Project Details
Description
Lung contusion is the commonest injury following blunt trauma to the chest that requires admission to the
hospital. The pathogenesis and cellular mechansims of lung contusion are not well understood in part due to
a lack of a reliable small animal model for isolated lung contusion . We have recently developed a
reproducible rat model for isolated bilateral lung contusion from blunt trauma in a closed chest to facilitate
mechanistic studies.This model is used here to examine the mechanistic inflammatory pathophysiology of
lung contusion, as well as its interaction with gastric aspiration, a frequent occurence in trauma patients.
Based on our preliminary studies, we hypothesize that acute inflammatory injury in isolated lung contusion
resolves by 7 days. In the presence of an additional "second hit"such as gastric aspiration, this injury
progresses to severe respiratory dysfunction (ALI/ARDS). The Specific Aim #1 examines in detail the cellular
mechanisms(role of neutrophils and alveolar macrophages) and specific chemokines(CINC-1, MIP-2 and
MCP-1) in the rat model. The Specific Aim # 2 studies the interaction of lung contusion with combination of
acid and particulate aspiration injury to the lung in rats. This aim examines the role of neutrophils, alveolar
macrophages and chemokines (CINC-1, MIP-2 and MCP-1) in the interaction of these two insults. In
addition, aim 2 uses genomic profiling (expression microarray complemented by quantitative RT-PCR) on
whole lung homogenates to identify other pathways that may be important in the pathogenesis of lung
contusion with/without gastric aspiration. Understanding lung contusion and its interaction with gastric
aspiration, two common insults suffered by trauma patients, will greatly aid the development of new
diagnostic and therapeutic modalities.
| Status | Finished |
|---|---|
| Effective start/end date | 02/1/06 → 07/4/08 |
Funding
- National Institute of General Medical Sciences: $417,246.00
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