Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Application of a kind of cerebroside compound

A technology of cerebrosides and compounds, applied in the field of preparation of drugs for the treatment of post-ischemic brain injury, can solve problems such as separation and purification difficulties, achieve significant therapeutic effects, high yield, and reduce mortality

Inactive Publication Date: 2011-12-21
NANJING MEDICAL UNIV +2
View PDF0 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Coupled with its similar structure, it brings great difficulties to the separation and purification

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Application of a kind of cerebroside compound
  • Application of a kind of cerebroside compound
  • Application of a kind of cerebroside compound

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0032] The method for preparing cerebroside A and cerebroside B from Gallus pilosulae, the concrete steps are:

[0033] (1) Pulverization: the dried Gallinarum gallinarum sample (1.5kg) (Yanyuan County, Sichuan Province) is pulverized to 100~10 orders;

[0034] (2) Solvent extraction: the pulverized gallinaceous fungus is packed into a 15-liter container, and methanol (7.5 liters) is shaken and extracted in a shaker for 3 days to obtain the gallinaceous fungus extract (151.3g); Subsequently, the extract was solvent-distributed with 90% aq.MeOH and n-hexane, and the obtained 90% aq.MeOH solution was concentrated and then solvent-distributed with water and n-butanol, and the n-butanol solution was concentrated under reduced pressure to obtain n-butanol layer sample (16.0 g);

[0035] (3) separation and purification: n-butanol layer sample with ODS open column (solvent system is MeOH: H 2 (0=90:10, 95:5, 100:0) separation; then, the sample containing the target compound (95% aq...

Embodiment 2

[0037] The physicochemical characteristics and the qualitative identification of chemical structure of cerebroside A and cerebroside B that embodiment 1 obtains:

[0038] Physicochemical properties of cerebroside A: [α] 25 D +4.5 (c 0.46, MeOH); Infrared spectrum (KBr) values: 3371, 2921, 2853, 1643, 1536, 1468, and 1081cm-1; m / z 728 (M+H)+;, chemical shift values:

[0039]C(150MHz, DMSO+2%D2O): 173.91, 135.08, 131.26, 131.05, 123.61, 103.56, 77.00, 76.63(76.62, CH-OD), 73.49(73.46), 71.20(71.17), 70.81(70.71), 70.25 (70.20), 68.86, 61.33 (61.21), 53.04 (53.00, CH-ND-), 39.90, 34.53, 32.23, 31.36, 29.10, 28.98, 28.74, 27.49, 27.38, 24.61, 22.14, 15.83, and 13.95.

[0040] Cerebroside B: The chemical structure of cerebroside B was determined using the same method as that of cerebroside A, and it was found that the difference between cerebroside B and A in structure (including three-dimensional structure) is that B is in the fatty chain There are two more methylene groups tha...

Embodiment 3

[0042] The animal pharmacology experiments of cerebroside A (JNGZ-A) and cerebroside B (JNGZ-B) described in the present invention are carried out to prove their application in the preparation of medicines for treating brain injury after ischemia.

[0043] The degree of neurological damage due to different forms of cerebral ischemia varies. The main pathological manifestations of middle cerebral artery occlusion are infarction and cerebral edema in the striatum, cerebral cortex, and hippocampus, which have a very high mortality and disability rate. Global cerebral ischemia selectively damages central nervous cells sensitive to hypoxia (such as nerve cells in the CA1 area of ​​the hippocampus), resulting in memory loss. Therefore, the present invention will use the classic middle cerebral artery occlusion (middle cerebral artery occlusion, MCAO) operation to simulate cerebral apoplexy, establish an animal model of global cerebral ischemia with vertebral artery and common caroti...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

No PUM Login to View More

Abstract

The present invention provides an application of cerebroside compounds (cerebroside A and cerebroside B) extracted and prepared from Gallus gallus in the preparation of a medicine for treating brain injury after cerebral ischemia. The present invention proves through pharmacological experiments that the cerebroside compound has a significant therapeutic effect on ischemic brain injury, can pass through the blood-brain barrier, reduce the size of cerebral infarction caused by cerebral ischemia, alleviate cerebral edema, and reduce neurological damage. Cell death, while promoting the recovery of motor and cognitive functions after stroke, and reducing stroke mortality. The invention develops new drug application of cerebroside compound, and provides new therapeutic drug for treating cerebral apoplexy.

Description

technical field [0001] The invention belongs to the field of natural medicinal chemistry. The invention mainly relates to the application of cerebroside compound extracted from Gallus pilosulae in the preparation of medicine for treating post-ischemic brain injury. Background technique [0002] Cerebral ischemic disease is one of the most common clinical diseases, with the characteristics of high morbidity, disability and mortality, which seriously threatens human health. With the gradual aging of the world's population, the incidence of ischemic brain injury is increasing year by year, but so far there is still a lack of effective prevention and treatment measures at home and abroad. The high sensitivity of central nervous cells to hypoxic injury and the lack of regenerative ability are considered to be the main reasons for the sequelae of stroke. Ischemic brain injury mainly includes (1) partial cerebrovascular occlusion (cerebral infarction) and (2) reduction or interru...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
Patent Type & Authority Patents(China)
IPC IPC(8): A61K31/7032A61P9/10C07H15/10C07H1/08
Inventor 陈玲戚建华戚智白银阳孙恺悦张卓高丽娟
Owner NANJING MEDICAL UNIV
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products

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