首页> 美国卫生研究院文献>Evidence-based Complementary and Alternative Medicine : eCAM >Effects of Shen-Fu Injection on the Expression of T-Cell-Specific Transcription Factors T-bet/Gata-3 in Porcine Postresuscitation Lung Injury
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Effects of Shen-Fu Injection on the Expression of T-Cell-Specific Transcription Factors T-bet/Gata-3 in Porcine Postresuscitation Lung Injury

机译:参附注射液对猪肺复苏后T细胞特异性转录因子T-bet / Gata-3表达的影响

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摘要

Shen-Fu injection (SFI) derived from the ancient traditional Chinese medicine. In this study, the effects of SFI on the expression of T-bet/GATA-3 and its potential mechanisms causing the shift of T cells from Th2 to Th1 on postresuscitation lung injury were examined in a porcine model of cardiac arrest. 30 pigs were randomly divided into SHAM (n = 6) and three return of spontaneous circulation (ROSC) groups (n = 8 per group); 24 pigs were subjected to 8 min of electrically induced cardiac arrest and 2 min of basic life support, which received central venous injection of Shen-Fu (SFI), epinephrine (EP) or saline (SA). After successful ROSC, 18 surviving pigs were sacrificed at 24 h after ROSC (n = 6 per group). The levels of serum and lung tissue interleukin (IL)-4 and interferon (IFN)-γ were measured by ELISA, and the protein and mRNA levels of GATA-3 and T-bet in the lung tissue were determined by western blotting and quantitative real-time polymerase chain reaction, respectively. Compared with the EP and SA groups, SFI treatment reduced the levels of IL-4 (P < 0.05), increased levels of IFN-γ (P < 0.05), and induced T-bet mRNA upregulation and GATA-3 mRNA downregulation (P < 0.05). SFI attenuated lung injury and regulated lung immune disorders. Therefore, SFI could protect postresuscitation lung injury by modulating a Th1/Th2 imbalance.
机译:申福注射液(SFI)源于古代传统中药。在这项研究中,在心脏骤停的猪模型中检查了SFI对T-bet / GATA-3表达的影响及其引起T细胞从Th2转移到Th1对复苏后肺损伤的潜在机制。 30只猪随机分为SHAM组(n = 6)和三组自发循环(ROSC)组(每组n = 8); 24只猪接受了8分钟的电诱导心脏骤停和2分钟的基本生命支持,接受了中心静脉注射申福(SFI),肾上腺素(EP)或生理盐水(SA)。成功进行ROSC后,在ROSC后24h将18只存活的猪处死(每组n = 6)。 ELISA法测定血清和肺组织白细胞介素(IL)-4和干扰素(IFN)-γ的水平,蛋白质印迹和定量测定肺组织中GATA-3和T-bet的蛋白质和mRNA水平实时聚合酶链反应。与EP和SA组相比,SFI治疗可降低IL-4水平(P <0.05),增加IFN-γ水平(P <0.05),并诱导T-bet mRNA上调和GATA-3 mRNA下调(P <0.05)。 SFI减轻了肺损伤并调节了肺免疫功能。因此,SFI可以通过调节Th1 / Th2不平衡来保护复苏后肺部损伤。

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