Uses of 5-cholesten-3β-ol sulfate
A technology of alcohol sulfate and cholestene, applied in the field of 5-cholestene-3β-alcohol sulfate salt, can solve the problems such as unpublished treatment effect of type I diabetes mellitus
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1、5
[0022] The preparation of embodiment 1,5-cholestene-3β-alcohol sulfate injection
[0023] Dissolve CS in DMSO to prepare a 50 mg / mL solution, then add co-solvent Tween 20, and finally dissolve the above mixture in normal saline to prepare CS injection. Among them, the concentration of CS is 5mg / L, DMSO is 10%, and Tween 20 is 2%, which is prepared and used now.
[0024] The beneficial effects of the present invention are demonstrated through experimental examples below.
experiment example 1、5
[0025] Experimental example 1, the inhibitory effect of 5-cholesten-3β-ol sulfate on the hyperglycemia of type I diabetes induced by STZ
[0026] 1. Experimental method
[0027] The C57 / 6J mice were divided into 4 groups, namely vehicle group, CS group, STZ group and CS+STZ group.
[0028] (1) Preparation of solution:
[0029] Preparation of DMSO injection: Dissolve DMSO and Tween 20 in normal saline to make an injection with 10% DMSO and 2% Tween 20, ready for immediate use.
[0030] Preparation of STZ citric acid buffer solution: Add 2.1g of citric acid to 100mL of double distilled water to make solution A (0.1mol / L), add 2.94g of sodium citrate to 100mL of double distilled water to make solution B (0.1mol / L) . Mix liquid A and liquid B at a ratio of 1:1.32, measure the pH value with a pH meter, adjust the pH=4.2-4.5, and finally dissolve STZ in the above mixed liquid to prepare STZ citric acid injection with a concentration of 8 mg / L. Ready to use
[0031] (2) Mouse pr...
experiment example 2、5
[0043] Experimental Example 2, Effect of 5-cholesten-3β-ol sulfate on pancreatic islet β cells
[0044] 1. STZ treatment of NIT-1 flow cytometry apoptosis experiment:
[0045] NIT-1 cells were plated overnight and pretreated with corresponding concentrations of CS solution (0 μM, 5 μM, 10 μM, DMSO as solvent) for 6 hours, and then added with corresponding concentrations of STZ solution (10 mM, 20 mM) and CS (0 μM, 5 μM, 10 μM , DMSO as solvent) for 24 hours. Apoptosis detection kit (Cat: FXP023) of Beijing Sizhengbai Biotechnology Company was used to detect cell apoptosis.
[0046] 2. Edu proliferation experiment:
[0047] NIT-1 cells were plated overnight and then treated with corresponding concentrations of CS (0 μM, 10 μM, 20 μM, DMSO as solvent) for 24 hours, and the cell proliferation was detected with Ruibo Edu detection kit (Cat: C10320-1).
[0048] 3. Insulin and glucagon staining experiment:
[0049] The fresh pancreatic tissues of the mice in each experimental gr...
PUM
Property | Measurement | Unit |
---|---|---|
quality score | 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