机构地区:[1]江西中医药大学,南昌330004
出 处:《中药药理与临床》2015年第1期5-9,共5页Pharmacology and Clinics of Chinese Materia Medica
基 金:国家自然科学基金项目;基金号:81160423
摘 要:目的:探讨温胆汤含药血清在谷氨酸(Glu)环境条件下对星形胶质细胞P38MAPK和PKC表达的影响。方法:将40只SD大鼠随机分为5组:正常组、氯氮平20mg/kg组、温胆汤40g/kg组、温胆汤30g/kg组、温胆汤20g/kg组,每组8只。正常组用等量生理盐水ig,氯氮平组ig 20 mg/kg,ig温胆汤生药40、30、20 g/kg,1次/d,8天后处死取血,制备含药血清。胶质原纤维酸性蛋白免疫染色法鉴定培养的星形胶质细胞纯度。星形胶质细胞在谷氨酸(0、5、10μmol/ml)条件下经含药血清处理,即谷氨酸对照组、正常血清组、氯氮平20mg/kg含药血清组、温胆汤40g/kg、30g/kg、20g/kg血清组,处理24h、36h和48h后,采用四甲基偶氮唑盐(MTT)法检测细胞存活率;ELISA法检测P38MAPK磷酸化和非磷酸化及PKC蛋白表达的影响。结果:培养的星形胶质细胞纯度在95%以上。谷氨酸(0μmol/ml)条件下,温胆汤40g/kg、30g/kg含药血清组在3个时间段不同程度增加星形胶质细胞存活率;谷氨酸(5、10μmol/ml)条件下,温胆汤含药血清处理24h、36h后,温胆汤40g/kg、30g/kg、20g/kg含药血清组不同程度增加的细胞存活率;48h后,温胆汤40g/kg含药血清组增加的细胞存活率。谷氨酸(0、5、10μmol/ml)条件下,氯氮平20mg/kg含药血清组、温胆汤30g/kg含药血清组能显著上调星形胶质细胞P38MAPK蛋白磷酸化和非磷酸化的表达。谷氨酸(0、5μmol/ml)条件下,温胆汤40g/kg、30g/kg、20g/kg含药血清组显著降低星形胶质细胞PKC表达;谷氨酸(10μmol/ml)条件下,温胆汤40g/kg含药血清组显著降低星形胶质细胞PKC表达。结论:一定谷氨酸环境下温胆汤能不同程度的增加星形胶质细胞的存活率,能上调P38MAPK磷酸化和非磷酸化的表达及降低PKC蛋白的表达,从而间接反映出温胆汤能调节星形胶质细胞GJIC(细胞缝隙连接)的功能。Objective: To research the effect of serum containing Wendan decoction on P38 MAPK and PKC of astrocytes in glutamate( Glu) environmental conditions. Methods: 40 SD rats were randomly divided into five groups: normal group,clozapine 20 mg / kg group,Wendan decoction 40 g / kg group,Wendan decoction 30 g / kg group and Wendan decoction 10 g / kg group,egivenht rats in each group. normal group groups were given normal saline every day,clozapine 20 mg / kg group given orgiveninal drug clozapine 20 mg / kg,the Wendan decoction 40 g / kg,Wendan decoction 30 g / kg and Wendan decoction 10 g / kg groups were respectively given Wendan decoction( 40,20,10 g / kg),1 times / d,After 8 days,the rats were sacrificed to preparation containing serum. Glial fibrillary acidic protein immunostaining identified cultured astrocytes purity.Astrocytes in glutamate( 0,5,10μmol / ml) conditions treated by the medicated serum drugs,namely glutamate in the control group,normal serum containing group,clozapine 20 mg / kg serum containing group,Wendan decoction 40 g / kg,30 g / kg,20 g / kg serum containing group,after 24 h,36h and 48 h treatment,Using tetrazolium salt( MTT) assay to detect cell viability; The contents of serum P38 MAPK phosphorylated and non-phosphorylated,PKC were detected by double antibody clip ELASA method. Results: cultured astrocytes purity of more than 95%. Under glutamate( 0μmol / ml) conditions,Wendan decoction 40 g / kg group containing serum significantly increased the survival rate of astrocytes in three time periods( P 0. 05); Under glutamate( 5,10μmol / ml) conditions,Wendan decoction containing serum treatment 24 h,and 36 h,Wendan decoction 30 g / kg,20 g / kg medicated serum cell viability was significantly increased; 48 h later,Wendan decoction 40 g / kg medicated serum cells was significantly increased. After the first treatment with serum containing 24 h,Under glutamate( 0,5,10μmol / ml) conditions,clozapine 20 mg / kg medicated serum group,Wendan decoction 30
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