats weighing 300 to 350 gram. Provide rat chow and water ad libitum.Perform all experiment between six AM and 12 PM.The animal care comedy of the Ben-Gurion University of the Negev, Israel approved all treatment and testing procedure used in this protocol. Maintain rats at room temperature of 22 Celsius degree with 12 hour lights and 12 hour dark cycles. Cannulate the tail vein with a 22 gauge catheter.Collect blood samples at baseline. Blood biochemical analysis include the measurement of serum GOT, GPT, and total bilirubin. Examination of liver enzymes and total bilirubin level were carried out in the biochemical laboratory of Soroka Medical Center.Caution:exposure to high concentration of carbon tetrachloride, including vapor or skin absorption can affect the central nervous system, degenerate the liver and kidney, and prolonged exposure may lead to coma or death. Prepare a 50 percent solution of carbon tetrachloride mixed with olive oil as vehicle in one to one ratio. Induce the pathotoxicity in vivo by carbon tetrachloride administration via an orogastric tube.Insert an orogastric tube through the oral cavity of the rat. Expose the rats to different doses of carbon tetrachloride. One milliliter per kilo for mild acute liver injury, two point five milliliter per kilo for moderate acute liver injury, or five milliliter per kilo for severe acute liver injury.For sham group, expose the rats to five milliliter per kilo only olive oil. Collect blood samples at 24 hours from carbon tetrachloride exposure. Blood biochemical analysis include the measurement of serum GOT, GPT, and total bilirubin.Place dead rat on dissecting board in dorsal recombinant with the abdominal facing upwards and shave her abdomen. Using scalpel, incise the full length of the ventrum from the anus to the chin. Reflect the skin.With the scalpel, incise the abdominal wall from the anus to the xiphoid cartilage to expose the abdominal viscera. Transfer the liver into a petri dish. Perform a hematoxylin and eosin staining.Examine the slices under microscope magnification of 200 times with a 20 millimeters objective length. The liver section should be graded by a specialized pathologist, blinded to the treatment protocol. The score of zero indicates no liver abnormalities, one to two indicates mild liver injury, three to four indicates moderate liver injury, and five to six indicates severe liver injury.The various groups of rats at different times are shown on the scheme. 24 hours after inducing acute liver injury, there was a significant increase in GOT, GPT, and total bilirubin levels, depending on the carbon tetrachloride exposed as compared to the control group. P value was less than zero point zero zero one.Histopathological changes were observed after 24 hours in all groups after carbon tetrachloride intoxication in various doses. Histological grading score at 24 hours between all three interventional groups to the control group was significantly higher. P value was less than zero point zero five.Our research group presented the common and physical method of induced acute liver injury in rats via carbon tetrachloride exposure through orogastric tube. This method is used to investigate the pathophysiology of acute liver injury and to test different about the protective strategy. Thank you very much for your attention.

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