Activation and Clinical Significance of p38 MAPK Signaling Pathway in Patients With Severe Trauma

被引:33
作者
Wang, Yi Xin [2 ]
Xu, Xin Yun [1 ]
Su, Wen Li [2 ]
Wang, Qiang [1 ]
Zhu, Wen Xian [2 ]
Chen, Fen [2 ]
Jin, Ge [2 ]
Liu, Yu Jian [3 ]
Li, Yi Dong [3 ]
Sun, Yan Ping [1 ]
Gao, Wen Chao [1 ]
Ruan, Can Ping [1 ]
机构
[1] Second Mil Med Univ, Chang Zheng Hosp, Dept Gen Surg, Shanghai 200003, Peoples R China
[2] Shanghai Univ Tradit Chinese Med, Shanghai Putuo Hosp, First Aid Ctr, Shanghai, Peoples R China
[3] Second Mil Med Univ, Inst Pathophysiol, Shanghai 200003, Peoples R China
关键词
trauma; signal pathway; p38; MAPK; IL-6; TNF alpha; PROTEIN-KINASE; IN-VITRO; INJURY; REPERFUSION; INHIBITION; INDUCTION; APOPTOSIS; MOUSE; VIVO; PIG;
D O I
10.1016/j.jss.2008.10.030
中图分类号
R61 [外科手术学];
学科分类号
100210 [外科学];
摘要
Background. Organ dysfunction or multiple organ dysfunction syndrome caused by developing immunological dysfunction and subsequent sepsis or the systemic inflammatory response syndrome after trauma is the leading cause of death in trauma patient. It is believed that mitogen-activated protein kinase) (p38MAPK) is one of the most important kinases in inflammatory signaling. In this study, the change of p38 MAPK signaling pathway in trauma patient with different severity and its clinical significance in trauma inflammation were investigated. Methods. One hundred fifty major trauma patients were included in the study and divided into three groups according to injury severity score (ISS). All data required to calculate ISS and determine organ function were registered on admission and during the ICU-stay. Peripheral blood samples were collected from trauma patients 6 h, 1 d, 3 d, 5 d, and 7 d after injury. RQ-PCR and Western blot was used to examine the changes in gene expression, protein expression, and activation level of leukocyte p38 MAPK. Plasma IL-6 and TNF alpha were assayed by ELISA. Results. Organ dysfunction in 33 trauma patients developed and eight deaths occurred after 24 h in ICU. The causes of death included severe ARDS, MODS, and irreversible brain injury. Incidence of organ dysfunction was related to the increase of injury severity (P < 0.01). Compared with healthy control, the gene expression of p38 MAPK in trauma patients increased significantly 6 h after injury (P < 0.05), and reached a maximum in 1 d (P < 0.01). The expression maintained a high level for 7 d (P < 0.05). One day after injury, significant elevation was observed in protein expression and activation level of p38 MAPK (P < 0.05), as well as the plasma TNF alpha and IL-6 level (P < 0.01). Further investigation found that the gene expression, protein expression, and activation levels of p38 MAPK increased with higher ISS (P < 0.05), and the elevation of plasma TNF alpha and IL-6 level was associated with the increase of activated p38 MAPK and ISS (P < 0.05). Conclusion. p38 MAPK signal pathway was activated in trauma patients. The severity of trauma had highly positive correlation with the expression and activation of p38 MAPK, as well as the elevation of plasma TNF alpha and IL-6 expression. These findings indicate that p38 MAPK signaling pathway plays an important role in the pathological mechanism of trauma. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:119 / 125
页数:7
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