Reduction of neutrophil activity decreases early microvascular injury after subarachnoid haemorrhage

• Published in: Journal of neuroinflammation 2011-08, Vol.8 (1), p.103-103, Article 103
• Main Authors: Friedrich, Victor, Flores, Rowena, Muller, Artur, Bi, Weina, Peerschke, Ellinor Ib, Sehba, Fatima A
• Format: Article
• Language: English
• Subjects: Animals; Antioxidants - metabolism; Antioxidants - pharmacology; Biomarkers - metabolism; Brain - anatomy & histology; Brain - drug effects; Brain - metabolism; Brain - pathology; Capillary Permeability; Care and treatment; Diagnosis; Endothelium, Vascular - pathology; Endothelium, Vascular - physiopathology; Humans; Male; Microcirculation; Neutrophil Activation; Neutrophil Infiltration; Neutrophils; Neutrophils - cytology; Neutrophils - drug effects; Neutrophils - physiology; Physiological aspects; Proline - analogs & derivatives; Proline - metabolism; Proline - pharmacology; Random Allocation; Rats; Rats, Sprague-Dawley; Risk factors; Subarachnoid hemorrhage; Subarachnoid Hemorrhage - pathology; Subarachnoid Hemorrhage - physiopathology; Thiocarbamates - metabolism; Thiocarbamates - pharmacology; Tubulin Modulators - pharmacology; Vinblastine - pharmacology; Wounds and injuries
• ISSN: 1742-2094; 1742-2094
• DOI: 10.1186/1742-2094-8-103

Subarachnoid haemorrhage (SAH) elicits rapid pathological changes in the structure and function of parenchymal vessels (≤ 100 μm). The role of neutrophils in these changes has not been determined. This study investigates the role of neutrophils in early microvascular changes after SAH METHOD: Rats were either untreated, treated with vinblastine or anti-polymorphonuclear (PMN) serum, which depletes neutrophils, or treated with pyrrolidine dithiocarbamate (PDTC), which limits neutrophil activity. SAH was induced by endovascular perforation. Neutrophil infiltration and the integrity of vascular endothelium and basement membrane were assessed immunohistochemically. Vascular collagenase activity was assessed by in situ zymography. Vinblastine and anti-PMN serum reduced post-SAH accumulation of neutrophils in cerebral vessels and in brain parenchyma. PDTC increased the neutrophil accumulation in cerebral vessels and decreased accumulation in brain parenchyma. In addition, each of the three agents decreased vascular collagenase activity and post-SAH loss of vascular endothelial and basement membrane immunostaining. Our results implicate neutrophils in early microvascular injury after SAH and indicate that treatments which reduce neutrophil activity can be beneficial in limiting microvascular injury and increasing survival after SAH.