XIE Xin-mei, PANG Xiao-bin, ZHAO Yan, WANG Bao-quan, CHEN Ruo-yun, DU Guan-hua. Neuroprotective effects of the effective components group of Xiaoshuantongluo against oxygen-glucose deprivation in primary cultured rat cortical neuronsJ. Acta Pharmaceutica Sinica, 2014,49(8): 1130-1135.
Citation: XIE Xin-mei, PANG Xiao-bin, ZHAO Yan, WANG Bao-quan, CHEN Ruo-yun, DU Guan-hua. Neuroprotective effects of the effective components group of Xiaoshuantongluo against oxygen-glucose deprivation in primary cultured rat cortical neuronsJ. Acta Pharmaceutica Sinica, 2014,49(8): 1130-1135.

Neuroprotective effects of the effective components group of Xiaoshuantongluo against oxygen-glucose deprivation in primary cultured rat cortical neurons

  • This study is to investigate the effect of the effective components group of Xiaoshuantongluo (XECG) on neuronal injury induced by oxygen-glucose deprivation (OGD) in primary cortical cultures isolated from SD rat cortex at day 3 and the possible mechanism. Cells were divided into control group, OGD model group and XECG group (1, 3 and 10 mg·L-1). The cell viability was assessed with MTT assay and the LDH release rate was measured by enzyme label kit. The cell apoptosis was analyzed using Hoechst staining. RT-PCR was applied to detect the mRNA levels of JAK2 and STAT3. Western blotting was used to detect the expressions of Bcl-2, Bax, p-JAK2 and p-STAT3 proteins. Results showed that XECG resulted in an obvious resistance to oxygen-glucose deprivation-induced cell apoptosis and decrement of cell viability, decrease the cell LDH release rate. XECG could adjust the expression of Bcl-2 and Bax proteins and increase Bcl-2/Bax ratio, up-regulate the expression of p-JAK2 and p-STAT3. In conclusion, XECG could protect against the neuronal injury cells exposed to OGD, which may be relevant to the promotion of JAK2/STAT3 signaling pathway, and impact the expression of Bax and Bcl-2.
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