Mouse Model for Alcoholic Hepatitis (AH)
Alcoholic Liver Disease
- Product No.DSI531Mu01
- Organism SpeciesMus musculus (Mouse) Same name, Different species.
- Prototype SpeciesHuman
- SourceAcute alcoholic liver disease(ALD) model induced by alcohol intake
- Model Animal StrainsKM Mice (SPF), healthy ,male, bodyweight:18g~22g.
- Modeling GroupingRandomly divided into six group: Control group, Model group, Positive drug group (Tiopronin) and Test drug group (three doses)
- Modeling Period15d
- Modeling Method1. Except for normal group, the other groups were in the morning with 50% ethanol by 12ml/kg gavage 1 times, continuous 15d, at the same time, the daily afternoon drug group mice were divided into low, middle and high dose administered to give the corresponding drugs, positive control group 30mg/kg treated with Tiopronin suspension, were 1 times a day, in normal model group was given the same volume of distilled water.
2. After the last irrigation, fasting and free drinking water 16h, pick the eye for blood and extract the serum, into the -80 degree for storage. The liver was removed and the mass was calculated. At the same time, part of the left lobe of the liver in 10% neutral formalin solution for pathological examination, a portion of the left lobe of the liver in liquid nitrogen frozen for molecular biological examination. - ApplicationsUsed to study the pathogenesis of acute alcoholic liver disease and screen the drugs for prevention and treatment of ALD
- Downloadn/a
- UOM Each case
- FOB
For more details, please contact local distributors! US$ 200
Model Evaluation
1. Liver coefficient: liver coefficient = organ wet mass / body mass.
2. Determination of blood biochemical parameters: the level of serum alanine aminotransferase (ALT), aspartate aminotransferase (AST) activity and triglyceride (TG) were measured by automatic biochemical analyzer.
Pathological Results
The pathological changes of liver: HE staining showed that there was no obvious fatty degeneration in the liver of the normal group, and the hepatic lobule structure was normal. In the model group, the liver was filled with a lot of fat degeneration.
Cytokines Level
The contents of TG, TC, MDA, GSH in liver tissue were detected.
Statistical Analysis
SPSS software is used for statistical analysis, measurement data to mean ± standard deviation (x ±s), using t test and single factor analysis of variance for group comparison, P<0.05 indicates there was a significant difference, P<0.01 indicates there are very significant differences.
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INCREMENT SERVICES
- Tissue/Sections Customized Service
- Serums Customized Service
- Immunohistochemistry (IHC) Experiment Service
- Small Animal In Vivo Imaging Experiment Service
- Small Animal Micro CT Imaging Experiment Service
- Small Animal MRI Imaging Experiment Service
- Small Animal Ultrasound Imaging Experiment Service
- Transmission Electron Microscopy (TEM) Experiment Service
- Scanning Electron Microscope (SEM) Experiment Service
- Learning and Memory Behavioral Experiment Service
- Anxiety and Depression Behavioral Experiment Service
- Drug Addiction Behavioral Experiment Service
- Pain Behavioral Experiment Service
- Neuropsychiatric Disorder Behavioral Experiment Service
- Fatigue Behavioral Experiment Service
- Nitric Oxide Assay Kit (A012)
- Nitric Oxide Assay Kit (A013-2)
- Total Anti-Oxidative Capability Assay Kit(A015-2)
- Total Anti-Oxidative Capability Assay Kit (A015-1)
- Superoxide Dismutase Assay Kit
- Fructose Assay Kit (A085)
- Citric Acid Assay Kit (A128 )
- Catalase Assay Kit
- Malondialdehyde Assay Kit
- Glutathione S-Transferase Assay Kit
- Microscale Reduced Glutathione assay kit
- Glutathione Reductase Activity Coefficient Assay Kit
- Angiotensin Converting Enzyme Kit
- Glutathione Peroxidase (GSH-PX) Assay Kit
- Cloud-Clone Multiplex assay kits
Catalog No. | Related products for research use of Mus musculus (Mouse) Organism species | Applications (RESEARCH USE ONLY!) |
DSI531Mu02 | Mouse Model for Alcoholic Hepatitis (AH) | n/a |
DSI531Mu01 | Mouse Model for Alcoholic Hepatitis (AH) | Used to study the pathogenesis of acute alcoholic liver disease and screen the drugs for prevention and treatment of ALD |