Application of silymarin in preparation of drugs for preventing and/or treating neuronal injury after cerebral ischemia
A technology for neuron damage and silymarin, which is applied in the application field of silibinin in the preparation of drugs for preventing and/or treating neuron damage after cerebral ischemia, can solve the problems of no report on the preventive effect and the like, and achieves the Effects of treating neuronal damage and death, inhibiting neuronal damage
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Embodiment 1
[0020] Example 1 Silyjinin inhibits the killing effect of oxygen-glucose deprivation (OGD) on human SH-SY5Y cells
[0021] Silyjining (purchased from Chengdu Ruifensi Company) was formulated into a mother solution with DMSO during use, and administered after dilution.
[0022] Human SH-SY5Y cells (purchased from China Jikai Biotechnology Co., Ltd.), using oxygen-glucose deprivation (OGD) to make a cell model of "neuron injury and death after cerebral ischemia", LDH (lactate dehydrogenase) release method to detect cell injury and death.
[0023] Human SH-SY5Y cells were inoculated in DMEM medium in 96-well plates, incubated overnight in a carbon dioxide incubator, and incubated with different concentrations of silymarin (2.0mmol / L and 4.0mmol / L) 1 hour in advance, and oxygen After 24 hours of sugar deprivation, the release degree of lactate dehydrogenase (LDH) was detected.
[0024] Experimental results such as figure 1 shown. The results showed that the OD values of LDH ...
Embodiment 2
[0032] Example 2 Silyjinin inhibits AIF nuclear translocation in human SH-SY5Y cells induced by oxygen-glucose deprivation (OGD)
[0033] The release of AIF (Apoptosis inducing factor) from mitochondria and into the nucleus is one of the main causes of programmed cell death. In order to elucidate the inhibitory effect of silymarin on the death of human SH-SY5Y cells induced by oxygen-glucose deprivation (OGD), in this experiment, human SH-SY5Y cells were inoculated in DMEM medium in a culture dish and incubated overnight in a carbon dioxide incubator. Incubate with different concentrations of silymarin (2.0mmol / L and 4.0mmol / L) 1 hour in advance. After 24 hours of oxygen-glucose deprivation, the cells are collected, and after lysis, the mitochondrial components and nuclei are separated by differential centrifugation. Then, Western blot analysis was used to detect the effect of silymarin on the nuclear translocation of AIF induced by oxygen-glucose deprivation (OGD).
[0034] ...
Embodiment 3
[0035] Example 3 Silyjinin inhibits oxygen-glucose deprivation (OGD)-induced DNA double-strand scission in human SH-SY5Y cells
[0036] DNA is the carrier of genetic information, and DNA double-strand breaks are the basis for DNA dissolution and cell death. In order to illustrate the protective effect of silymarin on cells, this experiment detected the effect of silymarin on DNA double-strand breaks in human SH-SY5Y cells induced by oxygen-glucose deprivation (OGD) by Western blot.
[0037] Experimental results such as image 3 shown. The results showed that oxygen-glucose deprivation (OGD) could significantly up-regulate the protein level of γ-H2AX, a marker of DNA double-strand breaks, but silymarin inhibited γ-H2AX induced by oxygen-glucose deprivation (OGD) in a concentration-dependent manner. expression up-regulated. This shows that silymarin can inhibit DNA double-strand damage caused by oxygen-glucose deprivation (OGD) in human SH-SY5Y cells.
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