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Extract of leontopodic acid plant and application of active ingredients thereof in treating hepatitis

A plant extract, Edelweiss technology, applied in the directions of organic active ingredients, medical preparations containing active ingredients, drug combinations, etc., can solve the problem that there are no antihepatitis drugs of Edelweiss compounds.

Inactive Publication Date: 2010-10-13
CHINA JILIANG UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Literature search shows that so far, there is no report of edelweisin compounds and plant extracts containing edelweisin compounds for treating hepatitis and preparing anti-hepatitis drugs

Method used

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  • Extract of leontopodic acid plant and application of active ingredients thereof in treating hepatitis
  • Extract of leontopodic acid plant and application of active ingredients thereof in treating hepatitis
  • Extract of leontopodic acid plant and application of active ingredients thereof in treating hepatitis

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0020] Example 1: Inhibition of Edelweiss plant extracts on HepG2.2.15 cells secreting hepatitis B virus surface antigen (HBsAg), hepatitis B virus E antigen (HBeAg) and hepatitis B virus DNA (HBV-DNA).

[0021] Determination of the inhibitory effect of the sample on the growth of HepG2.2.15 cells: the cells were digested with trypsin-EDTA and diluted to 1×10 5 / mL, added to a 96-well cell culture plate, 100uL per well, placed in CO 2cultured in an incubator. After 24 hours of inoculation, discard the medium, add the sample diluted with the medium, 200ul per well, add 3 wells for each concentration, add 5mg / ml MTT to the cell culture wells after 72 hours of culture, 10ul per well, and place at 37°C After incubation for 3 hours, 150ul of DMSO was added to completely dissolve the formazan, and a microplate reader was used for colorimetry at a wavelength of 570nm. Calculate the median toxic concentration of the sample on the growth of HepG2.2.15 cells.

[0022] Determination o...

Embodiment 2

[0027] Example 2 Effects of Edelweiss plant extracts on D-GalN-induced liver cell damage

[0028] Human normal liver cell line HL-7702, placed at 37°C in CO 2 Culture in an incubator; after the hepatocytes adhered to the wall, replace the culture medium, add 200mmol / l D-GalN, and act for 8h; then discard the culture medium, and add 200μl of different concentrations of the test drug solution, each concentration was set at 6 Repeat wells, set solvent and positive control at the same time; continue to cultivate for 48 hours, add 10 μl MTT (5 mg / ml) to each well, act for 4 hours, aspirate and discard the supernatant, add 150 μl DMSO, shake and mix well; Determine the A value.

[0029] Protection evaluation: calculation of protection rate (%) and proliferation index.

[0030] Note 1:

[0031] Note 2: Proliferation index = sample group (A) / injury group (A)

[0032] Table 2 Effects of Edelweiss plant extracts on D-GalN-induced normal human liver cell damage

[0033]

[0034...

Embodiment 3

[0035] Example 3 Protective effect of edelweiss plant extract on D-GalN-induced acute liver injury model in mice

[0036] Materials: 20-25g male ICR mice were randomly divided into groups according to body weight, 10 mice in each group. A normal control group, an injury control group, a positive control group and high, medium and low dose groups of the test drug were set up. Animals in the drug group were given prophylactic administration once a day for 7 consecutive days. The normal control group and the injury control group were given an equal volume of solvent, and the positive control group was given 50 mg / kg of silymarin. One hour after the last administration, animals in each group except the normal group were injected with 650 mg / kg galactosamine (D-GalN) intraperitoneally to cause toxicity. 24 hours after the last administration, the serum was separated to measure aspartate aminotransferase (AST) and alanine aminotransferase (ALT). At the same time, liver tissue was...

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Abstract

The invention relates to application of Leontopodic acid and a plant extract and a composition containing the Leontopodic acid in treating hepatitis. The leontopodic acid and the plant extract and the composition containing the leontopodic acid have obvious effects on resisting hepatitis virus, resisting inflammation, protecting the liver and regulating immunity, and can be used for treating hepatitis.

Description

technical field [0001] The present invention relates to the application of a plant extract and its active ingredients in the treatment of hepatitis, especially the edelweiss plant extract containing edelweisin compounds, edelweissin and its derivatives, and the drug combination containing edelweisin The use of the compound in the preparation of medicines for treating hepatitis B. Background technique [0002] Hepatitis is a general term for inflammatory diseases of the liver. According to the etiology, it can be divided into viral, alcoholic, drug-induced and autoimmune hepatitis. Viral hepatitis is the most common, of which hepatitis B is the main one, and hepatitis C next. Hepatitis B is a very harmful worldwide epidemic infectious disease caused by hepatitis B virus (HBV). According to statistics, there are currently about 350 million HBV carriers in the world, and China is a high-infection area of ​​HBV. HBV carriers Patients account for as high as 10% to 15% of the to...

Claims

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Application Information

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IPC IPC(8): A61K31/216A61P1/16A61P31/20A61P37/02C07C69/732C07C67/48
Inventor 伍义行郝冰洁
Owner CHINA JILIANG UNIV
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