Compositions and methods for treating inflammation and inflammation-related disorders by plectranthus amboinicus extracts
A composition and extract technology, applied in the direction of drug combination, medical raw materials derived from angiosperms, anti-inflammatory agents, etc.
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Embodiment 1
[0136] Example 1: Anti-inflammatory activity of PA extract
[0137] The effect of PA on LPS (lipopolysaccharide)-induced expression of 17 cytokines and 5 chemokines is shown in Table 1. Human umbilical vein endothelial (HUVEC) cells were co-incubated with LPS with or without 1 mg / ml PA crude extract. Cytokine expression profiles were determined using Luminex. The results showed that PA crude extract significantly reduced the expression of cytokines IL-6, IL-8, IL-12, MCP-1, and RANTES.
[0138] Table 1. Effect of PA extract on LPS-induced expression
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Embodiment 2
[0141] Example 2: Inhibition of AP-1 binding activity with PA extract
[0142] Since AP-1 activity is involved in inflammatory signaling, the effect of PA crude extract on AP-1 / DNA binding activity was examined. Such as figure 1 As shown, the effect of PA crude extract on the DNA binding activity of the AP-1 transcription factor was determined using an ELISA-based assay. Nuclear extracts prepared from TPA-activated HeLa or K562 cells were used as a source of AP-1 protein. After colocalization with oligonucleotides containing the AP-1 binding site, the AP-1 / DNA complex was detected with an anti-c-Fos antibody complexed with HRP. It was found that the in vitro DNA binding activity of AP-1 was inhibited by PA crude extract, and these effects were dose-dependent.
Embodiment 3
[0143] Example 3: Inhibition of AP-1 Binding Activity with Fraction 10, CHM9102, and Rosmarinic Acid
[0144] The PA crude extract was further fractionated by preparative HPLC using a C18 column. Such as figure 2 As shown, it separates the crude extract of P. chinensis into 16 fractions. Fraction 10 showed an inhibitory effect against AP-1 binding. This fraction was further purified on another C18 column using a solvent gradient from 2% acetonitrile to 90% acetonitrile containing 0.1% trifluoroacetic acid. The main peak is collected, and then its structure is determined by MASS and NMR analysis, such as image 3 shown. These studies lead to structural deduction for the active component CHM9102. Rosmarinic acid (an analog of CHM9102) was also tested for AP-1 inhibitory activity.
[0145] Although the methods and reagents have been described in terms of what are presently considered to be the most practical and preferred implementations, it should be understood that the...
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