Uses of triptolide for treating obesity and fatty liver
A kind of triptolide ketone, fat technology, applied in the field of triptolide ketone treatment of obesity and fatty liver
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0062] Example 1 The weight loss effect of triptolide ketone treatment on obese mice
[0063] (1) Experimental materials
[0064] (1) Experimental animals:
[0065] Strain: ICR mice, male and female;
[0066] Source: Experimental Animal Center of Soochow University School of Medicine;
[0067] Certificate of Conformity: Experimental animal production license number: XCYK (Su) 2002-0008, experimental animal use license number: SYXK (Su) 2002-0037;
[0068] Weight: 18-22g;
[0069] Number of animals in each group: 8.
[0070] (2) Mouse feed formula: maltodextrin (12%), sucrose (18%), cholesterol (2%), imported lard (21%), casein (21%), whole milk powder (5%) , Alfalfa Powder (3%), Corn Starch (8.5%), L-Cystine (0.5%), Vegetable Oil (3%), Premix (6%).
[0071] (3) Test drug: Triptolide was diluted with normal saline to the desired concentration.
[0072] (2) Experimental method
[0073] 24 ICR mice, weighing 18-22g. They were randomly divided into three groups with 8 rat...
Embodiment 2
[0093] Example 2 triptolide inhibits fat accumulation in obese model mice
[0094] (1) Experimental materials
[0095] Mouse fat and liver tissues were from Example 1; the hematoxylin-eosin staining kit was purchased from Nanjing Jiancheng Biology Co., Ltd.
[0096] (2) Experimental method
[0097] The fixed tissue was dehydrated with graded ethanol, and the xylene was transparent for 1 hour, then the xylene in the tissue was replaced with paraffin to harden the tissue, and soaked in wax overnight at 55°C. Embed the wax-soaked tissue block in fresh paraffin to make a wax block. The wax dipping temperature is 66°C. After the paraffin is solidified, it is cooled and solidified immediately, and it is solidified at -20°C. After it is fully solidified, the wax block is taken out. The embedded tissue was fixed on a paraffin microtome for sectioning. Before dewaxing, place the tissue slices at room temperature in a 60°C incubator and bake for 30 minutes, soak the tissue slices in ...
Embodiment 3
[0100] Embodiment 3 oil red dyeing experiment
[0101] (1) Experimental materials
[0102] Mouse fat and liver tissues were obtained from Example 1; the oil red staining kit was purchased from Nanjing Jiancheng Biological Co., Ltd.
[0103] (2) Experimental method
[0104] Take out the frozen section, warm it up at room temperature, wash off the embedding agent with distilled water; soak in 60% isopropanol for 2 minutes, rinse in advance to facilitate oil red o staining; stain with oil red o working solution for 2-5 minutes, adjust with 60% isopropanol Coloring needs to be completed with the help of a microscope to adjust the appropriate color; after the coloring is completed, wash it with water immediately; counterstain with hematoxylin for 1 minute, the running water turns blue, and observe under the microscope; seal the slide with water-based mounting agent; take pictures with an upright microscope as soon as possible , Statistics of oil red o staining results.
[0105] ...
PUM
Property | Measurement | Unit |
---|---|---|
Weight | aaaaa | aaaaa |
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com