Mouse Model for Hypoxic Ischemic Encephalopathy (HIE)

HIBD; NE; Hypoxic-ischemic brain damage; Neonatal encephalopathy

  • Product No.DSI685Mu01
  • Organism SpeciesMus musculus (Mouse) Same name, Different species.
  • Prototype SpeciesHuman
  • SourceInduced by Intermittent hypoxic (CHI)
  • Model Animal StrainsC57BL/6 Mice (SPF level), male, healthy, 6~8weeks
  • Modeling GroupingRandomly divided into groups: Control group, Model group, Positive drug group and Test drug group, 15 mice per group
  • Modeling Period4~6w
  • Modeling MethodMouse were exposed to chronic intermittent hypoxia (CIH) or air (IAA) and were fed a high-fat, high-cholesterol diet. CIH was handled as FIO2 cycling from 21 to 6.5%, 60 times/h, 9:00 A.M. to 9:00 P.M. Under a restricted feeding, each rat was provided with 13g food at 1week and increase 2g every week thereafter until 4 weeks. Twice supply everyday, no longer added after eating. No food in the course of intermittent hypoxia and rest time were in the cage. Meanwhile the non-CIH group was placed in the same size animal capsule, and provided with air pulse instead of intermittent hypoxia.
  • ApplicationsDisease Model
  • Download n/a
  • UOM Each case
  • FOB US$ 320
    For more details, please contact local distributors!
  • Mouse Model for Hypoxic Ischemic Encephalopathy (HIE) Packages (Simulation)
  • Mouse Model for Hypoxic Ischemic Encephalopathy (HIE) Packages (Simulation)
  • DSI685Mu01.png Fig. Intermittent hypoxic (CHI) equipment for animals
  • Certificate ISO9001: 2008, ISO13485: 2003 Registered

Model Evaluation of the Mouse Model for Hypoxic Ischemic Encephalopathy (HIE)

Pathological Results of the Mouse Model for Hypoxic Ischemic Encephalopathy (HIE)

Observation of arterial plaque
1. HE stain
Take the blood vessel specimen, 4% poly formaldehyde solution fixed, embedded to make the paraffin section, HE staining and the staining resluts are used for the observation of aortic arch atherosclerosis and analysis of total plaque cross-sectional area and plaque necrosis area.
2.IHC
IHC detection of CD68 expression in mouse aortic plaques.
3.Observation of arterial plaque under the scanning electron microscope
Kill animals by bloodletting, dissect the abdominal aorta, take abdominal aorta samples quickly, and cut up to 0.5-1.0cm. Longitudinally dissecting the vascular cavity with a corneal scissors, and wash with PBS buffer for 3 times. Fixed on filter paper and fully expose the surface of intravascular cavity. And rapidly transfer it to precooled 2.5% glutaraldehyde solution, fixed with a refrigerator at 4℃ for 3-4 hours. Then treated with gradient alcohol and acetone dehydration, place the specimen endothelial upward on the platform of the scanning electron microscope, adjust the voltage to 20 kV to observe whether there was plaque rupture and tarombokinesis in each experimental groups.

Cytokines Level of the Mouse Model for Hypoxic Ischemic Encephalopathy (HIE)

Tissue detection
1.RT-PCR
mRNA levels of FIH-1 and HIF-1 in epididymal fat pad and heart tissue were detected.
2.Western blot
The protein levels of FIH-1 and HIF-1 in epididymal fat pad and heart tissue were detected.

Statistical Analysis of the Mouse Model for Hypoxic Ischemic Encephalopathy (HIE)

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.

Related products

Catalog No. Organism species: Mus musculus (Mouse) Applications (RESEARCH USE ONLY!)
DSI685Mu01 Mouse Model for Hypoxic Ischemic Encephalopathy (HIE) Disease Model
DSI685Mu02 Mouse Model for Hypoxic Ischemic Encephalopathy (HIE) Disease Model
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