Effects of Shen-Fu Injection on the Expression of T-Cell-Specific Transcription Factors T-bet/Gata-3 in Porcine Postresuscitation Lung Injury

被引:17
作者
Gu, Wei [1 ]
Li, ChunSheng [1 ]
Yin, WenPeng [1 ]
Hou, XiaoMin [1 ]
Zhang, Da [1 ]
机构
[1] Capital Med Univ, Beijing Chaoyang Hosp, Dept Emergency Med, Beijing 100020, Peoples R China
关键词
CARDIAC-ARREST; MYOCARDIAL DYSFUNCTION; FACTOR GATA-3; CYTOKINE; MODEL; TH1; ISCHEMIA;
D O I
10.1155/2013/464650
中图分类号
R [医药、卫生];
学科分类号
10 ;
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)-gamma 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-gamma (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.
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页数:8
相关论文
共 29 条
[11]   Reduction of Plasma Gelsolin Levels Correlates with Development of Multiple Organ Dysfunction Syndrome and Fatal Outcome in Burn Patients [J].
Huang, Li-feng ;
Yao, Yong-ming ;
Li, Jin-feng ;
Dong, Ning ;
Liu, Chen ;
Yu, Yan ;
He, Li-xin ;
Sheng, Zhi-yong .
PLOS ONE, 2011, 6 (11)
[12]   Ischemia-reperfusion and immediate T cell responses [J].
Huang, Yanfei ;
Rabb, Hamid ;
Womer, Karl L. .
CELLULAR IMMUNOLOGY, 2007, 248 (01) :4-11
[13]   The endothelial response to oxygen deprivation: biology and clinical implications [J].
Karimova, A ;
Pinsky, DJ .
INTENSIVE CARE MEDICINE, 2001, 27 (01) :19-31
[14]  
[李玮 LI Wei], 2006, [基础医学与临床, Basic Medical Sciences and Clinics], V26, P362
[15]   TH1 AND TH2 CD4(+) T-CELLS IN THE PATHOGENESIS OF ORGAN-SPECIFIC AUTOIMMUNE-DISEASES [J].
LIBLAU, RS ;
SINGER, SM ;
MCDEVITT, HO .
IMMUNOLOGY TODAY, 1995, 16 (01) :34-38
[16]   THE CLINICAL IMPLICATIONS OF CONTINUOUS CENTRAL VENOUS OXYGEN-SATURATION DURING HUMAN CPR [J].
RIVERS, EP ;
MARTIN, GB ;
SMITHLINE, H ;
RADY, MY ;
SCHULTZ, CH ;
GOETTING, MG ;
APPLETON, TJ ;
NOWAK, RM .
ANNALS OF EMERGENCY MEDICINE, 1992, 21 (09) :1094-1101
[17]   XANTHINE OXIDASE-DERIVED OXYGEN RADICALS INCREASE LUNG CYTOKINE EXPRESSION IN MICE SUBJECTED TO HEMORRHAGIC-SHOCK [J].
SCHWARTZ, MC ;
REPINE, JE ;
ABRAHAM, E .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1995, 12 (04) :434-440
[18]   TISSUE OXYGEN DEBT AS A DETERMINANT OF LETHAL AND NONLETHAL POSTOPERATIVE ORGAN FAILURE [J].
SHOEMAKER, WC ;
APPEL, PL ;
KRAM, HB .
CRITICAL CARE MEDICINE, 1988, 16 (11) :1117-1120
[19]   A novel transcription factor, T-bet, directs Th1 lineage commitment [J].
Szabo, SJ ;
Kim, ST ;
Costa, GL ;
Zhang, XK ;
Fathman, CG ;
Glimcher, LH .
CELL, 2000, 100 (06) :655-669
[20]   Serum concentrations of interleukin-4 and interferon-gamma in relation to severe left ventricular dysfunction in patients with acute myocardial infarction undergoing percutaneous coronary intervention [J].
Szkodzinski, Janusz ;
Hudzik, Bartosz ;
Osuch, Marcin ;
Romanowski, Wojciech ;
Szygula-Jurkiewicz, Bozena ;
Polonski, Lech ;
Zubelewicz-Szkodzinska, Barbara .
HEART AND VESSELS, 2011, 26 (04) :399-407