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45 kcal% High Fat Diet

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Catalog No. TYD-04289

The 45 kcal% High Fat Diet is a type of high-fat model feed designed to induce obesity and type 2 diabetes in animal models.

45 kcal% High Fat Diet

45 kcal% High Fat Diet

😃Good
Catalog No. TYD-04289
The 45 kcal% High Fat Diet is a type of high-fat model feed designed to induce obesity and type 2 diabetes in animal models.
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Product Introduction

Bioactivity
Description
The 45 kcal% High Fat Diet is a type of high-fat model feed designed to induce obesity and type 2 diabetes in animal models.
In vivo
Before conducting formal experiments, it is recommended to use preliminary trials to determine optimal conditions, such as animal strain, age, dosage, frequency, duration, and time and indices for testing. A 45 kcal% High Fat Diet is effective for developing animal models for obesity and type 2 diabetes.

1. Obesity Induction Mechanism: High-fat diets increase the size and number of fat cells, thereby inducing obesity. Specific methods for modeling include: Rats: Sprague-Dawley • Male • 3 weeks old, feeding daily for 15 weeks. Mice: C57BL/6J • Male • 1 month old, feeding daily for 5 months. Note: 1) It is advised to adjust diets using a 24-hour fasting method or a gradual 7-day dietary change. 2) Replace feed every 2-3 days, discard old feed. 3) Use wood shavings bedding, changed 1-2 times a week. 4) Store refrigerated.

Indicators for Successful Modeling: Body weight in the high-fat (HF) diet group is 37% heavier compared to the normal diet group. Serum biochemistry shows elevated blood glucose, AST, and ALT. Fat metabolism indicators such as total cholesterol (T-CHO), triglycerides (TG), high-density lipoprotein cholesterol (HDL-C), low-density lipoprotein cholesterol (LDL-C), and free fatty acids (FFA) are significantly increased. Histopathology reveals more frequent cytoplasmic microvacuolation in hepatocytes at the liver lobule center in high-fat diet rats. Mild inflammatory infiltration by neutrophils and monocytes, fibrosis, and severe hepatocyte ballooning degeneration are observed. Other indicators include consistently higher liver and fat pad weights in the high-fat diet group compared to the normal diet group. Related Products: 60 kcal% High Fat Diet. Countermeasure Products: /

2. Type 2 Diabetes Induction Mechanism: A combination of a high-fat diet and Streptozotocin injection is a common method for establishing rodent models of type 2 diabetes (T2DM) and has recently been used in research on diabetes-related cognitive disorders. Specific methods for modeling include: Rats: Sprague-Dawley • Male • 4 weeks old, with a feeding regimen of 4 weeks on a high-fat diet followed by a single injection of 30 mg/kg Streptozotocin. Note: 1) It is suggested to use a 24-hour fasting method or a gradual 7-day dietary adjustment. 2) After 4 weeks of high-fat diet feeding, administer intraperitoneal injection of a single dose of Streptozotocin (30 mg/kg) after overnight fasting. 3) Rats with tail vein blood glucose exceeding 16.7 mmol/L after 7 and 14 days post-injection are considered diabetic.

Indicators for Successful Modeling: Blood glucose levels exceed 300 mg/dL (16.7 mmol/L). There is a significant decline in weight following STZ administration.
Chemical Properties
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year

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Please enter your animal experiment information in the following box and click Calculate to obtain the mother liquor preparation method and in vivo formula preparation method:
TargetMol | Animal experimentsFor example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . TargetMol | Animal experiments A total of 10 animals were administered, and the formula you used is 5% TargetMol | reagent DMSO+30% PEG300+5% Tween 80+60% Saline/PBS/ddH2O. So your working solution concentration is 2 mg/mL。
Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSOTargetMol | reagent (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
Preparation method for in vivo formula: Take 50 μL DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLSaline/PBS/ddH2OTargetMol | reagent mix well and clarify
For Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
All types of co-solvents required for the protocol, such asDMSO, PEG300/ PEG400, Tween 80, SBE-β-CD, corn oil are available for purchase on the TargetMol website with a simple click.
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