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Objective:To study the inhibitory effects of andrographolide (Andro) on the proliferation,migration and clone formation ability of renal cell carcinoma (RCC) cells and the induction on the apoptosis,and to clarify their related mechanisms.Methods:The RCC cells were treated with different concentrations (5,10,20,40 and 80 μmol · L-1) of Andro as experimental groups,and 0μmol · L 1 Andro group was used as blank control group,MTS assay was used to detect the proliferation rates of RCC cells in various groups.The RCC cells were treated with different concentrations (0.50,1.25 and 2.50 μmol · L-1) of Andro as experimental groups,and 0 μmol · L 1Andro group was used as blank control group.Clonogenic assays was used to detect the colony formation ability of RCC cells in various groups.The RCC cells were treated with different concentrations (10,20and 40 μmol · L-1) of Andro as experimental groups,and 0 μmol · L-1 Andro group was used as blank control group.Wound healing assay was used to detect the migration ability of RCC cells in various groups.Flow cytometry was used to detect the apoptotic rates of RCC cells in various groups.Western blotting was performed to detect the expression levels of apoptosis related proteins in RCC cells in various groups.Results:Compared with blank control group,the proliferation rates of RCC cells in 10,20,40 and 80 μmol · L-1 Andro groups were markedly decreased (P＜0.05 or P＜0.01).Compared with blank control group,the colony formation rates of RCC cells in 0.50 and 1.25μmol · L-1 Andro groups were markedly decreased (P＜0.05 or P＜0.01).Compared with blank control group,the scratch healing rates of RCC cells in 10,20 and 40 μmol · L-1 Andro groups were markedly decreased (P＜0.01),and the apoptotic rates of RCC cells in 20 and 40 μmol · L-1 Andro groups were markedly increased (P＜0.01).Compared with blank control group,the expression level of γ-H2AX protein in 40μmol · L-1 Andro group was markedly increased (P＜0.01),the expression level of Caspase-8 protein was decreased (P＜0.05),and the expression level of cleaved Caspase-8 protein was markedly increased (P＜0.01).Conclusion:Andro can effectively suppress the proliferation,migration and colony formation ability of RCC cells and induce the apoptosis of RCC cells.The mechanism of apoptosis might be related to inducing the DNA damage and the apoptotic pathways induced by JNK / H2AX and Caspase-8.
RESUMO
Objective To study the renal protective effects of ulinastatin in rats with multiple organ dysfunction syndrome(MODS). Methods Thirty-six Wistar rats were divided into 3 groups:control group ,model group and treatment group. The MODS models were produced by injecting lipopolysaccharide(LPS) through the sublingual vein into the rats. Ulinastatin was injected into the sublingual vein of the rats in treatment group, LPS was injected into rats in the same way after 10 minutes. On the second hour and the sixth hour after treatment, serum and renal tissue samples were collected from the rats to determine the level of TNF-?,IL-6, IL-1?, iNOS by RIA.The pathologic changes of renal tissue was examined. Results The levels of TNF-?,IL-6, IL-1?, iNOS of serum and renal tissue in treatment group were obviously lower than in model group (P
RESUMO
Aim To study protective effects of ulinastatin on injury of organs in rats induced by endotoxin.Methods 36 Wistar rats were divided into 3 groups: control group,model group and treatment group.The model of injury of organs were induced by injecting lipopolysaccharide(LPS) through the sublingual vein into rats.Ulinastatin was injected into the sublingual vein of rats in treatment group,LPS was injected into rats in the same way after 10 minutes.At the second hour or the sixth hour after treatment,serum and lung,liver and renal samples were cellected from rats to determine levels of TNF-?,IL-6,IL-1?and iNOS by RIA.Pathologic changes of lung,liver and renal organ were examined.Results Levels of TNF-?,IL-6,IL-1?,iNOS of serum and renal organs in treatment group were obviously reduced than those in model group(P
