Application of oldenlandia diffusa acting on retinol X receptor
A technology of Hedyotis diffusa and retinol, which is applied to medical preparations, instruments, and drug combinations containing active ingredients, and can solve problems such as unclear anti-tumor mechanisms
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Embodiment 1
[0025] Example 1 , Preparation of BHP component of Hedyotis diffusa extract
[0026] Take the whole herb of Hedyotis diffusa (purchased from Wujiang Shanghai Caitongde Chinese Medicine Decoction Pieces Company), cut into pieces, soak in 95% ethanol, and reflux for 3 times for 2 hours each time, discard the dregs, combine and concentrate the filtrate, Obtain the crude extract of Hedyotis diffusa.
[0027] Suspend the crude extract of Hedyotis diffusa with water, extract 4 times with petroleum ether until the residual liquid is colorless, and obtain the extract, which is the BHP component (ie, the petroleum ether component of Hedyotis diffusa).
Embodiment 2
[0028] Example 2 : Combination of BHP fraction of Hedyotis diffusa extract and RXR
[0029] Get the Hedyotis diffusa extract BHP component obtained in Example 1, and detect its combination with RXR, the specific process is as follows:
[0030] Add 3H 9cis-RA, GST-RXR LBD, and different amounts of BHP components of Hedyotis diffusa extract to TEG buffer, so that the concentration of 3H 9cis-RA in the final reaction system is 1% (V / V), GST - The concentration of RXR LBD was 0.02 g / ml, and the concentrations of BHP components of Hedyotis diffusa extract were 0.1, 1, 10, 100, 1000 μg / mL, and BSA was used instead of GST-RXR LBD as a blank control.
[0031] Incubate the obtained reaction system at 4°C for 16 hours, add GST agarose gel beads, shake at room temperature for 1 hour, centrifuge at 1000 rpm for 1 minute, discard the supernatant, add TEG buffer to wash 3 times, centrifuge, and use Binding buffer to resuspend , add scintillation liquid, measure the cpm value with liquid ...
Embodiment 3
[0033] Example 3 : BHP fraction of Hedyotis diffusa extract inhibits the transcription of RXR
[0034] CV1 cells (purchased from ATCC) cultured in 10% DMEM (purchased from Hyclone) were divided into 2×10 4 Each well was placed in a 48-well plate, and after 24 hours, each well was co-transfected with the following plasmids with 25 μL Lipofectamine2000 liposomes:
[0035] 10 ng GFP-RXRa, 50 ng TREpal, 50 ng β-Gal, 390 ng pBluescript (purchased from ATCC).
[0036] 6 hours after transfection, use new DMEM medium to replace the medium. After the cells grow for 8 hours, add BHP components to treat for 24 hours. Discard the culture medium, wash with PBS buffer three times, and add 40ul Reporter Lysis Buffer to each well. Cells were lysed and freeze-thawed 3 times.
[0037] Then, detect β-Gal and CAT (chloramphenicol acetyltransferase) activity, the result is as follows figure 2 shown.
[0038] figure 2 The results showed that with the increase of the drug concentration, the...
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