Neutrophil mediated muscle injury of the diaphragm

Excessive loading, as seen in chronic respiratory diseases and experimentally produced by tracheal banding (TB) may result in injury to the myofibres of the diaphragm and hypercapnic ventilatory failure. Neutrophils (PMNs) are primary inflammatory cells that migrate to an area of injury in order...

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Main Author: Samrai, Baljit
Language:English
Published: 2009
Online Access:http://hdl.handle.net/2429/9747
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spelling ndltd-LACETR-oai-collectionscanada.gc.ca-BVAU.2429-97472014-03-14T15:43:39Z Neutrophil mediated muscle injury of the diaphragm Samrai, Baljit Excessive loading, as seen in chronic respiratory diseases and experimentally produced by tracheal banding (TB) may result in injury to the myofibres of the diaphragm and hypercapnic ventilatory failure. Neutrophils (PMNs) are primary inflammatory cells that migrate to an area of injury in order to phagocytose cellular debris and promote the inflammatory response. During this process, neutrophils may also amplify muscle injury. We hypothesized that neutrophil depletion would reduce diaphragm muscle injury in an animal model where diaphragm injury was induced by tracheal banding. Adult male Sprague-Dawley rats were randomly assigned to one of four groups: 1. control (C), 2. tracheal banded (TB), 3. control plus neutrophil depleted (C+ND), 4. tracheal banded plus neutrophil depleted (TB+ND). In the C+ND and TB+ND groups, neutrophils were depleted by administering anti-rat polymorphonuclear leukocyte antisera, beginning one day pre-surgery. After anaesthesia, the carotid artery was chronically cannulated, esophageal pressures (Pes) were measured and a cuff was tightened around the isolated trachea, until the Pes during tidal breathing (Pes[sub TV]) was 20% of the maximal Pes (Pes[sub Max]) during tracheal occlusion in the TB and TB+ND groups. Arterial blood gas (ABG) samples were taken daily from the awake animal. Three days later, following anaesthesia, in vivo measures of Pes were repeated and then the diaphragm and trachea were excised for histological and immunohistochemical analysis. The following parameters were investigated: (1) the presence of neutrophils in the diaphragm measured by neutrophil specific myeloperoxidase (MPO) activity and point counting H&E diaphragm cross-sections; (2) muscle injury as quantified by point counting H&E stained diaphragm cross-sections; (3) the presence of EDI positive macrophages in the diaphragm by using immunohistochemistry; and (4) ABGs measure daily post-surgery. The TB groups were hypercapnic (PaC0₂ > 45mmHg; p<0.001) and had a decreased tracheal cross sectional area (p<0.001). ND groups had PMN counts <0.5 million/mL. MPO activity tended to increase indicating an increased presence of neutrophils in the diaphragm of the TB group, and C values were similar to those in the TB+ND group. The TB group had the most abnormal and inflamed muscle (p<0.05), whereas, the TB+ND group was similar to C values. EDI positive macrophages per cross-sectional area was greater in the TB group compared to the C group, indicating that the macrophage population increased in response to muscle injury. We conclude that macrophages increase and neutrophils tend to increase in the injured diaphragm induced by tracheal banding. Neutrophil depletion decreased diaphragm injury induced by resistive loading. 2009-06-26T23:13:24Z 2009-06-26T23:13:24Z 1999 2009-06-26T23:13:24Z 1999-11 Electronic Thesis or Dissertation http://hdl.handle.net/2429/9747 eng UBC Retrospective Theses Digitization Project [http://www.library.ubc.ca/archives/retro_theses/]
collection NDLTD
language English
sources NDLTD
description Excessive loading, as seen in chronic respiratory diseases and experimentally produced by tracheal banding (TB) may result in injury to the myofibres of the diaphragm and hypercapnic ventilatory failure. Neutrophils (PMNs) are primary inflammatory cells that migrate to an area of injury in order to phagocytose cellular debris and promote the inflammatory response. During this process, neutrophils may also amplify muscle injury. We hypothesized that neutrophil depletion would reduce diaphragm muscle injury in an animal model where diaphragm injury was induced by tracheal banding. Adult male Sprague-Dawley rats were randomly assigned to one of four groups: 1. control (C), 2. tracheal banded (TB), 3. control plus neutrophil depleted (C+ND), 4. tracheal banded plus neutrophil depleted (TB+ND). In the C+ND and TB+ND groups, neutrophils were depleted by administering anti-rat polymorphonuclear leukocyte antisera, beginning one day pre-surgery. After anaesthesia, the carotid artery was chronically cannulated, esophageal pressures (Pes) were measured and a cuff was tightened around the isolated trachea, until the Pes during tidal breathing (Pes[sub TV]) was 20% of the maximal Pes (Pes[sub Max]) during tracheal occlusion in the TB and TB+ND groups. Arterial blood gas (ABG) samples were taken daily from the awake animal. Three days later, following anaesthesia, in vivo measures of Pes were repeated and then the diaphragm and trachea were excised for histological and immunohistochemical analysis. The following parameters were investigated: (1) the presence of neutrophils in the diaphragm measured by neutrophil specific myeloperoxidase (MPO) activity and point counting H&E diaphragm cross-sections; (2) muscle injury as quantified by point counting H&E stained diaphragm cross-sections; (3) the presence of EDI positive macrophages in the diaphragm by using immunohistochemistry; and (4) ABGs measure daily post-surgery. The TB groups were hypercapnic (PaC0₂ > 45mmHg; p<0.001) and had a decreased tracheal cross sectional area (p<0.001). ND groups had PMN counts <0.5 million/mL. MPO activity tended to increase indicating an increased presence of neutrophils in the diaphragm of the TB group, and C values were similar to those in the TB+ND group. The TB group had the most abnormal and inflamed muscle (p<0.05), whereas, the TB+ND group was similar to C values. EDI positive macrophages per cross-sectional area was greater in the TB group compared to the C group, indicating that the macrophage population increased in response to muscle injury. We conclude that macrophages increase and neutrophils tend to increase in the injured diaphragm induced by tracheal banding. Neutrophil depletion decreased diaphragm injury induced by resistive loading.
author Samrai, Baljit
spellingShingle Samrai, Baljit
Neutrophil mediated muscle injury of the diaphragm
author_facet Samrai, Baljit
author_sort Samrai, Baljit
title Neutrophil mediated muscle injury of the diaphragm
title_short Neutrophil mediated muscle injury of the diaphragm
title_full Neutrophil mediated muscle injury of the diaphragm
title_fullStr Neutrophil mediated muscle injury of the diaphragm
title_full_unstemmed Neutrophil mediated muscle injury of the diaphragm
title_sort neutrophil mediated muscle injury of the diaphragm
publishDate 2009
url http://hdl.handle.net/2429/9747
work_keys_str_mv AT samraibaljit neutrophilmediatedmuscleinjuryofthediaphragm
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