Medicine and functional food for preventing and treating post-traumatic stress syndrome
A functional food, post-traumatic stress technology, applied in the field of preparation of amino acid oral liquid, can solve the problem of no research report on the prevention and treatment of mental diseases and so on
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Embodiment 1
[0024] Example 1 SMLC enhances the antioxidant capacity of brain tissue
[0025] The luminol reaction was used to detect the total antioxidant capacity of brain tissue. We use the brain tissue-hydrogen peroxide-luminol luminescence system to observe the chemiluminescence produced by the reaction of hydrogen peroxide and luminol under the catalysis of some enzymes in the brain tissue. Hydrogen peroxide was purchased from Merck. Drugs such as luminol, SMLC and Trolox were purchased from Sigma Company with a purity of >99%. The detection instrument is a Bayer Centaur 240 automatic chemiluminescence instrument, 0.1mol / L PBS 135μL, 5mmol / L luminol 15μL, rat hippocampus tissue extract supernatant 10μL, and 20μL of different concentrations of SMLC were added to the measurement tube successively. Test solution (5mM, 1mM) or positive control strong antioxidant Trolox (62.5μM), mix well, put in the instrument at 37℃, add 20μL of hydrogen peroxide (100mM) to start the reaction, after a...
Embodiment 2
[0026] Example 2 SMLC reduces the accumulation of ROS in nerve cells
[0027] The fluorescent probe DCFH-DA was used to detect ROS in nerve cell line SH-SY5Y. DCFH-DA itself has no fluorescence and can freely pass through the cell membrane. After entering the cell, it can be hydrolyzed by intracellular lipase to generate DCFH. However, DCFH cannot permeate the cell membrane, so the probe can be easily loaded into the cell. Intracellular ROS can oxidize non-fluorescent DCFH to produce fluorescent DCF. The fluorescence of DCF represents the level of reactive oxygen species in the cells. The human neuroblastoma cell line SH-SY5Y was cultured in DMEM medium containing 15% fetal bovine serum in a 5% CO2 incubator at 37 degrees Celsius. Passage every 3-5 days. Seed SH-SY5Y into 6-well plates before the experiment. Nerve cell line SH-SY5Y treated with different drug concentrations of SMLC (0mM, 0.5mM, 1mM), cultured for 24 hours, added hydrogen peroxide 250μM for 1 hour, removed...
Embodiment 3
[0028] Example 3 SMLC reduces nerve cell damage caused by hydrogen peroxide
[0029] The human neuroblastoma cell line SH-SY5Y was cultured in DMEM medium containing 15% fetal bovine serum in a 5% CO2 incubator at 37 degrees Celsius. Passage every 3-5 days. Seed SH-SY5Y into a 96-well plate before the experiment. 250 μM hydrogen peroxide was used for 12 hours to create a cell model of oxidative stress injury. SMLC (1 mM and 0.5 mM) was added to the medium 2 hours before the addition of hydrogen peroxide and maintained until the end of the experiment. After the experiment, the cell viability was detected by MTT. Aspirate the culture supernatant in each well, add 200ul of serum-free cell culture medium containing 0.5mg / ml MTT and continue to incubate for 4 hours, terminate the culture, aspirate the culture supernatant in the well, add 100μl DMSO to each well, shake for 10 After fully melting the crystals, perform colorimetry immediately, the measuring wavelength is 570nm, an...
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