RESUMO
The purpose of this study was to define the relationship between cardiac depression and morphological and immunological alterations in cardiac tissue after multiple trauma. However, the mechanistic basis of depressed cardiac function after trauma is still elusive. In a porcine polytrauma model including blunt chest trauma, liver laceration, femur fracture and haemorrhage serial trans-thoracic echocardiography was performed and correlated with cellular cardiac injury as well as with the occurrence of extracellular histones in serum. Postmortem analysis of heart tissue was performed 72 h after trauma. Ejection fraction and shortening fraction of the left ventricle were significantly impaired between 4 and 27 h after trauma. H-FABP, troponin I and extracellular histones were elevated early after trauma and returned to baseline after 24 and 48 h, respectively. Furthermore, increased nitrotyrosine and Il-1ß generation and apoptosis were identified in cardiac tissue after trauma. Main structural findings revealed alteration of connexin 43 (Cx43) and co-translocation of Cx43 and zonula occludens 1 to the cytosol, reduction of α-actinin and increase of desmin in cardiomyocytes after trauma. The cellular and subcellular events demonstrated in this report may for the first time explain molecular mechanisms associated with cardiac dysfunction after multiple trauma.
Assuntos
Traumatismos Cardíacos/patologia , Traumatismos Cardíacos/fisiopatologia , Ventrículos do Coração/patologia , Traumatismo Múltiplo/patologia , Actinina/metabolismo , Animais , Apoptose/fisiologia , Conexina 43/metabolismo , Citosol/metabolismo , Citosol/fisiologia , Desmina/metabolismo , Ecocardiografia/métodos , Proteína 3 Ligante de Ácido Graxo/metabolismo , Traumatismos Cardíacos/metabolismo , Ventrículos do Coração/metabolismo , Histonas/metabolismo , Interleucina-1beta/metabolismo , Masculino , Traumatismo Múltiplo/metabolismo , Miócitos Cardíacos/metabolismo , Miócitos Cardíacos/patologia , Suínos , Troponina I/metabolismo , Proteína da Zônula de Oclusão-1/metabolismoRESUMO
The complement and neutrophil defence systems, as major components of innate immunity, are activated during inflammation and infection. For neutrophil migration to the inflamed region, we hypothesized that the complement activation product C5a induces significant changes in cellular morphology before chemotaxis. Exposure of human neutrophils to C5a dose- and time-dependently resulted in a rapid C5a receptor-1 (C5aR1)-dependent shape change, indicated by enhanced flow cytometric forward-scatter area values. Similar changes were observed after incubation with zymosan-activated serum and in blood neutrophils during murine sepsis, but not in mice lacking the C5aR1. In human neutrophils, Amnis high-resolution digital imaging revealed a C5a-induced decrease in circularity and increase in the cellular length/width ratio. Biomechanically, microfluidic optical stretching experiments indicated significantly increased neutrophil deformability early after C5a stimulation. The C5a-induced shape changes were inhibited by pharmacological blockade of either the Cl-/HCO3--exchanger or the Cl- -channel. Furthermore, actin polymerization assays revealed that C5a exposure resulted in a significant polarization of the neutrophils. The functional polarization process triggered by ATP-P2X/Y-purinoceptor interaction was also involved in the C5a-induced shape changes, because pretreatment with suramin blocked not only the shape changes but also the subsequent C5a-dependent chemotactic activity. In conclusion, the data suggest that the anaphylatoxin C5a regulates basic neutrophil cell processes by increasing the membrane elasticity and cell size as a consequence of actin-cytoskeleton polymerization and reorganization, transforming the neutrophil into a migratory cell able to invade the inflammatory site and subsequently clear pathogens and molecular debris.
Assuntos
Citoesqueleto de Actina/imunologia , Forma Celular/imunologia , Complemento C5a/metabolismo , Inflamação/imunologia , Neutrófilos/imunologia , Actinas/metabolismo , Trifosfato de Adenosina/metabolismo , Células Cultivadas , Quimiotaxia , Antiportadores de Cloreto-Bicarbonato/metabolismo , Complemento C5a/imunologia , Humanos , Ativação de Neutrófilo , Neutrófilos/patologia , Receptor da Anafilatoxina C5a/metabolismo , Receptores Purinérgicos P2X/metabolismo , Transdução de SinaisRESUMO
Chest trauma has a significant relevance on outcome after severe trauma. Clinically, impaired lung function typically occurs within 72 hours after trauma. However, the underlying pathophysiological mechanisms are still not fully elucidated. Therefore, we aimed to establish an experimental long-term model to investigate physiological, morphologic and inflammatory changes, after severe trauma. Male pigs (sus scrofa) sustained severe trauma (including unilateral chest trauma, femur fracture, liver laceration and hemorrhagic shock). Additionally, non-injured animals served as sham controls. Chest trauma resulted in severe lung damage on both CT and histological analyses. Furthermore, severe inflammation with a systemic increase of IL-6 (p = 0.0305) and a local increase of IL-8 in BAL (p = 0.0009) was observed. The pO2/FiO2 ratio in trauma animals decreased over the observation period (p < 0.0001) but not in the sham group (p = 0.2967). Electrical Impedance Tomography (EIT) revealed differences between the traumatized and healthy lung (p < 0.0001). In conclusion, a clinically relevant, long-term model of blunt chest trauma with concomitant injuries has been developed. This reproducible model allows to examine local and systemic consequences of trauma and is valid for investigation of potential diagnostic or therapeutic options. In this context, EIT might represent a radiation-free method for bedside diagnostics.
Assuntos
Traumatismos Torácicos/diagnóstico por imagem , Ferimentos não Penetrantes/diagnóstico por imagem , Animais , Líquido da Lavagem Broncoalveolar , Modelos Animais de Doenças , Impedância Elétrica , Hemodinâmica , Inflamação/patologia , Interleucina-6/metabolismo , Interleucina-8/metabolismo , Pulmão/fisiopatologia , Lesão Pulmonar/fisiopatologia , Masculino , Traumatismo Múltiplo/fisiopatologia , Choque Hemorrágico/patologia , Suínos , Traumatismos Torácicos/fisiopatologia , Tomografia , Tomografia Computadorizada por Raios X , Ferimentos não Penetrantes/fisiopatologiaRESUMO
BACKGROUND: The objective structured clinical exam (OSCE) has become an established form of examination. However, for general and orthopedic surgery it has barely been evaluated. Therefore, the present study was performed to analyze the OSCE in surgery by the students of the University of Ulm. MATERIAL AND METHODS: In total 304 medical students undertaking the OSCE were included in the study. The students were asked to fill out a standardized questionnaire which contained different evaluation parameters, such as test adequacy, comprehensibility, balance, difficulty, atmosphere and clinical relevance as well as self-assessment and overall rating. RESULTS: In the overall rating the OSCE was rated as having a clinical relevance. The preferred preparation strategies were the clinical traineeship and standard medical textbooks. Altogether, the OSCE was chosen as the preferred future examination method, followed by multiple choice testing and clinical practical examination. CONCLUSION: The evaluation of the OSCE by the medical students at the University of Ulm showed a high acceptance rate as well as a high clinical relevance.