Objective: To investigate the effect of Jinmaitong (筋脉通,JMT) serum on the proliferation of rat Schwann cells (SCs) primarily cultured in high glucose medium. Method: SOs were primarily cultured in Dulbecco's...Objective: To investigate the effect of Jinmaitong (筋脉通,JMT) serum on the proliferation of rat Schwann cells (SCs) primarily cultured in high glucose medium. Method: SOs were primarily cultured in Dulbecco's minmum essential medium (DMEM control), 50 mmol/L glucose medium (50 mmol/L Glu), 75 mmol/L glucose medium (75 mmol/L Glu), as well as 50 mmol/L glucose medium, with different concentrations of JMT serum (undiluted, 1:2 diluted and 1:8 diluted) and Neurotropin (Ntp), respectively. The proliferation of SCs under different conditions was detected by MTT. Result: SCs grew exuberantly in DMEM within 24-72 h, but slowed down at 96 h. The proliferation of SCs was inhibited in 50 mmol/L Glu and 75 mmol/L Glu after cultures of 48, 72 and 96 h, which showed that both were significantly different compared to the control group (P〈0.01). The inhibition was more significant in 75 mmol/L Glu than in 50 mmol/L Glu (P〈0.05). Spearman's rho analysis revealed that the proliferation of SCs had a negative correlation with the concentration of glucose (r=-0.471, P〈0.01). Excluding the time factor, partial correlation showed similar results (r =-0.679, P〈0.01). After 48 h, the proliferation of SCs increased significantly in JMT 1:2 and Ntp compared with 50 mmol/L Glu (control 0.437±0.019, 50 mmol/ L Glu 0.367±0.035, JMT1:2 0.426±0.024, Ntp 0.422±0.013; P〈0.01), and there were no statistically significant differences among the JMT groups, the Ntp group and the control group (P〉0.05). Conclusions: The proliferation of SCs was inhibited in high glucose medium, and the inhibition was reduced by different concentrations of JMT serum, especially at JMT1:2.展开更多
基金Supported by the Natural Science Foundation of China(No.30572438)
文摘Objective: To investigate the effect of Jinmaitong (筋脉通,JMT) serum on the proliferation of rat Schwann cells (SCs) primarily cultured in high glucose medium. Method: SOs were primarily cultured in Dulbecco's minmum essential medium (DMEM control), 50 mmol/L glucose medium (50 mmol/L Glu), 75 mmol/L glucose medium (75 mmol/L Glu), as well as 50 mmol/L glucose medium, with different concentrations of JMT serum (undiluted, 1:2 diluted and 1:8 diluted) and Neurotropin (Ntp), respectively. The proliferation of SCs under different conditions was detected by MTT. Result: SCs grew exuberantly in DMEM within 24-72 h, but slowed down at 96 h. The proliferation of SCs was inhibited in 50 mmol/L Glu and 75 mmol/L Glu after cultures of 48, 72 and 96 h, which showed that both were significantly different compared to the control group (P〈0.01). The inhibition was more significant in 75 mmol/L Glu than in 50 mmol/L Glu (P〈0.05). Spearman's rho analysis revealed that the proliferation of SCs had a negative correlation with the concentration of glucose (r=-0.471, P〈0.01). Excluding the time factor, partial correlation showed similar results (r =-0.679, P〈0.01). After 48 h, the proliferation of SCs increased significantly in JMT 1:2 and Ntp compared with 50 mmol/L Glu (control 0.437±0.019, 50 mmol/ L Glu 0.367±0.035, JMT1:2 0.426±0.024, Ntp 0.422±0.013; P〈0.01), and there were no statistically significant differences among the JMT groups, the Ntp group and the control group (P〉0.05). Conclusions: The proliferation of SCs was inhibited in high glucose medium, and the inhibition was reduced by different concentrations of JMT serum, especially at JMT1:2.