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Activation and clinical significance of p38 MAPK signaling pathway in patients with severe trauma.
J Surg Res 2010; 161(1):119-25JS

Abstract

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 TNFalpha 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 TNFalpha 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 TNFalpha 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 TNFalpha and IL-6 expression. These findings indicate that p38 MAPK signaling pathway plays an important role in the pathological mechanism of trauma.

Authors+Show Affiliations

First Aid Center, Shanghai Putuo Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai, China. Rcipng@hotmail.comNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article
Research Support, Non-U.S. Gov't

Language

eng

PubMed ID

19482318

Citation

Wang, Yi Xin, et al. "Activation and Clinical Significance of P38 MAPK Signaling Pathway in Patients With Severe Trauma." The Journal of Surgical Research, vol. 161, no. 1, 2010, pp. 119-25.
Wang YX, Xu XY, Su WL, et al. Activation and clinical significance of p38 MAPK signaling pathway in patients with severe trauma. J Surg Res. 2010;161(1):119-25.
Wang, Y. X., Xu, X. Y., Su, W. L., Wang, Q., Zhu, W. X., Chen, F., ... Ruan, C. P. (2010). Activation and clinical significance of p38 MAPK signaling pathway in patients with severe trauma. The Journal of Surgical Research, 161(1), pp. 119-25. doi:10.1016/j.jss.2008.10.030.
Wang YX, et al. Activation and Clinical Significance of P38 MAPK Signaling Pathway in Patients With Severe Trauma. J Surg Res. 2010 Jun 1;161(1):119-25. PubMed PMID: 19482318.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Activation and clinical significance of p38 MAPK signaling pathway in patients with severe trauma. AU - Wang,Yi Xin, AU - Xu,Xin Yun, AU - Su,Wen Li, AU - Wang,Qiang, AU - Zhu,Wen Xian, AU - Chen,Fen, AU - Jin,Ge, AU - Liu,Yu Jian, AU - Li,Yi Dong, AU - Sun,Yan Ping, AU - Gao,Wen Chao, AU - Ruan,Can Ping, Y1 - 2008/12/03/ PY - 2008/09/29/received PY - 2008/10/29/revised PY - 2008/10/30/accepted PY - 2009/6/2/entrez PY - 2009/6/2/pubmed PY - 2010/5/21/medline SP - 119 EP - 25 JF - The Journal of surgical research JO - J. Surg. Res. VL - 161 IS - 1 N2 - 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 TNFalpha 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 TNFalpha 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 TNFalpha 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 TNFalpha and IL-6 expression. These findings indicate that p38 MAPK signaling pathway plays an important role in the pathological mechanism of trauma. SN - 1095-8673 UR - https://www.unboundmedicine.com/medline/citation/19482318/Activation_and_clinical_significance_of_p38_MAPK_signaling_pathway_in_patients_with_severe_trauma_ L2 - https://linkinghub.elsevier.com/retrieve/pii/S0022-4804(08)00684-7 DB - PRIME DP - Unbound Medicine ER -