山东医药
山東醫藥
산동의약
SHANDONG MEDICAL JOURNAL
2014年
10期
10-13
,共4页
孙燕妮%承解静%杨晓燕%杨洁%王丽敏%刘军
孫燕妮%承解靜%楊曉燕%楊潔%王麗敏%劉軍
손연니%승해정%양효연%양길%왕려민%류군
大黄牡丹汤,含药血清%肺巨噬细胞%Toll样受体4%髓样分化因子88
大黃牡丹湯,含藥血清%肺巨噬細胞%Toll樣受體4%髓樣分化因子88
대황모단탕,함약혈청%폐거서세포%Toll양수체4%수양분화인자88
Dahuang Mudan decoction,drug-contained serum%pulmonary macrophage%Toll-like receptor 4%myeloid differentiation factor 88
目的:探讨大黄牡丹汤含药血清(以下简称含药血清)对脓毒症的治疗机制。方法体外培养小鼠肺巨噬细胞株RAW264.7并随机分为空白组,模型组,含药血清高、中、低浓度组,每组3个复孔。除空白组外,其余四组均予细菌脂多糖( LPS)5μg/mL刺激24 h,含药血清高、中、低浓度组分别同时给予高、中、低浓度的含药血清进行干预。干预后于37℃、5%CO2培养箱中培养24 h。分别采用半定量RT-PCR和Western blot法测定Toll样受体4(TLR4)及髓样分化因子88(MyD88)mRNA和蛋白表达。结果模型组TLR4和MyD88 mRNA和蛋白表达均显著高于空白组(P<0.01);含药血清中浓度组与高浓度组TLR4和MyD88表达无显著差异,但均显著低于模型组(P<0.01)。结论含药血清治疗脓毒症的机制可能为抑制TLR4和下游MyD88表达。
目的:探討大黃牡丹湯含藥血清(以下簡稱含藥血清)對膿毒癥的治療機製。方法體外培養小鼠肺巨噬細胞株RAW264.7併隨機分為空白組,模型組,含藥血清高、中、低濃度組,每組3箇複孔。除空白組外,其餘四組均予細菌脂多糖( LPS)5μg/mL刺激24 h,含藥血清高、中、低濃度組分彆同時給予高、中、低濃度的含藥血清進行榦預。榦預後于37℃、5%CO2培養箱中培養24 h。分彆採用半定量RT-PCR和Western blot法測定Toll樣受體4(TLR4)及髓樣分化因子88(MyD88)mRNA和蛋白錶達。結果模型組TLR4和MyD88 mRNA和蛋白錶達均顯著高于空白組(P<0.01);含藥血清中濃度組與高濃度組TLR4和MyD88錶達無顯著差異,但均顯著低于模型組(P<0.01)。結論含藥血清治療膿毒癥的機製可能為抑製TLR4和下遊MyD88錶達。
목적:탐토대황모단탕함약혈청(이하간칭함약혈청)대농독증적치료궤제。방법체외배양소서폐거서세포주RAW264.7병수궤분위공백조,모형조,함약혈청고、중、저농도조,매조3개복공。제공백조외,기여사조균여세균지다당( LPS)5μg/mL자격24 h,함약혈청고、중、저농도조분별동시급여고、중、저농도적함약혈청진행간예。간예후우37℃、5%CO2배양상중배양24 h。분별채용반정량RT-PCR화Western blot법측정Toll양수체4(TLR4)급수양분화인자88(MyD88)mRNA화단백표체。결과모형조TLR4화MyD88 mRNA화단백표체균현저고우공백조(P<0.01);함약혈청중농도조여고농도조TLR4화MyD88표체무현저차이,단균현저저우모형조(P<0.01)。결론함약혈청치료농독증적궤제가능위억제TLR4화하유MyD88표체。
Objective To investigate the therapeutic mechanism of Dahuang Mudan decoction-contained serum ( here-inafter referred to as the drug contained serum ) in the treatment of sepsis .Methods Mouse pulmonary macrophage cell line RAW264 .7 was cultured in vitro , and then the cells were randomly divided into the blank group , model group , high-, moderate-and low-concentration drug-contained serum groups , each group of 3 holes.Except the blank group , other four groups were stimulated with bacterial lipopolysaccharide ( LPS) 5 μg/mL, then were treated with different concentrations of drug-contained serum for 24 h.After the intervention , the cells were cultured in 5%CO2 at 37℃for 24 h.Then the mR-NA expression of Toll-like receptor 4( TLR4) and myeloid differentiation factor 88( MyD88) was measured by semi-quanti-tative reverse transcription-polymerase chain reaction ( RT-PCR ) , and their protein expression was analyzed by Western blotting .Results The protein and mRNA expression of TLR 4 and MyD88 in the model group was significantly higher than that of the blank group (P<0.01), but the protein and mRNA expression of TLR4 and MyD88 in the high-and moderate-concentration drug-contained serum groups was significantly lower than that of the model group (P<0.01), and no signifi-cant differences was found between the high-and moderate-concentration drug-contained serum groups .Conclusion The therapeutic mechanism of Dahuang Mudan decoction-contained serum in the treatment of sepsis may be related to the inhibi-tion of TLR4 and down-regulation of MyD88 expression.