Application of sesamin in preparation of product for treating and/or preventing lymphoma
A technology of sesamin and lymphoma, applied in the field of lymphoma treatment, can solve the problem of little research on lymphoma
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Embodiment 1
[0037] 5×10 5 EL4 cells were subcutaneously injected into the right axilla of 6-8 week-old BALB / c female mice to establish a mouse T-cell lymphoma model. When the average tumor volume is about 100mm 3 At that time, the tumor-bearing mice were randomly divided into two groups for follow-up treatment. The mice in the treatment group were intraperitoneally injected with 10 mg / kg sesamin every 2 days, diluted with sterile phosphate buffered saline (PBS). Control group (NC) mice were intraperitoneally injected with the same volume of PBS solution. All mice were housed under specific pathogen-free (SPF) conditions and had free access to water and food. Tumor volumes were measured every two days. After 21 days, the mice were sacrificed, and the tumor tissues were collected and weighed. The result is as figure 1 shown. The tumor volume of the mice in the sesamin treatment group was significantly smaller than the tumor volume of the mice in the control group from about 11 days a...
Embodiment 2
[0039] The cell viability was determined by the CCK-8 method, and the specific method was as follows: 100 μL of cell suspension was prepared in a 96-well plate, with 2000 EL4 cells per well. The culture plate was pre-incubated for 24 h in the incubator (37°C, 5% CO 2 ). After 24h, stimulate with 10 μ M, 20 μ M and 40 μ M sesamin (dissolve sesamin in dimethyl sulfoxide (DMSO), and dilute sesamin with RPMI-1640 medium according to the experimental requirements to a final concentration of 10 μ M, 20 μ M and 50 μ M) Mouse T-cell lymphoma cell line EL4 cells (purchased from American ATCC Company) 48, 72 and 96h, EL4 cells in RPMI- 1640 medium at 37°C, 5% CO 2 cultured in a humidified incubator. After the specified time, add 10 μL of CCK8 solution to each well. The culture plate was incubated in the incubator for 1-4h, the absorbance at 450nm was measured with a microplate reader, and the cell viability was calculated according to the absorbance. If the OD value is not measured...
Embodiment 3
[0045] First, EL4 cells were treated with 10 μM, 20 μM and 40 μM sesamin for 72 hours, and the total protein of each group was extracted, and the protein expression levels of apoptosis-related markers in each group were detected by western blot method, including Bax, Bcl-2 and Caspase-3, internal reference For β-Tubulin, the specific method is the same as in Example 2, the only difference is that the primary antibody is Caspase-3 (1:1000), Bax (1:1000), Bcl-2 (1:1000), β-Tubulin (1:3000 ), the secondary antibody is the corresponding secondary antibody.
[0046] The result is as image 3 A and image 3 As shown in B, compared with the control group, the protein expression levels of apoptosis markers (Bax / Bcl-2 and cleaved-Caspase3) in different doses of sesamin treatment groups were significantly increased.
[0047] Secondly, EL4 cells were treated with 10 μM, 20 μM and 40 μM sesamin for 72 hours, and the apoptotic ratio (Annexin V+PI- and AnnexinV+PI+) of the EL4 cells treat...
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